|
| VAERS ID: |
48199 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1992-11-27 |
| Onset: | 1992-12-04 |
| Days after vaccination: | 7 |
| Submitted: |
1992-12-08 |
| Days after onset: | 4 |
| Entered: |
1992-12-18 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / PFIZER/WYETH |
4928115 / UNK |
- / IM A |
Administered by: Private Purchased by: Private Symptoms: Osteoarthritis,
Paraesthesia,
Pruritus SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Arthritis (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: erythromycin/Naprosyn Allergies: Diagnostic Lab Data: CBC, lytes, ESR-all nl; CDC Split Type:
Write-up: joint swellings-hands, itchy feet w/tingling; |
|
| VAERS ID: |
48755 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1992-10-23 |
| Onset: | 1992-10-24 |
| Days after vaccination: | 1 |
| Submitted: |
1992-12-14 |
| Days after onset: | 51 |
| Entered: |
1993-01-08 |
| Days after submission: | 25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
2F31117 / 1 |
LA / IM |
Administered by: Public Purchased by: Private Symptoms: Injection site hypersensitivity,
Pruritus,
Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: HTN med, Cardigem CD Current Illness: leg wound-resulting from boiling H20 Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt descrives onset of redness @ inject site, LD w/rash occuring & spread to forearms, shoulder, chest, groins; denies fever or rash on face, no resp distress, no neuro deficit; rash described as, prickly, raised, dry, rough & itchy; |
|
| VAERS ID: |
57615 (history) |
| Form: |
Version 1.0 |
| Age: |
28.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1993-10-19 |
| Onset: | 1993-10-20 |
| Days after vaccination: | 1 |
| Submitted: |
1993-11-10 |
| Days after onset: | 21 |
| Entered: |
1993-11-22 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Other Purchased by: Other Symptoms: Nausea,
Palpitations,
Tachycardia,
Vasodilatation SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: BCP''s; Current Illness: NONE Preexisting Conditions: endometrosis Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: nausea, flushed, palpitats/tachycardia; |
|
| VAERS ID: |
58134 (history) |
| Form: |
Version 1.0 |
| Age: |
46.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1993-10-18 |
| Onset: | 1993-11-08 |
| Days after vaccination: | 21 |
| Submitted: |
1993-11-22 |
| Days after onset: | 14 |
| Entered: |
1993-12-13 |
| Days after submission: | 21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / PFIZER/WYETH |
4938089 / 1 |
RA / IM |
Administered by: Public Purchased by: Other Symptoms: CSF test abnormal,
Guillain-Barre syndrome,
Laboratory test abnormal,
Paraesthesia SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: Clinoril Current Illness: UNKNOWN Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: 893333003J
Write-up: 2 wks p/vax pt devel numbness of legs below knees & numbness in fingers; admitted to hosp to rule out GBS; |
|
| VAERS ID: |
69651 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1994-11-14 |
| Onset: | 1994-11-14 |
| Days after vaccination: | 0 |
| Submitted: |
1994-12-02 |
| Days after onset: | 18 |
| Entered: |
1994-12-16 |
| Days after submission: | 14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Private Purchased by: Private Symptoms: Agitation,
Asthenia,
Central nervous system stimulation,
Condition aggravated,
Hypersensitivity,
Hypothermia,
Malaise SMQs:, Angioedema (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (broad), Hostility/aggression (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: in pt,same event occured last yr,pt thought it was flu vax;lasted 1 day;~ ()~~~In patient Other Medications: none; Current Illness: Preexisting Conditions: allergic to mercury, since early 1980''s; Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt recvd vax in pm;noc,began feeling bad & by next am was sick,t 97.7;agitation & fatigue,called "erethism";inc in sinus/nasal allergy sxs;allergic rxn to thimerosal;pt allergic to mercury & flu vax contained mercury preservatives; |
|
| VAERS ID: |
78528 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1995-10-25 |
| Onset: | 1995-10-25 |
| Days after vaccination: | 0 |
| Submitted: |
1995-10-25 |
| Days after onset: | 0 |
| Entered: |
1995-10-31 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
5F61127 / UNK |
LA / - |
Administered by: Public Purchased by: Other Symptoms: Chills,
Cough,
Nausea,
Pharyngitis,
Pyrexia,
Rhinitis SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Agranulocytosis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal infections (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Gly burde, chlorthazidine, APAP Current Illness: Otitis Media Preexisting Conditions: HTN DM Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: sudden onset fever, chill, coryza, nausea, scratching throat, coughing |
|
| VAERS ID: |
79723 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1995-10-25 |
| Onset: | 1995-10-29 |
| Days after vaccination: | 4 |
| Submitted: |
1995-11-18 |
| Days after onset: | 20 |
| Entered: |
1995-11-27 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Public Purchased by: Unknown Symptoms: Asthenia,
Chills,
Diarrhoea,
Headache,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: "start of virus" Preexisting Conditions: low immunity Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: feel very tired on 29OCT-30OCT fever, chills, h/a, diarrhea had it 10-12 days; fever 100-101;flu shot given 25OCT95 still feel tired;nurse told pt that she had ''start of virus'' when vaxed, made it ''twice as diff'' |
|
| VAERS ID: |
83943 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1995-10-17 |
| Onset: | 1995-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
1995-10-20 |
| Days after onset: | 2 |
| Entered: |
1996-02-26 |
| Days after submission: | 129 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4958138 / 2 |
- / IM A |
Administered by: Private Purchased by: Private Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: 895304005L
Write-up: pt recv vax 17OCT95 & 18OCT95 devel a diffuse rash characterized as red,punctate & w/a halo around it;pt was tx w/DPH;addtl info recv 30NOV95: pt was dx w/pseudomonas rash |
|
| VAERS ID: |
93537 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1996-10-18 |
| Onset: | 1996-10-19 |
| Days after vaccination: | 1 |
| Submitted: |
1996-12-04 |
| Days after onset: | 46 |
| Entered: |
1997-01-03 |
| Days after submission: | 30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4968170 / UNK |
RA / IM |
Administered by: Private Purchased by: Other Symptoms: Laboratory test abnormal,
Myasthenic syndrome,
Myelitis,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Malignancy related conditions (narrow), Guillain-Barre syndrome (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: MRI of entire spine; CT scan head WNL. LP-high protein, al IgG. EMG WNL CDC Split Type: VT96004
Write-up: ascending paresthesias, left leg weakness w/ transverse myelitis: hosp for 5 days sudomedrol. sx occurred w. 36 hr of influenza vax; no other expandable cause for sx. |
|
| VAERS ID: |
93538 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1996-10-15 |
| Onset: | 1996-10-18 |
| Days after vaccination: | 3 |
| Submitted: |
1996-12-02 |
| Days after onset: | 45 |
| Entered: |
1997-01-03 |
| Days after submission: | 32 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / MEDEVA PHARMA, LTD. |
E3036GA / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Asthenia,
Guillain-Barre syndrome,
Hypokinesia,
Myasthenic syndrome,
Paraesthesia SMQs:, Peripheral neuropathy (narrow), Malignancy related conditions (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (narrow), Demyelination (narrow), Hypotonic-hyporesponsive episode (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 29 days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: since 11oct96 biaxin for bronchitis/ pneumonia Current Illness: recovering from pneumonia/bronchitis Preexisting Conditions: Allergies: Diagnostic Lab Data: GBS CDC Split Type: VT96005
Write-up: 18oct96 woke w/ tingling in legs, weakness, worked all day. 20oct96 went to MD w/ above complaints "legs going on me" 21oct96 went to ER-admitted. 22oct96 transferred to diff hosp. Dx: GBS |
|
| VAERS ID: |
93539 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1996-11-08 |
| Onset: | 1996-11-18 |
| Days after vaccination: | 10 |
| Submitted: |
1996-12-02 |
| Days after onset: | 14 |
| Entered: |
1997-01-03 |
| Days after submission: | 32 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4968170 / UNK |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Back pain,
Guillain-Barre syndrome,
Headache,
Hypokinesia,
Myasthenic syndrome,
Pain SMQs:, Peripheral neuropathy (narrow), Retroperitoneal fibrosis (broad), Malignancy related conditions (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (narrow), Demyelination (narrow), Hypotonic-hyporesponsive episode (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 10 days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: GBS CDC Split Type: VT96006
Write-up: 18nov96- headache, legs and back ache;20dec96- went to MD for complaints; 22nov96- again went to MD for same complaints & weakness in legs-using walker; 23nov96-went to ER, unable to walk at all; pt admitted; still in ICU 02dec96; GBS |
|
| VAERS ID: |
93540 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1996-11-15 |
| Onset: | 1996-11-29 |
| Days after vaccination: | 14 |
| Submitted: |
1996-12-24 |
| Days after onset: | 25 |
| Entered: |
1997-01-03 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
6F71221 / UNK |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Guillain-Barre syndrome,
Hypokinesia,
Myasthenic syndrome,
Paraesthesia SMQs:, Peripheral neuropathy (narrow), Malignancy related conditions (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (narrow), Demyelination (narrow), Hypotonic-hyporesponsive episode (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 25 days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: albuterol, alupent, calan premarin, theophylline Current Illness: none Preexisting Conditions: chronic obstructive pulmonary disease; hypertension Allergies: Diagnostic Lab Data: GBS CDC Split Type: VT96007
Write-up: 29nov96- woke up feeling fine, w/in hr felt picky numbness, muscle weakness & eventually could not stand;went to med outpatient ctr; 30nov96- sx worse- went to ER admitted & still hospitalized; GBS |
|
| VAERS ID: |
98771 (history) |
| Form: |
Version 1.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1995-11-09 |
| Onset: | 1995-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
1997-02-06 |
| Days after onset: | 455 |
| Entered: |
1997-04-18 |
| Days after submission: | 70 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
5F61024 / 1 |
- / IM A |
Administered by: Other Purchased by: Other Symptoms: Conjunctivitis,
Cough,
Dry mouth,
Lacrimal disorder,
Laryngospasm,
Myalgia,
Pruritus,
Pyrexia SMQs:, Rhabdomyolysis/myopathy (broad), Severe cutaneous adverse reactions (broad), Anaphylactic reaction (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dystonia (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Eosinophilic pneumonia (broad), Conjunctival disorders (narrow), Lacrimal disorders (narrow), Ocular infections (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: allergy to tetracycline Allergies: Diagnostic Lab Data: CDC Split Type: CO6327
Write-up: eyes very red, itchy & watery;dry mouth, felt like object in throat 1hr p/vax;persistent cough;BP fine, P=fine;called MD who sent to ER;tx w/DPH;throat better;6PM devel temp 100.6 & was achy;nothing unusual to eat or drink; |
|
| VAERS ID: |
104039 (history) |
| Form: |
Version 1.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
1997-10-21 |
| Days after onset: | 4 |
| Entered: |
1997-10-29 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
7F81754 / 1 |
LA / - |
Administered by: Other Purchased by: Public Symptoms: Chills,
Nausea,
Pyrexia,
Tremor SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: NONE~ ()~~~In patient Other Medications: oral contraceptive;Loestrin Current Illness: NONE Preexisting Conditions: endometriosis Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: 8 1/2hr p/vax pt devel sl nausea, followed by uncontrollable shaking & teeth chattering;p/a period of rest pt devel a fever;T max 102 orally;had one other episode of violent shaking w/in the next 12hr;temp remained elevated for 36hr; |
|
| VAERS ID: |
104296 (history) |
| Form: |
Version 1.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
1997-11-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Oedema peripheral,
Pain,
Pruritus,
Vasodilatation SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: 5/8" needle provided by Wyeth for IM flu vax; CDC Split Type:
Write-up: pt states arm turned red, swelling up, itching, burn; reporter states 5/8" needle provided by Wyeth for IM flu vax; |
|
| VAERS ID: |
104297 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
1997-10-28 |
| Days after onset: | 10 |
| Entered: |
1997-11-03 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4978193 / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Oedema peripheral,
Pruritus,
Vasodilatation SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: allergies-colitis (ulcerative) Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: large reddened, raised area on deltoid, heat filled;ice applied;lasted 4+ days then resolved;spot was also very itchy during rxn;reporter feels the vax was given SC instead of IM because 5/8" needle provided by Wyeth; |
|
| VAERS ID: |
104298 (history) |
| Form: |
Version 1.0 |
| Age: |
29.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
1997-10-28 |
| Days after onset: | 10 |
| Entered: |
1997-11-03 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Other Purchased by: Private Symptoms: Oedema peripheral,
Vasodilatation SMQs:, Cardiac failure (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: NONE~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: NA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt arm swelled up turned very hot & red;pt put ice on it;it took 4 days to go back to nl;3 by 4 in wide raised;reporter states pt has large arms there fore 5/8" needle provided on tubex did not go IM; |
|
| VAERS ID: |
104299 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
1997-10-23 |
| Days after onset: | 5 |
| Entered: |
1997-11-03 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
LA / SC |
Administered by: Unknown Purchased by: Unknown Symptoms: Injection site mass,
Injection site pain,
Pruritus SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: pt exp itchy, hard, red wheal w/flu vax in 1996;~ ()~~~In patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: PCN Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: devel a 4inch x 2inch itchy, hard, red wheal @ site of the inj-varied between locally sore & locally very itchy till today 23OCt97;pt has recv vax other yr including last year w/rxn;reporter states 5/8" needle went SC not IM; |
|
| VAERS ID: |
104300 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
1997-10-28 |
| Days after onset: | 11 |
| Entered: |
1997-11-03 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
LA / SC |
Administered by: Unknown Purchased by: Unknown Symptoms: Injection site hypersensitivity,
Injection site mass,
Injection site oedema,
Oedema peripheral,
Pruritus,
Rash,
Vasodilatation SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: NONE~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: large red rash/swelling/itching/hot & was a hard ball where it was given;d/t 5/8" needle provided by Wyeth this inj probably went SC; |
|
| VAERS ID: |
104301 (history) |
| Form: |
Version 1.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 1997-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
1997-10-28 |
| Days after onset: | 10 |
| Entered: |
1997-11-03 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
LA / - |
Administered by: Other Purchased by: Unknown Symptoms: Oedema,
Pain,
Skin nodule,
Vasodilatation SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: area about size of a tennis ball that was swollen very red & hot very sore for 3 days;flu vax recv in individual doses from wyeth w/ 5/8" needle; |
|
| VAERS ID: |
104302 (history) |
| Form: |
Version 1.0 |
| Age: |
40.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-20 |
| Onset: | 1997-10-20 |
| Days after vaccination: | 0 |
| Submitted: |
1997-10-24 |
| Days after onset: | 4 |
| Entered: |
1997-11-03 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / 1 |
RA / SC |
Administered by: Other Purchased by: Other Symptoms: Injection site hypersensitivity,
Injection site mass,
Pain,
Vasodilatation SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: NA~ ()~~~In patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: NA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: rt upper arm, deltoid area became hot to touch w/tenderness, along w/a hard raised rash of 3" inches in circumference around the inj site;reporter states flu vax provided by Wyeth tubex prepared w/ 5/8" for Im shot; |
|
| VAERS ID: |
106438 (history) |
| Form: |
Version 1.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 0000-00-00 |
| Submitted: |
1998-01-12 |
| Entered: |
1998-01-16 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
7F81788 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Pain,
Tendon disorder SMQs:, Tendinopathies and ligament disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: diabetes Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt reported persistent soreness in lt arm & devel of tendonitis since flu shot;feels nurse gave shot too far back in arm;pt has been seen by MD & can not find cause for tendonitis-? flu shot only started since recv vax; |
|
| VAERS ID: |
106439 (history) |
| Form: |
Version 1.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1997-10-17 |
| Onset: | 0000-00-00 |
| Submitted: |
1998-01-12 |
| Entered: |
1998-01-16 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
7F81894 / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Injection site mass SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: pt exp abscess p/vax;~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: unk CDC Split Type:
Write-up: pt reported persistent lump about the size of walnut from flu shot; |
|
| VAERS ID: |
109228 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
1997-10-22 |
| Entered: |
1998-03-26 |
| Days after submission: | 155 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
- / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site reaction SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: unk Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: 897314036L
Write-up: several pt devel exaggerated inj site rxn p/vax;reporter unable to specify the number of people who exp this event; |
|
| VAERS ID: |
109292 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
1997-11-06 |
| Entered: |
1998-03-26 |
| Days after submission: | 140 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
- / UNK |
- / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site hypersensitivity,
Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: unk Current Illness: unk Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: 897344032L
Write-up: pt recv vax & devel an inj site rxn characterized by pain & redness; |
|
| VAERS ID: |
115161 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1998-10-07 |
| Onset: | 1998-10-08 |
| Days after vaccination: | 1 |
| Submitted: |
1998-10-14 |
| Days after onset: | 6 |
| Entered: |
1998-10-21 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4988203 / UNK |
RA / - |
Administered by: Private Purchased by: Private Symptoms: Malaise,
Pharyngitis,
Pyrexia,
Tinnitus SMQs:, Agranulocytosis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal infections (narrow), Hearing impairment (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: VT98002
Write-up: ringing ears, sore throat, malaise, elevated temp; |
|
| VAERS ID: |
115707 (history) |
| Form: |
Version 1.0 |
| Age: |
49.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 1988-10-27 |
| Submitted: |
1998-10-23 |
| Days after onset: | 3648 |
| Entered: |
1998-11-04 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Anorexia,
Asthenia,
Facial palsy,
Guillain-Barre syndrome,
Hyperhidrosis,
Hypokinesia,
Myasthenic syndrome,
Pain,
Paraesthesia,
Speech disorder SMQs:, Peripheral neuropathy (narrow), Neuroleptic malignant syndrome (broad), Dementia (broad), Malignancy related conditions (narrow), Parkinson-like events (broad), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Demyelination (narrow), Hearing impairment (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt recv vax & exp sweat, numbness in feet & hands;pt then put in hosp;GBS 3 days later in ICU;had bell''s palsy;had to learn to talk, eat, walk again;pt states was in perfect health a/shot; |
|
| VAERS ID: |
116306 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1998-10-13 |
| Onset: | 1998-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
1998-10-15 |
| Days after onset: | 2 |
| Entered: |
1998-11-09 |
| Days after submission: | 25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUOGEN) / PARKDALE PHARMACEUTICALS |
02298P / 1 |
- / IM |
Administered by: Private Purchased by: Private Symptoms: Chest pain,
Conjunctivitis,
Cough,
Dyspnoea,
Face oedema SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (narrow), Angioedema (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Conjunctival disorders (narrow), Ocular infections (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: UNK~ ()~~~In patient Other Medications: UNK Current Illness: UNK Preexisting Conditions: UNK Allergies: Diagnostic Lab Data: UNK CDC Split Type: FLU88121098
Write-up: Pt recv vax on 10/13/98; post vax pt exp increased cough, tight chest, red/puffy eyes & difficulty breathing |
|
| VAERS ID: |
116307 (history) |
| Form: |
Version 1.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1998-10-14 |
| Onset: | 1998-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
1998-10-15 |
| Days after onset: | 1 |
| Entered: |
1998-11-09 |
| Days after submission: | 25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUOGEN) / PARKDALE PHARMACEUTICALS |
02298P / 2 |
- / IM |
Administered by: Private Purchased by: Private Symptoms: Dysphonia,
Laryngospasm,
Rash maculo-papular SMQs:, Anaphylactic reaction (broad), Dystonia (broad), Parkinson-like events (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: UNK~ ()~~~In patient Other Medications: UNK Current Illness: UNK Preexisting Conditions: UNK Allergies: Diagnostic Lab Data: UNK CDC Split Type: FLU88131098
Write-up: Pt recv vax on 10/14/98; post vax pt exp tight throat, hoarse, red blotches on neck & chest |
|
| VAERS ID: |
117209 (history) |
| Form: |
Version 1.0 |
| Age: |
32.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1998-11-23 |
| Onset: | 1998-11-23 |
| Days after vaccination: | 0 |
| Submitted: |
1998-12-01 |
| Days after onset: | 8 |
| Entered: |
1998-12-08 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
0975780 / 2 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Chest pain,
Injection site hypersensitivity,
Injection site oedema,
Urticaria,
Vasodilatation SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: UNK~ ()~~~In patient Other Medications: UNK Current Illness: NONE Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: NONE CDC Split Type: MA9847
Write-up: Pt recv vax on 11/23/98; 3 min post vax pt exp red, warm, swollen vax site; hives on chest, neck; chest tight; tx=Benadryl, Epi kit |
|
| VAERS ID: |
118282 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1998-11-05 |
| Onset: | 0000-00-00 |
| Submitted: |
1998-12-12 |
| Entered: |
1999-01-22 |
| Days after submission: | 41 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
0984550 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Diarrhoea,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: unk CDC Split Type:
Write-up: pt reported a month p/vax has been sick w/diarrhea, nausea & h/a since inj;has not seen a MD;states there as few other @ office who were sick;encouraged pt to see MD; |
|
| VAERS ID: |
129872 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
1999-10-20 |
| Entered: |
1999-10-26 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Other Purchased by: Unknown Symptoms: Arthralgia,
Myalgia,
Vertigo SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Vestibular disorders (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: myalgia, arthralgia, vertigo; |
|
| VAERS ID: |
130175 (history) |
| Form: |
Version 1.0 |
| Age: |
0.3 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1999-10-19 |
| Onset: | 1999-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
1999-10-19 |
| Days after onset: | 0 |
| Entered: |
1999-11-02 |
| Days after submission: | 14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (INFANRIX) / SMITHKLINE BEECHAM |
911A1 / 2 |
RL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4998225 / 1 |
RL / IM |
| HIBV: HIB (HIBTITER) / PFIZER/WYETH |
P1113AA / 2 |
LL / IM |
| IPV: POLIO VIRUS, INACT. (POLIOVAX) / CONNAUGHT LTD. |
N08262 / 2 |
LL / SC |
Administered by: Private Purchased by: Public Symptoms: Injection site hypersensitivity,
Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: NONE~ ()~~~In patient Other Medications: Digixon;Lasix; Current Illness: NONE Preexisting Conditions: pre-mature, heart conditon;aeortic stenosis Allergies: Diagnostic Lab Data: NONE CDC Split Type: VT99004
Write-up: 5hr p/vax pt to MD office;has been crying since vax;remarkably tender, site rxn, erythema, pain in rt leg; |
|
| VAERS ID: |
132100 (history) |
| Form: |
Version 1.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1999-10-19 |
| Onset: | 1999-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
1999-11-01 |
| Days after onset: | 13 |
| Entered: |
1999-12-28 |
| Days after submission: | 57 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUOGEN) / PARKDALE PHARMACEUTICALS |
03179P / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Asthma,
Back pain,
Chills,
Dysphonia,
Injection site hypersensitivity,
Injection site mass,
Neck pain,
Vasodilatation SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Retroperitoneal fibrosis (broad), Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Lipitor,albuterol,Xanax,prednisone,Ambien Current Illness: NONE Preexisting Conditions: asthma,hypertension,elevated cholestrol,MVP,osteoarthritis Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: By 4p on 10/19/99, pt had a raised,bright red welt approx 2" x 3" in diam;hot to the touch at inj. site,neck,shoulder, & lower back pain w/ accompying chills.The next day,sx worsened.Tx w/ Benadryl & cephalexin. |
|
| VAERS ID: |
132261 (history) |
| Form: |
Version 1.0 |
| Age: |
23.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1999-11-03 |
| Onset: | 1999-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
1999-11-05 |
| Days after onset: | 2 |
| Entered: |
1999-12-28 |
| Days after submission: | 53 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
U0104AA / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Hypertonia,
Injection site hypersensitivity,
Injection site pain,
Laryngospasm,
Tongue oedema,
Vasodilatation SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Dystonia (broad), Parkinson-like events (narrow), Oropharyngeal allergic conditions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypokalaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: Allergy to tea tree oil, Asthma Allergies: Diagnostic Lab Data: NONE CDC Split Type: VT99008
Write-up: Vax. at worksite, continued at job, 3 1/2 hrs. later felt like throat had something stuck in it, felt constricted. Tongue felt tingly and thick. Felt flush, skin on chest, legs & arms was mottled, but not described as hives. Left arm at |
|
| VAERS ID: |
133301 (history) |
| Form: |
Version 1.0 |
| Age: |
46.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1991-10-14 |
| Onset: | 1999-10-08 |
| Days after vaccination: | 2916 |
| Submitted: |
1999-12-16 |
| Days after onset: | 69 |
| Entered: |
2000-01-13 |
| Days after submission: | 28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
U0104AA / 2 |
LA / IM |
Administered by: Private Purchased by: Unknown Symptoms: Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~ ()~~~In patient Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Brain MR scan normal. CDC Split Type:
Write-up: Tingly numbness rear L sole, heal, & rear arch. Spread 1/2 rear calf, then to include entire L palm, forearm while present in leg. 1 wk later numbness receded. Present only in L foot. Ruled out GBS. |
|
| VAERS ID: |
158300 (history) |
| Form: |
Version 1.0 |
| Age: |
27.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1999-10-12 |
| Onset: | 1999-10-12 |
| Days after vaccination: | 0 |
| Submitted: |
1999-10-22 |
| Days after onset: | 10 |
| Entered: |
2000-08-02 |
| Days after submission: | 285 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
U0145CA / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
U011H / 1 |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Erythema,
Feeling hot,
Oedema,
Skin nodule SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: 10/12, the same day as vax, the pt experienced redness, swelling and hot. 10/17 five days post vax, the pt experienced increased redness and warmth. Antibiotics were given. On 10/20, area was red and hard and an appointment with a private MD was made. 10/22, the pt is improved and continues on antibiotics. |
|
| VAERS ID: |
158302 (history) |
| Form: |
Version 1.0 |
| Age: |
32.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 1999-11-05 |
| Onset: | 1999-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
1999-11-05 |
| Days after onset: | 0 |
| Entered: |
2000-08-02 |
| Days after submission: | 270 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
U0145CA / 1 |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Chest discomfort,
Pharyngolaryngeal pain,
Pruritus SMQs:, Anaphylactic reaction (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: The pt complained of itching arms, legs with a rash. The pt experienced a burning throat, increased pressure in the chest. 911 was called. |
|
| VAERS ID: |
162053 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1999-10-13 |
| Onset: | 1999-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
1999-12-14 |
| Days after onset: | 62 |
| Entered: |
2000-10-06 |
| Days after submission: | 296 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4998212 / UNK |
- / IM |
| PPV: PNEUMO (PNU-IMUNE) / PFIZER/WYETH |
461144 / UNK |
- / IM |
Administered by: Private Purchased by: Other Symptoms: Injection site haemorrhage,
Injection site oedema,
Injection site pain SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNK Current Illness: NONE Preexisting Conditions: UNK Allergies: Diagnostic Lab Data: UNK CDC Split Type: HQ8314513DEC1999
Write-up: On the same day of vax, the pt developed an injection site reaction in the right arm characterized by swelling which extended over the upper arm and pain. The pt also developed ecchymotic areas in the upper arm and forearm. The pt recovered. |
|
| VAERS ID: |
162054 (history) |
| Form: |
Version 1.0 |
| Age: |
36.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1999-10-13 |
| Onset: | 1999-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
2000-03-15 |
| Days after onset: | 154 |
| Entered: |
2000-10-06 |
| Days after submission: | 204 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
4998212 / UNK |
- / IM |
| PPV: PNEUMO (PNU-IMUNE) / PFIZER/WYETH |
461144 / 1 |
- / IM |
Administered by: Private Purchased by: Other Symptoms: Injection site haemorrhage,
Injection site oedema,
Injection site pain SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: UNK Allergies: Diagnostic Lab Data: UNK CDC Split Type: HQ8314913DEC1999
Write-up: The same day of vaccination, the pt developed an injection site reaction characterized by upper arm pain and swelling to the Pnu-Imune site. The pt also developed bruising at the injection site. The pt recovered. |
|
| VAERS ID: |
162348 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 1999-10-14 |
| Onset: | 1999-10-31 |
| Days after vaccination: | 17 |
| Submitted: |
1999-12-29 |
| Days after onset: | 59 |
| Entered: |
2000-10-13 |
| Days after submission: | 288 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / CONNAUGHT LABORATORIES |
- / UNK |
- / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: MRI scan of right brain-nml CDC Split Type: U1999010150
Write-up: It was reported that a 56 year old male pt received a Fluzone UNSP ''99-''00 vaccination on 10/14/99. Reportedly, on 10/31/99, the pt developed paresthesia from sole of left foot with gradual increase to left leg, left side of body and left arm to the forearm. The paresthesia has faded in the same pattern it progressed. No right side involvement, pt''s reflexes were normal. Pt also developed paresthesia below right ankle at this time and is fading. The doctor has not confirmed dx with spinal tap or nerve conduction studies due to symptoms resolving at this time. No additional information was provided from correspondence returned on 12/17/99. |
|
| VAERS ID: |
161235 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2000-10-23 |
| Onset: | 2000-10-23 |
| Days after vaccination: | 0 |
| Submitted: |
2000-10-24 |
| Days after onset: | 1 |
| Entered: |
2000-11-01 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / MEDEVA PHARMA, LTD. |
E67360KA / 5 |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Headache,
Hyperhidrosis SMQs:, Neuroleptic malignant syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Prilosec, Lipitor, Bentyl, Lopressor Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 30 minutes post vax, the pt developed pounding headache and sweating. One hour post vax, the pt had headache only. 2 hours post vax, the pt had no symptoms. |
|
| VAERS ID: |
163762 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2000-12-05 |
| Onset: | 2000-12-06 |
| Days after vaccination: | 1 |
| Submitted: |
2000-12-13 |
| Days after onset: | 7 |
| Entered: |
2000-12-14 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUSHIELD) / PFIZER/WYETH |
40085190 / UNK |
- / IM |
Administered by: Private Purchased by: Unknown Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: reactive airway disease Allergies: Diagnostic Lab Data: CDC Split Type: VT00005
Write-up: One day post vax, the pt developed hives on arms, legs, face trunk. Still has them one week later. |
|
| VAERS ID: |
175571 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-09-17 |
| Onset: | 2001-09-18 |
| Days after vaccination: | 1 |
| Submitted: |
2001-09-19 |
| Days after onset: | 1 |
| Entered: |
2001-09-21 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (INFANRIX) / SMITHKLINE BEECHAM |
A997A2 / 5 |
RA / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UO598AA / 3 |
RA / IM |
| IPV: POLIO VIRUS, INACT. (POLIOVAX) / CONNAUGHT LTD. |
T0785 / 4 |
LA / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
1516K / 2 |
LA / SC |
Administered by: Private Purchased by: Private Symptoms: Injection site erythema,
Injection site oedema SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 6 x 9 inch irregular shaped red, swollen area right upper arm. |
|
| VAERS ID: |
177801 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-11-09 |
| Onset: | 2001-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2001-11-09 |
| Days after onset: | 0 |
| Entered: |
2001-11-16 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
E10821LA / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Dizziness,
Nausea,
Nervousness,
Pallor SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: The patient felt dizzy, nauseated, nervous and was very pale. The patient rested and was reassured. |
|
| VAERS ID: |
177824 (history) |
| Form: |
Version 1.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-11-05 |
| Onset: | 0000-00-00 |
| Submitted: |
2001-11-05 |
| Entered: |
2001-11-16 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
E10821LA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Injury SMQs:, Accidents and injuries (narrow), Hostility/aggression (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: UNK Preexisting Conditions: Allergic to Thimerosol. Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: The patient was injected with a needle on a syringe. There was no air or solution in it. |
|
| VAERS ID: |
178442 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-10-03 |
| Onset: | 2001-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
2001-11-05 |
| Days after onset: | 33 |
| Entered: |
2001-11-30 |
| Days after submission: | 25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U0600AA / UNK |
LA / SC |
Administered by: Public Purchased by: Private Symptoms: Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: The patient felt pain after the injection and had to lie down. It was several days until the whole body pain went away. |
|
| VAERS ID: |
178443 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2001-10-03 |
| Onset: | 2001-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2001-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U0600AA / UNK |
- / SC |
Administered by: Public Purchased by: Unknown Symptoms: Abdominal pain,
Dizziness,
Muscle spasms,
Pain SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: The patient had generalized pain, cramps, abdominal pain and dizziness for about 2 weeks. |
|
| VAERS ID: |
178444 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-10-14 |
| Onset: | 2001-10-15 |
| Days after vaccination: | 1 |
| Submitted: |
2001-11-21 |
| Days after onset: | 37 |
| Entered: |
2001-11-30 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U0600AA / UNK |
- / SC |
Administered by: Public Purchased by: Unknown Symptoms: Balance disorder,
Dizziness,
Ear discomfort,
Ear disorder,
Headache SMQs:, Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Post vax the patient''s ears started popping, she felt dizzy, her equilibrium was off all weekend, middle ear was stuffed and she had pressure in the head areas. |
|
| VAERS ID: |
178478 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-10-10 |
| Onset: | 2001-10-17 |
| Days after vaccination: | 7 |
| Submitted: |
2001-11-21 |
| Days after onset: | 35 |
| Entered: |
2001-12-03 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U0600AA / UNK |
- / SC |
Administered by: Public Purchased by: Other Symptoms: Hypokinesia,
Injection site pain,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hypotonic-hyporesponsive episode (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: The pt developed pain at the injection site, initially on 10/19/01, and the pain worsened. It went up the neck and down arms to chest and down hands to 4th and 5th digits which was prickly. Cannot move right arm. Seen MD and the flu vaccine could not be ruled out. It may be related. |
|
| VAERS ID: |
179733 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2001-10-31 |
| Onset: | 2001-10-31 |
| Days after vaccination: | 0 |
| Submitted: |
2001-12-29 |
| Days after onset: | 59 |
| Entered: |
2001-12-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
- / UNK |
- / - |
Administered by: Private Purchased by: Private Symptoms: Asthenia,
Chest pain,
Dizziness,
Dyspnoea,
Palpitations SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: HRT Current Illness: None Preexisting Conditions: Amoxicillian Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient c/o of painful cardiac palpitations, some SOB, lightheadedness and weakness (mod), which required her to sit and rest about 15 minutes. |
|
| VAERS ID: |
192310 (history) |
| Form: |
Version 1.0 |
| Age: |
51.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2002-10-22 |
| Onset: | 2002-10-23 |
| Days after vaccination: | 1 |
| Submitted: |
2002-10-25 |
| Days after onset: | 2 |
| Entered: |
2002-11-01 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
E35492KA / UNK |
- / IM |
Administered by: Private Purchased by: Unknown Symptoms: Early morning awakening,
Headache SMQs:, Depression (excl suicide and self injury) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: History of migraines Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Severe headache x 36-48 hrs. (migraine- like- acute onset 12 hrs after vaccine- awoke pt from sleep) |
|
| VAERS ID: |
193255 (history) |
| Form: |
Version 1.0 |
| Age: |
40.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2002-11-08 |
| Onset: | 2002-11-09 |
| Days after vaccination: | 1 |
| Submitted: |
2002-11-13 |
| Days after onset: | 4 |
| Entered: |
2002-11-14 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UO951AA / 1 |
LA / - |
Administered by: Other Purchased by: Private Symptoms: Injection site hypersensitivity,
Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: shellfish allergies Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: 24 hours influenza vaccination first time recipient reports itching at site x 3 days. |
|
| VAERS ID: |
210885 (history) |
| Form: |
Version 1.0 |
| Age: |
0.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2003-10-07 |
| Onset: | 2003-10-08 |
| Days after vaccination: | 1 |
| Submitted: |
2003-10-22 |
| Days after onset: | 14 |
| Entered: |
2003-10-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
765748 / 3 |
UN / IM |
Administered by: Public Purchased by: Public Symptoms: Asthenia,
Myalgia,
Pain,
Swelling SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Angioedema (broad), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNKNOWN Current Illness: UNKNOWN Preexisting Conditions: UNKNOWN Allergies: Diagnostic Lab Data: NONE KNOWN CDC Split Type:
Write-up: MUSCLE ACHES AND PAIN, GENERAL MALAISE AND EXTREME WEAKNESS.OUT OF WORK FOR 3 1/2 DAYS. HAD HAD VACCINE TWICE BEFORE AND HAD MODERATE LOCAL REACTIONS WITH ARM SWELLING AND PAIN. |
|
| VAERS ID: |
212109 (history) |
| Form: |
Version 1.0 |
| Age: |
30.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2003-11-04 |
| Onset: | 2003-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2003-11-04 |
| Days after onset: | 0 |
| Entered: |
2003-11-11 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
765954 / 1 |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Chest pain,
Pain,
Pallor,
Throat tightness SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Depoprovera Current Illness: NONE Preexisting Conditions: One sibling has egg allergy. Pt tolerate eggs. Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt presented 45 minutes after vaccination was at her work place. Reports discomfort/pain in chest and right axilla, "throat tightness," and is very pale. Medicated with Benadryl 50mg IM at 1245 by RN. Color improved. throat tightness lessened within 5 mins. Reports first onset of symptoms was within 20 mins of dose. Improved by 1330. |
|
| VAERS ID: |
213447 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2003-12-03 |
| Onset: | 2003-12-03 |
| Days after vaccination: | 0 |
| Submitted: |
2003-12-03 |
| Days after onset: | 0 |
| Entered: |
2003-12-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Asthenia,
Dyspnoea,
Heart rate increased,
Pallor SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: difficulty breathing, fast heartbeat, paleness, weakness |
|
| VAERS ID: |
213656 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2003-11-21 |
| Onset: | 2003-11-22 |
| Days after vaccination: | 1 |
| Submitted: |
2003-12-08 |
| Days after onset: | 16 |
| Entered: |
2003-12-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
765855 / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Arthralgia,
Injection site pain,
Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Extravasation events (injections, infusions and implants) (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Ritalin Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Burning/dysesthesia at vaccine site - same arm arthralgia and myalgias for two weeks |
|
| VAERS ID: |
213783 (history) |
| Form: |
Version 1.0 |
| Age: |
40.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2003-12-05 |
| Entered: |
2003-12-10 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / EVANS VACCINES |
765873 / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site pain,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Wellbutrin; Prednisone; Remeron; Neurontin; Trazodone; Current Illness: NONE Preexisting Conditions: History of allergy to Thimerosal. Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: After injection about 8-12 hours, noted increased injection site soreness and fever. |
|
| VAERS ID: |
214497 (history) |
| Form: |
Version 1.0 |
| Age: |
1.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2003-12-12 |
| Onset: | 2003-12-20 |
| Days after vaccination: | 8 |
| Submitted: |
2003-12-22 |
| Days after onset: | 2 |
| Entered: |
2003-12-30 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1133AA / 2 |
RL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (VIRIVAC) / MERCK & CO. INC. |
0611N / 1 |
LL / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
0896N / 1 |
RL / SC |
Administered by: Public Purchased by: Other Symptoms: Rash papular SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Rash over face and trunk; diffuse papular starting on 12/20/03. No fever or malaise. |
|
| VAERS ID: |
215451 (history) |
| Form: |
Version 1.0 |
| Age: |
38.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2002-11-06 |
| Onset: | 0000-00-00 |
| Submitted: |
2003-05-30 |
| Entered: |
2004-01-22 |
| Days after submission: | 237 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U0944AA / UNK |
- / - |
Administered by: Other Purchased by: Other Symptoms: Thought blocking SMQs:, Psychosis and psychotic disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: It was also reported that he had received influenza vaccine in the past with no problems. Allergies: Diagnostic Lab Data: NONE CDC Split Type: U200200977
Write-up: Information has been received concerning a 38 year old male who was administered Fluzone SV 2002-2003 USP (Lot # U0944aa) on 11/06/2002. Approximately 6 hours after vaccination, the pt experienced difficulty in verbalizing thoughts, which lasted for 2 to 3 hours. He was fully recovered. It was also reported that he had received influenza vaccine in the past with no problems. From additional information received on 04/10/03, from a nurse, it was reported that the pt, vaccine administrator and physician''s information be updated. No further information is anticipated, this case is closed. |
|
| VAERS ID: |
216845 (history) |
| Form: |
Version 1.0 |
| Age: |
89.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 2002-11-01 |
| Submitted: |
2004-02-16 |
| Days after onset: | 472 |
| Entered: |
2004-02-25 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Anxiety,
Chills,
Depression,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Depression (excl suicide and self injury) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Saw palmetto; Glucosamine; Chondrotin sulfates Current Illness: Preexisting Conditions: Back injury; Colorectal cancer; Fusion C5-6, incision bladder; Colon canser; Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Was given a flu shot have chills and fever ever since. Medical record states anxiety, depression. msv |
|
| VAERS ID: |
228125 (history) |
| Form: |
Version 1.0 |
| Age: |
64.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-10-14 |
| Onset: | 2004-10-19 |
| Days after vaccination: | 5 |
| Submitted: |
2004-10-20 |
| Days after onset: | 1 |
| Entered: |
2004-10-25 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1421AA / 5 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0740N / 1 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site erythema,
Injection site induration,
Injection site oedema,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: Right breast cancer; lymphactomy axillary dissectum, non ischemic cardiomyopathy. Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Very large area of redness, swelling, warmth and induration 15x15cm distal to right deltoid injection site of pneumococcal vaccine. Developed several hours after shot. As of next day, swelling somewhat diminished. |
|
| VAERS ID: |
228923 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2004-10-28 |
| Onset: | 2004-10-29 |
| Days after vaccination: | 1 |
| Submitted: |
2004-11-01 |
| Days after onset: | 3 |
| Entered: |
2004-11-08 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1439AA / UNK |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site swelling,
Injection site warmth,
Pyrexia,
Tenderness SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Pulmicort; Albuterol Current Illness: NONE Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Fever in evening $g100-101. Swelling injection site to elbow. Increased erythema and warmth injection site to most arm; slight tenderness. |
|
| VAERS ID: |
229232 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-11-04 |
| Onset: | 2004-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2004-11-11 |
| Days after onset: | 7 |
| Entered: |
2004-11-15 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500333P / UNK |
NS / IN |
Administered by: Private Purchased by: Unknown Symptoms: Chest discomfort,
Feeling abnormal,
Pain SMQs:, Anaphylactic reaction (broad), Dementia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: "Weird" feeling, aches, chest discomfort |
|
| VAERS ID: |
229234 (history) |
| Form: |
Version 1.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-11-04 |
| Onset: | 2004-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2004-11-11 |
| Days after onset: | 7 |
| Entered: |
2004-11-15 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500333P / UNK |
NS / IN |
Administered by: Private Purchased by: Unknown Symptoms: Chest pain,
Palpitations SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Fleeting episode of palpitations chest pain lasting 2 hours. |
|
| VAERS ID: |
229235 (history) |
| Form: |
Version 1.0 |
| Age: |
40.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2004-11-04 |
| Onset: | 2004-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2004-11-11 |
| Days after onset: | 7 |
| Entered: |
2004-11-15 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500333P / UNK |
NS / IN |
Administered by: Private Purchased by: Unknown Symptoms: Anxiety,
Palpitations SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Palpitations and felt anxious. Lasted 1/2 hours. |
|
| VAERS ID: |
229236 (history) |
| Form: |
Version 1.0 |
| Age: |
31.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-11-04 |
| Onset: | 2004-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2004-11-11 |
| Days after onset: | 7 |
| Entered: |
2004-11-15 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500333P / UNK |
NS / IN |
Administered by: Private Purchased by: Unknown Symptoms: Chest pain,
Feeling abnormal SMQs:, Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Felt "weird", left sided chest pain. |
|
| VAERS ID: |
229302 (history) |
| Form: |
Version 1.0 |
| Age: |
88.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-11-05 |
| Onset: | 2004-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2004-11-10 |
| Days after onset: | 5 |
| Entered: |
2004-11-16 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1557AA / UNK |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Anxiety,
Dyspnoea,
Eye swelling,
Flushing SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: post CVA, major depression, general anxiety and pa, mild COPD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient complained of feeling flushed: did not appear flushed. Complained of difficulty breathing. Observed by RN at site. Patient given Lorazepam 0.25 mg orally. Patient exhibited increasing shortness of breath with puffy eyes. Doctor called. Pt given epinephrine 0.3cLx1 at 2PM. 2:15 patient transported to Emergency Department by ambulance. No interventions at hospital ED. Pt recovered by time of arrival. Diagnosis: possible reaction to flu shot vs. anxiety. |
|
| VAERS ID: |
231173 (history) |
| Form: |
Version 1.0 |
| Age: |
39.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-12-09 |
| Onset: | 2004-12-09 |
| Days after vaccination: | 0 |
| Submitted: |
2004-12-15 |
| Days after onset: | 6 |
| Entered: |
2004-12-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500339P / 1 |
NS / IN |
Administered by: Unknown Purchased by: Unknown Symptoms: Erythema,
Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None reported Current Illness: None reported Preexisting Conditions: None reported Allergies: Diagnostic Lab Data: Unknown--contact hospital. CDC Split Type:
Write-up: Patient received full dose of FluMist. She waited 15 minutes without incident and left the clinic area. Approximately 20 minutes after leaving the clinic area, she returned c/o generalized pruritus, particularly on chest, arms, palms of hands. Erythema and diffuse papules were present on her chest only, in the lower sternal area extending approximately to mid-clavicular area. Dorsal thorax, stomach area, extremities negative for rash. Patient denied all symptoms except pruritus. Lungs and VS serially assessed over a period of 1/2 hour remained within normal limits (lungs clear, VS WNL). 50mg PO benadryl was administered. Phone consultation with primary care physician resulted in patient being transported to Emergency Dept. where she was assessed and released that day. Rx was benadryl PRN and prednisone 20mg x 2D. Treated at hospital. |
|
| VAERS ID: |
232190 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2004-12-01 |
| Onset: | 2004-12-11 |
| Days after vaccination: | 10 |
| Submitted: |
2005-01-06 |
| Days after onset: | 26 |
| Entered: |
2005-01-12 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
01457AA / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Eye irritation,
Facial palsy,
Upper respiratory tract infection,
Vomiting SMQs:, Acute pancreatitis (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Corneal disorders (broad), Hearing impairment (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: upper respiratory infection Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine given 12/01/2004 12/11/2004 - eye irritation, vomited and URI symptoms. 12/12/2004 - right side of face drooping. 12/12/2004 - seen ER Dx: Bell''s Palsy |
|
| VAERS ID: |
232772 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2003-10-17 |
| Onset: | 2003-10-21 |
| Days after vaccination: | 4 |
| Submitted: |
2005-01-21 |
| Days after onset: | 458 |
| Entered: |
2005-01-24 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U106888 / 5 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Discomfort,
Hypertrophy,
Injection site pain,
Laboratory test abnormal,
Myositis,
Shoulder pain SMQs:, Rhabdomyolysis/myopathy (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ASA; Zocor Current Illness: Preexisting Conditions: Patient''s pre-existing medical conditions include high cholesterol. He has no known allergies. He had no illnesses at the time of vaccination. The patient previously received four doses of influenza vaccine with no reactions reported. Allergies: Diagnostic Lab Data: The patient had an MRI completed in October of 2004. MRI results were not provided. From additional information received on 1/14/05, a radiology report was provided. The patient had an MRI of his right shoulder on 10/22/04 due to shoulder pain. The MRI showed marked AC joint hypertrophy with some secondary bone edema, especially at the distal clavicle. Some focal lucency was also noted at the site. The changes might have been due to osteoarthritis, but an erosive arthropathy could not be completely excluded and correlation with the patient''s history and involvement of other joints was recommended. There was impingement on the superior aspect of the supraspinatus, but no rotator cuff tear was seen. Other focal bony abnormality was not noted. There were changes of chronic impingement on the posterior aspect of the superolateral humerus. The physician also thought it relevant to know if the patient has a history of prior dislocation as there was some bony irregularity at the posteroinferior aspect of the glenoid labrum also seen with slight abnormality in bone signal change on the gradient images. The physician''s impression was marked AC joint hypertrophy, labrum intact and minor glenoid changes as described. CDC Split Type: 200403589
Write-up: From follow up information received on 1/14/05 the seriousness of this case was upgraded from non-serious to serious, as based upon medical judgement. From initial information received on 11/1/04 from a registered nurse regarding an adverse event occurring in the USA, it was reported that a 51 year old male patient received a dose of FLUZONE vaccine, lot number U106888, administered in the right deltoid on 10/17/03. Four days later, on 10/21/04, the patient developed lingering shoulder pain at the right deltoid site. The patient has seen an orthopedic shoulder specialist and has been through physical therapy. He also used non-steroidal anti-inflammatories with no beneficial effect. The orthopedic shoulder specialist thought that the patient may have developed some sort of myositis. Patient''s pre-existing medical conditions include high cholesterol. He has no known allergies. He did not have any illnesses at the time of vaccination. Concomitant medications at the time of vaccination included ASA and Zocor. The patient previously received four doses of influenza vaccine with no reactions reported. Reportedly, the discomfort, although it has waxed and waned somewhat, has not diminished significantly over the last several months. The patient has not recovered from these events. From additional information received on 1/14/05, from a physician, it was reported that the patient received a 0.5ml dose of FLUZONE, administered IM in the right deltoid. Reportedly, the patient had no illnesses at the time of vaccination. An MRI of the patient''s right shoulder was completed on 10/22/04 due to right shoulder pain. The MRI showed marked AC joint hypertrophy, labrum intact and minor glenoid changes. Per the reporter, the patient''s shoulder pain was somewhat improved as of the patient''s office visit on 12/23/04. The physician stated that he does not consider the adverse events to be a significant or permanent disability, but it was a cause of significant pain. Reportedly, the patient retained strength, range of motion and function of his shoulder. Contact information for the patient''s orthopedic specialist was provided. The adverse event coding for injection site pain was upgraded to shoulder pain. |
|
| VAERS ID: |
245678 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-10-18 |
| Onset: | 0000-00-00 |
| Submitted: |
2005-10-18 |
| Entered: |
2005-10-19 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA126BC / 1 |
RA / - |
Administered by: Private Purchased by: Private Symptoms: Unevaluable event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: NONE |
|
| VAERS ID: |
245784 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-10-12 |
| Onset: | 2005-10-14 |
| Days after vaccination: | 2 |
| Submitted: |
2005-10-18 |
| Days after onset: | 4 |
| Entered: |
2005-10-20 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1804AA / 4 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Feeling hot,
Injection site erythema,
Injection site mass,
Injection site pain,
Tenderness SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: On Zithromax for persistent otitis media. Current Illness: R A OM Preexisting Conditions: Amoxicillin rash 10/12/05, asthma. Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Had flu shot; c/o severe pain later that eve 10/12. When awoke 10/14 has 5-6cm sharply demarcated erythema with 2cm induration in center, very hot and tender. Rx with Duricef x 7 days. |
|
| VAERS ID: |
246234 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2005-10-25 |
| Onset: | 2005-10-26 |
| Days after vaccination: | 1 |
| Submitted: |
2005-10-27 |
| Days after onset: | 1 |
| Entered: |
2005-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1804AA / 1 |
LA / IM |
| PNC: PNEUMO (PREVNAR) / PFIZER/WYETH |
A56117K / 4 |
RA / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site hypersensitivity,
Injection site induration,
Injection site reaction,
Pruritus SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/O itchy, red, round knot on arm in area of PCV 7 injection. |
|
| VAERS ID: |
246497 (history) |
| Form: |
Version 1.0 |
| Age: |
94.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-10-21 |
| Onset: | 2005-10-22 |
| Days after vaccination: | 1 |
| Submitted: |
2005-10-27 |
| Days after onset: | 5 |
| Entered: |
2005-11-01 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Public Purchased by: Other Symptoms: Pyrexia,
Somnolence SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Shot on Friday- Friday night had fever 101.6 degrees. Slept most of Saturday - part of Sunday fever 99.5 degrees. Still not feel well 10/27/05 - onset of cold, perfect before flu shot |
|
| VAERS ID: |
246632 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2005-10-29 |
| Onset: | 2005-10-30 |
| Days after vaccination: | 1 |
| Submitted: |
2005-11-02 |
| Days after onset: | 3 |
| Entered: |
2005-11-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1823AA / 3 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Diabetes mellitus,
Hyperglycaemia,
Hypoglycaemia SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow), Hypoglycaemia (narrow), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2005-10-30
Days after onset: 0
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Insulin: Lentis 33 U BF Humulog B, L, D sliding scale Current Illness: NONE Preexisting Conditions: type 1 diabetes onset 7/03 Allergies: Diagnostic Lab Data: Autopsy being performed CDC Split Type: VT200510302005
Write-up: Patient vaccinated between 10am-1 Pm on October 30, 2005. Found dead in bed next morning at home by parents. Pt had type 1 diabetes with AC1 of 7.0 but having hypoglycemic episodes 1-2 times per week and not wanting to treat the symptoms per endocrinlogist. Term of DM removed from symtom list as per autopsy report rec''d 12/28/2005/sr This is tag-2 report. |
|
| VAERS ID: |
246892 (history) |
| Form: |
Version 1.0 |
| Age: |
86.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2005-11-03 |
| Onset: | 2005-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
2005-11-07 |
| Days after onset: | 4 |
| Entered: |
2005-11-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1815AA / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Cough,
Hypersensitivity,
Pharyngolaryngeal pain,
Pruritus SMQs:, Anaphylactic reaction (narrow), Angioedema (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No Previous Vaccinations: Other Medications: benadryl and steroids and albuterol udn and ipratropium udn Current Illness: n/a Preexisting Conditions: has hx of breast cancer among other things. (predominant hx) Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt developed allergic reaction to flu vaccine. sx=cough, sore throat, itching. tx= reversed c benadryl and steroids |
|
| VAERS ID: |
248373 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-10-25 |
| Onset: | 2005-10-26 |
| Days after vaccination: | 1 |
| Submitted: |
2005-11-21 |
| Days after onset: | 26 |
| Entered: |
2005-11-29 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1809AA / 4 |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Erythema,
Rash macular SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: tylenol Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 7 X 9 cm red/firm blotchy edges over left deltoid. No streaks, no central papule |
|
| VAERS ID: |
248377 (history) |
| Form: |
Version 1.0 |
| Age: |
57.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-11-18 |
| Onset: | 2005-11-18 |
| Days after vaccination: | 0 |
| Submitted: |
2005-11-21 |
| Days after onset: | 3 |
| Entered: |
2005-11-29 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1930AA / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Dysphagia,
Pharyngolaryngeal pain SMQs:, Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: allegra, nasalide Current Illness: Preexisting Conditions: Allergies: dust, pollen, cat dander Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine at state employee flu clinic. Called PHN at 4:30 pm reporting onset of rough throat and mild difficulty swallowing - denied rash, itching, hives. Subsequently seen at Hospital ER. Client reports he was given Benadryl and prednisone. Held for observation then releashed. |
|
| VAERS ID: |
248525 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2005-11-29 |
| Onset: | 2005-11-30 |
| Days after vaccination: | 1 |
| Submitted: |
2005-12-01 |
| Days after onset: | 1 |
| Entered: |
2005-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / - |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
RA / - |
| IPV: POLIO VIRUS, INACT. (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / - |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
- / UNK |
RA / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Headache,
Injection site erythema,
Injection site warmth,
Pruritus,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: She had 4 injections, 2 in each arm. Flu and MMR in her right arm and IPV and DTaP in her left. Today 2 days after her immunizations, the site of her left arm became 50% more swollen than before, very hot red and itchy. It has spread around the arm like an arm band. She had a very bad headache the day after her immunization. |
|
| VAERS ID: |
248641 (history) |
| Form: |
Version 1.0 |
| Age: |
31.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2005-11-10 |
| Onset: | 2005-11-10 |
| Days after vaccination: | 0 |
| Submitted: |
2005-11-21 |
| Days after onset: | 11 |
| Entered: |
2005-12-02 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U1816AA / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNK Current Illness: UNK Preexisting Conditions: UNK Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Client broke out into hives 10 minutes after receiving a flu shot. |
|
| VAERS ID: |
265578 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2006-10-17 |
| Onset: | 0000-00-00 |
| Submitted: |
2006-10-25 |
| Entered: |
2006-10-30 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2166AB / UNK |
LA / - |
Administered by: Private Purchased by: Public Symptoms: Eye oedema,
Face oedema SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Claritin, Flonase Current Illness: Preexisting Conditions: Allergic rhinitis, critical AS/aortic insufficiency Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lip/eye swelling following Fluzone. |
|
| VAERS ID: |
265579 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-10-24 |
| Onset: | 2006-10-24 |
| Days after vaccination: | 0 |
| Submitted: |
2006-10-25 |
| Days after onset: | 1 |
| Entered: |
2006-10-30 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
71210 / UNK |
LA / IM |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
1048F / 2 |
LA / SC |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Eye oedema,
Injection site oedema,
Injection site reaction,
Skin ulcer,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Albuterol, Nasonex, Ditrol LA Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: PT to f/u with allergy specialist and lab testing. CDC Split Type:
Write-up: Pt seen for Immunization administration. Returned to office 15 minutes later with swelling around eyes, 6cm diameter red, swelling, slight edema, around Varivax injection site, and few scattered urticarial lesions. Given Dexamethasone, Benadryl, Epi on hand. PT watches about 4 hours office released home. |
|
| VAERS ID: |
265857 (history) |
| Form: |
Version 1.0 |
| Age: |
1.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-10-27 |
| Onset: | 2006-10-28 |
| Days after vaccination: | 1 |
| Submitted: |
2006-10-30 |
| Days after onset: | 2 |
| Entered: |
2006-11-02 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U217UEA / 1 |
RL / - |
| MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
1091F / 1 |
LA / - |
Administered by: Private Purchased by: Public Symptoms: Injection site rash SMQs:, Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Tylenol Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: Allergy Testing CDC Split Type:
Write-up: Rash around inj site and on buttocks. Treated with Benadryl. |
|
| VAERS ID: |
267049 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2006-11-14 |
| Onset: | 2006-11-15 |
| Days after vaccination: | 1 |
| Submitted: |
2006-11-16 |
| Days after onset: | 1 |
| Entered: |
2006-11-17 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2243AA / 5 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Erythema,
Feeling hot,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Flovent, Albuterol Current Illness: NONE Preexisting Conditions: Allergies to feathers, animals Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Thirty-six hours following injection noted redness, swelling and warmth progressing over next 12 hours. No fever, systemic signs of illness. |
|
| VAERS ID: |
267300 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-11-13 |
| Onset: | 2006-11-14 |
| Days after vaccination: | 1 |
| Submitted: |
2006-11-15 |
| Days after onset: | 1 |
| Entered: |
2006-11-20 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
2F601511 / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Medication error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Post joint replacement 10/23/06 Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt received 2 influenza shots 5 days apart. No adverse symptoms, signs. 1st shot received 11/8/06 during home care visit. 2nd flu shot given 11/13/06 instead of Pneumonia shot, as had been planned. Vaccine was prepared by this writer and administered by home care RN. Error noted 11/14/06. Pt received Pneumonia shot next visit. |
|
| VAERS ID: |
268128 (history) |
| Form: |
Version 1.0 |
| Age: |
1.01 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-11-30 |
| Onset: | 2006-11-30 |
| Days after vaccination: | 0 |
| Submitted: |
2006-12-01 |
| Days after onset: | 1 |
| Entered: |
2006-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC21B056AA / 3 |
LL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U220FA / 2 |
RL / IM |
| HIBV: HIB (ACTHIB) / SANOFI PASTEUR |
UE946AA / 3 |
LL / IM |
| PNC: PNEUMO (PREVNAR) / PFIZER/WYETH |
B08503B / 3 |
RL / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Coma,
Condition aggravated,
Febrile convulsion,
Hypoventilation,
Respiratory disorder,
Sluggishness,
Strabismus,
Tachycardia,
Vomiting,
White blood cell count increased SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Acute central respiratory depression (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ocular motility disorders (narrow), Generalised convulsive seizures following immunisation (narrow), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Dehydration (broad), Hypokalaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No Previous Vaccinations: Other Medications: none Current Illness: None Preexisting Conditions: Febrile seizure history Birth HX: F/T vaginal, no complications. PMH: febrile seizures 8/06. Allergies: Diagnostic Lab Data: LABS: EEG was WNL. Blood cultures neg. Labs at initial hospital revealed WBC 24.1 CDC Split Type: 20061201
Write-up: Immunized yesterday after pe, last night 20 minutes after going to bed breathing funny, in emesis, unresponsive. Called 911. 73% O2 100% . Transport uneventful. Unresponsive to painful stimuli.T 98.9 at ER. O2 83% on room air. Resp shallow.Eyes deviated & sluggish to react. Tachycardiac @180. CXR nl. UA glucose. BS 171. Intubated.Ativan & rocephin admin. Then grand mal seizure. Improved after 20 min. WBC 20.10.Extubated prior to transfer. Transfered to hospital. "fine" "stable" Hx febrile seizure in past. 12/19/06 Received medical records from 2nd hospital which reveal patient admitted 12/1/06-12/2/06. At initial hospital patient was found to be actively seizing & was treated and transferred to PICU. Temp 102.5 on admit. Neuro exam at 2nd hospital found WNL & no further seizure activity noted. To be followed by peds neuro outpatient & have repeat MRI. Final DX: Febrile seizure. |
|
| VAERS ID: |
269019 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2006-12-14 |
| Entered: |
2006-12-18 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Anaphylactic reaction SMQs:, Anaphylactic reaction (narrow), Anaphylactic/anaphylactoid shock conditions (narrow), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: 200603455
Write-up: Seriousness criteria other medically significant (OMIC). Initial information received on 11 December 2006 from another manufacturer (no reference number provided). The information was originally provided to the other manufacturer by a health care professional. A patient (gender and birth date not reported) received a dose of influenza vaccine 20 years ago. The trade number, manufacturer and lot number were not reported. An unspecified amount of time later, the patient experienced an anaphylactic reaction. Per the reporter, no other information was available at the time of this report. It was not reported whether the patient recovered from the event. |
|
| VAERS ID: |
269039 (history) |
| Form: |
Version 1.0 |
| Age: |
82.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2006-11-14 |
| Onset: | 2006-11-14 |
| Days after vaccination: | 0 |
| Submitted: |
2006-12-13 |
| Days after onset: | 29 |
| Entered: |
2006-12-18 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
72008 / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0485F / UNK |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Chills,
Erythema,
Hyperhidrosis,
Lymphoedema SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Retroperitoneal fibrosis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Aspirin, Actonel, Lipotor,Noscor, retoprolol Current Illness: NONE Preexisting Conditions: No allergies, history of arteriosclerotic heart disease, prostate cancer Allergies: Diagnostic Lab Data: Patient has history cardiac cath Right anti-colital approach in distant past. CDC Split Type:
Write-up: Chills, sweats, erythema at shot site and lymphedema of entire Right upper arm. |
|
| VAERS ID: |
269040 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2006-11-22 |
| Onset: | 2006-11-23 |
| Days after vaccination: | 1 |
| Submitted: |
2006-12-16 |
| Days after onset: | 23 |
| Entered: |
2006-12-18 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA240AA / UNK |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0485F / 2 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Erythema,
Pain,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Lexapro, Lipitor, San Palmetto. Current Illness: NONE Preexisting Conditions: Macular degeneration Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Severe swelling, redness, pain at injection site accompanied by shaking rigors. (I did not see the patient, he described these symptoms to me on 12/8/06). |
|
| VAERS ID: |
273638 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-12-18 |
| Onset: | 2007-01-17 |
| Days after vaccination: | 30 |
| Submitted: |
2007-03-05 |
| Days after onset: | 47 |
| Entered: |
2007-03-08 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2164AA / UNK |
LA / - |
Administered by: Private Purchased by: Other Symptoms: Body temperature increased,
Diplopia,
Dysarthria,
Dysphagia,
Guillain-Barre syndrome,
Hypoaesthesia,
Intensive care,
Life support,
Mobility decreased,
Muscular weakness,
Neurological examination,
VIIth nerve paralysis SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Guillain-Barre syndrome (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Demyelination (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Hearing impairment (broad), Ocular motility disorders (broad), Respiratory failure (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow), Sexual dysfunction (broad)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 42 days
Extended hospital stay? Yes Previous Vaccinations: Other Medications: UNK Current Illness: NONE Preexisting Conditions: NONE records received 3/19/07-PMH:Hypothyroidism. Telangiectasia. Hyperlipidemia. Migraines. Depression. COPD. Allergies: Diagnostic Lab Data: Neurology Exam records received 3/19/07-CBC:normal. Sed rate 55. IGA deficiency. CSF glucose 62, protein 35, Streptococcal antigen negative. ANA titer 1:40 and RPR nonreactive. CSF cultures negative and lyme serology negative. MRI of brain negative. CXR negative. Barium swallow: showed a very weak swallow with evidence of penetration and this patient is at risk for aspiration. CDC Split Type:
Write-up: Onset 1/17/07 of weakness in legs ("rubbery feeling"), numbness in hands progressing to biceps - T-102 - neuro consult with diagnosis of Sensory Guillain Barre - in ICU on ventilator and receiving IVIG. In rehab 2-5 ---$g 2-28-07: discharged with diplopia; right 7th cranial nerve palsy; dysarthria; dysphagia and decreased mobility. 03/19/07-records received from facility for DOS-01/18/07-02/01/07 and acute rehabilitation from 02/05-02/28/07 DC DX: Guillain Barre Syndrome DC DX: Neurological disorder with acute inflammatory demyelinating polyneuropathy "Guillain-Barre Syndrome". Right VII cranial nerve palsy. Diplopia. Dysphagia. Dysarthria. Steroid versus ICU psychosis, resolved. Depression/Anxiety. Pulmonary issues, status post pneumonia, History of COPD and pulmonary involvment of AIDP. Decreased mobility. Decreased ADL. Admission to acute inpatient rehabilitation. Presented with C/O numbness in hands and weakness in legs. Noted a slight cough running nose and watery eyes recently. Temp of 102. Admitted. Continued to have muscular weakness, ataxia and difficulty with ambulation. Intubated and extubated. |
|
| VAERS ID: |
278822 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2006-12-01 |
| Onset: | 2007-01-01 |
| Days after vaccination: | 31 |
| Submitted: |
2007-05-14 |
| Days after onset: | 132 |
| Entered: |
2007-05-16 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / UN |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
- / UNK |
- / SC |
Administered by: Other Purchased by: Other Symptoms: Headache,
Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: (therapy unspecified) NEXIUM Current Illness: Hypersensitivity Preexisting Conditions: Fibromyalgia Allergies: Diagnostic Lab Data: None CDC Split Type: WAES0704USA02200
Write-up: Information has been received from a 68 year old female consumer with "hypersensitivity to many products" and a history of fibromyalgia in December 2006, was vaccinated SC with a dose of Zostavax. Concomitant vaccination included influenza virus vaccine (unspecified). Other concomitant therapy included Nexium and "thyroid medications". In January 2007, the patient experienced radiating pain from spinal column and headache. At the time of report the patient was not recovered from symptoms. No diagnostic laboratory procedures were undertaken. A product quality complaint was not involved. Additional information has been requested. |
|
| VAERS ID: |
294484 (history) |
| Form: |
Version 1.0 |
| Age: |
50.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2007-10-18 |
| Onset: | 2007-10-19 |
| Days after vaccination: | 1 |
| Submitted: |
2007-10-20 |
| Days after onset: | 1 |
| Entered: |
2007-10-25 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
80682 / 1 |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0698U / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Erythema nodosum,
Injection site reaction SMQs:, Hypersensitivity (narrow), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Advair; Lo/Ovral; Albuterol Current Illness: None Preexisting Conditions: Allergy: Pen. Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Erythema Nodosum Syndrome at site of injection ((R) upper arm) ? if this due to shot. |
|
| VAERS ID: |
297309 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2007-11-07 |
| Onset: | 2007-11-07 |
| Days after vaccination: | 0 |
| Submitted: |
2007-11-14 |
| Days after onset: | 7 |
| Entered: |
2007-11-19 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2492AA / 7+ |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
1344U / 2 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Body temperature increased,
Chills,
Headache,
Injection site swelling,
Injection site warmth,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Pt received annual Flu Shot and pneumovax at approx noon on 11/7. felt until dinner time when he began developing shaking chills, temperatures to 102-103 degrees F, severe headache, and his left deltoid became swollen red hot where injections were given. Symptoms lasted 48 hours. |
|
| VAERS ID: |
297411 (history) |
| Form: |
Version 1.0 |
| Age: |
30.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2007-11-12 |
| Onset: | 2007-11-14 |
| Days after vaccination: | 2 |
| Submitted: |
2007-11-20 |
| Days after onset: | 6 |
| Entered: |
2007-11-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA032AA / 1 |
LA / UN |
Administered by: Private Purchased by: Private Symptoms: Erythema,
Immunisation reaction,
Pruritus,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No concurrent medication Current Illness: Unknown Preexisting Conditions: The subject had no relevant medical history. Allergies: Diagnostic Lab Data: UNK CDC Split Type: A0695439A
Write-up: This case was reported by a healthcare professional and described the occurrence of systemic shot reaction in a 30-year-old male subject who was vaccinated with Flulaval for prophylaxis. The subject had no relevant medical history. There were no concurrent medications. No other vaccinations were administered on the date of receipt of Flulaval. The subject had not previously received a flu shot. On 12 November 2007 at 2:00 p.m., the subject received 1st dose of Flulaval (.5 ml, unknown, left arm). On 14 November 2007, 2 days after vaccination with Flulaval, the subject experienced a systemic reaction which included hives, redness and itching. The healthcare professional considered the events were clinically significant (or requiring intervention). The subject was treated with Benadryl and Claritin. At the time of reporting the events were unresolved. The healthcare professional considered the events were probably related to vaccination with Flulaval. |
|
| VAERS ID: |
297721 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2007-11-15 |
| Onset: | 2007-11-15 |
| Days after vaccination: | 0 |
| Submitted: |
2007-11-26 |
| Days after onset: | 11 |
| Entered: |
2007-11-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2479AA / 2 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Chest discomfort,
Chills,
Cough,
Headache,
Myalgia,
Palpitations,
Pyrexia,
Urticaria SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (narrow), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine administered about 1 pm. "Hives started in the afternoon/, fever, chills, muscle aches. Chest "fill up" almost like an asthma attack, chest congestion, coughing with heart racing lasting about 6 hours." Also developed headache, states gets migraines. |
|
| VAERS ID: |
298738 (history) |
| Form: |
Version 1.0 |
| Age: |
23.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2007-10-23 |
| Onset: | 2007-10-26 |
| Days after vaccination: | 3 |
| Submitted: |
2007-12-05 |
| Days after onset: | 40 |
| Entered: |
2007-12-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2448AA / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Asthenia,
Full blood count,
Injection site erythema,
Laboratory test,
Skin exfoliation SMQs:, Severe cutaneous adverse reactions (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: none~ ()~~0.00~Patient Other Medications: synthroid, methadone Current Illness: none Preexisting Conditions: hypothyroidism Allergies: Diagnostic Lab Data: CBC, CMP drawn today, results are pending. CDC Split Type:
Write-up: Red circle appeared 2-3 days after vaccine administration on Left Deltoid where vaccine was given. Skin changes noted and still evident 6 weeks later. Skin is rough and scaly, no masses or thickening noted at site. No enlarged L axillary nodes. Patient c/o feeling weak for last month. |
|
| VAERS ID: |
301793 (history) |
| Form: |
Version 1.0 |
| Age: |
30.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2007-11-15 |
| Onset: | 2007-11-16 |
| Days after vaccination: | 1 |
| Submitted: |
2008-01-07 |
| Days after onset: | 52 |
| Entered: |
2008-01-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2529AA / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Asthenia,
Fatigue,
Muscular weakness,
Myalgia,
Neuralgic amyotrophy,
Neurological examination abnormal,
Pyrexia,
Radiculitis brachial SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none. PMH: Mono (remote) and pneumonia. Allergies: Diagnostic Lab Data: Neurological exam on November 20, 2007 revealed normal tendon reflexes in the legs, diminished in arms. Electric reflex stimulation demonstrated conduction velocities in normal range. Clinical exam demonstrated complete loss of resistance to pull in distal flexors of left thumb and first 2 fingers, weakness on right side. Labs and Diagnostics: EMG and NCS 11/20/07 normal. H.pylori (-). CBC, UA and Chem WNL. CDC Split Type:
Write-up: Received Flu shot on November 15, 2007. Developed fever that night. On November 16, had fever and generalized muscle soreness, most pronounced in shoulders. November 17 and 18: progressive loss of strength and motor function in the hands, fatigue, continued fever and increasing muscle soreness. November 18th: fever resolved, but saw physician at clinic for continued soreness, fatigue, and loss of motor function in the hands. Referred to Neurology on November 20. Diagnosed with Parsonage-Turner Syndrome (acute brachial neuritis). Motor function in hands resolved without treatment within 2 weeks following visit with Dr., with minor residual weakness. Fatigue continued to present. 01/18/2008 MR received for Clinic visits 11/18/07 and 1/02/2008. Pt c/o fever, bil hand pain initially then hips and ankles, and muscle weakness. Weakness to hands (L$gR) noted on PE. Reflexes 1+ in upper extremities, 2+ lower. Seen by neurology 11/20/07 for EMG and NCS DX: Acute Brachial Neuritis. Seen again 01/02/08 with fatigue and nausea since visit in Nov. Exam WNL. Impression: Nausea, Possible GERD, Fatigue |
|
| VAERS ID: |
329616 (history) |
| Form: |
Version 1.0 |
| Age: |
15.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-10-22 |
| Onset: | 2008-10-22 |
| Days after vaccination: | 0 |
| Submitted: |
2008-10-22 |
| Days after onset: | 0 |
| Entered: |
2008-10-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2829AA / 1 |
LA / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AHAVB247AA / 1 |
RA / IM |
| MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR |
U273AA / 1 |
LA / IM |
| TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC52B020AA / UNK |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Grand mal convulsion,
Scan brain SMQs:, Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: PAMPRIN given 10/21/08 Current Illness: Preexisting Conditions: Chronic functional abdominal pain Allergies: Diagnostic Lab Data: CT Head CDC Split Type:
Write-up: Patient had clonic / tonic seizure lasting aproximately 60 seconds. |
|
| VAERS ID: |
329906 (history) |
| Form: |
Version 1.0 |
| Age: |
79.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-10-15 |
| Onset: | 2008-10-17 |
| Days after vaccination: | 2 |
| Submitted: |
2008-10-21 |
| Days after onset: | 4 |
| Entered: |
2008-10-24 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA207AA / UNK |
RA / UN |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C2938AA / UNK |
LA / UN |
Administered by: Private Purchased by: Public Symptoms: Hypersensitivity,
Injection site erythema,
Injection site pruritus,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Herpes zoster Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Per pt began as intense itching 2 days after w/ progressive redness to site. Seen today by MD - dx''d w/ allergic urticaria redness decreased to 3" area below deltoid and itching gone. |
|
| VAERS ID: |
330842 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-10-22 |
| Onset: | 2008-10-23 |
| Days after vaccination: | 1 |
| Submitted: |
2008-10-24 |
| Days after onset: | 1 |
| Entered: |
2008-10-31 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2829AA / 1 |
RA / IM |
| TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC14B06AA / 1 |
RA / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site pain,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Red hot deltoid 180 degrees around. Not circumferential; Tender to palp. Started 24 hrs after shot given Tdap. |
|
| VAERS ID: |
331418 (history) |
| Form: |
Version 1.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-10-31 |
| Onset: | 2008-10-31 |
| Days after vaccination: | 0 |
| Submitted: |
2008-11-05 |
| Days after onset: | 5 |
| Entered: |
2008-11-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
01849111A / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Cough,
Diarrhoea,
Wheezing SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Noninfectious diarrhoea (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Patient did not seek medical treatment. CDC Split Type: NH0814
Write-up: Patient c/o wheezing and coughinin that started within three hours after the immunization. She also states that she had mild diarrhea for the following two days. |
|
| VAERS ID: |
331854 (history) |
| Form: |
Version 1.0 |
| Age: |
40.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-06 |
| Onset: | 2008-11-06 |
| Days after vaccination: | 0 |
| Submitted: |
2008-11-10 |
| Days after onset: | 4 |
| Entered: |
2008-11-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
87877 / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pain in arm where the injection was given. Tx=Ibuprofen - one time 400mg. Hurt for 3 days. |
|
| VAERS ID: |
331884 (history) |
| Form: |
Version 1.0 |
| Age: |
0.83 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2008-11-07 |
| Onset: | 2008-11-07 |
| Days after vaccination: | 0 |
| Submitted: |
2008-11-10 |
| Days after onset: | 3 |
| Entered: |
2008-11-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2783CA / 1 |
LL / IM |
Administered by: Private Purchased by: Public Symptoms: Immediate post-injection reaction,
Pyrexia,
Rash SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: High fever (103) 10 mins after injection with rash shortly therafter |
|
| VAERS ID: |
331995 (history) |
| Form: |
Version 1.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-04 |
| Onset: | 2008-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2008-11-10 |
| Days after onset: | 6 |
| Entered: |
2008-11-11 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AALLA154AA / UNK |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Activities of daily living impaired,
Body temperature increased,
Chills,
Hyperhidrosis,
Myalgia,
Pain SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Dementia (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: TEMP~Influenza (Seasonal) (no brand name)~1~27.00~In Patient Other Medications: NONE Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Started with muscle aches, temperature @ 11pm was 103.8 degrees decreased 101.8 degrees with Tylenol, started having aches and chills, started sweating, continued with muscle aches and unable to get out of bed next day. |
|
| VAERS ID: |
332104 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2008-11-04 |
| Onset: | 2008-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2008-11-12 |
| Days after onset: | 8 |
| Entered: |
2008-11-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Private Purchased by: Unknown Symptoms: Asthenia,
Pain,
Pyrexia,
Upper respiratory tract congestion,
Wheezing SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none. Preexisting Conditions: none. Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Received flu vaccine at 3:30 p.m., felt chest congestion/wheezing by 5:30 p.m., high fever, weakness and genaeral body aches by 8:30 p.m., fever broke by 3:00 a.m. |
|
| VAERS ID: |
332958 (history) |
| Form: |
Version 1.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-11 |
| Onset: | 2008-11-12 |
| Days after vaccination: | 1 |
| Submitted: |
2008-11-20 |
| Days after onset: | 8 |
| Entered: |
2008-11-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA386AA / 1 |
RA / UN |
Administered by: Private Purchased by: Private Symptoms: Body temperature increased,
Cough,
Influenza like illness,
Pain SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Flu symptoms~Influenza (Seasonal) (no brand name)~1~40.00~In Sibling Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: ! day after receiving vaccine, had symptoms of achiness, flu-like symptoms, temperature 100.1(1 hour after TYLENOL) dry hackey cough. Put on antibiotics, ZITHROMAX 250mg by mouth times 7 days( 5days after vaccine administered. Patients brother had similar reaction). |
|
| VAERS ID: |
333287 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-11 |
| Onset: | 2008-11-12 |
| Days after vaccination: | 1 |
| Submitted: |
2008-11-25 |
| Days after onset: | 13 |
| Entered: |
2008-11-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None, but did have a UTI two weeks prior and was on Keflex for 10 days Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: My daughter had the LAIV (nasal spray) and had a severe reaction - hives from her head to her toes. She needed to be on steroids to bring relief. Not sure if doctor reported this reaction. |
|
| VAERS ID: |
337558 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-25 |
| Onset: | 2008-11-26 |
| Days after vaccination: | 1 |
| Submitted: |
2008-11-26 |
| Days after onset: | 0 |
| Entered: |
2008-12-18 |
| Days after submission: | 22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
IN500561P / UNK |
NS / IN |
Administered by: Public Purchased by: Public Symptoms: Chills,
Oropharyngeal pain,
Pyrexia,
Rhinorrhoea,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug (s) Not Reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0007561
Write-up: A non-serious spontaneous report of fever, vomiting, chills sore throat, and runny nose has been received from a nurse concerning a four- year old female subsequent to FLUMIST. This case is submitted in accordance with MedImmune''s post-marketing commitment on accelerated reporting for the newly indicated population of 2 years to 59 months of age for FLUMIST. Neither past medical history nor concomitant medications were reported. The patient received FLUMIST on 25-Nov-2008. The patient woke up on 26-Nov-2008 with a fever, vomiting, chills, sore throat, and runny nose. The outcome was not reported. The events of fever, vomiting, chills, sore throat, and runny nose resolved on approximately 03-Dec-2008, within one week after the onset of the events. Additional information received 08-Jan-2009 and incorporated into the case outcome and resolution date. |
|
| VAERS ID: |
337139 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-10-21 |
| Onset: | 2008-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2008-12-03 |
| Days after onset: | 43 |
| Entered: |
2009-01-13 |
| Days after submission: | 41 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U2787EA / 7+ |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Agitation,
Burning sensation,
Diarrhoea,
Hyperhidrosis,
Insomnia,
Lymphadenopathy,
Pruritus SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Pseudomembranous colitis (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Hypersensitivity (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Trazodone; Methacarbenol Current Illness: None Preexisting Conditions: Injectable iron; Celiac Disease; Fibromyalgia Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Burning itch over upper body, extremities + bottoms of feet. Felt very "hyper" "wired". Difficulty sleeping that night, diarrhea, sweats, swollen axillary lymph nodes. Symptoms resolved after 72 hours. |
|
| VAERS ID: |
337506 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2008-11-05 |
| Onset: | 2008-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2009-01-13 |
| Days after onset: | 69 |
| Entered: |
2009-01-15 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
02449111A / UNK |
RA / IM |
| TD: TD ADSORBED (TDVAX) / MASS. PUB HLTH BIOL LAB |
TD199 / UNK |
LA / IM |
Administered by: Private Purchased by: Unknown Symptoms: Chills,
Fatigue,
Myalgia,
Tremor SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Severe Shaking Chills myalgias for several hours. Resolved spontaneously. Fatigued the next day. |
|
| VAERS ID: |
338770 (history) |
| Form: |
Version 1.0 |
| Age: |
51.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-01-13 |
| Onset: | 2009-01-13 |
| Days after vaccination: | 0 |
| Submitted: |
2009-01-16 |
| Days after onset: | 3 |
| Entered: |
2009-02-02 |
| Days after submission: | 17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
89980 / 1 |
LA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C2865AA / 1 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Chills,
Muscle spasms,
Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dystonia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Began 5 hour after injcetion Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fever, Chills, and cramps, vomiting |
|
| VAERS ID: |
349532 (history) |
| Form: |
Version 1.0 |
| Age: |
1.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-03-18 |
| Onset: | 2009-03-28 |
| Days after vaccination: | 10 |
| Submitted: |
2009-06-18 |
| Days after onset: | 82 |
| Entered: |
2009-06-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT2792FA / 2 |
LL / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AHAVB329CA / 1 |
RL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
1506X / 1 |
LL / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
1397X / 1 |
RL / SC |
Administered by: Private Purchased by: Other Symptoms: Erythema,
Rash generalised,
Rash papular,
Rash pruritic,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: Conjunctivitis Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pt father reported "it looked like hives all over" - Rash-1wk- after MMR II, VARIVAX, HAVRIX given. Red itchy papules 2mm-1cm varying site and location. Lasted 1mo. No resp sx. No intercurrent illness. |
|
| VAERS ID: |
355575 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2008-11-25 |
| Onset: | 2008-11-26 |
| Days after vaccination: | 1 |
| Submitted: |
2008-11-26 |
| Days after onset: | 0 |
| Entered: |
2009-08-13 |
| Days after submission: | 259 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500561P / UNK |
NS / IN |
Administered by: Public Purchased by: Public Symptoms: Chills,
Oropharyngeal pain,
Pyrexia,
Rhinorrhoea,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug(s) Not Reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0007559
Write-up: A non-serious report of fever, vomiting, chills, sore throat, and runny nose has been received from a nurse concerning a 10-year-old female, subsequent to FLUMIST. No medical history nor concomitant medications were provided. The patient received FLUMIST on 25-Nov-2008. On the next morning, the patient woke up with symptoms of fever, vomiting, chills, sore throat, and runny nose. Outcome for the events not reported. |
|
| VAERS ID: |
358248 (history) |
| Form: |
Version 1.0 |
| Age: |
25.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-09-21 |
| Onset: | 2009-09-22 |
| Days after vaccination: | 1 |
| Submitted: |
2009-09-24 |
| Days after onset: | 2 |
| Entered: |
2009-09-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA25AA / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: depoprovera Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: pt broke outwith severe hives. Benedryl for treatment. |
|
| VAERS ID: |
359189 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-09-24 |
| Onset: | 2009-09-24 |
| Days after vaccination: | 0 |
| Submitted: |
2009-09-29 |
| Days after onset: | 5 |
| Entered: |
2009-10-02 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3207AA / 2 |
LA / IM |
Administered by: Public Purchased by: Private Symptoms: Chills,
Cough,
Dysphonia,
Dyspnoea,
Emergency care,
Hypersensitivity,
Ocular hyperaemia,
Pyrexia,
Swollen tongue SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Glaucoma (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: None~ ()~~0.00~Patient Other Medications: Zyrtec Current Illness: No illness Preexisting Conditions: Sulfa -$g hives Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Uncontrolled coughing, hoarseness, tongue started swelling, fever & chills, short of breath, red eyes; was seen in emergency dept at Rutland Regional Med Ctr & treated for allergic reaction. |
|
| VAERS ID: |
359654 (history) |
| Form: |
Version 1.0 |
| Age: |
15.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-09-30 |
| Onset: | 2009-09-30 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-06 |
| Days after onset: | 6 |
| Entered: |
2009-10-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
- / UNK |
- / - |
Administered by: Private Purchased by: Public Symptoms: Discomfort,
Erythema,
Facial pain,
Headache,
Oedema,
Rhinalgia SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Glaucoma (broad), Cardiomyopathy (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: no Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: given nasal flu vaccine - had nose pain, felling of needing to sneeze, later medial face discomfort left greater than right, no runny nose, no cough, some headache bilat temples and some throat clearing. Exam 10/6 reveals erythema and edema of nasal mucosa left $g right. treated with nasal steroid spray |
|
| VAERS ID: |
360147 (history) |
| Form: |
Version 1.0 |
| Age: |
45.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-06 |
| Days after onset: | 0 |
| Entered: |
2009-10-08 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA281AA / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Injection site pain,
Injection site swelling,
Oedema peripheral SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: loratadine; KLONIPIN; METHYLIN; PROZOSIN; PEPCID; METFORMIN; ZOCOR; glyburide Current Illness: Preexisting Conditions: Hyperlipidemia; DM; depression/agoraphobic; asthma; allergy-PENICILLIN; TRAMADOL Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Left arm deltoid tenderness, swelling, no redness with some left hand swelling requiring pt to remove ring from 4th digit. 25 mg PO BENADRYL and ice to L arm. |
|
| VAERS ID: |
360749 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-10 |
| Onset: | 2009-10-11 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-14 |
| Days after onset: | 3 |
| Entered: |
2009-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3177AA / 2 |
LL / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site pruritus,
Injection site urticaria SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Premature at 27 weeks gestation Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Woke up itching on legs, hives developed. Patients father denied any difficult with breathing, patient acting well otherwise. Hives improved with Benedryl. |
|
| VAERS ID: |
361365 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-09-23 |
| Onset: | 2009-09-23 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-07 |
| Days after onset: | 14 |
| Entered: |
2009-10-16 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3207AA / 2 |
LA / IM |
Administered by: Public Purchased by: Private Symptoms: Chills,
Cough,
Dry throat,
Hypersomnia,
Pain,
Pain in extremity,
Throat irritation SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Depression (excl suicide and self injury) (broad), Tendinopathies and ligament disorders (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Received flu vax on 9/23/09 @11A, throat started with dry, scratchy throat with cough @ 3p, had chills, went to sleep and slept till next day. had body aches and chills; vax arm was very sore. |
|
| VAERS ID: |
361506 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-01 |
| Onset: | 2009-10-02 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-19 |
| Days after onset: | 17 |
| Entered: |
2009-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUAU56AA / 1 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Musculoskeletal stiffness SMQs:, Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None stated Preexisting Conditions: unknown/ none stated Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/o ring finger and pinky finger stiffness that comes and goes. Has not been to Doctor. |
|
| VAERS ID: |
361988 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-13 |
| Onset: | 2009-10-18 |
| Days after vaccination: | 5 |
| Submitted: |
2009-10-21 |
| Days after onset: | 3 |
| Entered: |
2009-10-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT32531A / 3 |
LL / IM |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500759P / 1 |
NS / IN |
Administered by: Private Purchased by: Public Symptoms: Wheezing SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Asthma/bronchospasm (broad), Eosinophilic pneumonia (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Awoke Wheezing with no previous hx. Given Albuterol Nebulizer treatment and sent home with a machine. Went to ER later that day with increased symptoms |
|
| VAERS ID: |
362862 (history) |
| Form: |
Version 1.0 |
| Age: |
46.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-13 |
| Days after onset: | 6 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Fatigue SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Chiari malformation Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Severe fatigue x 1 day. |
|
| VAERS ID: |
362864 (history) |
| Form: |
Version 1.0 |
| Age: |
33.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-19 |
| Onset: | 2009-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-20 |
| Days after onset: | 1 |
| Entered: |
2009-10-26 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Feeling abnormal,
Feeling jittery,
Headache,
Pallor,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Dementia (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 2005~Influenza (Seasonal) (no brand name)~~29.00~Patient Other Medications: None Current Illness: None Preexisting Conditions: NKDA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Started feeling "jittery" and shakey. Headache, pale - "not felling myself". |
|
| VAERS ID: |
362866 (history) |
| Form: |
Version 1.0 |
| Age: |
24.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-19 |
| Days after onset: | 13 |
| Entered: |
2009-10-26 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Headache,
Pain,
Pyrexia,
Rhinorrhoea SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: PROZAC; VICODIN; BC pills Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Runny nose, achy, headache. It lasted 7 days and running a fever. |
|
| VAERS ID: |
362867 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-13 |
| Days after onset: | 7 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Fatigue SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No Preexisting Conditions: PCN; Codeine; Sulfa Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Sudden on set severe fatigue lasting 3 hrs - better after drinking bottle of mountain dew. |
|
| VAERS ID: |
362868 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-13 |
| Days after onset: | 7 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
RA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Asthenia,
Chills,
Diarrhoea,
Dizziness,
Headache,
Myalgia,
Nausea,
Oropharyngeal pain,
Pain in extremity,
Pyrexia,
Tremor,
Vomiting SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: DILANTIN Current Illness: No Preexisting Conditions: Seizure disorder; NKDA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Started with feeling dizzy, shaky, nausea, weakness, muscle aches, vomiting, diarrhea, sore throat, fever, chills, headache x 5 days. Sore arm. |
|
| VAERS ID: |
362869 (history) |
| Form: |
Version 1.0 |
| Age: |
45.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-13 |
| Days after onset: | 6 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Doxycycline Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: General muscle aching x 2 days. |
|
| VAERS ID: |
362870 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-13 |
| Days after onset: | 7 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Headache,
Myalgia,
Nausea,
Vomiting SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NAPROSYN; LIPITOR; DETROL LA; SYNTHROID Current Illness: None Preexisting Conditions: NKDA; hypothyroid; HTN; cholesterol Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Started with h.a., progressed to N/V and muscle aches x 2 days. |
|
| VAERS ID: |
362871 (history) |
| Form: |
Version 1.0 |
| Age: |
27.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-13 |
| Days after onset: | 6 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Nausea,
Pain SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: General body aching, worse from knees down, nausea. |
|
| VAERS ID: |
362872 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-13 |
| Days after onset: | 6 |
| Entered: |
2009-10-26 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: General body aches. |
|
| VAERS ID: |
362873 (history) |
| Form: |
Version 1.0 |
| Age: |
57.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-08 |
| Onset: | 2009-10-09 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-14 |
| Days after onset: | 5 |
| Entered: |
2009-10-26 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Arthralgia,
Headache,
Myalgia,
Rhinorrhoea SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Hypertension Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Headache, joint & muscle aches. Runny nose. |
|
| VAERS ID: |
362875 (history) |
| Form: |
Version 1.0 |
| Age: |
50.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-06 |
| Onset: | 2009-10-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-14 |
| Days after onset: | 8 |
| Entered: |
2009-10-26 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA456AA / UNK |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Chills,
Headache,
Myalgia,
Pyrexia,
Vomiting SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: DEPAKOTE; levothyroxine Current Illness: None Preexisting Conditions: Seizure disorder; hypothyroid Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Chills, h.a., vomiting, fever 101.9, muscle aches. H.A. lasted 3 days-other sx.-lasted 3 days. |
|
| VAERS ID: |
363299 (history) |
| Form: |
Version 1.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-22 |
| Onset: | 2009-10-26 |
| Days after vaccination: | 4 |
| Submitted: |
2009-10-27 |
| Days after onset: | 1 |
| Entered: |
2009-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1008133P / 1 |
GM / IM |
Administered by: Private Purchased by: Other Symptoms: Drug exposure during pregnancy,
Intra-uterine death,
Skin warm,
Ultrasound scan abnormal,
Vomiting SMQs:, Acute pancreatitis (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Prenatal vitamins Current Illness: Patient denied Preexisting Conditions: None-pregnancy. Allergies: NKDA Allergies: Diagnostic Lab Data: Ultrasound x 2 confirms diagnosis. Labs: Antibody screen, VDRL, Hepatitis B and C negative, Chlamydia and Gonorrhea screening negative Dx studies: Doppler, US CDC Split Type:
Write-up: 10/5/09 Seasonal flu vaccine. 10/14/09 Normal prenatal exam. 10/20/09 to 10/22/09 AM vomiting, "felt a little warm". 10/22/09 H1N1-afebrile. 10/26/09 Fetal demise at 30 5/7 weeks. 10/29/2009 hospital records for 10/26/-10/27/2009. patient at at 30 5/7 wks gestation, presented with c/o''s decreased fetal movement, hx of nausea/vomiting x 2 days which resolved. Per doppler and ultrasound no FHR noted, no amniotic fluid around the baby noted. Tx: induced labor with Misoprostol/epidual anesthesia. Autopsy requested. DC DX Intrauterine Death Unspecified ICD-9 Code 656.40 |
|
| VAERS ID: |
364021 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-27 |
| Onset: | 2009-10-28 |
| Days after vaccination: | 1 |
| Submitted: |
2009-10-30 |
| Days after onset: | 2 |
| Entered: |
2009-10-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Fatigue,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Student takes no medication, to my knowledge. I am unaware if the student had any other vaccines within 4 weeks. I have not notified the family of this report. I have notified the MD. Current Illness: Did not appear to be ill. Preexisting Conditions: N/A Allergies: Diagnostic Lab Data: At time of report I believe the student is at home resting and recovering and will be returning to school on Monday. CDC Split Type:
Write-up: Teacher noted fatigue in the AM. Fever checked at noon--103.3. Student was sent home with family for rest and care. MD notified and VDH called to inquire if this report was required. They advised "Yes." |
|
| VAERS ID: |
364228 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-29 |
| Onset: | 2009-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-01 |
| Days after onset: | 3 |
| Entered: |
2009-11-02 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Nausea,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Reported feeling nauseous following vaccination and then fainted. Responsive within minutes, cold compress applied to forehead. Remained supine for approx. 30 minutes then returned to classroom. |
|
| VAERS ID: |
364870 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-27 |
| Onset: | 2009-10-28 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-03 |
| Days after onset: | 6 |
| Entered: |
2009-11-04 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP10AA / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Fever~ ()~UN~0.00~Patient Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: 10/28/09-vomiting in evening. OK next day. 10/30/09-fever 103 degrees in evening-OK next day. |
|
| VAERS ID: |
364922 (history) |
| Form: |
Version 1.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-21 |
| Onset: | 2009-10-25 |
| Days after vaccination: | 4 |
| Submitted: |
2009-10-29 |
| Days after onset: | 4 |
| Entered: |
2009-11-04 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (UNKNOWN)) / UNKNOWN MANUFACTURER |
- / UNK |
UN / UN |
Administered by: Public Purchased by: Unknown Symptoms: Arthralgia,
Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: CELEXA; ibuprofen; mvi; O3; NEXIUM; PREMPRO; calcium Current Illness: None Preexisting Conditions: GERD; osteoarthritis; depression; migraines Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Significant muscle aches (myalgia) and joint pain of all joints: lasted 48 hrs. (gradual onset). Peaked during the night 10/25/09 until AM. Called MD, rec NSAIDS-call if worsened. |
|
| VAERS ID: |
364938 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-23 |
| Onset: | 2009-10-23 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-27 |
| Days after onset: | 4 |
| Entered: |
2009-11-04 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP001AA / 1 |
RL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3210AA / 4 |
LL / IM |
Administered by: Private Purchased by: Public Symptoms: Rash,
Urticaria,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Vacterl syndrome Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Vomited about 10 min. after vaccine and continued to vomit intermittently for 5 hrs. Developed hive-like rash on trunk and extremities within 1 hour of vaccine which persisted about 5 hrs. |
|
| VAERS ID: |
365047 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-26 |
| Onset: | 2009-10-26 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-26 |
| Days after onset: | 0 |
| Entered: |
2009-11-04 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Fall,
Muscle twitching SMQs:, Dyskinesia (broad), Dystonia (broad), Accidents and injuries (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Child received H1N1 vaccine, #1 dose, at 10:15 AM. Within 5 minutes patient dropped to the floor. This was not witnessed by an adult. Once observed by adult, within a minute, observer noted minor twitching of upper extremities. Heart rate was 80-88. |
|
| VAERS ID: |
365156 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-03 |
| Onset: | 2009-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-04 |
| Days after onset: | 1 |
| Entered: |
2009-11-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Headache,
Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: One hour after receiving vaccination had a headache. Reported to school nurse, rested and returned to class. Later in day around 2:30 PM experienced left sided numbness in arm and leg. Home at 2:45 reported numbness symptoms to parent who called primary physician. Parent instructed to take child to ED at local hospital. At Southwestern VT Medical Center, child seen in ED with continued left sided numbness in arm and leg. Vital signs & temp within normal limits. ED physician examined child and parent told no abnormal neurological symptoms found. Child released to home. On 11/04/09, child still experiencing left sides numbness in upper leg but not arm. Child returned to school 11-/4/09. Preexisting Conditions: NKA Allergies: Diagnostic Lab Data: Vital signs and temperature No tests done according to parent CDC Split Type:
Write-up: Headache one hour after vaccination, numbness left arm & leg 2:30 PM evaluation by ED physician No treatment |
|
| VAERS ID: |
365856 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-06 |
| Onset: | 2009-11-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-07 |
| Days after onset: | 1 |
| Entered: |
2009-11-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Chills,
Nausea,
Pyrexia,
Thirst,
Vomiting projectile SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fever, cold chills, nausea, excessive unquenchable thirst, projectile vomiting. |
|
| VAERS ID: |
366009 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-04 |
| Onset: | 2009-11-08 |
| Days after vaccination: | 4 |
| Submitted: |
2009-11-09 |
| Days after onset: | 1 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (UNKNOWN)) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Cough,
Pyrexia SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: no Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Cough, fever of 101.8, lethargy, cough syrup and Motrin. |
|
| VAERS ID: |
366010 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-04 |
| Onset: | 2009-11-05 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-09 |
| Days after onset: | 4 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (UNKNOWN)) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Cough,
Pyrexia,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies - dust mites, cats Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fever of 102.00, cough, vomiting. |
|
| VAERS ID: |
366013 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-05 |
| Onset: | 2009-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 4 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP008AA / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Oropharyngeal pain,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none reported Current Illness: none known Preexisting Conditions: no known allergies or pre-existing conditions Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Approximately 4 hours post vaccine, parent reports c/o sore throat. Fever (101-102F) developed, persisting to next day (none in early am, then recurrence around 10am 11/6), treated with Tylenol by family. h/o family illnesses earlier in the week. |
|
| VAERS ID: |
366015 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-05 |
| Onset: | 2009-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 4 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP008AA / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none known Current Illness: none known. h/o family illness earlier in the week Preexisting Conditions: none known Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: c/o nausea several hours following vaccine administration. Rest, sips of water, gradually resolved. |
|
| VAERS ID: |
366020 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-05 |
| Onset: | 2009-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 4 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP008AA / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Flushing,
Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: no Preexisting Conditions: receiving regularly scheduled allergy shots Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Facial flushing and sensed diffuse itching. No hives or rash. Treated with one dose of diphenhydramine (reaction consistent with response to allergy shots, and treatment chosen was usual treatment for those occurences) with no recurrence. |
|
| VAERS ID: |
366071 (history) |
| Form: |
Version 1.0 |
| Age: |
51.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-29 |
| Onset: | 2009-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-29 |
| Days after onset: | 0 |
| Entered: |
2009-11-09 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / UNK |
UN / UN |
Administered by: Other Purchased by: Public Symptoms: Injection site pruritus,
Injection site urticaria,
Pruritus generalised,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: Possible exposure to virus but no symptoms until after vaccine Preexisting Conditions: No Allergies: Diagnostic Lab Data: None performed CDC Split Type:
Write-up: Hives and itching on left arm from hand up (injection arm). Itching on face, L side. BENADRYL 50 mg PO with relief. |
|
| VAERS ID: |
366177 (history) |
| Form: |
Version 1.0 |
| Age: |
34.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-29 |
| Onset: | 2009-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 11 |
| Entered: |
2009-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1008133P / 1 |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Rash erythematous,
Throat tightness,
Wheezing SMQs:, Anaphylactic reaction (narrow), Angioedema (broad), Asthma/bronchospasm (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Severe persistent asthma; GERD; PCN; erythromycin; neomycin; NOROXIN; cephalosporins; sulfa; latex Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Red, raised all over body rash. Throat felt a little tight. Some wheezing. Over the course of 6 hours, 150 mg of BENADRYL taking to relieve symptoms. Prednisone 60 mg for 2 days, 40 mg 2 days, 20 mg for 3 days. |
|
| VAERS ID: |
366369 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-04 |
| Onset: | 2009-11-05 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-06 |
| Days after onset: | 1 |
| Entered: |
2009-11-10 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP008AA / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Hydrochlorothiazide Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Rash-upper torso red, flat, discrete, round lesions; began morning after, non-itching, no treatment. Hx similar episode with medication change-BP meds. |
|
| VAERS ID: |
366424 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-04 |
| Onset: | 2009-11-04 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-04 |
| Days after onset: | 0 |
| Entered: |
2009-11-10 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP008AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Body temperature increased,
Dry skin,
Headache,
Malaise,
Skin warm SMQs:, Neuroleptic malignant syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: EPIPEN prn; fluoride Current Illness: None reported Preexisting Conditions: Peanut allergies; tree nut allergies Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient received the vaccine at 11:00 AM. At 12:00 PM reports to school nurse that he felt "sick". Temp 102 degrees F, skin warm and dry, alert and oriented x 3. RR=28, pulse=120. Denies difficulty breathing or swallowing. No localized reaction at injection site. No hives. Complains of headache. Has a history of peanut allergies. |
|
| VAERS ID: |
367431 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-06 |
| Onset: | 2009-11-06 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-13 |
| Days after onset: | 7 |
| Entered: |
2009-11-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP013AA / 1 |
UN / IM |
Administered by: Other Purchased by: Unknown Symptoms: Muscle spasms,
Pain SMQs:, Dystonia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: N/A Preexisting Conditions: Crohns Disease Allergies: Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Cramps on the front side of upper thighs for four consecutive days. Pain level - moderate to severe. |
|
| VAERS ID: |
367931 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-13 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-16 |
| Entered: |
2009-11-17 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / UNK |
LA / UN |
Administered by: Public Purchased by: Other Symptoms: Inappropriate schedule of drug administration,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student received dose 2 with this clinic within 21 days of receiving prior H1N1 vaccine per mother of student. Verbal decline form parent failed to be reinforced with paperwork: consent did not get removed. Per mom and school nurse student never showed signs or an adverse reaction to date of form being completed. |
|
| VAERS ID: |
367990 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-09 |
| Onset: | 2009-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 0 |
| Entered: |
2009-11-17 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
- / IM |
Administered by: Public Purchased by: Unknown Symptoms: Feeling hot,
Immediate post-injection reaction,
Pallor SMQs:, Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student became hot/pale immediately after injection. He was given a cool towel for his fore head and put his head between his legs x5 min. Regained normal - temp color within 10 min. |
|
| VAERS ID: |
367991 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-09 |
| Onset: | 2009-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2009-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Erythema,
Headache,
Local swelling,
Pruritus SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Local swelling, redness, itching. Cold pack applied w/ some relief. Some headache. |
|
| VAERS ID: |
367992 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-09 |
| Onset: | 2009-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 0 |
| Entered: |
2009-11-17 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP01017AA / 1 |
AR / IM |
Administered by: Public Purchased by: Unknown Symptoms: Abdominal pain upper SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Stomach hurts. |
|
| VAERS ID: |
367996 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-09 |
| Onset: | 2009-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-09 |
| Days after onset: | 0 |
| Entered: |
2009-11-17 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
AR / IM |
Administered by: Public Purchased by: Unknown Symptoms: Chest pain,
Immediate post-injection reaction,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pat said she felt shaky and her chest hurt immediately after injection. No complaints weaken 20 min after injection. |
|
| VAERS ID: |
368039 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2009-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / 1 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Nausea,
Pallor,
Vertigo SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow), Hypotonic-hyporesponsive episode (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: - Vertigo, pallor, nausea x 1/2 hr. - Emergency Technician attended to Pt - offered juice -Pt returned to class approx 1/2 hr after injection. |
|
| VAERS ID: |
368043 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-13 |
| Entered: |
2009-11-17 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
UN / IM |
Administered by: Public Purchased by: Public Symptoms: Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea - short duration recovered. |
|
| VAERS ID: |
368097 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-09 |
| Entered: |
2009-11-17 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
AR / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Headache,
Immediate post-injection reaction SMQs:, Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient complained of a headache immediately after injections. Had water/rest. No complaints after 20 min. |
|
| VAERS ID: |
368108 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-12 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-13 |
| Entered: |
2009-11-17 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / 1 |
LL / IM |
Administered by: Other Purchased by: Public Symptoms: SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Novartis vaccine administered to 3 yo. Manufacturer''s insert states to be used for children 4 and older, i.e. as off-label use. |
|
| VAERS ID: |
368110 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-12 |
| Onset: | 2009-11-12 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-13 |
| Days after onset: | 1 |
| Entered: |
2009-11-17 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient complained of itchy ear, head, neck 15 minutes post vaccine observed for additional 15 minutes and the itchiness had resolved. |
|
| VAERS ID: |
368118 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-13 |
| Entered: |
2009-11-17 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
UN / IM |
Administered by: Public Purchased by: Public Symptoms: Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea - rested recovered |
|
| VAERS ID: |
368120 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-13 |
| Onset: | 2009-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-13 |
| Days after onset: | 0 |
| Entered: |
2009-11-17 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Malaise,
Nausea,
Vertigo SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vertigo; nausea. One hour later still not feeling well-school nurse sending home. |
|
| VAERS ID: |
368123 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-13 |
| Onset: | 2009-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-15 |
| Days after onset: | 2 |
| Entered: |
2009-11-17 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Vertigo SMQs:, Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Vertigo, 0. |
|
| VAERS ID: |
368216 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-16 |
| Onset: | 2009-11-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-17 |
| Days after onset: | 1 |
| Entered: |
2009-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 2 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Inappropriate schedule of drug administration,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: history of asthma Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: Student received 1st H1N1 vaccine 2 weeks prior. Student did not exhibit adverse symptoms. |
|
| VAERS ID: |
368368 (history) |
| Form: |
Version 1.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-10 |
| Onset: | 2009-11-11 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-18 |
| Days after onset: | 7 |
| Entered: |
2009-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
- / 1 |
NS / IN |
Administered by: Unknown Purchased by: Unknown Symptoms: Asthenia,
Blood test normal,
Chills,
Cough,
Dysphagia,
Dyspnoea,
Headache,
Oropharyngeal pain,
Postnasal drip,
Rhinorrhoea,
Tonsillar inflammation SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Patient is not on any medications. Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Blood tests were negative for Mono. She is still very sick. I am convinced that there might be a relationship between her illness and the Nasal H1N1 Vaccine. CDC Split Type:
Write-up: Sore throat, inflamed tonsils, cough, runny nose and post nasal drip, headache, difficulty swallowing and breathing, chills, overall weakness. |
|
| VAERS ID: |
368369 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-16 |
| Onset: | 2009-11-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-18 |
| Days after onset: | 2 |
| Entered: |
2009-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 2 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness,
Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Vestibular disorders (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: "Felt dizzy" Left arm and left leg felt numb and tingling--like it felt asleep. Observed for 45 minutes Checked VS within normal limits. Given juice and rested. Went to lunch with mother who works at the school the site of the public health H1N1 clinic. Preexisting Conditions: None Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Patient felt dizzy and numbness in left arm & left leg following the administration of H1N1 vaccine IM. Patient observed & rested for 45 minutes. Given juice. Symptoms resolved and patient went to lunch and then back to class. |
|
| VAERS ID: |
368380 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
VP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Headache,
Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Headache, nausea, pulse - 76. Sat down, had a snack. |
|
| VAERS ID: |
368382 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness,
Headache SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded. Headache - sat down. Pulse - 102. |
|
| VAERS ID: |
368383 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Asthenia,
Dizziness,
Nausea,
Pallor SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Felt faint, nauseated, pale, pulse 68, laid down, elevated feet, rested, still felt weak, laid down in nurse''s office. |
|
| VAERS ID: |
368385 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Headache SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded, headache, pulse 62. Sat down-put head down. |
|
| VAERS ID: |
368386 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-13 |
| Entered: |
2009-11-18 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
UN / IM |
Administered by: Public Purchased by: Public Symptoms: Vertigo SMQs:, Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vertigo-pt rested-recovered. |
|
| VAERS ID: |
368387 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / IM |
Administered by: Public Purchased by: Other Symptoms: Headache,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Headache, shaky, pulse -80, sat down - put head down |
|
| VAERS ID: |
368388 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-13 |
| Entered: |
2009-11-18 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
UN / IM |
Administered by: Public Purchased by: Public Symptoms: Vertigo SMQs:, Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vertigo - Rested - Recovered. |
|
| VAERS ID: |
368389 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizzy-lightheaded-occurred 1st, nausea, H/A, pulse 82-sat down, had a snack. |
|
| VAERS ID: |
368390 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Tingling in legs after receiving shot. Initial pulse 45, after 2min heart rate 60. Laid down, feet elevated, felt better after resting. |
|
| VAERS ID: |
368392 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fainted after shot, pulse 60, laid down feet elevated, rested, pulse 60, drank juice, felt better. |
|
| VAERS ID: |
368397 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-16 |
| Onset: | 2009-11-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-18 |
| Days after onset: | 2 |
| Entered: |
2009-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Crying,
Dizziness,
Emotional distress,
Fall,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Depression (excl suicide and self injury) (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Patient felt dizzy & shaky following vaccine shot fell to floor from sitting position. Nurse immediately responded to patient. Checked vital signs, patient awake crying very upset. Remained with nurse for one hour given fluids that were tolerated well. Patient did not have breakfast thus patient given juice and sent to lunch. Symptoms resolved and returned to class. Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Received H1N1 vaccine injection immediately felt dizzy & shaky fell to floor from a sitting position. Patient crying & upset Vital signs normal no mental status changes. given juice as patent had no eaten breakfast. Observed by a nurse for 1 hour and symptoms resolved and returned to class. |
|
| VAERS ID: |
368400 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-17 |
| Onset: | 2009-11-17 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-18 |
| Days after onset: | 1 |
| Entered: |
2009-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 2 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Rash erythematous,
Throat irritation SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Wihin 10 minutes after receiving the H1N1 vaccine injection, red raised rash appeared on left arm and "itchy" throat. With school nurse and given 1 teaspoon Benadryl and rash resolved. Returned to class. Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Within 10 minutes after receiving the H1N1 vaccination injection, red rash appeared on the left arm. Patient complained of an itchy throat. Patient given 1 teaspoon of Benadryl and rash resolved. Returned to class |
|
| VAERS ID: |
368410 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-02 |
| Days after onset: | 0 |
| Entered: |
2009-11-18 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Flushing,
Headache,
Heart rate decreased,
Nausea SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Felt faint, headache, nausea, laid down, elevated feet, pulse 40, rested, pulse rechecked 68, drank juice, still flushed but reports feeling better. |
|
| VAERS ID: |
368450 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-17 |
| Onset: | 2009-11-17 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-18 |
| Days after onset: | 1 |
| Entered: |
2009-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 2 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Headache,
Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Within 15 minutes of receiving the H1N1 vaccine injection, patient experienced a shooting pain down to fingers & had a "bad" headache. Given Tylenol by school nurse and symptoms resolved and child went back to class. Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: After receiving H1N1 vaccine injection in left arm, patient complained of shooting pain down to fingers in left arm and reported a bad headache. Patient observed by school nurse and given Tylenol. Symptoms resolved and child returned to class. |
|
| VAERS ID: |
368991 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-29 |
| Onset: | 2009-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-03 |
| Days after onset: | 5 |
| Entered: |
2009-11-20 |
| Days after submission: | 17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
UP008AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Palpitations SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: c/o fast/hard HR, HR auscuitated, reg + strong rate of 66, no trouble breathing monitored. |
|
| VAERS ID: |
368993 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-10-29 |
| Onset: | 2009-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-03 |
| Days after onset: | 5 |
| Entered: |
2009-11-20 |
| Days after submission: | 17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
JP008AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Rash papular SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Small raised dots around mouth. Not itchy/irritating, rechecked 1 hr later, without change. Msg left for mother. No difficulty breathing/no mouth involvement. |
|
| VAERS ID: |
369382 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-17 |
| Onset: | 2009-11-17 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-17 |
| Days after onset: | 0 |
| Entered: |
2009-11-23 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1009231P / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Abnormal sensation in eye,
Dizziness SMQs:, Anticholinergic syndrome (broad), Corneal disorders (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizzy and eyes felt funny |
|
| VAERS ID: |
369488 (history) |
| Form: |
Version 1.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-16 |
| Onset: | 2009-10-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-19 |
| Days after onset: | 34 |
| Entered: |
2009-11-23 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLL279AA / 1 |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Erythema,
Pruritus,
Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Evening after immunization - body became "itchy" esp. feet. Next day facial and chest rash - face very red. May have had temp. elevation - did not have thermometer. Took Ibuprofen for relief. Felt achy and tired by 10/20/09. Symptoms much less, face still red. From 10/16 - 10/20 denies throat tightness, sore throat, sneezing, cough. Patient/employee reported this reaction on 10/20/09 with phone call received by reporting nurse. This is the first seasonal flu shot this patient/employee received. Eggs tend to upset her stomach so she avoids them but does eat them occasionally. |
|
| VAERS ID: |
369508 (history) |
| Form: |
Version 1.0 |
| Age: |
34.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-10 |
| Onset: | 2009-11-10 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 10 |
| Entered: |
2009-11-23 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3262H / UNK |
RA / IM |
Administered by: Private Purchased by: Other Symptoms: Breast pain,
Fatigue,
Headache,
Incorrect dose administered,
Injection site swelling,
Malaise,
Mastitis,
Peripheral coldness,
Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Lipodystrophy (broad), Functional lactation disorders (narrow), Hypersensitivity (narrow), Medication errors (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: The patient was a breastfeeding mother at the time of vaccination. Preexisting Conditions: Patient had a history of asthma, fibromyalgia and known allergies to penicillin, sulfa and latex. The patient may have received a flu vaccination three years ago. She had no adverse events following prior vaccinations. Allergies: Diagnostic Lab Data: None CDC Split Type: 200904927
Write-up: Initial report received from a health care professional on 11 November 2009. This report involved a case of misuse where the patient received two pediatric doses of FLUZONE combined into one injection. A 35-year-old female patient with a history of asthma, fibromyalgia and known allergies to penicillin, sulfa and latex and who was breastfeeding mother at the time of vaccination, had received an intramuscular right deltoid injection of FLUZONE, lot number U3262HA on 10 November 2009 at 11:30 am and five minutes later, she developed injection site swelling and cold hands. Benadryl was administered and the patient was sent home. At 3:00 pm, the patient went to emergency room with complaints of hives, malaise, fatigue, headache and fever of 102F and was released. At 3:00 am, the patient returned to the emergency room with the same symptoms in addition to left breast pain. The patient was diagnosed with mastitis. The patient had no concurrent illness and she had not been taking any concomitant medications at the time of vaccination. She had no adverse events following prior vaccinations. At the time of the report, the patient''s recovery status was unknown. Documents held by sender: None. |
|
| VAERS ID: |
369565 (history) |
| Form: |
Version 1.0 |
| Age: |
0.35 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-19 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-23 |
| Days after onset: | 3 |
| Entered: |
2009-11-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT3178D / 2 |
RA / IM |
Administered by: Private Purchased by: Public Symptoms: Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Will be having allergy testing CDC Split Type:
Write-up: Hives at 2nd dose, given ZYRTEC. Low grade fever on face, L & R legs, left & R arms, buttocks. |
|
| VAERS ID: |
369692 (history) |
| Form: |
Version 1.0 |
| Age: |
1.27 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-12 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-11-18 |
| Entered: |
2009-11-24 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP022AA / 1 |
LL / IJ |
Administered by: Public Purchased by: Public Symptoms: Incorrect dose administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Received 0.5ml of H1N1 vaccine instead of 0.25mls. No adverse reaction reported by mom. No treatment needed. |
|
| VAERS ID: |
369733 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-10 |
| Onset: | 2009-10-11 |
| Days after vaccination: | 1 |
| Submitted: |
2009-11-13 |
| Days after onset: | 33 |
| Entered: |
2009-11-24 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC20B137AA / 5 |
LA / IM |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1009224P / UNK |
RA / IM |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500741P / 3 |
NS / IN |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site induration,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: In same arm that previously in 2/05 a BCG was given, a 10 x 14 cm, red swelling with slight enduration at site of BCG - not at site of DTaP/IPB was vigorous (was above site of BCG). |
|
| VAERS ID: |
370339 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-12 |
| Onset: | 2009-11-17 |
| Days after vaccination: | 5 |
| Submitted: |
2009-11-27 |
| Days after onset: | 10 |
| Entered: |
2009-11-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (CSL)) / CSL LIMITED |
00449611A / 2 |
UN / UN |
Administered by: Unknown Purchased by: Unknown Symptoms: Blood immunoglobulin G,
Blood immunoglobulin M,
Borrelia burgdorferi serology negative,
Facial palsy SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: postviral neuropathy since 1992 12/3/09 PMH:(10/02/09) left eye irritation with foreign body sensation. Allergies: Diagnostic Lab Data: LYME IgG/IgM NEGATIVE CDC Split Type:
Write-up: BELL''S PALSY OF RIGHT SIDE. 12/03/09 Medical record received for DOS: 10/2/02 and 11/17/09. DX: Bell''s Palsy Pt presented with rt. sided facial weakness and inability to close rt. eye |
|
| VAERS ID: |
370522 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/O "can''t feel Lt. arm". (Injection site Rt arm). Observation x 15". |
|
| VAERS ID: |
370526 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: "dizzy" - juice given; observed |
|
| VAERS ID: |
370529 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Felt faint - moved to floor. Given juice drink. Observation x 15". |
|
| VAERS ID: |
370532 (history) |
| Form: |
Version 1.0 |
| Age: |
17.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Nausea,
Vertigo SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/o head spinning, sl. nauseous 30" after immunization - hydrated well. T 97 degrees. |
|
| VAERS ID: |
370534 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
10208P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/O itchy Rt hand-site of wk stamp. Rx-observation x 15". |
|
| VAERS ID: |
370541 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea, T 98.5. Observed-hydrated, rested in nurse''s office. |
|
| VAERS ID: |
370559 (history) |
| Form: |
Version 1.0 |
| Age: |
17.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
- / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea, dizzy. Well hydrated. 97.5 T. |
|
| VAERS ID: |
370565 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/O dizziness, lightheaded. Well hydrated. 98.3. |
|
| VAERS ID: |
370567 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded after eating lunch. Observed - sent back to class x 15". |
|
| VAERS ID: |
370570 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness,
Dyspepsia SMQs:, Anticholinergic syndrome (broad), Gastrointestinal nonspecific dysfunction (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 30 minutes after injection - lightheaded + felt acid stomach. T 97.5. |
|
| VAERS ID: |
370572 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Head injury,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Same.~Vaccine not specified (no brand name)~UN~0.00~Patient Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fainted after injection. Hit Lt side of head on table. No c/o headache. Hydrated and observed x 20". 1040 AM T 99.5 / T. 99.8 1052 AM T 99.6 @ 1105. |
|
| VAERS ID: |
370573 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Abdominal pain upper,
Dizziness SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded + sl. stomach ache" onset 10:40 am Observed x15 "$g OK. T976 |
|
| VAERS ID: |
370575 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
LA / UN |
Administered by: Public Purchased by: Public Symptoms: Abdominal discomfort,
Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/o injection arm "numb. Upset stomach. Observation X 10 hours. |
|
| VAERS ID: |
370576 (history) |
| Form: |
Version 1.0 |
| Age: |
15.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness,
Fatigue,
Somnolence SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Tired, drowsy, lightheaded - 5" after injection. Felt tired this AM. T 98.3. Rx - hydration. |
|
| VAERS ID: |
370578 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-11-30 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102128P1 / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Dizziness,
Headache,
Sensation of heaviness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Rt arm "feels heavy" , dizzy, head hurts, T 97.4. Rx- hydration. Sent to class 10:14 a.m. |
|
| VAERS ID: |
370823 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-20 |
| Onset: | 2009-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-20 |
| Days after onset: | 0 |
| Entered: |
2009-12-01 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
LA102128P1 / 1 |
RA / IM |
Administered by: Public Purchased by: Other Symptoms: Blood pressure normal,
Dizziness,
Headache,
Heart rate normal SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: HR and BP WNL CDC Split Type:
Write-up: Initial dizziness then c/o headache. Headache continued x about 30 - 40 mins. Student layed down and slept - felt better afterwards. |
|
| VAERS ID: |
371215 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-30 |
| Onset: | 0000-00-00 |
| Submitted: |
2009-12-02 |
| Entered: |
2009-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500799 / UNK |
- / - |
Administered by: Unknown Purchased by: Unknown Symptoms: Inappropriate schedule of drug administration,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Unknown Preexisting Conditions: None per pt Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 60 yr old male received LAIV H1N1 Vaccine. |
|
| VAERS ID: |
371775 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-02 |
| Onset: | 2009-12-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-02 |
| Days after onset: | 0 |
| Entered: |
2009-12-07 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP027AB / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Feeling of body temperature change,
Injection site anaesthesia,
Injection site pain,
Oxygen saturation normal,
Pain in extremity SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Asthmatic Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pain in arm at at site of injection c/o hot & cold & numbness in area VS. & O2 sat WNL. |
|
| VAERS ID: |
371833 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-03 |
| Onset: | 2009-12-03 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-07 |
| Days after onset: | 4 |
| Entered: |
2009-12-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102130P1 / 2 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Cold sweat,
Eye swelling,
Feeling abnormal,
Pallor SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Dementia (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None known. Preexisting Conditions: None known. Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student became pale, clammy. After rest and hydration student continued to feel "off." His vital signs were WNL. Parents were called and he went home to rest. Parents reported he felt fine all day and night. The following AM student woke with swollen eyes. The parents were unclear if this was due to cat exposure and student''s allergy to cats or a flu shot reaction. Student referred to MD and was seen 22.5 hours after receiving the vaccine. Parent reported there was no swelling, redness at site of injection, no malaise felt. MD suggested Benadryl and monitoring at home. |
|
| VAERS ID: |
372033 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-30 |
| Onset: | 2009-11-30 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-01 |
| Days after onset: | 1 |
| Entered: |
2009-12-08 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Chills,
Dizziness,
Headache,
Nausea,
Pyrexia,
Somnolence SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ZYRTEC; ZYFLO; SINGULAIR; ADVAIR; PREVACID Current Illness: None Preexisting Conditions: Allergies (mold, dust mites, pollen, crabs), Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Horrible headache, naucious, dizzy, fever/chills. Slept from 3pm to 8am. |
|
| VAERS ID: |
372038 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-30 |
| Onset: | 2009-11-30 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-01 |
| Days after onset: | 1 |
| Entered: |
2009-12-08 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102124P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Dizziness,
Erythema,
Eye swelling,
Headache,
Lip swelling,
Paraesthesia oral,
Rash macular,
Swelling face,
Throat irritation SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None noted|| Reported? reaction to MIDOL on 11/28/09 Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: About 30 mins after vaccination - light-headed, sl headache, R hand redder than left. Tx''d with ibuprofen. @ 3pm student called mom @ work c/o tingling/swollen lips, 1 eye swelling. @ 430pm mom home - student with increased facial swelling, eyes swelling, throat itchy, "splotches all over" went to ER IV BENADRYL 12/1/09 8 am - eyes still sl swollen, few blotches - 10:30 am appears clear. |
|
| VAERS ID: |
372488 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-19 |
| Onset: | 2009-11-19 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-04 |
| Days after onset: | 15 |
| Entered: |
2009-12-10 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
1314Y / 2 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site erythema,
Injection site mass,
Injection site pain,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Methylphenidate HCI 20mg; Fluticasone Propionate SUSP 50mg; Omeprazole 20mg CPDR; Sinemet 25-100mg tabs; Advair Diskus 250-50mcg/dose MISC; Lisinopril-Hydrochlorothiazide 20-12.5mg tabs; Metaproterenol Sulfate 20mg tabs; Doxycycl HYC; Amox/ Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pain, swelling, redness of deltoid and "egg size" lump in axilla. Right arm. |
|
| VAERS ID: |
373485 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-11 |
| Onset: | 2009-12-11 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-11 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP037DA / 2 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Client complained of dizziness 10 minutes post vaccine administration. Recovered quickly after laying down in health office. Released to clinic area 15 minutes later. |
|
| VAERS ID: |
373490 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-10 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-10 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP077AB / 2 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizzy, headache, nausea resolved after 20 mins. Temp 99.5. |
|
| VAERS ID: |
373492 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-02 |
| Onset: | 2009-12-03 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2009-12-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Migraine SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Symptoms of a migraine H.A. next day. |
|
| VAERS ID: |
373494 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-11 |
| Onset: | 2009-12-11 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-11 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1013282P / 2 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Nausea,
Vertigo SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: - Vertigo and nausea following injection. - Lasting 1-2 hrs. |
|
| VAERS ID: |
373496 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-11 |
| Onset: | 2009-12-11 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-11 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP037DA / 1 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Body temperature increased,
Injection site anaesthesia,
Nausea,
Vertigo SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt c/o numbness at injection site. Persisting 2 hours after injection. 3 hrs after injection, Temp increased 99.3 and nausea and vertigo. Pt was sent home with mother. |
|
| VAERS ID: |
373528 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-10 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-10 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP027AB / 2 |
UN / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Chills,
Pallor,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pallor, chills, fever 100.5. 20 minutes after 1st Temp -99.5. -Student was sent home. |
|
| VAERS ID: |
373529 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-10 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-10 |
| Days after onset: | 0 |
| Entered: |
2009-12-16 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP027AB / 2 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Headache SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Headache, Tylenol 160 mg. |
|
| VAERS ID: |
373880 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-07 |
| Onset: | 2009-12-07 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-07 |
| Days after onset: | 0 |
| Entered: |
2009-12-17 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1013282P / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Cold sweat,
Fall,
Loss of consciousness,
Pallor SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Child briefly lost consciousness after dropping to the floor. Became alert spontaneously. B/P - 120/70 P. 80 Pale & clammy; alert & oriented. No incontinence or seizure activity. Was fine the next day. |
|
| VAERS ID: |
373916 (history) |
| Form: |
Version 1.0 |
| Age: |
17.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-17 |
| Onset: | 2009-12-17 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-17 |
| Days after onset: | 0 |
| Entered: |
2009-12-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Dizziness,
Feeling hot,
Head injury,
Headache,
Hyperhidrosis,
Loss of consciousness,
Nausea,
Syncope,
Visual impairment SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Cardiomyopathy (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: faint~Td Adsorbed (no brand name)~UN~0.00~Patient Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None known CDC Split Type:
Write-up: At 10:50 patient was in post vaccination area, states he felt faint, saw spots before his eyes and fainted. Hit head on table then floor. Witness states he was out for 15 sec. then came to. Alert and oriented x3. Warm, sweaty, nauseated pupils equal and reactive, hand and foot grasp equal and strong. HR 60 and regular. C/o HA. Mother called will follow-up with MD. |
|
| VAERS ID: |
373973 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-09 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 1 |
| Submitted: |
2009-12-17 |
| Days after onset: | 7 |
| Entered: |
2009-12-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U33352AA / 1 |
LL / IM |
Administered by: Private Purchased by: Unknown Symptoms: Convulsion SMQs:, Torsade de pointes/QT prolongation (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: seizure~Varicella (no brand name)~1~1.60~Patient Other Medications: Current Illness: None Preexisting Conditions: no Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: seizure |
|
| VAERS ID: |
374012 (history) |
| Form: |
Version 1.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-07 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 3 |
| Submitted: |
2009-12-17 |
| Days after onset: | 7 |
| Entered: |
2009-12-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP044AA / 2 |
LA / IJ |
Administered by: Public Purchased by: Public Symptoms: Myalgia,
Nausea,
Neck pain,
Pyrexia SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Verapamil Keppra Advair Flonase Amitriptylin albuterol Current Illness: no Preexisting Conditions: penicillin beta blockers asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea, fever, muscle aches, sore neck. |
|
| VAERS ID: |
374473 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / UNK |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded. Rested, food. |
|
| VAERS ID: |
374499 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP067AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Abdominal discomfort,
Dizziness,
Headache,
Hypotonia,
Pallor SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: PCH; SULFA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt became dizzy approx 5 min after receiving the injection. Her stomach was also upset and she complained of a headache. She appeared pale and limp when I had her rest on a mat. BP 112/72 home with dad feeling better @ 11:30. |
|
| VAERS ID: |
374500 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea, lightheaded, rested good |
|
| VAERS ID: |
374501 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP067AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Abdominal pain upper,
Headache,
Immediate post-injection reaction,
Injection site pruritus SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccinated-1005 immediate-stomach crampy, injection site itchy BP 90/60 headache. Rest-home with mother. Mom reports felt fine by noon. |
|
| VAERS ID: |
374502 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP067AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Pen Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt presented at the nurses office with nausea, dizziness and a headache. BP 95/66. Rested-home with mother @ 1pm. Starting to feel better at that time. |
|
| VAERS ID: |
374503 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Chest discomfort SMQs:, Anaphylactic reaction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: tightness in center chest after 15m wait time pulse 76 R - regular, no SOB |
|
| VAERS ID: |
374504 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102140P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Headache,
Hyperhidrosis,
Nausea SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: KNA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Felt faint @ 10:05. Palms sweaty. Nausea. Headache. Took student to a mat to lie down. Improved. Refused water. 10:20 escorted back to classroom. |
|
| VAERS ID: |
374506 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102140P1 / 1 |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Injection site erythema SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Redness, size of half dollar, at injection site. No other adverse symptoms after 15/20 minutes. |
|
| VAERS ID: |
374508 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-16 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-16 |
| Days after onset: | 0 |
| Entered: |
2009-12-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness,
Vertigo SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: vertigo, light headed, pulse about 80, resp about 16/18, improved after 25 minutes |
|
| VAERS ID: |
375093 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-21 |
| Onset: | 2009-12-21 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-21 |
| Days after onset: | 0 |
| Entered: |
2009-12-28 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102130P1 / 1 |
LA / UN |
Administered by: Unknown Purchased by: Unknown Symptoms: Anxiety,
Chest discomfort,
Nausea SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Anxiety related to needles Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nausea, "Tight chest" (Patient states normal anxiety reaction). |
|
| VAERS ID: |
375200 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-16 |
| Onset: | 2009-12-17 |
| Days after vaccination: | 1 |
| Submitted: |
2009-12-22 |
| Days after onset: | 5 |
| Entered: |
2009-12-29 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102139P1 / 1 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Malaise,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Seasonal allergies-none active at this time Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student had fever and malaise x3 days post vaccine (per dad). |
|
| VAERS ID: |
375233 (history) |
| Form: |
Version 1.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-06 |
| Days after vaccination: | 4 |
| Submitted: |
2009-11-23 |
| Days after onset: | 17 |
| Entered: |
2009-12-29 |
| Days after submission: | 36 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Injection site pain,
Neck pain,
Pain SMQs:, Extravasation events (injections, infusions and implants) (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Bulging discs at C4-6 Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: 4-5 days after admin. of vaccine, I experienced pain from bottom of left deltoid to behind left ear all the way up the side of my neck. Pain lasted x1 wk. Missed 1 day of work. |
|
| VAERS ID: |
375235 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-02 |
| Onset: | 2009-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-23 |
| Days after onset: | 21 |
| Entered: |
2009-12-29 |
| Days after submission: | 36 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP010AA / 1 |
LA / UN |
Administered by: Other Purchased by: Public Symptoms: Body temperature normal,
Cough,
Headache,
Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Fluoride; vitamins Current Illness: May have had a fever Preexisting Conditions: Skin reaction to swimming in chlorinated pools Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Patient c/o a headache 10 min. after shot admin. Temp was taken=102 degrees. Wet cough and fever x 3 days. 11/5 developed hives, afebrile. Hives x 5 days. Hives responded to CLARITAN. Cough x 3 wks. |
|
| VAERS ID: |
375443 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-08 |
| Onset: | 2009-12-09 |
| Days after vaccination: | 1 |
| Submitted: |
2009-12-29 |
| Days after onset: | 20 |
| Entered: |
2009-12-30 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP025AA / 1 |
LA / IM |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
0581Y / 2 |
RA / SC |
Administered by: Unknown Purchased by: Unknown Symptoms: Injection site erythema,
Injection site pruritus,
Injection site reaction,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: On 12/11/09 - patient''s mother called to report a local reaction at injection site of VARIVAX vaccine given to patient on 12/8/09. Mother only wanted it reported to facility-that area was reddened, swollen (approx. the size of a tangerine) with itchiness - and at time of phone call to us - resolving - patient''s mother refused offered appoint. for patient to be seen. |
|
| VAERS ID: |
376319 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2009-12-10 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-11 |
| Days after onset: | 1 |
| Entered: |
2010-01-08 |
| Days after submission: | 28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102140P1 / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Injection site erythema,
Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Received vaccine @ 10:12 am - arrived @ 10:37 a.m. redness/tenderness @ injection site. Iced/observed x 10 min. Ice off x 10 min. No change. Called mom. Gave 12.5mg BENADRYL. |
|
| VAERS ID: |
376877 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-01-13 |
| Onset: | 2010-01-13 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-14 |
| Days after onset: | 1 |
| Entered: |
2010-01-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / - |
Administered by: Public Purchased by: Private Symptoms: Chills,
Eye pruritus,
Lip swelling,
Myalgia,
Throat irritation SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Angioedema (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: NONE Preexisting Conditions: WASP STINGS Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: THICKENING OF THROAT, SWELLING OF LIPS, ITCHINESS OF EYES, CHILLS, NO FEVER, MUSCLE ACHES. TREATED WITH BENADRYL WHICH IMPROVED SYMPTOMS, STILL ITCHY NEXT DAY WITH ACHES BUT IMPROVING. |
|
| VAERS ID: |
376949 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-01-08 |
| Onset: | 2010-01-11 |
| Days after vaccination: | 3 |
| Submitted: |
2010-01-14 |
| Days after onset: | 3 |
| Entered: |
2010-01-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP089AA / 1 |
LA / IM |
Administered by: Military Purchased by: Military Symptoms: Asthenia,
Back pain,
Constipation,
Fatigue,
Muscular weakness,
Neck pain SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Retroperitoneal fibrosis (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: AMLODIPINE BESYLATE 10MG TAB TAKE ONE TABLET BY MOUTH ACTIVE DAILY FOR BLOOD PRESSURE/HEART, DO NOT TAKE WITH GRAPEFRUIT JUICE 2) BUPROPION HCL 75MG TAB TAKE ONE TABLET BY MOUTH TWICE ACTIVE DAILY FOR DEPRESSION 3) Current Illness: no Preexisting Conditions: Hepititis C Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt states that since receiving flu vaccine on 1/8/10, he has felt fatiqued, aching in neck and back. Feels that he is weaker in leg and in back. No fever no NVD. Has marked constipation, which he also dates to this. He states he has marked decrease in strength in arms and legs. |
|
| VAERS ID: |
377276 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-01-14 |
| Onset: | 2010-01-14 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-18 |
| Days after onset: | 4 |
| Entered: |
2010-01-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP099AA / 2 |
RA / IM |
Administered by: Other Purchased by: Public Symptoms: Confusional state,
Flushing,
Headache SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypersensitivity (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None known Preexisting Conditions: Tonsilectomy and ear tubes 06 Allergies: Diagnostic Lab Data: None VS WNL CDC Split Type:
Write-up: Vaccine administered (H1N1) @ approximately 9:15am. 10am - facial flushing and headache "confusion" stated by student but remained alert and oriented x 3. Vital signs WNL T99.5. 10:45am flushing headache and self stated confusion resolved. |
|
| VAERS ID: |
377477 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-31 |
| Onset: | 2010-01-10 |
| Days after vaccination: | 10 |
| Submitted: |
2010-01-14 |
| Days after onset: | 4 |
| Entered: |
2010-01-20 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP076AA / 1 |
RL / IM |
Administered by: Private Purchased by: Public Symptoms: Arthralgia,
Erythema multiforme,
Joint swelling,
Malaise,
Pyrexia,
Rash,
Urticaria SMQs:, Severe cutaneous adverse reactions (narrow), Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: OMNICEF Current Illness: Acute otitis media Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Severe sickness - like illness with fever, joint pain, ankle swelling, urticarial/erythema multiform type rash. |
|
| VAERS ID: |
377517 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-01-13 |
| Onset: | 2010-01-13 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-13 |
| Days after onset: | 0 |
| Entered: |
2010-01-20 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP099AA / 2 |
UN / IM |
Administered by: Public Purchased by: Unknown Symptoms: Dizziness,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: No rxn to #1 dose H1N1. Stated "this one hurt". CDC Split Type:
Write-up: Nausea, lightheadedness, allowed to rest, feet up, cold compress on head. After 10 min c/o of headache, at 30 min hungry-eating snack. (At 11:00 Mom picked up to take home). |
|
| VAERS ID: |
378265 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-01-20 |
| Onset: | 2010-01-20 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-20 |
| Days after onset: | 0 |
| Entered: |
2010-01-26 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP099AA / 1 |
RA / IM |
Administered by: Other Purchased by: Public Symptoms: Body temperature decreased,
Feeling hot,
Hyperhidrosis,
Nausea,
Pallor,
Somnolence SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: C/O SA/nausea. Pale, quiet-sweaty brow-had juice/gold fish, said feels hot, T 95.7, pulse 80-Rest in health office-9:45 TC to mom-she talked with son-encouraged try recess-Reassessed at 11:00, feeling fine. |
|
| VAERS ID: |
378449 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-12-02 |
| Onset: | 2009-12-02 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-07 |
| Days after onset: | 5 |
| Entered: |
2010-01-27 |
| Days after submission: | 51 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Injection site erythema,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Localized reaction at site of inj. swollen and red/mom gave her Benadryl. |
|
| VAERS ID: |
378450 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-13 |
| Onset: | 2009-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-13 |
| Days after onset: | 0 |
| Entered: |
2010-01-27 |
| Days after submission: | 75 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / UNK |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student stated he felt lightheaded and nauseous, ate crackers, water and rested x 15 min. before stating he felt better to go to class. |
|
| VAERS ID: |
378451 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-07 |
| Onset: | 2009-12-07 |
| Days after vaccination: | 0 |
| Submitted: |
2009-12-07 |
| Days after onset: | 0 |
| Entered: |
2010-01-27 |
| Days after submission: | 51 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
1013282P / 1 |
AR / IM |
Administered by: Public Purchased by: Public Symptoms: Confusional state,
Convulsion,
Feeling cold,
Pallor,
Syncope,
Urinary incontinence SMQs:, Torsade de pointes/QT prolongation (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none known Preexisting Conditions: none known Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Approximate 5 min after receiving H1N1 injection child reportedly fainted and had seizure like activity was incontinent of urine. Remained pale, cold and some confusion. Applied O2 and was transported to ER. He was observed and released. Questions of hx of seizures in the past. |
|
| VAERS ID: |
378452 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-11-18 |
| Onset: | 2009-11-18 |
| Days after vaccination: | 0 |
| Submitted: |
2009-11-18 |
| Days after onset: | 0 |
| Entered: |
2010-01-27 |
| Days after submission: | 70 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP022AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Unevaluable event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: None stated. |
|
| VAERS ID: |
378453 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-13 |
| Onset: | 2009-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2010-01-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (NOVARTIS)) / NOVARTIS VACCINES AND DIAGNOSTICS |
102042P1 / UNK |
LA / - |
Administered by: Public Purchased by: Other Symptoms: Dizziness SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Student stated he felt "woozy". Laid down x 10 minutes and ate crackers. Stated he felt better and resumed class. |
|
| VAERS ID: |
378658 (history) |
| Form: |
Version 1.0 |
| Age: |
25.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-28 |
| Onset: | 2009-10-31 |
| Days after vaccination: | 3 |
| Submitted: |
2010-01-13 |
| Days after onset: | 74 |
| Entered: |
2010-01-28 |
| Days after submission: | 15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
- / 1 |
UN / IJ |
Administered by: Other Purchased by: Other Symptoms: Abortion spontaneous,
Asthenia,
Chills,
Cough,
Diarrhoea,
Dizziness,
Drug exposure during pregnancy,
Dyspnoea,
Fatigue,
Headache,
Influenza,
Insomnia,
Nasal congestion,
Nausea,
Oropharyngeal pain,
Pyrexia,
Rhinorrhoea,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Reported fever, chills, fatigue, insomnia, shortness of breath, cough, sore throat, runny nose/nasal congestion, dizziness, diarrhea, nausea, vomiting, headache, weakness. Onset - 4 days post vaccination. Sought medical care. Hospitalized. Diagnosed with H1N1 infection about 1 week post vaccination. Had a miscarriage 1 week later, 2 weeks post vaccination. Patient was nine weeks pregnant at date of miscarriage. |
|
| VAERS ID: |
378941 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-01-26 |
| Onset: | 2010-01-26 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-26 |
| Days after onset: | 0 |
| Entered: |
2010-02-01 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP089AA / 2 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Abdominal discomfort,
Dizziness,
Feeling cold,
Headache,
Neck pain SMQs:, Anticholinergic syndrome (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheaded, felt cold, back of neck/head started to hurt, upset stomach. Home with parent. |
|
| VAERS ID: |
378942 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-01-26 |
| Onset: | 2010-01-26 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-26 |
| Days after onset: | 0 |
| Entered: |
2010-02-01 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP089AA / 2 |
RA / UN |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Feeling cold,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizzy - felt cold and shaky - Home with parent. |
|
| VAERS ID: |
378943 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-01-26 |
| Onset: | 2010-01-26 |
| Days after vaccination: | 0 |
| Submitted: |
2010-01-26 |
| Days after onset: | 0 |
| Entered: |
2010-02-01 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP089AA / 2 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Nausea,
Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Nauseated after received immun. (10:30am). Vomited at 1:40 pm. Home with parent. |
|
| VAERS ID: |
379653 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-02-01 |
| Onset: | 2010-02-01 |
| Days after vaccination: | 0 |
| Submitted: |
2010-02-05 |
| Days after onset: | 4 |
| Entered: |
2010-02-08 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UT0459A / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0611Y / 1 |
RA / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site induration,
Injection site pain,
Injection site swelling,
Oedema peripheral SMQs:, Cardiac failure (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: LLLeg open knee 12 cm Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Rt arm 1- site hard, painful 3 hrs post shot ice, pain killer recommended. 2- much of arm red, swollen, hot the next day, elevation, AUGMENTIN 875 BID x/8d |
|
| VAERS ID: |
379654 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-02-03 |
| Onset: | 2010-02-04 |
| Days after vaccination: | 1 |
| Submitted: |
2010-02-05 |
| Days after onset: | 1 |
| Entered: |
2010-02-08 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U32733A / 5 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Inflammation,
Injection site pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: FOCALIN 5 mg qd Current Illness: none Preexisting Conditions: ADHD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 2/4 itchiness @ site, sore 2/5 L arm red and inflamed below inject site. |
|
| VAERS ID: |
379862 (history) |
| Form: |
Version 1.0 |
| Age: |
64.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-03 |
| Onset: | 2009-12-06 |
| Days after vaccination: | 3 |
| Submitted: |
2010-02-09 |
| Days after onset: | 65 |
| Entered: |
2010-02-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (CSL)) / CSL LIMITED |
00147911A / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Arthralgia,
Borrelia burgdorferi serology negative,
C-reactive protein increased,
Full blood count normal,
Metabolic function test,
Musculoskeletal stiffness,
Red blood cell sedimentation rate normal SMQs:, Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Xopenex INH Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CR P elevated at 5.88; ESR - negative; Lyme - negative; CMP - negative; CBC - negative CDC Split Type:
Write-up: 3 days after injection he began with arthralgias & arthritic stiffness. This progressed to overt inflammatory arthritis of hands/knees/buttocks. Work up CR-P elevated at 5.88, ESR neg, Lyme neg, CMP neg, CBC neg. Condition resolved with steroid treatment x 3 wks. |
|
| VAERS ID: |
380936 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-02-11 |
| Onset: | 2010-02-12 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2010-02-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP033AB / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Arthralgia,
Chills,
Diarrhoea,
Myalgia,
Nausea,
Pyrexia,
Vomiting SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Arthritis (broad), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Known. Preexisting Conditions: States IDDM on Wed. Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Fever, chills, N/V/D, myalgias, arthralgias for 48 hours. |
|
| VAERS ID: |
381364 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-12-07 |
| Onset: | 2009-12-10 |
| Days after vaccination: | 3 |
| Submitted: |
2010-02-26 |
| Days after onset: | 78 |
| Entered: |
2010-02-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UT023AA / 2 |
LL / IJ |
Administered by: Public Purchased by: Public Symptoms: Abnormal behaviour,
Abnormal faeces,
Aggression,
Diarrhoea,
Incorrect dose administered SMQs:, Dementia (broad), Pseudomembranous colitis (broad), Psychosis and psychotic disorders (broad), Biliary system related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (narrow), Noninfectious diarrhoea (narrow), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: The doctor was not concerned about the shot and I do not think he reported my findings. On 2/24/10 I told the nurse about my concerns. She asked to see his shot record and what she found scared us both. On 12/07/09 she was given .5 of the H1N1 shot and on 01/08/10 he was given another .25. This is a total of .75 way more than an adult dose. My grandson was overdosed and may be damaged for life, because of this. I no longer have that genteel little boy. If you can give me advice on what to do, Please let me know. CDC Split Type:
Write-up: My grandson went from a genteel and loving child to an aggressive and unpredictable child, this is still continuing today. He had loose and smelly bowel movements for about two weeks after each H1N1 shot. |
|
| VAERS ID: |
382292 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2010-03-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UP017AA / 1 |
RA / UN |
Administered by: Unknown Purchased by: Unknown Symptoms: Throat tightness SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Known Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Approx 1/2 hour after injection c/o tightness in throat. B/P 88/0 64-18. No other symptoms. Able to drink, eat & talk without difficulty. |
|
| VAERS ID: |
396151 (history) |
| Form: |
Version 1.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2009-10-26 |
| Onset: | 2009-10-26 |
| Days after vaccination: | 0 |
| Submitted: |
2009-10-27 |
| Days after onset: | 1 |
| Entered: |
2010-08-16 |
| Days after submission: | 293 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
500723P / UNK |
NS / IN |
Administered by: Other Purchased by: Other Symptoms: Contraindication to vaccination,
No adverse event SMQs:, Medication errors (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug(s) Not Reported Current Illness: Asthma Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0009234
Write-up: A non-serious spontaneous report of inadvertent administration of FLUMIST to a 9-year-old with asthma was received from a registered nurse. The patient''s medical history included asthma. Concomitant medications included the Flu Shot given 22-Sep-2009. There was no adverse event associated with this medication error; therefore, treatment and reporter/sponsor causality assessments are not applicable, and the event is considered resolved. |
|
| VAERS ID: |
399017 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-09-16 |
| Onset: | 2010-09-16 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-16 |
| Days after onset: | 0 |
| Entered: |
2010-09-21 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC21B248CA / 3 |
LA / UN |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3566AA / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Crying,
Headache,
Injection site erythema,
Injection site pain,
Insomnia,
Pain,
Pyrexia,
Screaming SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Same.~Hib (no brand name)~3~0.50~Patient|Same.~Measles + Mumps + Rubella (no brand name)~1~1.50~Patient|Same.~DTaP + HepB + IPV Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Awake all night, screaming and crying; fever 101, began 3-4 hours after getting vaccine; complained of body and head hurting. Said (L) arm hurt more but bot equally red. |
|
| VAERS ID: |
400338 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-09-22 |
| Onset: | 2010-09-22 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-24 |
| Days after onset: | 2 |
| Entered: |
2010-09-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3566A3N / 3 |
LL / IM |
| HIBV: HIB (ACTHIB) / SANOFI PASTEUR |
AHIBC252C / 4 |
RL / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
913965NDO / 5 |
RL / IM |
Administered by: Unknown Purchased by: Public Symptoms: Injection site erythema,
Injection site pain,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: URI Preexisting Conditions: Spastic cerebral palsy, GERD, developmental delay, sensorineural hearing loss, congenital CMV exposure Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling and redness with pain at injection site on R upper thigh, which worsened over next 24 hours before improving. |
|
| VAERS ID: |
403092 (history) |
| Form: |
Version 1.0 |
| Age: |
36.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-12 |
| Onset: | 2010-10-12 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-13 |
| Days after onset: | 1 |
| Entered: |
2010-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (GSK)) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA536AA / UNK |
LA / IJ |
Administered by: Public Purchased by: Other Symptoms: Erythema,
Hypoaesthesia facial,
Hypoaesthesia oral,
Pruritus SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: no Allergies: Diagnostic Lab Data: no CDC Split Type:
Write-up: red & itchy face followed by lips & jaw going numb |
|
| VAERS ID: |
403494 (history) |
| Form: |
Version 1.0 |
| Age: |
74.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-07 |
| Onset: | 2010-10-07 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-15 |
| Days after onset: | 8 |
| Entered: |
2010-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
112946P1 / UNK |
UN / IM |
Administered by: Private Purchased by: Unknown Symptoms: Injection site erythema,
Injection site pruritus SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt described redness and itching at admin site that day and following day. Area approx 4" circ. Pt states she treated with BENADRYL x 1 dose with relief. No other treatment needed. |
|
| VAERS ID: |
403496 (history) |
| Form: |
Version 1.0 |
| Age: |
85.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-13 |
| Onset: | 2010-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-15 |
| Days after onset: | 2 |
| Entered: |
2010-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
112946P1 / UNK |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Unevaluable event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: B12 injection on same day opposite arm Current Illness: No Preexisting Conditions: PCN; MACRODANTIN; ASA; Fluticasone Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: None stated. |
|
| VAERS ID: |
403507 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-10-08 |
| Onset: | 2010-10-09 |
| Days after vaccination: | 1 |
| Submitted: |
2010-10-15 |
| Days after onset: | 6 |
| Entered: |
2010-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (SANOFI)) / SANOFI PASTEUR |
UH180AA / 2 |
RA / IM |
| MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR |
U330600AA / 1 |
LA / IM |
| TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC52B063AA / 1 |
RA / IM |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Oedema peripheral,
Pruritus SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: no Preexisting Conditions: no Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: right arm, redness, swollen, itchy, redness spreading from outside arm to inside of arm (7"w x 5.5"L) |
|
| VAERS ID: |
403898 (history) |
| Form: |
Version 1.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-09-27 |
| Onset: | 2010-09-28 |
| Days after vaccination: | 1 |
| Submitted: |
2010-10-14 |
| Days after onset: | 16 |
| Entered: |
2010-10-18 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH180AA / 2 |
LA / IM |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
0758Z / 2 |
LA / SC |
Administered by: Private Purchased by: Public Symptoms: Headache,
Injection site erythema,
Injection site warmth,
Local reaction,
Pruritus,
Pyrexia SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Lexapro; Mirena Current Illness: None Preexisting Conditions: Acne; Anxiety; Eczema; Obesity Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Red warm area at site; 9/29/10 - headache fever (not take) 10.5 cm x 14cm red, hot local reaction. Temp in office was normal 9/30/10 - local reaction now itching. |
|
| VAERS ID: |
404795 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-20 |
| Onset: | 2010-10-20 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-22 |
| Days after onset: | 2 |
| Entered: |
2010-10-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / UN |
Administered by: Unknown Purchased by: Private Symptoms: Burning sensation,
Eye pruritus,
Eye swelling,
Hypersensitivity,
Lacrimation increased,
Nasal discomfort,
Oropharyngeal pain,
Sneezing SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Peripheral neuropathy (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Lacrimal disorders (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: I have no way of knowing any of this information. My health care provider administered this. They didn''t disclose lot numbers or any kind or manufacturer. I was told it was Influenza 2010-2011 Current Illness: NO Preexisting Conditions: no Allergies: Diagnostic Lab Data: I contacted my Dr''s office and explained everything. The nurse I spoke to acting like this type of stuff wasn''t normal. She said she would note my medical file. CDC Split Type:
Write-up: First sign was a burning sensation in my arm that lasted over 1 hr. Then beginning at 4:30 pm I felt tickling in my nose. Blowing my nose ongoing until 8:00 pm then violent sneezing, eyes began itch and swollen. Eyes were running and throat felt very bad. I was experiencing what I would call a severe allergic reaction. I have never experienced anything like that. |
|
| VAERS ID: |
405028 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-10-07 |
| Onset: | 2010-10-07 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-23 |
| Days after onset: | 16 |
| Entered: |
2010-10-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / IJ |
Administered by: Public Purchased by: Other Symptoms: Dyspnoea SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Shortness of breath |
|
| VAERS ID: |
405054 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-20 |
| Onset: | 2010-10-22 |
| Days after vaccination: | 2 |
| Submitted: |
2010-10-24 |
| Days after onset: | 2 |
| Entered: |
2010-10-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Other Symptoms: Mobility decreased,
Pain in extremity,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: not yet CDC Split Type:
Write-up: Severe arm pain tingling in fingers. 5 days later severe pain unable to lift arm to get dressed. Little effect with pain meds. |
|
| VAERS ID: |
406654 (history) |
| Form: |
Version 1.0 |
| Age: |
34.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-21 |
| Onset: | 2010-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2010-10-27 |
| Days after onset: | 6 |
| Entered: |
2010-11-02 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U3719AA / 1 |
AR / IM |
Administered by: Private Purchased by: Private Symptoms: Arthralgia,
Chills,
Dyspnoea,
Pyrexia SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: YAZ (birth control) Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Approx 4 hrs after vaccination patient felt short of breath followed by joint pain, chills, and fever: 102.5 & duration 24 hrs. |
|
| VAERS ID: |
408151 (history) |
| Form: |
Version 1.0 |
| Age: |
27.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-11-09 |
| Onset: | 2010-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2010-11-09 |
| Days after onset: | 0 |
| Entered: |
2010-11-12 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT3568BA / 1 |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Feeling cold,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None known Current Illness: None Preexisting Conditions: No allergies to eggs, chicken or polmycin Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 3 pm - came back with c/o urticaria both forearms; skin felt cool and moist. Sat him down - BP 120/70. No other s/s. 330 pm took 50mg BENADRYL PO of his personal meds. Opted out of IM injection of diphenhydramine. 345 pm symptoms lessening. Reviewed vaccine info sheet to watch for further symptoms. Instructed to call 911 if they occur. He arranged for someone to drive him home. 4 pm symptoms gone - was okay to leave. |
|
| VAERS ID: |
408305 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-18 |
| Onset: | 2010-10-19 |
| Days after vaccination: | 1 |
| Submitted: |
2010-11-15 |
| Days after onset: | 27 |
| Entered: |
2010-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (UNKNOWN)) / UNKNOWN MANUFACTURER |
- / 1 |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Faecal incontinence,
Musculoskeletal pain,
Neck pain,
Paraesthesia,
Pruritus,
Skin warm SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Arthritis (broad), Noninfectious diarrhoea (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: seasonal allergies, eczema Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Pain in neck and shoulders, heat & severe pain radiating through bicep down to elbow, tingling through finger tips in both arms and sudden itching on palms of both hands. 10/20 09:00: uncontrollable bowels. |
|
| VAERS ID: |
408422 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2009-10-21 |
| Onset: | 2009-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-09 |
| Days after onset: | 323 |
| Entered: |
2010-11-15 |
| Days after submission: | 67 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500778P / UNK |
NS / IN |
Administered by: Other Purchased by: Other Symptoms: Drug administration error,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug (s) Not reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0009142
Write-up: A non-serious spontaneous report of administration of full dose of H1N1 2009 Monovalent Vaccine Live in one nostril was received from a certified medical assistant concerning an adult. The patient''s medical history and concomitant medications were not provided. There was no adverse event associated with this medication error; therefore, treatment and reporter/sponsor causality assessments are not applicable, and the event is considered resolved. |
|
| VAERS ID: |
408439 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2009-10-21 |
| Onset: | 2009-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-10 |
| Days after onset: | 324 |
| Entered: |
2010-11-15 |
| Days after submission: | 66 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500778P / UNK |
NS / IN |
Administered by: Other Purchased by: Other Symptoms: Drug administration error,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug(s) Not Reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0009152
Write-up: A non-serious spontaneous report of administration of full dose of H1N1 vaccine in one nostril was received from a certified medical assistant concerning an adult. The patient''s medical history and concomitant medications were not provided. There was no adverse event associated with this medication error; therefore, treatment and reporter/sponsor causality assessments are not applicable, and the event is considered resolved. |
|
| VAERS ID: |
408442 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2009-10-21 |
| Onset: | 2009-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-09 |
| Days after onset: | 323 |
| Entered: |
2010-11-15 |
| Days after submission: | 67 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500778P / UNK |
NS / IN |
Administered by: Other Purchased by: Other Symptoms: Drug administration error,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug (s) Not reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0009153
Write-up: A non-serious spontaneous report of administration of full dose of H1N1 2009 Monovalent Vaccine Live in one nostril was received from a certified medical assistant concerning an adult. The patient''s medical history and concomitant medications were not provided. There was no adverse event associated with this medication error; therefore, treatment and reporter/sponsor causality assessments are not applicable, and the event is considered resolved. |
|
| VAERS ID: |
408446 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2009-10-21 |
| Onset: | 2009-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-09 |
| Days after onset: | 323 |
| Entered: |
2010-11-15 |
| Days after submission: | 67 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN(H1N1): INFLUENZA (H1N1) (H1N1 (MONOVALENT) (MEDIMMUNE)) / MEDIMMUNE VACCINES, INC. |
500778P / UNK |
NS / IN |
Administered by: Other Purchased by: Other Symptoms: Drug administration error,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concomitant Drug (s) Not Reported Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: MEDI0009155
Write-up: A non-serious spontaneous report of administration of fall dose of H1N1 2009 vaccine in one nostril was received from a certified medical assistant concerning an adult. The patient''s medical history and concomitant medications were not provided. There was no adverse event associated with this medication error; therefore, treatment and reporter/sponsor causality assessments are not applicable, and the event is considered resolved. |
|
| VAERS ID: |
409399 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-09-29 |
| Onset: | 0000-00-00 |
| Submitted: |
2010-11-01 |
| Entered: |
2010-11-19 |
| Days after submission: | 18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
111796P1 / 1 |
UN / SC |
Administered by: Other Purchased by: Private Symptoms: Discomfort,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 4 weeks after received vaccine, pt couldn''t raise arm without it being sore and very uncomfortable. Pt went to physician. No treatment at this time. MD wants to wait to see if body will reabsorb at site. Office visit Oct. 22. |
|
| VAERS ID: |
411621 (history) |
| Form: |
Version 1.0 |
| Age: |
0.57 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2009-11-09 |
| Onset: | 2009-11-09 |
| Days after vaccination: | 0 |
| Submitted: |
2010-09-27 |
| Days after onset: | 321 |
| Entered: |
2010-11-23 |
| Days after submission: | 57 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1009225PA / 1 |
LG / IM |
Administered by: Other Purchased by: Other Symptoms: Inappropriate schedule of drug administration,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No other medications Current Illness: Unknown Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: PHHY2009US64097
Write-up: Case previously recorded as MA2009-4085. Initial case report received from a nurse on 09 NOV 2009. A 6-month-old male patient was vaccinated with 0.5 mL FLUVIRIN (batch no. 1009225PA) i.m into the thigh on 09 NOV 2009. No adverse events were reported. Reference no: NA09-07868. |
|
| VAERS ID: |
410686 (history) |
| Form: |
Version 1.0 |
| Age: |
32.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-11-19 |
| Onset: | 2010-11-23 |
| Days after vaccination: | 4 |
| Submitted: |
2010-11-30 |
| Days after onset: | 7 |
| Entered: |
2010-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA525BA / 2 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Urticaria,
Vaccine positive rechallenge SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Hives~Influenza (Seasonal) (no brand name)~~31.00~Patient Other Medications: Current Illness: No Preexisting Conditions: Developed hives after 2009 flu vaccination which slowly improved throughout the year but did not resolve. Otherwise healthy. Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Developed a severe chronic hive outbreak following flu vaccine. No known allergy to eggs or chicken. No history of hives prior to receiving the 2009 flu shot. In 2009 hives developed several days after receiving the flu shot. Medication was prescribed and the condition could be controlled by the medicine. Several days after receiving the 2010 flu shot, the condition has returned with a vengeance and cannot be controlled even with medication. I suspect that the flu shot has created a chronic hive condition that will not be easily resolved. |
|
| VAERS ID: |
412731 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-10-11 |
| Onset: | 2010-10-13 |
| Days after vaccination: | 2 |
| Submitted: |
2010-12-14 |
| Days after onset: | 62 |
| Entered: |
2010-12-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT3644AA / 1 |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Dyspnoea SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No illness at that time. Preexisting Conditions: COPD, CHF, DM Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Noticed his breathing was worse a few days later, and he feels as though his breathing''s been worse ever since the vaccine was administered. |
|
| VAERS ID: |
412988 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-09-16 |
| Onset: | 2010-09-19 |
| Days after vaccination: | 3 |
| Submitted: |
2010-12-10 |
| Days after onset: | 82 |
| Entered: |
2010-12-16 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
501017P / 1 |
NS / IN |
Administered by: Private Purchased by: Public Symptoms: Lymphadenopathy SMQs:, Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lymphadenopathy R cervical & submand. nodes torticolis TYLENOL & Ibuprofen. |
|
| VAERS ID: |
413028 (history) |
| Form: |
Version 1.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-11-17 |
| Onset: | 2010-11-18 |
| Days after vaccination: | 1 |
| Submitted: |
2010-12-12 |
| Days after onset: | 24 |
| Entered: |
2010-12-17 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT3568BA / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Injected limb mobility decreased,
Musculoskeletal pain SMQs:, Rhabdomyolysis/myopathy (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Painful left shoulder following influenza vaccine increasing in intensity over time affect her ability to move arm. Followed up with her provider. Receiving physical therapy. |
|
| VAERS ID: |
413227 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-11-18 |
| Onset: | 2010-12-10 |
| Days after vaccination: | 22 |
| Submitted: |
0000-00-00 |
| Entered: |
2010-12-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U3632AA / UNK |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Borrelia test negative,
Chest X-ray,
Computerised tomogram,
Hypoaesthesia facial,
Laboratory test normal,
VIIth nerve paralysis,
Visual impairment SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Hearing impairment (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Vitamins Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Labs and lyme test; CT scan; chest x-ray CDC Split Type:
Write-up: 12/10/10 - pt. experienced difficulty with vision in (R) eye and numbness in (R) side of face. 12/11/10 - E.D. visit; diagnosed with Bell''s Palsy - Rx: Prednisone x 7 days and antiviral meds, Lyme test - neg., CT scan, bloodwork - neg. |
|
| VAERS ID: |
414164 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2010-12-07 |
| Onset: | 2010-12-08 |
| Days after vaccination: | 1 |
| Submitted: |
2011-01-05 |
| Days after onset: | 28 |
| Entered: |
2011-01-06 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
111822P1 / 1 |
LA / UN |
Administered by: Private Purchased by: Private Symptoms: Injection site erosion,
Injection site erythema,
Injection site pain,
Injection site scar,
Injection site vesicles SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ZOCOR; Indomethacin; CYMBALTA; ACTOS; Atenolol; HUMULIN N Current Illness: Preexisting Conditions: IDDM; Depression; LDD; HTN; Hyperlipidemia Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt developed a red blister over area of injection the next day. Pt states it popped and left a gaping hole. On exam today, area of slight erosion & scarring. Mild tenderness at site of injection. No treatment. |
|
| VAERS ID: |
415352 (history) |
| Form: |
Version 1.0 |
| Age: |
29.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-01-24 |
| Onset: | 2011-01-25 |
| Days after vaccination: | 1 |
| Submitted: |
2011-01-25 |
| Days after onset: | 0 |
| Entered: |
2011-01-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
- / 1 |
LA / IM |
Administered by: Unknown Purchased by: Private Symptoms: Chills,
Dyspnoea,
Headache,
Pain,
Pyrexia,
Tremor SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalopathy/delirium (broad), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: I received the Flu Vaccine yesterday. In the middle of the night I woke up with a fever, chills, shortness of breath, body aches, headache, and uncontrollable shaking. This lasted for one hour. This morning I still have a fever. |
|
| VAERS ID: |
415738 (history) |
| Form: |
Version 1.0 |
| Age: |
28.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-01-25 |
| Onset: | 2011-01-25 |
| Days after vaccination: | 0 |
| Submitted: |
2011-01-26 |
| Days after onset: | 1 |
| Entered: |
2011-01-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT3656BA / UNK |
RA / UN |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0466Z / UNK |
LA / UN |
Administered by: Private Purchased by: Public Symptoms: Injection site pain,
Injection site swelling,
Pain SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt developed severe pain 10/10 and swelling at injection site, pt states pain started soon after injection and got much worse from day of injection. Pt given Methylprednisolone Pak and TYLENOL #3. |
|
| VAERS ID: |
417883 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-02-07 |
| Onset: | 2011-02-09 |
| Days after vaccination: | 2 |
| Submitted: |
2011-02-24 |
| Days after onset: | 15 |
| Entered: |
2011-03-02 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLAA614AA / 1 |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0932Z / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Body temperature increased,
Chills,
Diarrhoea,
Erythema,
Fatigue,
Oedema peripheral,
Tremor SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Pseudomembranous colitis (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Redness & swelling in (R) arm within hours of shot - Temp 102, chills, tremors, fatigue, diarrhea redness and swelling from (R) axilla to mid forearm treated with KEFLEX and antihistamine. |
|
| VAERS ID: |
424358 (history) |
| Form: |
Version 1.0 |
| Age: |
69.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2010-10-07 |
| Onset: | 2010-10-07 |
| Days after vaccination: | 0 |
| Submitted: |
2011-05-31 |
| Days after onset: | 236 |
| Entered: |
2011-05-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA615AA / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Pain,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: No Preexisting Conditions: Unknown Allergies: Diagnostic Lab Data: Went to PCP CDC Split Type:
Write-up: Received shot high on arm. Has pain in left arm and has difficulty in moving arm without pain. Has been to neurologist and had physical therapy for past 3 weeks. Slight improvement. |
|
| VAERS ID: |
434406 (history) |
| Form: |
Version 1.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-06 |
| Onset: | 2011-09-07 |
| Days after vaccination: | 1 |
| Submitted: |
2011-09-14 |
| Days after onset: | 7 |
| Entered: |
2011-09-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UH452AB / 1 |
RA / IM |
Administered by: Other Purchased by: Public Symptoms: Body temperature increased,
Nausea,
Oropharyngeal pain,
Skin warm SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Lorazepam, fluticasone nasal spray. Current Illness: non, seasonal allergies Preexisting Conditions: Anxiety Allergies: Diagnostic Lab Data: none available, patient was not seen by a medical professional CDC Split Type:
Write-up: Patient was warm, with a slightly raised body temperature, she had mild nausea and a sore throat. This lasted for 24 hours. |
|
| VAERS ID: |
434641 (history) |
| Form: |
Version 1.0 |
| Age: |
24.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-14 |
| Onset: | 2011-09-17 |
| Days after vaccination: | 3 |
| Submitted: |
2011-09-18 |
| Days after onset: | 1 |
| Entered: |
2011-09-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UH470AD / UNK |
LA / IM |
Administered by: Unknown Purchased by: Other Symptoms: Chills,
Dyspnoea,
Pain,
Pyrexia,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: fever, chills, aches, short of breath, syncope, |
|
| VAERS ID: |
435009 (history) |
| Form: |
Version 1.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-20 |
| Onset: | 2011-09-20 |
| Days after vaccination: | 0 |
| Submitted: |
2011-09-20 |
| Days after onset: | 0 |
| Entered: |
2011-09-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
49281038965 / UNK |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Buttock crushing,
Dizziness,
Fall,
Head injury SMQs:, Anticholinergic syndrome (broad), Accidents and injuries (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Forteo, Ambien Current Illness: no Preexisting Conditions: osteoporosis, irregular heartbeat Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: After check-out I was looking over the sales slip and re-arranging items in cart. I took one step backwards and tripped over the "barrier" cone in front of the customer service desk. I fell over backwards, landing on right buttocks and head. It''s possible that I fell as result of dizziness from the vaccine shot, but more likely that I was simply not watching my step. I''m in good physical shape and in fact just before the vaccine I participated in an aerobics class. Alerted doctor''s office and advised to use ice on buttock injury. |
|
| VAERS ID: |
435338 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-14 |
| Onset: | 2011-09-15 |
| Days after vaccination: | 1 |
| Submitted: |
2011-09-22 |
| Days after onset: | 7 |
| Entered: |
2011-09-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH454AA / 1 |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site rash SMQs:, Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None (radiation about 5 yrs. ago) Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Half moon rash (bumps) at injection site moving up arm to shoulder. |
|
| VAERS ID: |
435793 (history) |
| Form: |
Version 1.0 |
| Age: |
36.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-11 |
| Onset: | 0000-00-00 |
| Submitted: |
2011-09-27 |
| Entered: |
2011-09-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH475AB / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Bursitis,
Drug administered at inappropriate site SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: None Preexisting Conditions: None given Allergies: Diagnostic Lab Data: Unknown at this time CDC Split Type:
Write-up: Patient says injection administered too high and she believes the bursa. She now has bursitis that won''t resolve. Patient states may need cortisone injection to resolve. |
|
| VAERS ID: |
436166 (history) |
| Form: |
Version 1.0 |
| Age: |
76.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-23 |
| Onset: | 2011-09-24 |
| Days after vaccination: | 1 |
| Submitted: |
2011-09-29 |
| Days after onset: | 5 |
| Entered: |
2011-09-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UH436AA / UNK |
AR / IM |
Administered by: Unknown Purchased by: Other Symptoms: Cellulitis,
Dermatitis allergic,
Erythema,
Malaise,
Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: High blood pressure (controlled). Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Patient complained the following day she got the shot saying her arm is itching and red. I counseled her to apply BENADRYL/ZnO cream but she didn''t feel well the 2nd day. Visited her PCP who diagnosed her with cellulitis and allergic skin reaction followed vaccine. Treated with CIPRO 500 mg tab for 1 week and fluconazole 150 for 1 day. |
|
| VAERS ID: |
436670 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-15 |
| Onset: | 0000-00-00 |
| Submitted: |
2011-10-03 |
| Entered: |
2011-10-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH475AB / 1 |
UN / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Mobility decreased,
Pain in extremity SMQs:, Parkinson-like events (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt complaining of left arm pain, & can''t lift the arm up. |
|
| VAERS ID: |
436717 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-10-03 |
| Onset: | 2011-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-04 |
| Days after onset: | 1 |
| Entered: |
2011-10-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH476AC / 6 |
RA / IM |
Administered by: Private Purchased by: Unknown Symptoms: Arthralgia,
Body temperature SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pt c/o temp and joint aches after Influenza vaccine - Mom request report be made. |
|
| VAERS ID: |
436720 (history) |
| Form: |
Version 1.0 |
| Age: |
64.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-10 |
| Onset: | 2011-09-10 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-04 |
| Days after onset: | 24 |
| Entered: |
2011-10-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH475AB / 1 |
LA / - |
Administered by: Public Purchased by: Other Symptoms: Hypokinesia,
Pain,
Pain in extremity,
Periarthritis SMQs:, Parkinson-like events (broad), Guillain-Barre syndrome (broad), Hypotonic-hyporesponsive episode (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: asacol, fluoxetine, simvastatin, fish oil, multivitamin, calcium, Current Illness: None Preexisting Conditions: none Allergies: Diagnostic Lab Data: Have seen an orthopedic PA for review. Recommended PT perhaps cortisone later. CDC Split Type:
Write-up: Pain in movement of arm, frozen shoulder, difficulty moving arm and lifting items. Pain continues after 4+ weeks with no improvement. |
|
| VAERS ID: |
437347 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-10-04 |
| Onset: | 2011-10-06 |
| Days after vaccination: | 2 |
| Submitted: |
2011-10-08 |
| Days after onset: | 2 |
| Entered: |
2011-10-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT445AA / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
1011AA / 1 |
RA / IM |
Administered by: Unknown Purchased by: Private Symptoms: Chills,
Injection site erythema,
Injection site pain,
Injection site swelling,
Injection site warmth,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Xanax, asa, Vantin, diltiazem, dofetilide, Pepcid, Lortab, multivitamin, omega-3 fatty acid, Lexapro, Lamictal Current Illness: No Preexisting Conditions: Heart Arrythmias; Seizure d/o; Depression Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling, warmth, tenderness, erythema spreading from site over the next several days, fevers and rigors. |
|
| VAERS ID: |
438007 (history) |
| Form: |
Version 1.0 |
| Age: |
74.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-10-04 |
| Onset: | 2011-10-07 |
| Days after vaccination: | 3 |
| Submitted: |
2011-10-13 |
| Days after onset: | 6 |
| Entered: |
2011-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA616AA / 4 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Asthenia,
Dysphagia,
Fatigue,
Headache,
Lymphadenopathy,
Tenderness SMQs:, Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: BCP Current Illness: None Preexisting Conditions: Allergic to "deer meat" Allergies: Diagnostic Lab Data: Temp 97.7 10/13/11 CDC Split Type:
Write-up: Felt tired & weak for a few days headache, tender throat, discomfort swallowing (L) side of neck has swollen lymph node. |
|
| VAERS ID: |
438214 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2011-10-13 |
| Entered: |
2011-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
N56506A / UNK |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Headache,
Injection site erythema,
Injection site rash,
Injection site swelling,
Pain,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: NKA Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 2 days after vaccine administered - came into pharmacy with rash red swollen at site of injection - and complained of headache, fever and aches since shot given. |
|
| VAERS ID: |
438256 (history) |
| Form: |
Version 1.0 |
| Age: |
49.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-10-12 |
| Onset: | 2011-10-12 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-14 |
| Days after onset: | 2 |
| Entered: |
2011-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Other Purchased by: Private Symptoms: Activities of daily living impaired,
Chills,
Pyrexia,
Tremor,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Had uncontrollable violent shaking for about an hour, then fever and chills all night and the next day with vomiting. Missed 2 days of work. |
|
| VAERS ID: |
439045 (history) |
| Form: |
Version 1.0 |
| Age: |
49.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-10-17 |
| Onset: | 2011-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-19 |
| Days after onset: | 2 |
| Entered: |
2011-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT491AA / 2 |
LA / IJ |
Administered by: Other Purchased by: Public Symptoms: Burning sensation,
Chills,
Disorientation,
Dizziness,
Headache,
Heart rate increased,
Influenza like illness,
Nasal congestion,
Pain,
Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (narrow), Arrhythmia related investigations, signs and symptoms (broad), Dementia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: N/A CDC Split Type:
Write-up: I became achy and feverish flu like sysmptoms. Apporx 9:30pm at my residents Ibegan to experince chills, Fever, soreness and dizziness. Approx. 11:30pm I was experincing an extremely high temp. (106*)severe chills, dizziness, disorientation, rapid heart beat and vomiting. Throughout time line I was drinking water and taking 800ml of Ibuprofen. Approx 1:30am on 10/18/11 my Fever and symptoms started to reside. Temp dropped (104*) chills started to subside and Vomiting stopped. Approx 3:00am body temp was down (101*) chills almost gone and hot burning sensation disappeared too. Approx. 5:45am awoke after a couple of hours of sound sleep. Except for light headedness and feeling of being tired all sysmptoms had gone. Approx 7:00am on 10/18/11 I had only a bad headache and nasal stuffiness type feeling left. Approx 9:00am I called my Doctor reported reaction event and was advised to continue Tylenol or Ibuprofen. Approx 5:30pm on 10/18/11 all symptoms gone. Felt fine. |
|
| VAERS ID: |
439514 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-16 |
| Onset: | 2011-09-16 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-21 |
| Days after onset: | 35 |
| Entered: |
2011-10-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
111 / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Blood test,
Bronchoscopy,
Platelet count decreased,
Pulmonary haemorrhage,
Thrombocytopenia,
White blood cell count decreased SMQs:, Haematopoietic leukopenia (narrow), Haematopoietic thrombocytopenia (narrow), Haemorrhage terms (excl laboratory terms) (narrow), Systemic lupus erythematosus (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Immune-mediated/autoimmune disorders (broad)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
Extended hospital stay? No Previous Vaccinations: bleeding~Influenza (Seasonal) (Fluzone High-Dose)~1~67.00~Patient Other Medications: Metoprolol 25 mcg Timolol eye drops Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: Bronchoscopy, blood drawings CDC Split Type:
Write-up: I got my Flu shot around 3 in the afternoon on Sept 16th, and was in our local ER bleeding from my lung that night. Doc''s at hospital (was shipped via ambulance from our local hospital) came in next day telling me my WHITE BLOOD CELL COUNT WAS LOW AND CONCERNED THEM (I highlighted in Red the first ''reaction'' shown in the box below)...So for a short ''window of time'' after the Flu shot (approx. 24 hours all told), these things happened. Thrombocytopenia (abnormally low platelet count, which can result in abnormal bleeding) My note: this is what happened to me after getting Flu shot earlier in the day...I had a LOW white cell count that concerned Docs the following day! And was bleeding from my left lung! One of the Serious adverse events in your package insert. I definitely will never get another Flu shot of any kind for any reason. I was NOT informed that the shot I was getting was 4 times the amount of flu bug as the regular shots...I feel like a guinea pig being used for experimentation without my knowledge or consent! Apparently the injection set my white cells on the attack due to your products invasion, and I could not produce them fast enough, resulting in the LOW cell count, resulting in the bleeding... |
|
| VAERS ID: |
439536 (history) |
| Form: |
Version 1.0 |
| Age: |
1.35 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-10-20 |
| Onset: | 2011-10-21 |
| Days after vaccination: | 1 |
| Submitted: |
2011-10-23 |
| Days after onset: | 2 |
| Entered: |
2011-10-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LL / IM |
Administered by: Unknown Purchased by: Private Symptoms: Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: Child vomited. Fever 101 to 103 degrees lasting 24 hours. Children''s Tylenol 1.5 ML every 4 hours to control fever. |
|
| VAERS ID: |
439711 (history) |
| Form: |
Version 1.0 |
| Age: |
20.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2011-10-05 |
| Onset: | 2011-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2011-10-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH475AB / UNK |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Headache,
Pallor,
Vertigo SMQs:, Vestibular disorders (narrow), Hypotonic-hyporesponsive episode (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Pale; vertigo; headache Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vertigo, pale, headache. |
|
| VAERS ID: |
440085 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-20 |
| Onset: | 2011-09-20 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2011-10-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH454AA / 1 |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0614AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Back pain,
Chest pain,
Musculoskeletal pain,
Myalgia,
Neck pain SMQs:, Rhabdomyolysis/myopathy (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Extreme muscle soreness on Right arm w/in min of rec. Pain spread to shoulder, neck, chest, back by mid-afternoon. Resolved after 9 days. |
|
| VAERS ID: |
440387 (history) |
| Form: |
Version 1.0 |
| Age: |
85.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-10-21 |
| Onset: | 2011-10-22 |
| Days after vaccination: | 1 |
| Submitted: |
2011-10-27 |
| Days after onset: | 5 |
| Entered: |
2011-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UH459AB / UNK |
AR / IM |
Administered by: Other Purchased by: Other Symptoms: Pruritus,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: BETIMOL 0.5% eye; TRAVATAN Z 0.004% eye Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Hives on legs & arms that is "really itchy". |
|
| VAERS ID: |
440798 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-10-28 |
| Onset: | 2011-10-28 |
| Days after vaccination: | 0 |
| Submitted: |
2011-10-31 |
| Days after onset: | 3 |
| Entered: |
2011-10-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA652AA / 2 |
LA / IM |
| MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR |
U3837AA / 1 |
LA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C3900AA / UNK |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Respiratory arrest SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Respiratory failure (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 2 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: PCN; asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Resp. arrest after exposure to "fog machine" at school dance, then cold air - occurred within 6 hours after immunization. H/O bad asthma. |
|
| VAERS ID: |
441626 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-11-02 |
| Onset: | 2011-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
2011-11-03 |
| Days after onset: | 1 |
| Entered: |
2011-11-07 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA678AA / 1 |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0811AA / 1 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Injection site erythema,
Injection site pain,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Oxycodone; BONIVA; Baclofen; ENBREL; LYRICA; LUNESTA Current Illness: Back pain Preexisting Conditions: Osteoporosis; Psoriasis; Esophageal reflux; Allergy to PCN Allergies: Diagnostic Lab Data: No temperature increase CDC Split Type:
Write-up: Left deltoid reddened, tender and slightly swollen Pt. reports worsened overnight. Erythema to upper left arm that extends to inner aspect arm halfway toward elbow. Advised to elevate and take ibuprofen for pain. |
|
| VAERS ID: |
442671 (history) |
| Form: |
Version 1.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-11-09 |
| Onset: | 2011-11-10 |
| Days after vaccination: | 1 |
| Submitted: |
2011-11-16 |
| Days after onset: | 6 |
| Entered: |
2011-11-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA636BA / 1 |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Chills,
Contusion,
Pain,
Pain in extremity,
Palpitations,
Pyrexia SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Sore arm Low Grade Fever~Influenza (Seasonal) (no brand name)~~41.00~Patient Other Medications: Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: none CDC Split Type:
Write-up: 24 hours after the vaccine was administered, patient developed a low grade fever and sore arm. She took Advil. At 3:30 pm she spiked a fever and had chills. 6:30 pm her heart was racing, temp 103.5. She called her MD on call. He recommended Benadryl (patient did not have any) and cold compresses. 8:30 pm Temp 102. 11-11-11 2 Am Had chills and temp 102. Took Tylenol. Woke in am with achiness and continued painful right arm. Temp now gone but arm painful with resistence. She said the arm does not have redness or swelling but there is a bruise. She said it does not appear infected. I recommended she follow up with her provider if the arm does not improve and could try warm compresses or ice (which ever felt better to her to help decrease the pain. On a scale of 1-10, at it''s worst the pain was a 7 and now is a 2. |
|
| VAERS ID: |
442808 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-10-20 |
| Onset: | 2011-11-14 |
| Days after vaccination: | 25 |
| Submitted: |
2011-11-16 |
| Days after onset: | 2 |
| Entered: |
2011-11-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1100901 / 2 |
- / IM |
Administered by: Private Purchased by: Private Symptoms: Ataxia,
CSF test abnormal,
Computerised tomogram abnormal,
Hypoaesthesia,
Miller Fisher syndrome,
Nerve conduction studies abnormal,
Paraesthesia,
VIIth nerve paralysis SMQs:, Peripheral neuropathy (narrow), Anticholinergic syndrome (broad), Guillain-Barre syndrome (narrow), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad), Ocular motility disorders (narrow), Immune-mediated/autoimmune disorders (broad), Sexual dysfunction (broad)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, ? days
Extended hospital stay? No Previous Vaccinations: Other Medications: Amiloride-HCTZ, Atenolol, Simvastatin, Enalapril, Ibuprofen, Potassium, Centrum Silver Current Illness: None Preexisting Conditions: Diabetes, Hypertension, Hyperlipidemia, elevated PSA Allergies: Diagnostic Lab Data: NCS, CSF, CT all consistent with Miller-Fisher Variant of Guillain Barre. CDC Split Type:
Write-up: Started 11/14 with numbness and Tingling in toes and fingers. Progressed to waist and then on Saturday, Nov 12, developed a Bell''s Palsy and ataxia. |
|
| VAERS ID: |
443658 (history) |
| Form: |
Version 1.0 |
| Age: |
50.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-11-08 |
| Onset: | 2011-11-14 |
| Days after vaccination: | 6 |
| Submitted: |
2011-11-16 |
| Days after onset: | 2 |
| Entered: |
2011-11-22 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
N57117 / UNK |
UN / IM |
Administered by: Other Purchased by: Public Symptoms: Chills,
Diarrhoea,
Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Gabapentin; Paroxetine; Lisinopril; bupropion; DEXILANT; Hydroxyzine; Nitrostat; Metoprolol Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 6 days after vaccine patient developed fever, chills, vomiting & diarrhea. |
|
| VAERS ID: |
443733 (history) |
| Form: |
Version 1.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-11-15 |
| Onset: | 2011-11-15 |
| Days after vaccination: | 0 |
| Submitted: |
2011-11-16 |
| Days after onset: | 1 |
| Entered: |
2011-11-22 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT4197B / 7+ |
LA / IM |
| HPV4: HPV (GARDASIL) / MERCK & CO. INC. |
0692AA / 1 |
RA / IM |
| MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR |
U4008AA / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Chest discomfort,
Dyspnoea,
Rash erythematous,
Rash pruritic,
Sensory loss SMQs:, Anaphylactic reaction (narrow), Peripheral neuropathy (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: FLOVENT; PRO-AIR; SINGULAIR Current Illness: Physical Preexisting Conditions: Asthma; Seasonal allergies Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Had below imms on 11/15/11. That eve - red, itchy rash bil hands. Then chest tight. Took to ER - given BENADRYL. They thought possibly viral. Slept well. Next AM SOB, chest tight, no feeling (R) hand. Rash continues. On BENADRYL and her albuterol (has asthma). Site of injection WNL, no erythema, no edema. |
|
| VAERS ID: |
443877 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-11-18 |
| Onset: | 2011-11-19 |
| Days after vaccination: | 1 |
| Submitted: |
2011-11-23 |
| Days after onset: | 4 |
| Entered: |
2011-11-28 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT414CA / 4 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Arthralgia,
Erythema nodosum,
Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Erythema nodosum, myalgia, arthralgias started 48 hours after immunization. |
|
| VAERS ID: |
443916 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-11-24 |
| Onset: | 2011-11-24 |
| Days after vaccination: | 0 |
| Submitted: |
2011-11-24 |
| Days after onset: | 0 |
| Entered: |
2011-11-28 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH462AC / 1 |
AR / IM |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Seizure like phenomena,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: end stage cold symptoms Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Lightheadedness, with seizure like symptoms, then fainting, lasted approx 10 sec 911 called; I laid her down on floor with feet raised, the 911 techs took over, ambulance & tech took her from store. |
|
| VAERS ID: |
444950 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-12-02 |
| Onset: | 2011-12-03 |
| Days after vaccination: | 1 |
| Submitted: |
2011-12-08 |
| Days after onset: | 5 |
| Entered: |
2011-12-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH476AD / UNK |
LA / IM |
Administered by: Unknown Purchased by: Other Symptoms: Autopsy,
Culture negative,
Death,
Dyspnoea,
Influenza like illness,
Lethargy,
Microscopy,
Pain,
Pyrexia,
Resuscitation,
Unresponsive to stimuli SMQs:, Anaphylactic reaction (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2011-12-06
Days after onset: 3
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: no Preexisting Conditions: no Allergies: Diagnostic Lab Data: Gross Autopsy negative. Preliminary cultures negative Pending Microscopic examination CDC Split Type:
Write-up: Went for well child check 12/2 no issues flu vaccination given. Next day developed flu like illness with fever 102.3, body aches lethargy, treated with Tylenol and Motrin, symptoms waxed and waned got significantly worse Tuesday 12/6/11 with dyspnea. Patient went unresponsive on way to pediatrician emergent resuscitation and died 12/6/11. |
|
| VAERS ID: |
446077 (history) |
| Form: |
Version 1.0 |
| Age: |
54.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-12-15 |
| Onset: | 2011-12-15 |
| Days after vaccination: | 0 |
| Submitted: |
2011-12-20 |
| Days after onset: | 5 |
| Entered: |
2011-12-22 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1100701 / 1 |
LA / UN |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
1138AA / 1 |
RA / UN |
Administered by: Public Purchased by: Public Symptoms: Injection site erythema,
Injection site reaction,
Injection site swelling,
Rash macular SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Red blotchy area on upper arm where injection was given with slight swelling. |
|
| VAERS ID: |
447037 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-10-24 |
| Onset: | 2011-10-24 |
| Days after vaccination: | 0 |
| Submitted: |
2012-01-02 |
| Days after onset: | 70 |
| Entered: |
2012-01-09 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN3: INFLUENZA (SEASONAL) (FLUMIST) / MEDIMMUNE VACCINES, INC. |
501105P / 2 |
NS / IN |
| HPV4: HPV (GARDASIL) / MERCK & CO. INC. |
0692AA / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Adverse reaction,
Hypoaesthesia,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Paresthesias - numbness, tingling involving both upper and lower extremities - Sx come and go but started on day of vaccine. Then more sx 2 wks later then again 2 wks later. Episodes last upwards of 1 hr - no known HA at time of attacks. |
|
| VAERS ID: |
447082 (history) |
| Form: |
Version 1.0 |
| Age: |
1.13 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-01-04 |
| Onset: | 2012-01-06 |
| Days after vaccination: | 2 |
| Submitted: |
2012-01-09 |
| Days after onset: | 3 |
| Entered: |
2012-01-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT4159CA / 1 |
UN / UN |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
0853AA / 1 |
LL / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
0605AA / 1 |
LL / SC |
Administered by: Private Purchased by: Public Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Recent amox for AOM - completed 12/24 Preexisting Conditions: No Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: 3 immunizations given 1/4/11. On 1/6 developed diffuse urticarial appearing rash without symptoms. No target lesions or purpura. No joint swelling. Minimal response to 1.2 mg/kg dose of BENADRYL given multiple times. Resolved nearly completely by 1/9/11. |
|
| VAERS ID: |
447886 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2011-12-12 |
| Onset: | 2011-12-12 |
| Days after vaccination: | 0 |
| Submitted: |
2012-01-24 |
| Days after onset: | 43 |
| Entered: |
2012-01-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC20B171CA / 1 |
RL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA614BA / 5 |
LL / IM |
Administered by: Private Purchased by: Other Symptoms: Chills,
Pain in extremity,
Pyrexia,
Tremor,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Began with a fever at 4pm-ish. Woke up at 12:00 AM shaking with chills and fever of 101. Vomited once. Leg hurt. Fever spiked to 103.4 at 12:15AM. 12:30AM fever at 104.0. Motrin given at 12:30 so we waited to see if it came down. Fever at 103 at 1:00AM. Fever at 101.3 at 1:30 AM. Put him to bed. He maintained a low grade 100 degree fever which lowered slowly over the next few days. Visited the doctor to check him out with fever on 12/14 or 12/15/2011. They said to watch him and come back if fever worsened. His fever went away the next day and we have had no further issues. |
|
| VAERS ID: |
449723 (history) |
| Form: |
Version 1.0 |
| Age: |
0.52 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-02-10 |
| Onset: | 2012-02-11 |
| Days after vaccination: | 1 |
| Submitted: |
2012-02-16 |
| Days after onset: | 5 |
| Entered: |
2012-02-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR |
C4045AA / 3 |
RL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UT4149CA / 1 |
RL / IM |
| HEP: HEP B (ENGERIX-B) / GLAXOSMITHKLINE BIOLOGICALS |
AHBVC022DA / 3 |
LL / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
F17155 / 3 |
LL / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site rash SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: TRIVISOL po daily Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Red raised rash on both thighs, has happened before at 6 wk vaccines & 4 month vaccines. Same shots given except flu given 2-10-12 her first time. |
|
| VAERS ID: |
463464 (history) |
| Form: |
Version 1.0 |
| Age: |
77.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-08-26 |
| Onset: | 2012-08-27 |
| Days after vaccination: | 1 |
| Submitted: |
2012-08-28 |
| Days after onset: | 1 |
| Entered: |
2012-08-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH715AA / UNK |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Erythema,
Skin warm,
Tenderness SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Localized redness on left arm. Pt states area is warm and tender. |
|
| VAERS ID: |
465725 (history) |
| Form: |
Version 1.0 |
| Age: |
25.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-09-18 |
| Onset: | 2012-09-18 |
| Days after vaccination: | 0 |
| Submitted: |
2012-09-18 |
| Days after onset: | 0 |
| Entered: |
2012-09-20 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
P58406 / UNK |
LA / SYR |
Administered by: Other Purchased by: Private Symptoms: Hypoaesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Sertraline; Trazodone; Lithium; LOW-OGESTREL Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Within 10 min. of having the shot, her face went numb on her cheek just below her left eye down to her neck. |
|
| VAERS ID: |
465985 (history) |
| Form: |
Version 1.0 |
| Age: |
23.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-09-20 |
| Onset: | 2012-09-21 |
| Days after vaccination: | 1 |
| Submitted: |
2012-09-21 |
| Days after onset: | 0 |
| Entered: |
2012-09-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
D58507 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Headache,
Pyrexia,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ORTHO TRI CYCLEN LO; Citalopram Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: About 7 hours after administration patient had high fever (103.5), shaking and headache. Was examined, treated & released from medical center after about 1 hour & told to rest for 2 days. |
|
| VAERS ID: |
466774 (history) |
| Form: |
Version 1.0 |
| Age: |
89.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2012-09-19 |
| Onset: | 2012-09-19 |
| Days after vaccination: | 0 |
| Submitted: |
2012-09-27 |
| Days after onset: | 8 |
| Entered: |
2012-09-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4490AA / UNK |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Balance disorder,
Chills,
Feeling cold,
Nausea,
Nervousness SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: BENICAR; CRESTOR Current Illness: None Preexisting Conditions: High cholesterol & high blood pressure Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Appx 6 hours after vaccination, patient felt nausea, had shivers & cold chills, felt shaky, unsteady. Feelings persisted until next morning. |
|
| VAERS ID: |
467627 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-09-28 |
| Onset: | 2012-09-29 |
| Days after vaccination: | 1 |
| Submitted: |
2012-10-04 |
| Days after onset: | 5 |
| Entered: |
2012-10-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC20B187AA / UNK |
UN / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U4483AA / 7+ |
RL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
0497AE / 2 |
UN / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
H010853 / 2 |
UN / SC |
Administered by: Private Purchased by: Public Symptoms: Injection site swelling,
Lethargy,
Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Asthma Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: High fever & lethargy 24 hrs after. Urticaria 5 days after. Swollen IZ site. |
|
| VAERS ID: |
468520 (history) |
| Form: |
Version 1.0 |
| Age: |
38.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-10-04 |
| Onset: | 2012-10-04 |
| Days after vaccination: | 0 |
| Submitted: |
2012-10-09 |
| Days after onset: | 5 |
| Entered: |
2012-10-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1203901 / UNK |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
H010515 / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Axillary pain,
Diarrhoea,
Erythema,
Injection site streaking SMQs:, Anaphylactic reaction (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (broad), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: H/O Asthma Preexisting Conditions: H/O Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pain in the armpit, red streaking ascending the left arm into the armpit and around the collar bone. Also experienceing diarrhea. |
|
| VAERS ID: |
469829 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-09-17 |
| Onset: | 2012-10-04 |
| Days after vaccination: | 17 |
| Submitted: |
2012-10-12 |
| Days after onset: | 8 |
| Entered: |
2012-10-15 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4499AA / UNK |
AR / IM |
Administered by: Other Purchased by: Other Symptoms: Injected limb mobility decreased,
Tenderness SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient described original "tenderness" after shot then that went away. Approx. 2 to 3 weeks later pt felt that the arm where the shot was given became lame and had some restriction of mobility but experienced NO tenderness. Since fully resolved over the next 2 days. NO tenderness, redness, rash, or trouble breathing reported. |
|
| VAERS ID: |
469833 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-09-17 |
| Onset: | 2012-10-04 |
| Days after vaccination: | 17 |
| Submitted: |
2012-10-12 |
| Days after onset: | 8 |
| Entered: |
2012-10-15 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4499AA / UNK |
AR / IM |
Administered by: Other Purchased by: Other Symptoms: Injected limb mobility decreased,
Injection site reaction,
Tenderness SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient described original "tenderness" after shot, then went away. Approx. 2-3 weeks later pt felt that arm where shot was given was lame and had decreased mobility but without tenderness. Resolved all symptoms over the next 2 days. No tenderness, redness, rash or trouble breathing reported. |
|
| VAERS ID: |
469802 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-10-11 |
| Onset: | 2012-10-14 |
| Days after vaccination: | 3 |
| Submitted: |
2012-10-16 |
| Days after onset: | 2 |
| Entered: |
2012-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
06749211A / UNK |
RA / IM |
| TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
C4136BA / UNK |
LA / IM |
Administered by: Private Purchased by: Unknown Symptoms: Injection site cellulitis SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ProAir, Azithromycin, Robitussin AC Current Illness: Community Acquired Pneumonia Preexisting Conditions: Allergies to PCN, Sulfa, Iodine and Fish Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Cellulitis at injection site; Treated with Keflex. |
|
| VAERS ID: |
470048 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-10-08 |
| Onset: | 2012-10-11 |
| Days after vaccination: | 3 |
| Submitted: |
2012-10-15 |
| Days after onset: | 4 |
| Entered: |
2012-10-16 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
AFLLA739AA / UNK |
RA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C4034AA / UNK |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Erythema,
Local reaction,
Pruritus,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Venlafexine; Naproxen; LOTREL; LIPITOR; Atenolol; Omeprazole; NAMENDA; Donepezil; Clonazepam Current Illness: None Preexisting Conditions: HTN; Hyperlipidemia; Depression; Anxiety Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Local reaction - erythema, swelling, itching. Treatment - ibuprofen, BENADRYL, cold packs. |
|
| VAERS ID: |
471558 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-10-18 |
| Onset: | 2012-10-18 |
| Days after vaccination: | 0 |
| Submitted: |
2012-10-19 |
| Days after onset: | 1 |
| Entered: |
2012-10-24 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4525AA / 1 |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Asthenia,
Dizziness,
Dyspnoea,
Heart rate increased SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Labored breathing, weak, fast heart rate, dizziness lasting about 1 min at 9PM night after receiving shot. No treatment needed. |
|
| VAERS ID: |
471525 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-23 |
| Onset: | 2011-09-23 |
| Days after vaccination: | 0 |
| Submitted: |
2012-10-25 |
| Days after onset: | 398 |
| Entered: |
2012-10-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1101001 / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Injection site pain,
Nerve injury,
Pain in extremity SMQs:, Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNKNOWN what medications patient takes. Current Illness: No Preexisting Conditions: Rheumatoid arthritis Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Patient received a flu shot last year and developed pain down the left arm soon after which has lasted to this day. There was soreness at the site after vaccine was given in 2011, then pain down the arm and it has still not gone away. Patient''s physician said there may be some nerve damage. No treatment done. |
|
| VAERS ID: |
471722 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-10-23 |
| Onset: | 2012-10-23 |
| Days after vaccination: | 0 |
| Submitted: |
2012-10-27 |
| Days after onset: | 4 |
| Entered: |
2012-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / SYR |
Administered by: Private Purchased by: Private Symptoms: Dizziness,
Dyspnoea,
Fatigue,
Injection site erythema,
Injection site haematoma,
Injection site pruritus,
Injection site rash,
Musculoskeletal pain SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Extravasation events (injections, infusions and implants) (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Toprol XL 100mg, Hyzaar 100/25 No other different meds or vaccines for months. Current Illness: None. Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizziness first evening. Next morning woke with shoulder pain, trouble breathing and fatigue. Used heating pad on shoulder still having trouble breathing. Rested all day. Felt relief next day. Then had a large 2-3" itchy, red blotchy area at injection site. Itchiness lasted 3 days. Still have a bruise type area remaining but itching is gone. I have had many flu shots and NEVER had any reaction whatsoever. This is a complete mystery. |
|
| VAERS ID: |
472420 (history) |
| Form: |
Version 1.0 |
| Age: |
46.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-10-24 |
| Onset: | 2012-10-24 |
| Days after vaccination: | 0 |
| Submitted: |
2012-10-31 |
| Days after onset: | 7 |
| Entered: |
2012-10-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Public Purchased by: Unknown Symptoms: Asthenia,
Body temperature decreased,
Dyspnoea,
Haemorrhage subcutaneous,
Injection site haematoma,
Oedema peripheral,
Rash,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac failure (broad), Anaphylactic reaction (narrow), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: TBD CDC Split Type:
Write-up: Fainting, weakness, difficulty breathing, entire arm swollen to the point of dimpling flesh, rash around throat and chest, shocky low body temperature for 36 hours. Gradual decrease over $g3 days. Massive bruise at administration site appeared after 24 hours, doubled in size each day for three days; evidence of fresh subcutaneous bleeding continues to develop more than one week later. |
|
| VAERS ID: |
473645 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2011-09-26 |
| Onset: | 2011-09-26 |
| Days after vaccination: | 0 |
| Submitted: |
2012-11-06 |
| Days after onset: | 407 |
| Entered: |
2012-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH452AC / UNK |
RA / SYR |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
0454AA / UNK |
RA / UN |
Administered by: Private Purchased by: Private Symptoms: Malaise,
Nausea,
Syncope,
Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: HTN; Hyperlipidemia; Obesity Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: The night of vaccine given, patient had nausea, vomiting, syncope and then malaise for a couple days. |
|
| VAERS ID: |
474479 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2012-11-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4490AA / 1 |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Losartan-HCTZ Current Illness: None Preexisting Conditions: Hypertension Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient reports muscle aches for 2 weeks after flu shot. |
|
| VAERS ID: |
474540 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-11-07 |
| Onset: | 2012-11-08 |
| Days after vaccination: | 1 |
| Submitted: |
2012-11-09 |
| Days after onset: | 1 |
| Entered: |
2012-11-14 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC20B204AA / UNK |
LA / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U4483AA / 4 |
RA / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
0683AE / 1 |
RA / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
H015137 / 1 |
LA / SC |
Administered by: Other Purchased by: Public Symptoms: Injection site erythema,
Injection site mass,
Injection site pain,
Injection site swelling,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Amoxicillin Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: (L) arm red/swollen/painful. Lump at site of KINRIX. Fever 103 degrees. |
|
| VAERS ID: |
475381 (history) |
| Form: |
Version 1.0 |
| Age: |
46.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-11-14 |
| Onset: | 2012-11-15 |
| Days after vaccination: | 1 |
| Submitted: |
2012-11-27 |
| Days after onset: | 12 |
| Entered: |
2012-11-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1205301 / 2 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None reported Current Illness: None reported Preexisting Conditions: None reported Allergies: Diagnostic Lab Data: Patient contacted MD. Clinician has left several follow up messages to see outcome. Pt has not returned calls to date. CDC Split Type:
Write-up: Rash developed in the middle of pts back. By days end the rash had spread across the back with some spots on shoulders and arms. No other symptoms. |
|
| VAERS ID: |
475542 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-11-25 |
| Onset: | 2012-11-26 |
| Days after vaccination: | 1 |
| Submitted: |
2012-11-27 |
| Days after onset: | 1 |
| Entered: |
2012-11-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
P50708 / UNK |
LA / IM |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
H011332 / 1 |
LA / SC |
Administered by: Other Purchased by: Other Symptoms: Injection site erythema SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine administered on Sun 11/25/12. Patient contacted pharmacy at 8 am on 11/27/12 to say she had a red, round area around vaccination site about the size of a silver dollar. |
|
| VAERS ID: |
477167 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-11-09 |
| Onset: | 2012-11-16 |
| Days after vaccination: | 7 |
| Submitted: |
2012-12-08 |
| Days after onset: | 22 |
| Entered: |
2012-12-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / UN |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U4482BA / UNK |
UN / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AHAVB523AA / 2 |
LL / IM |
Administered by: Private Purchased by: Other Symptoms: Blood test normal,
Electroencephalogram abnormal,
Epilepsy,
Fear,
Grand mal convulsion,
Nuclear magnetic resonance imaging abnormal,
Pyrexia,
Screaming,
Staring SMQs:, Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hostility/aggression (broad), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Azithromycin for a sinus infection. Current Illness: Yes, he was on medicine for a sinus infection. Preexisting Conditions: He was diagnosed with epilepsy on November 22, 2012. He was born with full body petechiae. Allergies: Diagnostic Lab Data: He was tested for leukodystrophy among many other things, but all of his blood tests came back okay. He had an MRI and an EEG which confirmed epilepsy. CDC Split Type:
Write-up: He starting running a fever on November 16th, that night he woke up screaming several times, his eyes were all glazed over, and he was petrified. I thought they were just nightmares. The morning of November 18th, he was taken by ambulance to the hospital following a grand mal seizure. He went on to have multiple seizures at the hospital, and was transferred to another facility. At first they were calling them febrile seizures until they diagnosed him with epilepsy. The cause of his fever is still unknown, but I believe the vaccines he had on Nov.9 may have caused the fever, and brought on the seizures. |
|
| VAERS ID: |
477393 (history) |
| Form: |
Version 1.0 |
| Age: |
29.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-11-20 |
| Onset: | 2012-11-21 |
| Days after vaccination: | 1 |
| Submitted: |
2012-12-10 |
| Days after onset: | 19 |
| Entered: |
2012-12-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
RA / SYR |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
- / 1 |
LA / SYR |
Administered by: Public Purchased by: Other Symptoms: Asthenia,
Blood test abnormal,
Chills,
Decreased appetite,
Feeling of body temperature change,
Infection,
Influenza virus test negative,
Injection site erythema,
Injection site pain,
Injection site rash,
Injection site warmth,
Malaise,
Nausea,
Pyrexia,
Somnolence,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: acetaminophen (TYLENOL) 500 mg tablet; aspirin 325 mg EC tablet; multivitamin Iron-Ca-FA-Min (THERAPEUTIC-M) 27-0.4 mg tablet; senna-docusate; (ICOLACE) 8.6-50 mg per tablet; HYDROmorphone (DILAUDID) 2 mg tablet; modafinil (PROVIGIL) 200 m Current Illness: Preexisting Conditions: Had knee realignment surgery on 11/19/2012. Hypertension. Allergies: Diagnostic Lab Data: Flu shot: negative; Blood work for infection: positive CDC Split Type:
Write-up: On 11/21/2012 woke up with 101.5 temperature. I was able take Tylenol to bring it down, but the fever kept fluctuating between normal and fever. Had nausea, uncontrollable chills, was cold and hot, very sleepy, vomiting, weakness also had loss of appetite. I had had knee surgery on 11/19/2012 for knee realignment. PNEUMOVAX was given to me on 11/20/2012 in my left shoulder. Also Influenza Split injection was given in my right shoulder. I had a rash on my left shoulder that grew from the injection site to the elbow and shoulder that was very sore, red and hot. Started as small and grew. I kept getting worse and On 11/23/2012 woke up with 102.5 temperature and was really sick I was able to get the temperature down with Tylenol but my Dr advised me to go to the to the emergency room. The ER did test for the flu and came back negative. The Dr also checked my leg for infection and did not see any sign on the incision of infection and said looked really good. Also did blood tests found that came back as had infection somewhere. The ER Dr said she thought I had a infection in my left arm near the injection site and put me on antibiotic. My temperature and side effects went away on 11/25/2012 but the rash remained for another week or so. |
|
| VAERS ID: |
478104 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-11-29 |
| Onset: | 2012-11-29 |
| Days after vaccination: | 0 |
| Submitted: |
2012-12-07 |
| Days after onset: | 8 |
| Entered: |
2012-12-14 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4499AA / UNK |
UN / IM |
Administered by: Other Purchased by: Public Symptoms: Chills,
Cough,
Pyrexia SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Cough, fever, chills for about 24 hours then pt was fine, started a few hours after administration. |
|
| VAERS ID: |
478206 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-12-12 |
| Onset: | 2012-12-15 |
| Days after vaccination: | 3 |
| Submitted: |
2012-12-15 |
| Days after onset: | 0 |
| Entered: |
2012-12-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Nausea,
Vertigo SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: I got vaccine for free at walk-in service at Medical Center. Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Sudden onset of nausea and vertigo. Worst with bodily movement or bending. Continuing at time of this report. Reviewed forum posting. Apparently this is being reported by others. |
|
| VAERS ID: |
478589 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2012-12-18 |
| Onset: | 2012-12-18 |
| Days after vaccination: | 0 |
| Submitted: |
2012-12-18 |
| Days after onset: | 0 |
| Entered: |
2012-12-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLU707AA / UNK |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Chills SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Acetaminophen PO, ASA, cefazolin, chlorthalidone, docusate, gabapentin, glipizide, metformin, metoprolol, oxycodone, rosuvastatin, sitagliptin, NS IV fluids Current Illness: None Preexisting Conditions: Diabetes, hypertension, atherosclerosis, hyperlipidemia, recent L4-5 fusion (12/17) Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt had onset of rigors about 1 hr after administration of vaccine. |
|
| VAERS ID: |
478874 (history) |
| Form: |
Version 1.0 |
| Age: |
35.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-12-19 |
| Onset: | 2012-12-19 |
| Days after vaccination: | 0 |
| Submitted: |
2012-12-20 |
| Days after onset: | 1 |
| Entered: |
2012-12-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
33332001201 / 1 |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Chills,
Musculoskeletal pain,
Neck pain,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None. Current Illness: None Preexisting Conditions: Allergic to PCN & Sulfa drugs Allergies: Diagnostic Lab Data: None. CDC Split Type:
Write-up: My arm began to get very sore about an hour after the shot and then my neck on the same side as the shot started to hurt all the way through my shoulder about an hour an a half after the shot. I went to bed around 9 p.m. and then got the chills and shivers. I took Advil and Tylenol, threw on another blanket and turned up the heat and went to sleep. I did not have a fever. When I got up this morning, all symptoms were gone, except the sore arm. |
|
| VAERS ID: |
480013 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-11-09 |
| Onset: | 2012-11-10 |
| Days after vaccination: | 1 |
| Submitted: |
2012-12-31 |
| Days after onset: | 51 |
| Entered: |
2012-12-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
P50808 / 1 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Chills,
Cough,
Diarrhoea,
Pain,
Pyrexia,
Respiratory tract congestion SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 1993~Influenza (Seasonal) (no brand name)~UN~0.00~Patient Other Medications: See attached Current Illness: None Preexisting Conditions: See attached Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt was ill with body aches, cough, diarrhea, fever/chills, chest congestion. Pt receives a split dose vaccine #1 given 11/9/12 #2 on 11/29/12. |
|
| VAERS ID: |
480617 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-12-20 |
| Onset: | 2012-12-20 |
| Days after vaccination: | 0 |
| Submitted: |
2013-01-02 |
| Days after onset: | 13 |
| Entered: |
2013-01-08 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH746AC / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Burning sensation,
Cough,
Erythema,
Lacrimation increased,
Pruritus SMQs:, Anaphylactic reaction (narrow), Peripheral neuropathy (broad), Lacrimal disorders (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Extremely red, itchy, burning, water eyes, cough (annoying). |
|
| VAERS ID: |
481789 (history) |
| Form: |
Version 1.0 |
| Age: |
38.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-01-12 |
| Onset: | 2013-01-13 |
| Days after vaccination: | 1 |
| Submitted: |
2013-01-17 |
| Days after onset: | 4 |
| Entered: |
2013-01-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE INTRADERMAL) / SANOFI PASTEUR |
UT4470BA / UNK |
UN / ID |
Administered by: Other Purchased by: Other Symptoms: Infection,
Injection site erythema,
Injection site rash SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Rizatriptan; citalopram; Zolpidem; clonazepam; amlodipine Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient developed large, raised red area at site of injection. She consulted her physician who placed her on antibiotics for suspicion of infection. |
|
| VAERS ID: |
481997 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-01-02 |
| Onset: | 2013-01-02 |
| Days after vaccination: | 0 |
| Submitted: |
2013-01-20 |
| Days after onset: | 18 |
| Entered: |
2013-01-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH746AC / UNK |
AR / IM |
Administered by: Other Purchased by: Other Symptoms: Cough,
Oral pain,
Oropharyngeal pain SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown -$g answered no on survey Preexisting Conditions: Unknown Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Approx 4 hours post vaccine patient reports coughing for 30-60 minutes followed by a sore throat and mouth that lasted for approx 3-4 hours. Was not bad enough to keep her from falling asleep that night. By the next morning all signs and symptoms had fully resolved. |
|
| VAERS ID: |
483324 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-10-19 |
| Onset: | 2012-10-28 |
| Days after vaccination: | 9 |
| Submitted: |
2012-11-06 |
| Days after onset: | 9 |
| Entered: |
2013-02-04 |
| Days after submission: | 90 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
- / 1 |
LA / UN |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
- / 1 |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Herpes zoster SMQs:, Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Dx shingles CDC Split Type:
Write-up: Rec''d shingles vaccine 10/19/2012 came down with shingles 9 days later on 10/28/2012. |
|
| VAERS ID: |
497381 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-09-29 |
| Onset: | 2012-09-29 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2013-07-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH718AA / UNK |
AR / IM |
Administered by: Other Purchased by: Private Symptoms: Incorrect route of drug administration,
Rotator cuff syndrome SMQs:, Drug abuse and dependence (broad), Tendinopathies and ligament disorders (narrow), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: July 10, 2013 my doc. said "I have tendinitis/cuff and thickening of acromion, but no way to tell if it''s life, or improper vaccination. Received flu" shot 9/2012 into my shoulder top, instead of muscle. Enclosed copy or signature and date at pharmacy. Please notify fellow to stop administering vaccinations this way! Thank you! |
|
| VAERS ID: |
501086 (history) |
| Form: |
Version 1.0 |
| Age: |
86.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-08-28 |
| Onset: | 2013-08-28 |
| Days after vaccination: | 0 |
| Submitted: |
2013-08-29 |
| Days after onset: | 1 |
| Entered: |
2013-08-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4713AA / UNK |
LA / SYR |
Administered by: Other Purchased by: Public Symptoms: Injection site pain,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling at the injection site and severe pain. |
|
| VAERS ID: |
501688 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-08-19 |
| Onset: | 2013-08-19 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2013-09-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4713AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Injection site pruritus,
Lip swelling SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Blood pressure Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Within 5 mins after administering the shot patient had itching around the injection site and after few minutes she had dizziness and her lips started swelling. She went to the ER right away where she got prednisone shot and she is fine after that. |
|
| VAERS ID: |
504744 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-09-18 |
| Onset: | 2013-09-18 |
| Days after vaccination: | 0 |
| Submitted: |
2013-09-19 |
| Days after onset: | 1 |
| Entered: |
2013-09-30 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4713AA / 1 |
LA / UN |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
H016283 / 2 |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Nausea,
Pyrexia,
Tremor SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Hypothyroidism; Penicillin allergy; High BP Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Evening of shots, extreme nausea from 8:00 to 10:00 PM. Then uncontrollable violent shaking, cont ''d thru night, around 1:00 AM 99.8 fever, 5:00 AM 99.3 fever, still shakes, 8:00 AM 98.6 fever and ok. |
|
| VAERS ID: |
505403 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2013-10-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4762BA / UNK |
UN / UN |
Administered by: Unknown Purchased by: Unknown Symptoms: Cellulitis SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Cellulitis. |
|
| VAERS ID: |
505410 (history) |
| Form: |
Version 1.0 |
| Age: |
87.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-09-24 |
| Onset: | 2013-09-24 |
| Days after vaccination: | 0 |
| Submitted: |
2013-10-02 |
| Days after onset: | 8 |
| Entered: |
2013-10-03 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4781AA / 2 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Convulsion,
Local swelling SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Angioedema (broad), Systemic lupus erythematosus (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 4 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Atorvastatin; PAXIL; FLONASE; NAMENDA; SEROQUEL; COZAAR; Hydralazine; Lisinopril; Metformin; Atenolol; CLARINEX; Z-PAK Current Illness: Finished ZPAK - 500mg 1 day prior to shot Preexisting Conditions: NKA; Dementia; High blood pressure; High cholesterol (All that I know) Allergies: Diagnostic Lab Data: At pharmacy CDC Split Type:
Write-up: Patient''s caregiver came to the pharmacy 8 days after patient received flu shot, explaining how she was rushed to the emergency room about 3 hours after the flu shot. The patient was having a seizure (caregiver could not say which kind), and stayed in the hospital for 4 days. Patient also has some leg swelling that has not gone away, she has a follow-up for Wed. |
|
| VAERS ID: |
505994 (history) |
| Form: |
Version 1.0 |
| Age: |
78.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-09-25 |
| Onset: | 2013-09-27 |
| Days after vaccination: | 2 |
| Submitted: |
2013-10-05 |
| Days after onset: | 8 |
| Entered: |
2013-10-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4781AA / UNK |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Injection site erythema,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 9/27/13: raised, warm and red at site; 9/28/13: pt saw doctor prior to travel to foreign country, did not feel it was infected; cold compress and Benadryl. Advised to have next yr flu shot at doctor office. |
|
| VAERS ID: |
506108 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-09-30 |
| Onset: | 2013-09-30 |
| Days after vaccination: | 0 |
| Submitted: |
2013-10-02 |
| Days after onset: | 2 |
| Entered: |
2013-10-07 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
45BL3 / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
J004064 / 2 |
RA / IM |
Administered by: Public Purchased by: Private Symptoms: Blood calcium,
Blood creatinine,
Blood electrolytes,
Blood folate,
Blood glucose,
Blood urea,
Differential white blood cell count,
Erythema,
Full blood count,
Hepatitis A virus test,
Hepatitis B virus test,
Hepatitis C virus test,
Liver function test normal,
Pain in extremity,
Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: LASIX; KCl; CARDIZEM; ASA; thiamine; PROTONIX; Mg; folic acid; SPIRIVA Current Illness: None acute Preexisting Conditions: HTN; emphysema; ETOH abuse/cirrhosis; polycythemia; increased cholesterol; mult episodes cellulitis; PVD; Afib Allergies: Diagnostic Lab Data: 9/30 OV - LFTs, BUN/Cr, Ca++, CBC diff, lytes, folate, glu, hepatitis screen CDC Split Type:
Write-up: A few hrs after vaccination pt noted redness, pain, itching to both arms - spreading. (R) arm area distal and proximal to injection site approximately 3 in diam. (L) arm area distal to injection site approximately 3 1/2 in diam BENADRYL 25-50mg every 4h-6hr PRN - treatment. |
|
| VAERS ID: |
506441 (history) |
| Form: |
Version 1.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-09-29 |
| Onset: | 2013-09-29 |
| Days after vaccination: | 0 |
| Submitted: |
2013-10-03 |
| Days after onset: | 4 |
| Entered: |
2013-10-08 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH908AA / UNK |
LA / UN |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
U4617AA / UNK |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Contusion,
Erythema,
Local swelling,
Nausea,
Pain in extremity SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Temperature and BP - WNL CDC Split Type:
Write-up: 9-29-13 in evening had a swollen and sore arm. On Mon. 9-30-13 in the AM there was a large bruise (quarter size) continued to swell and hurt. Went to urgent care on 10/2/13 temperature and BP were OK. Was given Cephalexin 500mg for 1 week. Continues to have nausea, but the redness and swelling are decreasing. |
|
| VAERS ID: |
506776 (history) |
| Form: |
Version 1.0 |
| Age: |
79.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-09 |
| Onset: | 2013-10-09 |
| Days after vaccination: | 0 |
| Submitted: |
2013-10-09 |
| Days after onset: | 0 |
| Entered: |
2013-10-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U42628A / UNK |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Malaise,
Vomiting SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine administered at approx. 10h30AM. Call from daughter at approx. 4h10PM reporting patient vomiting and unwell. Patient referred to MD or hospital ER. |
|
| VAERS ID: |
507690 (history) |
| Form: |
Version 1.0 |
| Age: |
96.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-07 |
| Onset: | 2013-10-07 |
| Days after vaccination: | 0 |
| Submitted: |
2013-10-13 |
| Days after onset: | 6 |
| Entered: |
2013-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4764AA / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Dizziness,
Fall,
Feeling cold SMQs:, Anticholinergic syndrome (broad), Accidents and injuries (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atenolol; HCTZ Current Illness: Unknown Preexisting Conditions: Unknown, patient said none Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: That evening after the shot, the patient felt very cold, dizzy, and ended up falling at her home. No hospitalization reported and no other symptoms since. |
|
| VAERS ID: |
507289 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-09-20 |
| Onset: | 2013-09-22 |
| Days after vaccination: | 2 |
| Submitted: |
2013-10-10 |
| Days after onset: | 18 |
| Entered: |
2013-10-15 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
R55208 / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Arthritis bacterial,
Blood culture negative,
Chills,
Full blood count,
Incisional drainage,
Influenza virus test negative,
Injection site bruising,
Injection site haematoma,
Injection site joint movement impairment,
Injection site pain,
Injection site swelling,
Joint injury,
Laboratory test normal,
Nuclear magnetic resonance imaging abnormal,
Pain in extremity,
Red blood cell sedimentation rate increased,
Tremor,
Urine analysis normal,
White blood cell count increased SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Noninfectious myocarditis/pericarditis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 3 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Metoprolol; Omeprazole; Simvastatin; Aspirin; CELEBREX; Glucosamine; Acetaminophen Current Illness: No Preexisting Conditions: Diabetes; Joint pain; Hypertension; Hyperlipidemia Allergies: Diagnostic Lab Data: 9/29 Chest neg, Flu swab neg, U/A NL, WBC 13.4, ESR 9. Bld cult neg after 5 days; 9/30 WBC - 20.5, ESR 77; 10/2 MRI - lg fluid collection CDC Split Type: NH1010201317
Write-up: 9/24 ER visit w/ c/o shoulder injury, bruise over (L) deltoid site of injection, has hematoma. 9/29 Return to ER w/ chills, persistent arm pain. 9/30 pt called MD office - shaking, chills. Advised to go to ER CBC and ESR repeated, decreased ROM, pain and swelling (L) shoulder. Discharged to see Ortho MD today (later in day) ER MD spoke to Ortho surgeon. Sent home. Returned on 10/5 to Ortho surg and admitted to hospital w septic arthritis. I and D x 2. |
|
| VAERS ID: |
508340 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-16 |
| Onset: | 2013-10-17 |
| Days after vaccination: | 1 |
| Submitted: |
2013-10-20 |
| Days after onset: | 3 |
| Entered: |
2013-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
R54407 / UNK |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Asthenia,
Dizziness,
Dyskinesia,
Fatigue,
Grip strength decreased SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dyskinesia (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Temazepam; Pravastatin; ZYRTEC; Cyproheptadine; Levothyroxine; Tuminifen; ACIPHEX Current Illness: None Preexisting Conditions: CIDP-Chronic Inflammatory Demyelinating Peripheral Neuropathy; Left mastectomy Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt awoke with light headedness and fatigue. Experienced "jerking" in trunk area, had to rest on floor several time on way to kitchen. Was very weak and dropped two glasses while trying to get a drink. Had to rest on floor several times while returning to bed. Pt went back to sleep and felt better in afternoon. Felt fully recovered by following morning. |
|
| VAERS ID: |
508495 (history) |
| Form: |
Version 1.0 |
| Age: |
8.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-10-14 |
| Onset: | 2013-10-15 |
| Days after vaccination: | 1 |
| Submitted: |
2013-10-18 |
| Days after onset: | 3 |
| Entered: |
2013-10-21 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH900AC / UNK |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Abdominal pain,
Vomiting SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Fever~Influenza (H1N1) (H1N1 (MONOVALENT) (UNKNOWN))~2~5.00~Patient Other Medications: Symbicort Current Illness: None Preexisting Conditions: Asthma; Probable ibuprofen allergy Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Severe abdominal pain, persistent vomiting in middle of night (3AM) until mid am after imm given late after noon (5:00 pm) imm given. Stopped vomiting at noon next day. |
|
| VAERS ID: |
509500 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2013-10-25 |
| Entered: |
2013-10-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
AR / UN |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
- / UNK |
AR / UN |
Administered by: Other Purchased by: Other Symptoms: Injection site pain,
Injection site swelling,
Pruritus SMQs:, Anaphylactic reaction (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No other medications Current Illness: Drug hypersensitivity Preexisting Conditions: Heparin Allergies: Diagnostic Lab Data: CDC Split Type: WAES1310USA008104
Write-up: This spontaneous report as received from a consumer refers to a 73 year old male patient with no pertinent medical history. On 22-SEP-2013 the patient was vaccinated with a dose of PNEUMOVAX23 and a dose of influenza virus vaccine (manufacture unknown) in the same arm (dose number, dose, frequency, route and lot# not reported). On the same day, the patient received his allergy shots (manufacture unknown) in his other arm (dose number, dose, frequency, route and lot# not reported). After receiving PNEUMOVAX23 and influenza virus vaccine (manufacture unknown) in the same arm, on an unknown date in 2013 the patient experienced pain and swelling at the injection site. The patient also experienced some itching after receiving allergy shots (manufacture unknown). The patient did not receive any treatment and any lab diagnostic studies. The patient also did not seek any medical attention. On an unspecified date, the outcome of all events was reported as recovered on therapy. The patient was not reintroduced. The patient reported TYLENOL, OXYCONTIN and oxycodone did not work for him and he was allergic to them. The patient was also allergic to heparin. Additional information has been requested. |
|
| VAERS ID: |
511654 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-10-24 |
| Onset: | 2013-10-24 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-06 |
| Days after onset: | 13 |
| Entered: |
2013-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
- / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
- / 1 |
LA / IM |
Administered by: Public Purchased by: Private Symptoms: Activities of daily living impaired,
Headache,
Injection site reaction,
Malaise,
Pyrexia,
Rash erythematous SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Notes: This was the first dose of Pneumovax I have received. The reaction was much stronger than past flu vaccines. Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 101.7 fever for two days (in bed-malaise). Red rash around Pneumococcal vaccine injection site. Mild headaches for about 10 days. |
|
| VAERS ID: |
511823 (history) |
| Form: |
Version 1.0 |
| Age: |
28.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2012-11-15 |
| Onset: | 2012-12-10 |
| Days after vaccination: | 25 |
| Submitted: |
2013-11-07 |
| Days after onset: | 332 |
| Entered: |
2013-11-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
AFLUA715BA / UNK |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Asthenia,
Electromyogram,
Exposure during pregnancy,
Hypoaesthesia,
Lumbar puncture,
Paraesthesia,
Tremor SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 7 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Multivitamins Current Illness: Pregnancy Preexisting Conditions: Pregnancy Allergies: Diagnostic Lab Data: Electromyography, Spinal tap CDC Split Type:
Write-up: Tingling, numbness and loss of strength involving fingers and toes. Tremors around eyes. |
|
| VAERS ID: |
513336 (history) |
| Form: |
Version 1.0 |
| Age: |
87.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-20 |
| Onset: | 2013-10-20 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-01 |
| Days after onset: | 12 |
| Entered: |
2013-11-15 |
| Days after submission: | 14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4764AA / UNK |
UN / IM |
Administered by: Other Purchased by: Public Symptoms: Vaccination site pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atorvastatin; Lisinopril; Amlodipine Current Illness: No Preexisting Conditions: Hypertension; High cholesterol Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Site of vaccination still sore 26 days after administration. |
|
| VAERS ID: |
513457 (history) |
| Form: |
Version 1.0 |
| Age: |
1.2 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-11-01 |
| Onset: | 2013-11-08 |
| Days after vaccination: | 7 |
| Submitted: |
2013-11-15 |
| Days after onset: | 7 |
| Entered: |
2013-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U4692BA / 3 |
LL / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AHAVB641AA / 1 |
RL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
J002866 / 1 |
LL / IM |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
J006114 / 1 |
LL / SC |
Administered by: Private Purchased by: Public Symptoms: Convulsion,
Febrile convulsion,
Postictal state,
Pyrexia,
Tachycardia,
Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Generalised convulsive seizures following immunisation (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: TYLENOL PRN Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Patient had a fever 11-8-13. Later in day had a 5 minute seizure at dinner. EMS called, went to ED. Vomited once, febrile 39.3, tachycardic given 150 mg TYLENOL, observed. Short post-ictal period. No further seizure, dx: Febrile seizure, time of admit to ED 18:02, time of discharge to home 20:56. |
|
| VAERS ID: |
513769 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2013-11-18 |
| Entered: |
2013-11-19 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / UN |
Administered by: Other Purchased by: Other Symptoms: Death,
Headache,
Laboratory test,
Pyrexia,
Respiratory arrest SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Hypersensitivity (broad), Respiratory failure (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? Yes
Birth Defect? No
Died? Yes
Date died: 0000-00-00
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: UNK Preexisting Conditions: No pre-existing health conditions and was a very healthy child Allergies: Diagnostic Lab Data: Lab tests unknown CDC Split Type: 2013SA118114
Write-up: Initial report was received on 07 November 2013 from a non-health care provider from an unverified internet source. The reporter for this case is the same as case number 2013SA114788. A 7 year-old female patient (date of birth not reported) had received an Influenza vaccine (manufacturer, lot number, route, site and date of administration not reported) at her annual checkup. The patient was reported to have no pre-existing health conditions and was a very healthy child. The patient developed a severe headache and fever one day after vaccination. Three days later, the patient stopped breathing and died without warning in her mother''s arm. Diagnostic and laboratory testing were not reported. No further details were available at the time of the report. The patient''s outcome was fatal. Documents held by sender: None. |
|
| VAERS ID: |
513837 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-11-06 |
| Onset: | 2013-11-06 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-19 |
| Days after onset: | 13 |
| Entered: |
2013-11-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4784AA / UNK |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Body temperature decreased,
Dizziness,
Malaise SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Tamsulosin; Bupropion SR Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient reports feeling ill since he got flu shot on 11/06/13. He has been feeling dizzy, has low temperature 95 degrees. |
|
| VAERS ID: |
513843 (history) |
| Form: |
Version 1.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-21 |
| Onset: | 2013-10-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2013-11-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
39TFS / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: C-reactive protein,
Differential white blood cell count,
Full blood count,
Incorrect route of drug administration,
Injected limb mobility decreased,
Injection site joint pain,
Laboratory test,
Red blood cell sedimentation rate,
X-ray SMQs:, Drug abuse and dependence (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Endometriosis; hyperinsulinemia; reactive hypoglycemia Allergies: Diagnostic Lab Data: CBC with diff; ESR; CRP CDC Split Type:
Write-up: Vaccine was injected into my left shoulder joint instead of deltoid muscle. Now having severe joint pain and decreased mobility. Have had labs, x-rays, MD appointments and now seeing orthopedics. |
|
| VAERS ID: |
514284 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-11-07 |
| Onset: | 2013-11-07 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-21 |
| Days after onset: | 14 |
| Entered: |
2013-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4784AA / UNK |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Hyperhidrosis,
Malaise SMQs:, Neuroleptic malignant syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Info not available to me Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient described excessive perspiration and general malaise after flu shot and for 1-2 days after. |
|
| VAERS ID: |
514433 (history) |
| Form: |
Version 1.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-11-20 |
| Onset: | 2013-11-21 |
| Days after vaccination: | 1 |
| Submitted: |
2013-11-22 |
| Days after onset: | 1 |
| Entered: |
2013-11-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH917AB / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Rash pruritic SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: Unknown CDC Split Type:
Write-up: Patient received influenza vaccine on 11/20/13 at a flu clinic for employees staffed by nurses from another facility. Patient called facility the next morning to report that she woke up with an "itchy rash" on her chest and face. She denied any difficulty breathing or shortness of breath. Patient was encouraged to take a Benadryl and contact her PCP. The Lead RN contacted the patient x 2 on 11/21/13. Pt. reported that she was at work and that the symptoms had not worsened and she had not taken any Benadryl. She had contacted her PCP and was awaiting a return phone call. She continued to deny shortness of breath/difficulty breathing and no emergent care was deemed to be necessary. |
|
| VAERS ID: |
514803 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-11-21 |
| Onset: | 2013-11-21 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-26 |
| Days after onset: | 5 |
| Entered: |
2013-11-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
T3959 / UNK |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Arthralgia,
Dizziness,
Headache,
Myalgia,
Oropharyngeal pain,
Productive cough,
Pyrexia SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Eosinophilic pneumonia (broad), Vestibular disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Low-grade fever, dizziness, muscle/joint aches, productive cough, sore throat, headache. Started with dizziness < 6 hours after vaccination. Has never been vaccinated for influenza before. |
|
| VAERS ID: |
514848 (history) |
| Form: |
Version 1.0 |
| Age: |
74.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-25 |
| Onset: | 2013-10-25 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-26 |
| Days after onset: | 32 |
| Entered: |
2013-11-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4717AA / UNK |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Asthenia,
Bedridden,
Myalgia,
Pyrexia SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: COPD Preexisting Conditions: COPD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Over the course of 24 hours developed fever, muscle pain and weakness that resulted in her being bedridden. Lasted 24 hours. |
|
| VAERS ID: |
515025 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-10-28 |
| Onset: | 2013-10-29 |
| Days after vaccination: | 1 |
| Submitted: |
2013-11-27 |
| Days after onset: | 29 |
| Entered: |
2013-11-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
13443P / UNK |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Injected limb mobility decreased,
Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 1 month of pain close to injection site, with reduced ROM, tenderness to palpation. |
|
| VAERS ID: |
515155 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2013-11-19 |
| Onset: | 2013-11-19 |
| Days after vaccination: | 0 |
| Submitted: |
2013-11-27 |
| Days after onset: | 8 |
| Entered: |
2013-11-29 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
HZ5EX / UNK |
NS / IN |
Administered by: Public Purchased by: Public Symptoms: Incorrect route of drug administration,
No adverse event SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pt was given FLUARIX (IM form of influenza) nasally to left nare - nurses made error thinking it was FLUMIST. No ill effect no adverse symptoms occurred. Mother was with child. Error caught minutes after pt left. Parent notified, state, and appropriate forms filled out. |
|
| VAERS ID: |
515253 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-10-17 |
| Onset: | 2013-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2013-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
FJ94N / UNK |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Feeling abnormal,
Flushing,
Injection site erythema,
Injection site rash,
Injection site warmth,
Malaise,
Vision blurred SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Dementia (broad), Extravasation events (injections, infusions and implants) (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Hypersensitivity (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None known Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Pt c/o IM site became very hot flush to face rash and redness at IM site size of baseball pt describes rush feeling not feeling well sl blurred vision denied SOB B/P 120/80 HR 78 remains talking no SE of anaphylaxis applied cool compress to site IM inc increased fluids observed 15 min symptoms slowly dissipated. |
|
| VAERS ID: |
515356 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-11-08 |
| Onset: | 2013-11-09 |
| Days after vaccination: | 1 |
| Submitted: |
2013-12-02 |
| Days after onset: | 23 |
| Entered: |
2013-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4784AA / UNK |
RA / IM |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
J006827 / UNK |
LA / SC |
Administered by: Other Purchased by: Private Symptoms: Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Enalapril; HCTZ; Simvastatin Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Sore arm for weeks after shot, still having a sore arm, no swelling or redness (right arm). |
|
| VAERS ID: |
517544 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-12-11 |
| Onset: | 2013-12-13 |
| Days after vaccination: | 2 |
| Submitted: |
2013-12-23 |
| Days after onset: | 10 |
| Entered: |
2013-12-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH894AB / 7+ |
RA / IM |
Administered by: Private Purchased by: Other Symptoms: Fatigue,
Headache,
Muscle fatigue,
Pain SMQs:, Rhabdomyolysis/myopathy (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Extreme fatigue onset, headache next am and continued fatigue x approx. 32 hours then body aches head to toe and muscle fatigue that continued for approx 6 more days with intermittent headaches. |
|
| VAERS ID: |
517580 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2013-12-10 |
| Onset: | 2013-12-12 |
| Days after vaccination: | 2 |
| Submitted: |
2013-12-24 |
| Days after onset: | 12 |
| Entered: |
2013-12-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
13471P / UNK |
UN / IM |
Administered by: Unknown Purchased by: Other Symptoms: Injection site erythema,
Local reaction SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: SYMBICORT; PROAIR; SINGULAIR; SPIRIVA Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: None (negative) CDC Split Type:
Write-up: Local site reaction, redness 1 cm above injection site. |
|
| VAERS ID: |
518643 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-01-07 |
| Onset: | 2014-01-07 |
| Days after vaccination: | 0 |
| Submitted: |
2014-01-07 |
| Days after onset: | 0 |
| Entered: |
2014-01-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
TK5ME / 1 |
RA / SYR |
Administered by: Other Purchased by: Private Symptoms: Angioedema,
Idiopathic angioedema,
Local reaction,
Swollen tongue,
Throat tightness SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt having angioedema (rear of tongue), complained of tightness in throat. Pt has had idiopathic angioedema in past. The patient came back approximately 10 minutes after I gave her the shot and said she was having angioedema (specifically tongue swelling toward the back of tongue) and that she felt like her throat was closing. She did not have swelling, redness or warmth at site of injection. She said she had had angioedema in the past and said that her doctor said when she had it to use an epipen but did not have one. She stated that last year she got a localized reaction last year when she got a flu shot but attributed that to "the person giving the shot" I administered epinephrine 0.3 mg into the muscle of right thigh. Pt said she thought swelling had gone down and was feeling better. Pt stayed in area with me for approximately 20 minutes so I could assess whether or not shot working. Declined ambulance/ driving her home. Epipen lot 2mg670 exp 5/14. |
|
| VAERS ID: |
518941 (history) |
| Form: |
Version 1.0 |
| Age: |
28.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-01-05 |
| Onset: | 2014-01-05 |
| Days after vaccination: | 0 |
| Submitted: |
2014-01-05 |
| Days after onset: | 0 |
| Entered: |
2014-01-10 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
T3959 / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Head injury,
Loss of consciousness,
Myalgia,
Pallor,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Rhabdomyolysis/myopathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None listed consent form Preexisting Conditions: None listed on consent form Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient was given vaccination, was fine after the vaccination, then complained of muscle soreness. Patient then went pale and fainted, hitting his head on pharmacy counter. Regained consciousness and was A and O x 3. Left with paramedics for precautionary reasons. |
|
| VAERS ID: |
518998 (history) |
| Form: |
Version 1.0 |
| Age: |
39.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-01-11 |
| Onset: | 2014-01-12 |
| Days after vaccination: | 1 |
| Submitted: |
2014-01-12 |
| Days after onset: | 0 |
| Entered: |
2014-01-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH895AA / 1 |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None known or apparent Preexisting Conditions: Hot pepper allergy and sulfa drugs Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt HAD HIVES ON LEGS STOMACH AND BACK AFTER WAKING 14 HOURS AFTER FLUSHOT. I INSTRUCTED HER TO TAKE BENADRYL AND WATCH FOR FURTHER SIGNS OF ANAPHYLAXIS AND TO TREAT AS AN EMERGENCY IF SIGNS WORSEN. I ALSO ASKED IF THERE MAY BE ANYTHING ELSE COINCIDENTAL THAT MAY HAVE TRIGGERED, SHE WOULD THINK ABOPUT AND LET US KNOW... |
|
| VAERS ID: |
519992 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-01-10 |
| Onset: | 2014-01-10 |
| Days after vaccination: | 0 |
| Submitted: |
2014-01-13 |
| Days after onset: | 3 |
| Entered: |
2014-01-21 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UH888AA / UNK |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Injection site erythema,
Injection site pruritus,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Diabetes Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Redness, swelling, itching, warmth on arm at site of injection beginning within hours after injection. Applied diphenhydramine cream and symptoms have decreased. |
|
| VAERS ID: |
527605 (history) |
| Form: |
Version 1.0 |
| Age: |
24.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-04-02 |
| Onset: | 2014-04-02 |
| Days after vaccination: | 0 |
| Submitted: |
2014-04-04 |
| Days after onset: | 2 |
| Entered: |
2014-04-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / SYR |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / SYR |
Administered by: Private Purchased by: Other Symptoms: Fatigue,
Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Paroxetine HCL 10 MG; Clonazepam 0.5 MG; Loperamide 2 MG Current Illness: No Preexisting Conditions: Myotonic Muscular Dystrophy Type 1 Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Severe pain where the shot was given lasting several days, tiredness. |
|
| VAERS ID: |
542844 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-08-19 |
| Onset: | 0000-00-00 |
| Submitted: |
2014-08-28 |
| Entered: |
2014-09-08 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4995AA / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Chills,
Hyperaesthesia,
Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Oxycodone; Chlorthalidone; Zolpidem; VYVANSE Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient complained of full body aches/chills and skin sensitivity which lasted a few days after receiving the vaccine. |
|
| VAERS ID: |
543686 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-11 |
| Onset: | 2014-09-11 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-12 |
| Days after onset: | 1 |
| Entered: |
2014-09-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U5019AA / 2 |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site erythema,
Injection site inflammation,
Injection site pain,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Latex Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Extreme redness and inflammation originating at the site of injection. Area is hot to touch and slightly painful. |
|
| VAERS ID: |
543711 (history) |
| Form: |
Version 1.0 |
| Age: |
83.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-12 |
| Onset: | 2014-09-12 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-13 |
| Days after onset: | 1 |
| Entered: |
2014-09-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4995AA / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Allergy test,
Erythema,
Feeling hot,
Pain SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Allergy CDC Split Type:
Write-up: Redness/sore and hot. Had BENADRYL 25mg tab. |
|
| VAERS ID: |
544040 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-09-15 |
| Onset: | 2014-09-15 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-15 |
| Days after onset: | 0 |
| Entered: |
2014-09-17 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. |
CH2023 / 1 |
NS / IN |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
T9J3M / 2 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Epistaxis,
Underdose SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Medication errors (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt received 1/2 dose in (L) nostril, following 1/4 dose in (R) nostril began to bleed from (R) nostril. Dr examined and could not determine site of bleed. |
|
| VAERS ID: |
544483 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-12 |
| Onset: | 2014-09-12 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-12 |
| Days after onset: | 0 |
| Entered: |
2014-09-19 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U5016AA / 1 |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Chills,
Hypoaesthesia,
Pyrexia,
Tremor SMQs:, Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: ~Pneumo (Pneumovax)~1~0.00~Patient Other Medications: LANTUS SOLOSTAR; Lorazepam; Levothyroxine; Gabapentin Current Illness: None Preexisting Conditions: Diabetes; Thyroid problem; Anxiety; Pain Allergies: Diagnostic Lab Data: Unknown CDC Split Type:
Write-up: Patient received flu shot (Hi dose) on 9-12-14 at about 9:23AM. She started having high fever (about 101.4 degrees F), shivering (shaking), numbness in fingers, chilling all at about 5:30 PM after she came back from work. Feeling better the next day. |
|
| VAERS ID: |
544706 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-18 |
| Onset: | 2014-09-18 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-20 |
| Days after onset: | 2 |
| Entered: |
2014-09-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
T57906 / 1 |
LL / UN |
Administered by: Other Purchased by: Private Symptoms: Hypoaesthesia,
Immediate post-injection reaction,
Muscle contractions involuntary,
Muscular weakness,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Supraventricular tachycardia Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Immediately upon injection the patient complained of a loss of muscle control and pain and numbness in left arm. Symptoms started to improve within minutes and within 24 hours the only remaining symptom was some muscle weakness. Patient has refused medical care. |
|
| VAERS ID: |
545323 (history) |
| Form: |
Version 1.0 |
| Age: |
45.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-23 |
| Onset: | 2014-09-24 |
| Days after vaccination: | 1 |
| Submitted: |
2014-09-24 |
| Days after onset: | 0 |
| Entered: |
2014-09-26 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1411301 / 1 |
AR / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
J004196 / 1 |
AR / IM |
Administered by: Other Purchased by: Private Symptoms: Chills,
Injection site reaction,
Rash macular SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Oxycodone; Ropinirole; Morphine ER; Perphenazine; Cyclobenzaprine; Ondansetron; Perphenazine Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Pt was seen at ER then discharfed home same day. CDC Split Type:
Write-up: Patient''s husband reported that pat experienced chills and had a series of red blotches around the site where the injection occurred. Symptoms occurred approx 24 hrs after vaccine. |
|
| VAERS ID: |
545874 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-24 |
| Onset: | 2014-09-25 |
| Days after vaccination: | 1 |
| Submitted: |
2014-09-26 |
| Days after onset: | 1 |
| Entered: |
2014-09-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U5017AA / 1 |
LA / UN |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
K009105 / 1 |
RA / UN |
Administered by: Other Purchased by: Other Symptoms: Erythema,
Injection site reaction,
Local reaction,
Pain SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Local reaction at the injection site. Very very painful and redness. |
|
| VAERS ID: |
545465 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-12 |
| Onset: | 2014-09-13 |
| Days after vaccination: | 1 |
| Submitted: |
2014-09-28 |
| Days after onset: | 15 |
| Entered: |
2014-09-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
145402 / 1 |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Rash on vaccine arm (left) and underarm - lasted ~5 days given antihistamine by RPh. |
|
| VAERS ID: |
546206 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-18 |
| Onset: | 2014-09-18 |
| Days after vaccination: | 0 |
| Submitted: |
2014-09-23 |
| Days after onset: | 5 |
| Entered: |
2014-09-30 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U5042AA / 1 |
LA / IM |
Administered by: Other Purchased by: Public Symptoms: Influenza like illness,
Rash erythematous SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Glipizide; Bupropion; Montelukast; Simvastatin; Omeprazole; Ferrous sulfate; LANTUS Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Red rash; flu like symptoms for several hours. |
|
| VAERS ID: |
547562 (history) |
| Form: |
Version 1.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-01 |
| Onset: | 2014-10-02 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-02 |
| Days after onset: | 0 |
| Entered: |
2014-10-06 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
T59106 / 2 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Losartan; Metoprolol; HCTZ; Iron; Tramadol; ATIVAN; Naproxen; Omeprazole; PEPCID Current Illness: None Preexisting Conditions: Environmental allergies Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: A little itchy when went to bed 10/1/14. Woke up very, very itchy, on right side, right arm, arm pit, breast, shoulder, up neck and right side of scalp and ear. Took 25 mg of BENADRYL 9:30 am 10/2. T 99.1 - rx dr. |
|
| VAERS ID: |
548155 (history) |
| Form: |
Version 1.0 |
| Age: |
74.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-09-18 |
| Onset: | 2014-09-21 |
| Days after vaccination: | 3 |
| Submitted: |
2014-09-28 |
| Days after onset: | 7 |
| Entered: |
2014-10-07 |
| Days after submission: | 9 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4995AA / UNK |
UN / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
K007773 / UNK |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Erythema,
Pain,
Pruritus,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling, redness, pain, itching. |
|
| VAERS ID: |
548211 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-09-18 |
| Onset: | 2014-09-21 |
| Days after vaccination: | 3 |
| Submitted: |
2014-09-25 |
| Days after onset: | 4 |
| Entered: |
2014-10-07 |
| Days after submission: | 12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U4995AA / UNK |
UN / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
K007773 / UNK |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Contusion,
Pain,
Pruritus,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemorrhage terms (excl laboratory terms) (narrow), Accidents and injuries (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling, bruising, pain, itching. |
|
| VAERS ID: |
550715 (history) |
| Form: |
Version 1.0 |
| Age: |
50.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-09 |
| Onset: | 2014-10-11 |
| Days after vaccination: | 2 |
| Submitted: |
2014-10-14 |
| Days after onset: | 3 |
| Entered: |
2014-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI169AA / 1 |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Injection site rash,
Rash,
Viral rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Triamterene/HCTZ; metoprolol; omeprazole Current Illness: None Preexisting Conditions: Hypertension; reflux Allergies: Diagnostic Lab Data: Patient was examined by dermatologist CDC Split Type:
Write-up: Approximately 2 days after receiving vaccine, patient noticed generalized rash at site of injection as well as opposite arm and torso. Dermatologist diagnosed him with vaccine related "viral exanthem". Not allergic reaction. No hives, no urticaria. |
|
| VAERS ID: |
550743 (history) |
| Form: |
Version 1.0 |
| Age: |
21.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-08-17 |
| Onset: | 2014-08-18 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-14 |
| Days after onset: | 57 |
| Entered: |
2014-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
T58706 / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Pain,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Shooting pain whenever I lifted my left arm. Severe for about 6 weeks. For the past 2 weeks it has been more minor pain with movement. |
|
| VAERS ID: |
547966 (history) |
| Form: |
Version 1.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-13 |
| Onset: | 2014-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
2014-10-15 |
| Days after onset: | 2 |
| Entered: |
2014-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 2 |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Injection site erythema,
Injection site induration,
Injection site pruritus,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: similar but larger area~Influenza (Seasonal) (no brand name)~1~28.00~Patient Other Medications: Depo provera, Sudafed, Vit B12, Glucophage, Singulair, Nasacort Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Itching and redness around injection site. Redness continued to expand to 6 cm x 8cm over next few hours. Became hot and firm. |
|
| VAERS ID: |
548217 (history) |
| Form: |
Version 1.0 |
| Age: |
1.72 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-14 |
| Onset: | 2014-10-15 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-16 |
| Days after onset: | 1 |
| Entered: |
2014-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AC7AG / 4 |
LL / IM |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5018BA / 3 |
LL / IM |
| HIBV: HIB (ACTHIB) / SANOFI PASTEUR |
UI11AA / 4 |
RL / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
H65738 / 4 |
RL / IM |
Administered by: Private Purchased by: Unknown Symptoms: Dyskinesia,
Irritability,
Pyrexia,
Staring,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dyskinesia (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: IRRITABILITY~ ()~~0.00~Patient Other Medications: Current Illness: NONE Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: NONE CDC Split Type:
Write-up: PARENTS REPORT IRRITABILITY, FEVER AND PROLONGED STARING SPELL WHILE PATIENT WAS SITTING UP. HER NECK HAD ABNORMAL MOVEMENTS - DESCRIBED AS SMALL AND INVOLUNTARY AND JERKING BY HER PARENTS. VOMITED THE MORNING ON 10/16/2014. |
|
| VAERS ID: |
549261 (history) |
| Form: |
Version 1.0 |
| Age: |
10.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-10 |
| Onset: | 2014-10-10 |
| Days after vaccination: | 0 |
| Submitted: |
2014-10-13 |
| Days after onset: | 3 |
| Entered: |
2014-10-21 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. |
CJ2105 / 2 |
NS / IN |
| HPV4: HPV (GARDASIL) / MERCK & CO. INC. |
K001631 / 2 |
LA / UN |
Administered by: Private Purchased by: Public Symptoms: Fall,
Head injury,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Around 1520 patient was standing with brother against the wall waiting for mom to finish in bathroom. Both gave staff a high 5 and about 5 seconds later patient fell and hit his head on opposite wall. Patient was carried back to room 3 and Dr rushed in to exam him. Syncopal event shortly after receiving vaccines. |
|
| VAERS ID: |
550037 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-24 |
| Onset: | 2014-10-25 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-26 |
| Days after onset: | 1 |
| Entered: |
2014-10-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
33332-0014-1 / 1 |
LA / IM |
Administered by: Public Purchased by: Private Symptoms: Dizziness,
Dysphonia,
Fatigue,
Oropharyngeal pain,
Sinus congestion SMQs:, Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Sore throat; hoarseness; mild dizziness; fatigue; sinus congestion. |
|
| VAERS ID: |
550272 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-22 |
| Onset: | 2014-10-22 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2014-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
14625P / UNK |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Hives on legs noted 5 hours after flu vaccination; resolved spontaneously after 1 hour. |
|
| VAERS ID: |
550386 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-09-22 |
| Onset: | 2014-09-25 |
| Days after vaccination: | 3 |
| Submitted: |
2014-10-17 |
| Days after onset: | 22 |
| Entered: |
2014-10-28 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1412201 / 1 |
LA / UN |
Administered by: Public Purchased by: Private Symptoms: Chest X-ray abnormal,
Death,
Fungal test positive,
Gun shot wound,
Influenza A virus test negative,
Influenza B virus test,
Influenza virus test negative,
Intensive care,
Intentional self-injury,
Pneumonia,
Sputum abnormal,
White blood cell count increased SMQs:, Suicide/self-injury (narrow), Neuroleptic malignant syndrome (broad), Accidents and injuries (narrow), Hostility/aggression (broad), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (narrow), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2014-09-26
Days after onset: 1
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Multiple see print out Current Illness: None Preexisting Conditions: SULFACET-R, Rash; ALEVE, unknown; Bee Sting, anaphylaxis Allergies: Diagnostic Lab Data: CXR showed multifocal pneumonia of (R) lung; Sputum light growth yeast; Rapid flu negative for flu A and B; CBC, WBC 14.2 CDC Split Type:
Write-up: Patient ended up hospitalized 3 days later with severe pneumonia he was hospitalized on 9/25/14 and placed in ICU. He signed out AMA on 9/26/14 and died of self inflicted gun shot. |
|
| VAERS ID: |
551051 (history) |
| Form: |
Version 1.0 |
| Age: |
20.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-25 |
| Onset: | 2014-10-26 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-28 |
| Days after onset: | 2 |
| Entered: |
2014-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI171AC / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Axillary pain,
Injection site erythema,
Injection site swelling,
Pain SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient had redness and swelling at site next day but then 2 days after injection also experienced soreness and pain under arm hurts to move arm. Patients PCP was consulted and did not advise treatment. |
|
| VAERS ID: |
551924 (history) |
| Form: |
Version 1.0 |
| Age: |
18.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-11 |
| Onset: | 2014-10-11 |
| Days after vaccination: | 0 |
| Submitted: |
2014-10-28 |
| Days after onset: | 17 |
| Entered: |
2014-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI169AA / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Axillary pain,
Injection site erythema,
Injection site pain,
Pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced redness and soreness at site but 3 days later developed pain under arm, it hurt to move arm. Pain lasted appx 24 hrs then resolved. Patient''s PCP was consulted, she did not advise treatment. |
|
| VAERS ID: |
550773 (history) |
| Form: |
Version 1.0 |
| Age: |
43.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-10-24 |
| Onset: | 2014-10-25 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-29 |
| Days after onset: | 4 |
| Entered: |
2014-10-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / SYR |
Administered by: Other Purchased by: Other Symptoms: Blister,
Erythema SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atorvastatin 20 mg tablet aspirin chewable 81 mg tablet metFORMIN 500 mg ER tablet lisinopril 10 mg tablet Current Illness: No Preexisting Conditions: Diabetes Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Blister a little smaller than a dime. Has since grown a little and gotten very red including a dark red ring around it. |
|
| VAERS ID: |
551089 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-26 |
| Onset: | 2014-10-27 |
| Days after vaccination: | 1 |
| Submitted: |
2014-10-29 |
| Days after onset: | 2 |
| Entered: |
2014-10-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI171AC / UNK |
AR / IM |
Administered by: Other Purchased by: Private Symptoms: Discomfort,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced a very sore arm even at rest, she was in discomfort. |
|
| VAERS ID: |
551963 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-18 |
| Onset: | 2014-10-19 |
| Days after vaccination: | 1 |
| Submitted: |
2014-11-05 |
| Days after onset: | 17 |
| Entered: |
2014-11-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Other Symptoms: Activities of daily living impaired,
Axillary pain,
Back pain,
Impaired driving ability,
Mobility decreased,
Muscular weakness,
Musculoskeletal pain,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Retroperitoneal fibrosis (broad), Dementia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None. Preexisting Conditions: None Allergies: Diagnostic Lab Data: Went to doctor and chiropractor CDC Split Type:
Write-up: Arm and shoulder pain and weakness, radiating down arm, into armpit, into back. Very painful and movement & use impaired. Can''t lift arm. Trouble driving and daily routines such as dressing. Doctor said nerve may have been hit. Chiropractor said muscles involved too. Treatment is gentle exercises to maintain motion and NSAIDs. 18 days out, my left arm is still VERY PAINFUL, can''t be used properly, and symptoms continue to worsen. |
|
| VAERS ID: |
552252 (history) |
| Form: |
Version 1.0 |
| Age: |
73.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-09-29 |
| Onset: | 2014-09-30 |
| Days after vaccination: | 1 |
| Submitted: |
2014-11-05 |
| Days after onset: | 36 |
| Entered: |
2014-11-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
65023BA / UNK |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Muscle spasms,
Pain in extremity,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Dystonia (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced a sore arm and tingling in his fingers and cramping in muscle. Symptoms began after receiving the vaccine and for 3-4 weeks. |
|
| VAERS ID: |
552813 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-11-03 |
| Onset: | 2014-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
2014-11-10 |
| Days after onset: | 7 |
| Entered: |
2014-11-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Private Symptoms: Chills,
Heart rate increased,
Hypoaesthesia,
Muscular weakness,
Nausea,
Tinnitus SMQs:, Rhabdomyolysis/myopathy (broad), Acute pancreatitis (broad), Peripheral neuropathy (broad), Neuroleptic malignant syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hearing impairment (narrow), Dehydration (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No known illnesses at the time of vaccination. Preexisting Conditions: No pre-existing conditions. Allergies: Diagnostic Lab Data: At a follow-up visit on 11/6/2014, no tests were given. CDC Split Type:
Write-up: Nausea, limb weakness, ringing in ears, facial numbness, chills, rapid heart beat. |
|
| VAERS ID: |
552893 (history) |
| Form: |
Version 1.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-01 |
| Onset: | 2014-10-05 |
| Days after vaccination: | 4 |
| Submitted: |
2014-11-10 |
| Days after onset: | 36 |
| Entered: |
2014-11-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
T58106 / 1 |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Pain in extremity,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Vaccinated on 10.1.2014 Left arm. Approximately 2-3 days later felt pain in arm tingling to hand. Noticed after massage therapy and has not subsided. Used Ice and warm pack with no relief. Had appointment with Chiropractor no relief. Called physician on 10.27.14 talked with Nurse. 11.4.14 Seen by physician and placed on prednisone. Feels better in morning but hurts toward evening. (As reported to me by patient) |
|
| VAERS ID: |
552903 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-11-05 |
| Onset: | 2014-11-05 |
| Days after vaccination: | 0 |
| Submitted: |
2014-11-10 |
| Days after onset: | 5 |
| Entered: |
2014-11-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
T58106 / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Chills,
Decreased appetite,
Headache,
Injection site pain,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Fever, Chills, Headache and no appeite lasting till 11.08.2014. Patient stated that she had slight head ache before vaccination. Arm at site remains tender. |
|
| VAERS ID: |
553451 (history) |
| Form: |
Version 1.0 |
| Age: |
21.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2014-11-12 |
| Entered: |
2014-11-13 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1414101 / UNK |
RA / IM |
Administered by: Public Purchased by: Private Symptoms: Pruritus,
Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Fluoxetine; SPRINTEC (BC) Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: Patient responded to prednisone at ER. CDC Split Type:
Write-up: Patient received Flu shot 9am and became very itchy hours later. A rash appeared on arm and neck on side where she got the shot. After taking BENADRYL 50 mg at 12 pm she was brought to the ER in town to get further care. Fine the next day. |
|
| VAERS ID: |
554082 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-11-16 |
| Onset: | 2014-11-17 |
| Days after vaccination: | 1 |
| Submitted: |
2014-11-17 |
| Days after onset: | 0 |
| Entered: |
2014-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
U5055AA / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Lip swelling SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/a Current Illness: Cancer Preexisting Conditions: Allergy to sulfa drugs Allergies: Diagnostic Lab Data: N/a CDC Split Type:
Write-up: Lip swelling. Took Benadryl, symptoms resolved 15 minutes later. |
|
| VAERS ID: |
554137 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-29 |
| Onset: | 2014-11-01 |
| Days after vaccination: | 3 |
| Submitted: |
2014-11-06 |
| Days after onset: | 5 |
| Entered: |
2014-11-17 |
| Days after submission: | 11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / SYR |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Herpes zoster,
Immune system disorder,
Induration,
Local swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Aspirin; IMITREX; Theophylline; Asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: I reacted by my arm swelling up, getting really red and hard, Dr said it also attacked my immune system which triggered shingles. ER Dr said that. |
|
| VAERS ID: |
556265 (history) |
| Form: |
Version 1.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2014-09-19 |
| Onset: | 0000-00-00 |
| Submitted: |
2014-12-01 |
| Entered: |
2014-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC3: INFLUENZA (SEASONAL) (FLUCELVAX) / NOVARTIS VACCINES AND DIAGNOSTICS |
015021A / UNK |
LA / UN |
Administered by: Other Purchased by: Unknown Symptoms: Infective tenosynovitis SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Customer states that a tendon became infected, resulting in cortisone injections. |
|
| VAERS ID: |
557396 (history) |
| Form: |
Version 1.0 |
| Age: |
77.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-10 |
| Onset: | 2014-10-11 |
| Days after vaccination: | 1 |
| Submitted: |
2014-12-09 |
| Days after onset: | 59 |
| Entered: |
2014-12-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC3: INFLUENZA (SEASONAL) (FLUCELVAX) / NOVARTIS VACCINES AND DIAGNOSTICS |
014011A / UNK |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Death,
Diarrhoea SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2014-10-22
Days after onset: 11
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Lantus; Metformin; Citalopram; Lisinopril; Immodium; Gabapentin; Acetaminophen Current Illness: None evident at time of vaccination, other than pre-existing conditions. Preexisting Conditions: Diabetes, COPD, arthritis, depression Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt. had diarrhea during nap. Increased Immodium, no other complaints following. Patient was found deceased 9:30 AM 10/22/2014. Was normal with no problems 5 PM previous evening. |
|
| VAERS ID: |
557505 (history) |
| Form: |
Version 1.0 |
| Age: |
3.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-12-03 |
| Onset: | 2014-12-03 |
| Days after vaccination: | 0 |
| Submitted: |
2014-12-04 |
| Days after onset: | 1 |
| Entered: |
2014-12-09 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR |
C4642AA / 1 |
LA / IM |
| FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. |
CK2057 / 1 |
NS / IN |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
H65738 / 1 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site urticaria SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No known illness Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Parent reported small hives on area of arm at injection site. Possibly had a slight fever last evening. |
|
| VAERS ID: |
558288 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-12-11 |
| Onset: | 2014-12-11 |
| Days after vaccination: | 0 |
| Submitted: |
2014-12-12 |
| Days after onset: | 1 |
| Entered: |
2014-12-15 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1411501 / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
K004483 / 1 |
LA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C4565AA / 1 |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Erythema,
Local swelling,
Lymphadenopathy,
Malaise,
Rash SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ZITHROMAX; FLAGYL; CHANTIX; SUBOXONE; CONCERTA; NEURONTIN; Albuterol MDI; IMITREX Current Illness: None Preexisting Conditions: Bilateral galactorrhea x 6+ mos. seen by gyn 12/15/14 -$g FLAGYL (+) Bl on PAP; DJD; Pneumonia; ADHD; anxiety; opiates dependence; asthma Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt became ill with malaise 12/11 evening, noticed in 12/12 AM rash at axillary (L), swollen (L) axillary nodes. Area is swollen and erythematous. Came to office at 2:30 pm with same rash sx, feeling better over in regard to malaise. Treated with azithromycin 250 mg tab (2 tabs x 1 day, then 1 tab x 4 days). Told to call with worsening sx. |
|
| VAERS ID: |
561382 (history) |
| Form: |
Version 1.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-11-07 |
| Onset: | 2014-11-08 |
| Days after vaccination: | 1 |
| Submitted: |
2015-01-13 |
| Days after onset: | 66 |
| Entered: |
2015-01-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
U499ODA / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Anxiety,
Depression,
Dizziness,
Electromyogram,
Headache,
Hypoaesthesia,
Malaise,
Muscular weakness,
Nuclear magnetic resonance imaging brain,
Nuclear magnetic resonance imaging spinal,
Paraesthesia SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Depression (excl suicide and self injury) (narrow), Vestibular disorders (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Prenatal multivitamin, vitamin C, vitamin D, Fish "More milk plus" (an herbal supplement for lactation). Current Illness: No Preexisting Conditions: 8 weeks postpartum, allergic to PCN and latex, Celiac disease. Allergies: Diagnostic Lab Data: EMG, MRI brain and C-spine. CDC Split Type:
Write-up: Please see physician records; acute onset of headache, dizziness, general malaise followed by acute bilateral upper extremity paresthesias (numbness and tingling, mild component of weakness). Symptoms listed first were gone within 48 hours of the vaccine administration time. However, upper extremity paresthesias persisted- very intense for about 1-2 weeks with a gradual decrease in symptoms at 2-3 weeks and minimal symptoms after 3-4 weeks and nearly complete resolution of symptoms about 5-6 weeks later. Also caused anxiety and depression, secondary to symptoms. |
|
| VAERS ID: |
561962 (history) |
| Form: |
Version 1.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-14 |
| Onset: | 2014-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
2014-10-14 |
| Days after onset: | 0 |
| Entered: |
2015-01-21 |
| Days after submission: | 99 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / 4 |
LA / IM |
Administered by: Public Purchased by: Unknown Symptoms: Flushing,
Paraesthesia SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: RA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Tingling in finger tips. Flushed feeling. BP 138/88. F/U with primary care MD reported no action needed at time. Continued to monitor. Retake BP -$g 128/80. F/U with patient at 15:00. Denies any needs. Reports no symptoms. F/U on 10/16/14 -rpt no symptoms. |
|
| VAERS ID: |
563351 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-15 |
| Onset: | 2014-10-15 |
| Days after vaccination: | 0 |
| Submitted: |
2015-01-29 |
| Days after onset: | 106 |
| Entered: |
2015-01-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLULAVAL) / GLAXOSMITHKLINE BIOLOGICALS |
9X3L3 / UNK |
AR / UN |
Administered by: Other Purchased by: Other Symptoms: Injection site pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No other medications Current Illness: Unknown Preexisting Conditions: Influenza vaccine, No reaction on previous exposure to drug Allergies: Diagnostic Lab Data: CDC Split Type: US2014GSK033320
Write-up: This case was reported by a nurse and described the occurrence of injection site pain in a 48-year-old female patient who received FLULAVAL QUADRIVALENT (batch number 9X3L3, expiry date 30th June 2015). Previously administered products included flu vaccine with an associated reaction of no reaction to previous exposure to drug. On 15th October 2014, the patient received FLULAVAL QUADRIVALENT. On 15th October 2014, 0 min after receiving FLULAVAL QUADRIVALENT, the patient experienced injection site pain. On an unknown date, the outcome of the injection site pain was not recovered/not resolved. It was unknown if the reporter considered the injection site pain to be related to FLULAVAL QUADRIVALENT. Additional information received: Nurse reported that a patient complained about pain in her arm and where she received the vaccine. |
|
| VAERS ID: |
573073 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-28 |
| Onset: | 2014-10-28 |
| Days after vaccination: | 0 |
| Submitted: |
2015-04-03 |
| Days after onset: | 157 |
| Entered: |
2015-04-08 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
AR / SYR |
Administered by: Private Purchased by: Unknown Symptoms: Activities of daily living impaired,
Drug administered at inappropriate site,
Injection site discomfort,
Insomnia,
Nuclear magnetic resonance imaging,
Pain in extremity,
Ultrasound scan SMQs:, Dementia (broad), Drug abuse and dependence (broad), Tendinopathies and ligament disorders (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: Ultrasound, MRI CDC Split Type:
Write-up: Received flu shot on 10/28/14 9:30 am, arm hurt around 10:30 am - could not sleep on it, push door open, lift it, get dressed etc. Called after 1 week, 2 weeks, got PT script after 3 weeks. Injection was high in arm. I am a thin female. Its been 5 months, improved but still some discomfort at injection site. |
|
| VAERS ID: |
574463 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-21 |
| Onset: | 2014-12-06 |
| Days after vaccination: | 46 |
| Submitted: |
2015-04-19 |
| Days after onset: | 133 |
| Entered: |
2015-04-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UI190AC / 1 |
AR / SYR |
Administered by: Unknown Purchased by: Unknown Symptoms: Allergy test,
Anaemia,
Antineutrophil cytoplasmic antibody,
Antinuclear antibody,
Arthralgia,
Autoimmune disorder,
Biopsy skin abnormal,
Blood immunoglobulin A,
Blood immunoglobulin G,
C-reactive protein,
Complement factor C3,
Complement factor C4,
Creatinine urine,
Differential white blood cell count,
Fatigue,
Full blood count,
Gait disturbance,
Inflammation,
Joint range of motion decreased,
Juvenile idiopathic arthritis,
Metabolic function test,
Mononucleosis heterophile test negative,
Myalgia,
Neutrophil count,
Rash,
Red blood cell sedimentation rate increased,
Rheumatoid factor increased,
Serum ferritin,
Urine analysis,
Vasculitis,
Viral infection,
Weight bearing difficulty,
Weight decreased,
X-ray limb normal SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Haematopoietic erythropenia (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Anticholinergic syndrome (broad), Malignancy related therapeutic and diagnostic procedures (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Eosinophilic pneumonia (broad), Vasculitis (narrow), Skin tumours of unspecified malignancy (broad), Hypersensitivity (narrow), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow), Noninfectious myocarditis/pericarditis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Multi vitamin Current Illness: No Preexisting Conditions: Allergic to Sulfa Meds, supra and septra Allergies: Diagnostic Lab Data: 1/13/15 - ANC, Anti Nuclear Antibody, Comprehensive Metabolic panel, Hemagram & differential, Mono-test, Rheumatoid factor, Sedrate: Westergren. 1/16/15 - skin biopsy 1/28/15 - ANCA, Anti Nuclear Antibody, C-Reactive Protein, C3 Complement, C4 Complement, Comprehensive Metabolic Panel, Creatinine Urine Random, Ferritin, Hemagram and Differential, Proteinase 3 antibody, Sed. Rate: Westergren, Total protein urine random & Urinalysis. 2/27/15 - xrays of both wrists 4/1/15 - C-Reactive Protein High Sensitivity, Food Panel I IgG4, Food Panel II IgG, Gliadin AB Panel, IgA, IgG, Comprehensive Metabolic Panel, Ferritin & Sed. Rate: Westergren CDC Split Type:
Write-up: My daughter has always been healthy with the exception of ear infections when she was younger. She played soccer, did cheerleading and currently dances twice a week. My daughter received her first dose of the Gardasil HPV vaccine on 7/22/14 and a second dose on 7/22/14. On 12/6/14 she woke up with a rash on her thighs, stomach, arms and back. We took her to the doctors and they diagnosed her with Pityriasis Rosea. On the evening 12/7/14 she started experiencing muscle pain and could barely walk on her legs. We took her back to the doctors on 12/8/14 and was told that she did not have Pityriasis Rosea and that what she most likely had was a virus. Her symptoms, rash and muscle pain, continued to worsen and we took her back to the doctors on 12/10/14. We were told that she appeared to have a viral infection and it needed to run its course. On 1/13/15 we took her back to the doctors as she was still having her rash, was tired all the time and was still having muscle pain her legs, arms and wrists. Weight loss also became a concern. On 12/8/14 weight was 110 pounds on 1/13/15 she was down to 99 pounds 8 ounces. Blood was drawn results were negative for mono, a weak positive for autoimmune, SED RATE showed inflammation and positive for anemia. On 1/16/15 saw a dermatologist for a skin biopsy which came back as vasculitis. On 1/28/15 we saw a Rheumatoid Arthritis specialist who diagnosed her with undefined Juvenile Idiopathic Arthritis and prescribed her 125 mg Naproxen 2 times a day. As Naproxen was not working on 2/6/15 Prednisone was prescribed at 3 tablets of 10 mg of prednisone a day for 1 week, than 2 tablets for a week and then 1 tablet for a week. Follow up with RA specialist on 2/27/15. Continues to have rash and joint pain in her legs and arms. Was left on taking 10 mg of Prednisone daily and went for x-rays on wrist. Wrists x-rays came back good. On 4/1/15 follow up with RA specialist. Range of motion better in legs and arms. Still pain and limited range in both wrists. Steroid injection into joint of left wrist and Prednisone was reduced to 7.5 mg daily. As I am writing this on 4/19/15 she still is experiencing a rash on her legs, arms, stomach and back. The rash comes and goes. She is still having pain in her wrists more in the right as she had the steroid injection in the left. She is unable to put pressure or support her weight on her hands. There is once again a loss of range of motion in her right arm. She cannot straighten her arm as it hurts too much. |
|
| VAERS ID: |
576957 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-01 |
| Onset: | 2014-10-01 |
| Days after vaccination: | 0 |
| Submitted: |
2015-05-05 |
| Days after onset: | 216 |
| Entered: |
2015-05-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
LY2FS / UNK |
- / - |
Administered by: Other Purchased by: Other Symptoms: Injected limb mobility decreased,
Injection site pain,
Rotator cuff syndrome SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: sore arm~Influenza (Seasonal) (no brand name)~~51.00~Patient Other Medications: Advil Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Flu shot given in upper left arm. After the shot left arm has been very sore and now has an impingement that has caused limited range of motion and severe stabbing pains. Went to my doctor who diagnosed the impingement and referred to Physical Therapy. Have been going to Physical Therapy for 13 weeks and my arm has not gotten better. |
|
| VAERS ID: |
596792 (history) |
| Form: |
Version 1.0 |
| Age: |
66.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-15 |
| Onset: | 2015-09-15 |
| Days after vaccination: | 0 |
| Submitted: |
2015-09-18 |
| Days after onset: | 3 |
| Entered: |
2015-09-22 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI436AA / 1 |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
L53938 / 1 |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site erythema,
Injection site induration,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: At site of injection, red, hot, hard, swollen. Patient went to MD. MD treated with CLARITIN. MD told patient to monitor, and call MD if redness spreads or feels fever/chills/nausea. |
|
| VAERS ID: |
596952 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-16 |
| Onset: | 2015-09-17 |
| Days after vaccination: | 1 |
| Submitted: |
2015-09-21 |
| Days after onset: | 4 |
| Entered: |
2015-09-22 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI4355AA / UNK |
UN / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
L87117 / UNK |
UN / IM |
Administered by: Other Purchased by: Private Symptoms: Injection site erythema,
Injection site pruritus,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Furosemide Current Illness: Preexisting Conditions: NKA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Localized redness, swelling, warm to touch, mild itching of left deltoid. |
|
| VAERS ID: |
596955 (history) |
| Form: |
Version 1.0 |
| Age: |
92.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-17 |
| Onset: | 2015-09-17 |
| Days after vaccination: | 0 |
| Submitted: |
2015-09-22 |
| Days after onset: | 5 |
| Entered: |
2015-09-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI442AB / UNK |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Feeling cold,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt developed chills, shaking. Brought to ER by daughter. |
|
| VAERS ID: |
597283 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-24 |
| Onset: | 2015-09-24 |
| Days after vaccination: | 0 |
| Submitted: |
2015-09-25 |
| Days after onset: | 1 |
| Entered: |
2015-09-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. |
FJ2099 / 1 |
NS / IN |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Acute URI Preexisting Conditions: Milk and environmental allergies Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: On-call physician took call from mom at 10:15pm. Within 45 min of vaccine face was red, then at night developed large hive on (L) cheek. Mom gave BENADRYL and child went to sleep. Never had any respiratory symptoms. |
|
| VAERS ID: |
601520 (history) |
| Form: |
Version 1.0 |
| Age: |
84.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-24 |
| Onset: | 2015-09-25 |
| Days after vaccination: | 1 |
| Submitted: |
2015-10-08 |
| Days after onset: | 13 |
| Entered: |
2015-10-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
UI428AB / UNK |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
U361230 / 1 |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Erythema,
Injection site pruritus SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Amlodipine; BENICAR; CENTRUM; B12; DITROPAN; EVISTA; KLOR-CON; MIROLAX; NEXIUM; Loratidine Current Illness: None Preexisting Conditions: GERD; HTN Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Right upper extremity erythema, pruritis surrounding injection site. Onset 12 hours after vaccination. Improving with BENADRYL, loratadine added. Erythema persistent $g 1 week after vaccination. |
|
| VAERS ID: |
601795 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-15 |
| Onset: | 2014-10-15 |
| Days after vaccination: | 0 |
| Submitted: |
2015-10-10 |
| Days after onset: | 360 |
| Entered: |
2015-10-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
T58106 / UNK |
UN / UN |
Administered by: Public Purchased by: Private Symptoms: Muscular weakness,
Nuclear magnetic resonance imaging,
Pain in extremity,
Rotator cuff syndrome,
X-ray SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Tendinopathies and ligament disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: CALCIUM, FISH OIL Current Illness: NO Preexisting Conditions: NONE Allergies: Diagnostic Lab Data: MRI AND XRAY CDC Split Type:
Write-up: PAIN AND WEAKNESS OF RIGHT ARM. HURT FOR SEVERAL WEEKS. TOOK IBUPROPHEN. TOLD DOCTOR AT NEXT VISIT. PAIN SUBSIDED, BUT CONTINUOUS. IN FEBRUARY, ROTATOR CUFF TORE AFTER SIMPLE MOVEMENT OF ARM. XRAYS AND MRI - YEAR LATER STILL HURTS. |
|
| VAERS ID: |
602186 (history) |
| Form: |
Version 1.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-30 |
| Onset: | 2015-10-01 |
| Days after vaccination: | 1 |
| Submitted: |
2015-10-05 |
| Days after onset: | 4 |
| Entered: |
2015-10-13 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
VI459AB / 2 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Chills,
Dizziness,
Fatigue,
Headache,
Pain,
Vertigo SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Levothyroxine; Estradiol; IMMODIUM; Probiotic; TYLENOL Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Dizziness, vertigo, chills, headache, fatigue, soreness. Onset the following evening after administration 10-1-15 lasting continuously through 10-5-15. |
|
| VAERS ID: |
602622 (history) |
| Form: |
Version 1.0 |
| Age: |
39.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2015-10-09 |
| Onset: | 2015-10-10 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2015-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5309AA / UNK |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
K007826 / UNK |
RA / IM |
Administered by: Public Purchased by: Public Symptoms: Erythema,
Local swelling,
Pain,
Pruritus SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Regualr Diabetes visit Preexisting Conditions: Allergy to sulfa; Diagnosis of Diabetes Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Local swelling/redness/itching achyness. |
|
| VAERS ID: |
602792 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-09 |
| Onset: | 2015-10-11 |
| Days after vaccination: | 2 |
| Submitted: |
2015-10-15 |
| Days after onset: | 4 |
| Entered: |
2015-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
93T79 / UNK |
LA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Musculoskeletal pain,
Neck pain,
Pain,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt initially felt no pain when vaccine administered on Friday 10/9/15. Sunday 10/11/15 in the evening arm started to hurt. By Monday patient was in "agony" and saw physician. Pt said she couldn''t move her arm without pain at this time. Pain also sometimes radiates through shoulder into neck. MD prescribed muscle relaxant and Tylenol with codeine. Pt did not take Tylenol with codeine but did take muscle relaxant at night and took 600 mg of ibuprofen which she said helped. Spoke with patient on Wed 10/14 and again on Thurs 10/15/15. She said pain is getting lesser every day but still present somewhat. Advised massaging the muscle, moving it as much as possible and icing it if necessary. |
|
| VAERS ID: |
602820 (history) |
| Form: |
Version 1.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-08 |
| Onset: | 2015-10-09 |
| Days after vaccination: | 1 |
| Submitted: |
2015-10-15 |
| Days after onset: | 6 |
| Entered: |
2015-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
U58808 / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
L001311 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Injection site erythema,
Injection site reaction,
Injection site swelling,
Injection site warmth,
Mobility decreased,
Pain,
Pain in extremity SMQs:, Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Metoprolol, losartan, ventolin, estradiol, spironolactone Current Illness: None Preexisting Conditions: Hypertension, hyperaldosterone, anxiety, asthma; Allegies to penicillin and aspirin Allergies: Diagnostic Lab Data: n/a CDC Split Type:
Write-up: The patient had a sore arm and inability to raise it. She iced it and used ibuprofen. The next day the arm became swollen, red and hot to the touch from the administration site to the elbow with a burning type pain. The patient continued to ice, used Benadryl and loratadine and over the course of the next few days the reaction dissipated. |
|
| VAERS ID: |
603232 (history) |
| Form: |
Version 1.0 |
| Age: |
80.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-13 |
| Onset: | 2015-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
2015-10-17 |
| Days after onset: | 4 |
| Entered: |
2015-10-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7HZ73 / 1 |
LA / SYR |
Administered by: Other Purchased by: Other Symptoms: Injection site pain,
Musculoskeletal stiffness,
Neck pain SMQs:, Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 10/13/15 Immunization given about 4:28 pm. 10/15/15 9:58 am patients daughter called and said patient was experiencing pain and stiffness from injection site of left deltoid up shoulder to back of neck. Pt applied ice and had taken ALEVE and at afternoon was not getting worse and doing better. At 8:00 pm patients daughter said patient was feeling better. |
|
| VAERS ID: |
603233 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-10-03 |
| Onset: | 2015-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
2015-10-17 |
| Days after onset: | 14 |
| Entered: |
2015-10-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI456AA / 2 |
LA / UN |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
J67646 / 1 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Injection site pain,
Musculoskeletal stiffness,
Neck pain SMQs:, Dystonia (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: High blood pressure Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 10/3/15 had immunization at retail pharmacy. 10/5/15 came into pharmacy and described having pain and stiffness going from site of injection up arm, across shoulders and up neck; pharmacist called covering MD who verified no red line from injection site and gave pager # if needed and advised ER if condition worsens. Pt iced and took acetaminophen and reported continuing improvement/complete recovery. |
|
| VAERS ID: |
603305 (history) |
| Form: |
Version 1.0 |
| Age: |
16.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-10-14 |
| Onset: | 2015-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
2015-10-16 |
| Days after onset: | 2 |
| Entered: |
2015-10-19 |
| Days after submission: | 3 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5309AA / 1 |
RA / IM |
| MNQ: MENINGOCOCCAL CONJUGATE (MENACTRA) / SANOFI PASTEUR |
U5178AA / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site discomfort,
Injection site erythema,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: XOPENEX HFA Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Significant redness, swelling and discomfort of left shoulder area. |
|
| VAERS ID: |
603499 (history) |
| Form: |
Version 1.0 |
| Age: |
75.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-02 |
| Onset: | 2015-10-02 |
| Days after vaccination: | 0 |
| Submitted: |
2015-10-20 |
| Days after onset: | 18 |
| Entered: |
2015-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
L94EX / 3 |
UN / UN |
Administered by: Private Purchased by: Unknown Symptoms: Dyspnoea,
Muscular weakness,
Pain in extremity,
Restless legs syndrome SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 10 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Leg pain, restless legs, progressive weakness of extremities, neck, difficulty breathing. |
|
| VAERS ID: |
604128 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-19 |
| Onset: | 2015-10-20 |
| Days after vaccination: | 1 |
| Submitted: |
2015-10-21 |
| Days after onset: | 1 |
| Entered: |
2015-10-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / UN |
| VARZOS: ZOSTER (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
RA / UN |
Administered by: Private Purchased by: Unknown Symptoms: Injection site reaction,
Local reaction SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Local reaction - zoster vaccine (R) deltoid. Recommended Topical hydrocortisone. |
|
| VAERS ID: |
604519 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-10-09 |
| Onset: | 2015-10-19 |
| Days after vaccination: | 10 |
| Submitted: |
2015-10-23 |
| Days after onset: | 4 |
| Entered: |
2015-10-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
43E97 / 2 |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / 1 |
- / SYR |
Administered by: Unknown Purchased by: Unknown Symptoms: Wrong drug administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Depression, reflux, CAD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient is 52 years old and has CAD. He is indicated for the Pneumovax. Nurse was not aware of the two different pneumococcal vaccines. Ended up grabbing Prevnar 13 from the refrigerator and gave him the injection. She did not notice it was not the correct vaccine until she was unable to document the vaccination in the chart. The lot number, etc.. is not available for me to report. He also received a flu shot on the same day. |
|
| VAERS ID: |
608028 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-20 |
| Onset: | 2015-10-21 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-06 |
| Days after onset: | 16 |
| Entered: |
2015-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7754S / UNK |
RA / UN |
Administered by: Private Purchased by: Private Symptoms: Back pain,
Fatigue,
Headache,
Pain in extremity SMQs:, Retroperitoneal fibrosis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Urinary tract infection Preexisting Conditions: Meperidine allergy Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Arm soreness, fatigue, headache, back pain - no treatment necessary. |
|
| VAERS ID: |
608049 (history) |
| Form: |
Version 1.0 |
| Age: |
59.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-11-02 |
| Onset: | 2015-11-04 |
| Days after vaccination: | 2 |
| Submitted: |
2015-11-05 |
| Days after onset: | 1 |
| Entered: |
2015-11-06 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5310CA / 2 |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Injection site erythema SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Nasal congestion/Cough Preexisting Conditions: Penicillin Allergy Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Erythema at injection site (4 x 5 cm) nontender. Full function of (L) arm. Given Rx for BENADRYL 25 mg QHS. |
|
| VAERS ID: |
609536 (history) |
| Form: |
Version 1.0 |
| Age: |
1.36 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-26 |
| Onset: | 2015-11-04 |
| Days after vaccination: | 9 |
| Submitted: |
2015-11-05 |
| Days after onset: | 1 |
| Entered: |
2015-11-13 |
| Days after submission: | 8 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5319DA / 1 |
LL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
K024036 / 1 |
LL / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
L023593 / 1 |
RL / SC |
Administered by: Private Purchased by: Public Symptoms: Pyrexia,
Rash generalised,
Seizure SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Convulsions (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Generalised convulsive seizures following immunisation (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Fever, rash (all over body). Seizure. |
|
| VAERS ID: |
609655 (history) |
| Form: |
Version 1.0 |
| Age: |
52.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-11-10 |
| Onset: | 2015-11-11 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-13 |
| Days after onset: | 2 |
| Entered: |
2015-11-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7DT2Y / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
L021367 / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Erythema,
Fatigue,
Nausea,
Pain in extremity,
Pyrexia,
Skin tightness SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Amitriptyline; tramadol; furosemide; enalapril; amlodipine; Lantus; meloxicam; metformin; Novolog; Vitamin D Current Illness: No patient reports feeling well Preexisting Conditions: Diabetes, Neuropathy Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Began to feel feverish, tired, nausea. Redness began to spread over upper arm Wed evening: pain and tightness in upper arm, by Thursday the redness had covered most of upper arm to elbow. The patient saw a NP at his physicians office around 4:00PM Thursday and she prescribed a ZPAK. |
|
| VAERS ID: |
609748 (history) |
| Form: |
Version 1.0 |
| Age: |
82.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-11-09 |
| Onset: | 2015-11-12 |
| Days after vaccination: | 3 |
| Submitted: |
2015-11-13 |
| Days after onset: | 1 |
| Entered: |
2015-11-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI520AA / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site erythema,
Injection site pain,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Redness, swelling, tenderness at injection site. Treated with KEFLEX 250 mg PO QID x 5 days. |
|
| VAERS ID: |
609696 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-11-02 |
| Onset: | 2015-11-06 |
| Days after vaccination: | 4 |
| Submitted: |
2015-11-15 |
| Days after onset: | 9 |
| Entered: |
2015-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / UN |
Administered by: Private Purchased by: Other Symptoms: Herpes zoster SMQs:, Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Ursodiol, 300 mgs 1x/day; Diazepam 4.75mg/day; Metoprolol XL 25mg 1x/day; Propranolol 5mg 1x/day Current Illness: No. On slow, medically supervised benzodiazepine withdrawal plan. Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Onset of shingles. |
|
| VAERS ID: |
610424 (history) |
| Form: |
Version 1.0 |
| Age: |
41.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-10-14 |
| Onset: | 2015-10-15 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-18 |
| Days after onset: | 34 |
| Entered: |
2015-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI439AB / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Influenza SMQs:, Infective pneumonia (broad), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: No CDC Split Type:
Write-up: Severe flu symptoms, called out of work. Lasted 24-36 hours. Did not seek medical help. Slept for the most part of the day. |
|
| VAERS ID: |
610543 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-11-06 |
| Onset: | 2015-11-08 |
| Days after vaccination: | 2 |
| Submitted: |
2015-11-18 |
| Days after onset: | 10 |
| Entered: |
2015-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Unknown Purchased by: Private Symptoms: Insomnia,
Pain SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Started as dull ache and has continued to increase to a more intense ache... taking Advil to be able to sleep. |
|
| VAERS ID: |
610603 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-06 |
| Onset: | 2015-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-18 |
| Days after onset: | 42 |
| Entered: |
2015-11-19 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5310CA / UNK |
RA / IM |
Administered by: Private Purchased by: Unknown Symptoms: Haematoma,
Laboratory test normal,
Pain in extremity SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Diabetes Allergies: Diagnostic Lab Data: Exam normal CDC Split Type:
Write-up: Hematoma, arm pain. Next day continuous. |
|
| VAERS ID: |
611220 (history) |
| Form: |
Version 1.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-09-03 |
| Onset: | 2015-09-05 |
| Days after vaccination: | 2 |
| Submitted: |
2015-10-05 |
| Days after onset: | 30 |
| Entered: |
2015-11-19 |
| Days after submission: | 45 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI428AB / 1 |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Injection site erythema,
Injection site mass,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: UNK Preexisting Conditions: Unknown Allergies: Diagnostic Lab Data: Lab tests unknown CDC Split Type: 2015SA136221
Write-up: Initial unsolicited report received from a pharmacist on 05 September 2015. This case involves a 67-year-old female patient who was vaccinated with first dose of FLUZONE HD (batch number: UI428AB, expiry date: 19 March 2016) via intramuscular route in right deltoid on 03 September 2015. Reporter denied any illness at time of vaccination, pre-existing physician-diagnosed allergies, birth defects, medical conditions. Concomitant medications were not reported. On 05 September 2015, two days post vaccination, the patient developed redness at injection site, lump at site, warmth and red ring around injection site. Laboratory data and corrective treatments were not reported. At the time of this report, the outcome of the events was unknown. List of documents held by sender: none. |
|
| VAERS ID: |
612051 (history) |
| Form: |
Version 1.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-10-20 |
| Onset: | 2015-10-21 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-26 |
| Days after onset: | 36 |
| Entered: |
2015-11-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
LA / IM |
Administered by: Public Purchased by: Other Symptoms: Injection site pain,
Muscle spasms,
Muscle tightness SMQs:, Dystonia (broad), Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: TYLENOL; NEXIUM; Gabapentin; SYNTHROID; CADUET; Citalopram; ADVAIR; CLARITIN Current Illness: None Preexisting Conditions: Sciatic; Allergy - NSAIDS OTC and prescription, Tramadol; KEFLEX, Clindamycin; Seasonal allergies; Codeine Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Employee flu, vaccine give left upper arm. Hurt a little as fluid injected, but seemed normal injection, achy as usual following day. With 1-2 days it continued to be nagging, but was having spasms/tightness. After a couple of weeks spread to tightness in shoulder and neck, incorporated left shoulder blade. I first thought it would go away. Taking TYLENOL 2-3 x day since beginning, recently tried muscle relaxants; routine visit with chiropractor suggest PT and see PCP for continued spasms/tightening-$g saw PCP starting PT scan and PCP said I should call Employee Health. |
|
| VAERS ID: |
611953 (history) |
| Form: |
Version 1.0 |
| Age: |
34.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2014-10-14 |
| Onset: | 2014-10-15 |
| Days after vaccination: | 1 |
| Submitted: |
2015-11-29 |
| Days after onset: | 410 |
| Entered: |
2015-11-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
LA / SYR |
Administered by: Public Purchased by: Other Symptoms: Exercise tolerance decreased,
Impaired work ability,
Joint range of motion decreased,
Musculoskeletal pain SMQs:, Rhabdomyolysis/myopathy (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Shoulder pain after influenza vaccination provided at my employer. Initially very painful and limited ROM. This lasted at least a couple impacting my ability to work and exercise. Pain and limited ROM lasted for about 9 months. |
|
| VAERS ID: |
613328 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-12-03 |
| Onset: | 2015-12-04 |
| Days after vaccination: | 1 |
| Submitted: |
2015-12-06 |
| Days after onset: | 2 |
| Entered: |
2015-12-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
15722P / UNK |
UN / IM |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
L012478 / UNK |
UN / SC |
Administered by: Other Purchased by: Private Symptoms: Rash erythematous,
Rash pruritic SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Rash and red, itchy spots after getting ZOSTAVAX vaccine. |
|
| VAERS ID: |
615709 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-12-01 |
| Onset: | 2015-12-02 |
| Days after vaccination: | 1 |
| Submitted: |
2015-12-19 |
| Days after onset: | 17 |
| Entered: |
2015-12-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI459AB / 1 |
RA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
M20639 / 1 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Injected limb mobility decreased,
Lymphadenopathy SMQs:, Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Clonazepam; Doxepin; PREMPRO Current Illness: Preexisting Conditions: Chronic fatigue syndrome; Possible Lyme Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient followed up with pharmacy a week after receiving immunizations to state she had swollen lymph nodes in arm that received flu shot and that she couldn''t raise that arm initially. And she was in bed for several days. |
|
| VAERS ID: |
617881 (history) |
| Form: |
Version 1.0 |
| Age: |
36.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-01-06 |
| Onset: | 2016-01-06 |
| Days after vaccination: | 0 |
| Submitted: |
2016-01-07 |
| Days after onset: | 1 |
| Entered: |
2016-01-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
AT3CC / 1 |
RA / IM |
Administered by: Unknown Purchased by: Unknown Symptoms: Dizziness,
Vomiting SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Husband of client received IIV4 Flulaval at 2:25 pm on 1/6/16 during a clinic visit with wife and 4 week old infant. This client is a 36 year old male with no history of illness and no history of chronic illness. Client was asked all required and necessary questions regarding past experience with vaccinations, allergies to eggs and/or vaccine components. Client stated no negative events occurred from vaccinations, the last vaccination being a TD. This was his first flu shot he was receiving to protect his 4 week old daughter. Flulaval (Lot: AT3CC, NCD 19515-898-11), 0.5ml, was administered IM to right deltoid at 2:25pm. Fifteen minutes following vaccination with Flulaval client reports going into bathroom, feeling lightheaded, lowering himself to the floor and then vomited. He returned to office and then reported to another nurse that he had nearly passed out when he had a vaccination in the past. Vital signs were taken, 108/76, Pulse regular 80. Client appeared pale and was sat at table, provided a drink, and asked to remain in place for monitoring. At 3:30pm this client desired to leave with wife/baby reporting he felt better. His pulse was 80 regular. At time of event the Nursing Supervisor was informed and present for entire follow up monitoring. Client was advised at time of department from office to seek medical attention for further symptoms. A follow up telephone call was made to client at 4 pm, he was attempting to eat, but reports vomiting what he had eaten. This RN instructed patient to have wife drive him home, and to lay down. |
|
| VAERS ID: |
619856 (history) |
| Form: |
Version 1.0 |
| Age: |
1.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-01-15 |
| Onset: | 2016-01-17 |
| Days after vaccination: | 2 |
| Submitted: |
2016-01-20 |
| Days after onset: | 3 |
| Entered: |
2016-01-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U5338BA / 2 |
RL / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
294X9 / 1 |
LL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
K074036 / 1 |
RL / SC |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
L026405 / 1 |
LL / SC |
Administered by: Public Purchased by: Public Symptoms: Altered state of consciousness,
Tremor,
Vomiting SMQs:, Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: About 30 hrs after getting MMR, V, Hep A, Flu vaccine, pt has brief period of altered level of consciousness while bathing, possible mild seizure (mom reported some brief shaking), f/b vomiting and then promptly fell asleep. Responsive at time of mom''s call with NL breathing and temp. |
|
| VAERS ID: |
622962 (history) |
| Form: |
Version 1.0 |
| Age: |
15.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-02-10 |
| Onset: | 2016-02-12 |
| Days after vaccination: | 2 |
| Submitted: |
2016-02-17 |
| Days after onset: | 5 |
| Entered: |
2016-02-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE) / SANOFI PASTEUR |
U5304AB / 7+ |
LA / IM |
| HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. |
L019297 / 3 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Aggression,
Headache,
Vision blurred SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Hostility/aggression (narrow), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Concerta 36mg; Ventolin HFA Current Illness: Preexisting Conditions: ADHD; Cough Variant Asthma; Migraine Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Blurry vision, headache, combative. |
|
| VAERS ID: |
626980 (history) |
| Form: |
Version 1.0 |
| Age: |
20.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-03-14 |
| Onset: | 2016-03-14 |
| Days after vaccination: | 0 |
| Submitted: |
2016-03-14 |
| Days after onset: | 0 |
| Entered: |
2016-03-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI440AB / 4 |
RA / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
793JR / 1 |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Expired product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: GAVE HEP A VACCINE WHICH HAD EXPIRED LAST MONTH. |
|
| VAERS ID: |
646932 (history) |
| Form: |
Version 1.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2015-12-04 |
| Onset: | 2015-12-04 |
| Days after vaccination: | 0 |
| Submitted: |
2016-08-09 |
| Days after onset: | 248 |
| Entered: |
2016-08-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI524AA / UNK |
LA / UN |
Administered by: Other Purchased by: Unknown Symptoms: Dysgeusia SMQs:, Taste and smell disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Comments: None Allergies: Diagnostic Lab Data: CDC Split Type: USSA2015SA208185
Write-up: Initial unsolicited report received from a non-healthcare professional on 07 December 2015. This case involves a 72-years old female patient who was vaccinated with a dose of FLUZONE HD (batch number: UI524AA, dose, dose in series and route of administration was not reported) in the left arm on 04 December 2015. The patient''s illness at time of vaccination, pre-existing physician diagnosed allergies, birth defects, medical conditions were reported as none and denied any other vaccinations within four weeks of vaccinations. The patient''s concomitant medications were not reported. On 04 December 2015, thirty minutes following the vaccination, the patient had developed metallic taste. Laboratory data and corrective treatment was not reported. On an unknown date, the patient was recovered from the event (after 1.5 day). List of documents held by sender: none. |
|
| VAERS ID: |
651156 (history) |
| Form: |
Version 1.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-08-31 |
| Onset: | 2016-09-01 |
| Days after vaccination: | 1 |
| Submitted: |
2016-09-03 |
| Days after onset: | 2 |
| Entered: |
2016-09-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI620AB / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
L022262 / UNK |
RA / IM |
Administered by: Other Purchased by: Private Symptoms: Injection site erythema,
Injection site pain,
Injection site pruritus,
Injection site rash SMQs:, Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergy to cephalosporin Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Sore arm, redness, rash, and itchy arm where flu shot was administered for 3 days. |
|
| VAERS ID: |
654453 (history) |
| Form: |
Version 1.0 |
| Age: |
30.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-09-12 |
| Onset: | 2016-09-14 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2016-09-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
A3AD2 / 1 |
RA / IM |
Administered by: Private Purchased by: Private Symptoms: Injection site erythema,
Injection site swelling,
Injection site warmth,
Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Redness, swelling, warmth at injection site. Hive-like. Lasted 2-3 days. Pt. became febrile and was seen for office visit. S/S resolved. |
|
| VAERS ID: |
658584 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-10-03 |
| Onset: | 2016-10-04 |
| Days after vaccination: | 1 |
| Submitted: |
2016-10-07 |
| Days after onset: | 3 |
| Entered: |
2016-10-11 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
165803 / 1 |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
M94708 / 1 |
RA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Asthenia,
Blood pressure increased,
Blood test normal,
Cardiac stress test normal,
Chest discomfort,
Electrocardiogram,
Fatigue,
Feeling cold,
Heart rate increased,
Injection site erythema,
Injection site swelling,
Pyrexia,
Tremor,
Vaccination complication,
Ventricular extrasystoles,
White blood cell count increased SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Ventricular tachyarrhythmias (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypertension (narrow), Cardiomyopathy (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Dehydration (broad), Hypokalaemia (broad), Noninfectious myocarditis/pericarditis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atorvastatin; Losartan; Levothyroxine; Clobetasol Current Illness: No Preexisting Conditions: Hypertension; Hyperlipidemia; Hypothyroidism Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: At approximately 3:00am on 10/04/16, patient awoke with her chest feeling heavy. She felt that her heart was beating heavily. She went back to sleep then awoke again shaking and feeling cold, heart still felt like it was beating fast/strong. She again fell back to sleep. She awoke at 6:00 AM(when she normally would prepare for work) but felt very tired and weak, her chest still felt heavy. She had recently (7/30/16) suffered a stroke so she was worried that something serious was happening. Her right arm at the site where she had received the PREVNAR 13 vaccine was red and raised. She measured her blood pressure and found it to be 144/102 (her usual reading would be 135/75), her heart rate was 113 (her usual was appx 70). She took her blood pressure medication and a low dose aspirin. She called 911. The EMT found her to have a low grade fever (100.3). She was given an EKG. She was told that she was having PVC''s at the rate of 1 every 5 seconds. Her blood work and stress test were normal. She had an elevated WBC which was expected due to her fever. Doctor diagnosed her to have had an adverse reaction to her PREVNAR 13 vaccine. Over time, (2-3 hours) she felt better and her symptoms went away. She was discharged. |
|
| VAERS ID: |
659506 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-10-13 |
| Onset: | 2016-10-16 |
| Days after vaccination: | 3 |
| Submitted: |
2016-10-16 |
| Days after onset: | 0 |
| Entered: |
2016-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 3 |
LA / SYR |
| VARZOS: ZOSTER (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
RA / SYR |
Administered by: Private Purchased by: Other Symptoms: Injection site erythema,
Injection site pruritus,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: No Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Bright red, swollen area warm to touch around injection area. About 2 1/2" in diameter. Lighter pink area, slightly swollen radiating from injection area about 5" from injection site to arm area above elbow. Extremely itchy directly around injection site. |
|
| VAERS ID: |
660055 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-10-06 |
| Onset: | 2016-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2016-10-08 |
| Days after onset: | 1 |
| Entered: |
2016-10-18 |
| Days after submission: | 10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI678AD / UNK |
LA / IM |
Administered by: Private Purchased by: Other Symptoms: Injection site erythema,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: local reaction, red, swelling, itchy Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Area is red, swollen, warm to the touch left Deltoid to almost elbow. |
|
| VAERS ID: |
661476 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-09-30 |
| Onset: | 0000-00-00 |
| Submitted: |
2016-10-25 |
| Entered: |
2016-10-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1620201 / 2 |
LA / IM |
Administered by: Other Purchased by: Unknown Symptoms: Injection site reaction,
Pain in extremity,
Skin tightness SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient describes her arm feels like there is a cuff around her bicep area. She reports it is constant. Full range of motion for patient. No clear discoloration on patient''s arm to date (10/25/2016) patient reports no pain on injection site rather arm below injection site. |
|
| VAERS ID: |
661707 (history) |
| Form: |
Version 1.0 |
| Age: |
75.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-09-28 |
| Onset: | 2016-10-03 |
| Days after vaccination: | 5 |
| Submitted: |
0000-00-00 |
| Entered: |
2016-10-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI691AB / 7+ |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
N16560 / 1 |
RA / IM |
Administered by: Other Purchased by: Other Symptoms: Eczema,
Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: No Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Rash on hands 5 days after - mild. Seen 2nd time - 10/25/16 - Eczematous rash, hands, arms, torso. |
|
| VAERS ID: |
661899 (history) |
| Form: |
Version 1.0 |
| Age: |
74.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-10-17 |
| Onset: | 2016-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
2016-10-19 |
| Days after onset: | 2 |
| Entered: |
2016-10-26 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
C54L3 / 5 |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
M026317 / 1 |
LA / IM |
Administered by: Private Purchased by: Private Symptoms: Vaccination site erythema SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ZOCOR; Aspirin; Omeprazole Current Illness: Cough likely R/T GERD Preexisting Conditions: NKDA Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Large (greater than 20 cm) area of erythema surrounding vaccine site and traveling down to elbow. |
|
| VAERS ID: |
662102 (history) |
| Form: |
Version 1.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-10-23 |
| Onset: | 2016-10-23 |
| Days after vaccination: | 0 |
| Submitted: |
2016-10-27 |
| Days after onset: | 4 |
| Entered: |
2016-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1619521 / UNK |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Dizziness,
Hypersensitivity,
Pharyngeal oedema,
Pruritus,
Urticaria SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Anticholinergic syndrome (broad), Oropharyngeal allergic conditions (narrow), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: lamotrigine, risperidone, atorvastatin, atenolol ,Depakote, irbesartan Current Illness: none reported Preexisting Conditions: none reported Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: PATIENT CAME IN AT 5PM AND STATED HE HAD FELT DIZZY, WOOSY WHEN HE GOT HOME FROM PHARMACY. LAID DOWN AND NAPPED. REPORTED NO SWELLING OF THROAT, ITCHING, HIVES ETC LIKE AN ALLERGIC REACTION. |
|
| VAERS ID: |
662545 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-10-26 |
| Onset: | 2016-10-26 |
| Days after vaccination: | 0 |
| Submitted: |
2016-10-28 |
| Days after onset: | 2 |
| Entered: |
2016-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U5J99AC / 3 |
RL / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site erythema,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: URI Preexisting Conditions: Asthma; Microcephaly; Congenital hearing loss; Dev. delay Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Notified by nurse triage on 10/27 at 8:15 pm that family was calling due to continued swelling and redness on leg at site of flu shot. No fever, no induration. Recommended cool compresses, pain med if needed, call office in AM for eval if worsening. |
|
| VAERS ID: |
662645 (history) |
| Form: |
Version 1.0 |
| Age: |
50.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-10-21 |
| Onset: | 2016-10-23 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2016-10-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
4A2E2 / UNK |
LA / IM |
| VARZOS: ZOSTER LIVE (ZOSTAVAX) / MERCK & CO. INC. |
M027117 / 1 |
RA / SC |
Administered by: Other Purchased by: Other Symptoms: Activities of daily living impaired,
Burning sensation,
Hypoaesthesia,
Injection site rash,
Injection site swelling,
Pain,
Pain in extremity,
Peripheral swelling SMQs:, Cardiac failure (broad), Angioedema (broad), Peripheral neuropathy (broad), Dementia (broad), Guillain-Barre syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Acyclovir Current Illness: Preexisting Conditions: Herpes Simplex with complication noted on 10/18/15 Allergies: Diagnostic Lab Data: Pt. does have noted history of Herpes Simplex with complication noted 10/18/15 CDC Split Type:
Write-up: 10/23/16 - pt. woke up to her right arm being numb. This subsided through out the morning. Swelling with rash near the injection site extending down close to the elbow. Painful to close fingers - had little strength in hand. She couldn''t make a fist with right hand, difficulty removing a ring that was worn. 10/25/16 - pain and difficulty brushing teeth, chopping vegetables, lifting tea pot. Burning sensation in upper arm where rash is. 10/24/16 - pt. was seen for OV. Ibuprofen 400 mg - 600 mg every 6 hrs recommended. 10/31/16 - still mild hand/finger swelling. |
|
| VAERS ID: |
664115 (history) |
| Form: |
Version 1.0 |
| Age: |
82.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-09-02 |
| Onset: | 2016-09-02 |
| Days after vaccination: | 0 |
| Submitted: |
2016-11-03 |
| Days after onset: | 62 |
| Entered: |
2016-11-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI659AA / UNK |
LA / UN |
Administered by: Other Purchased by: Private Symptoms: Abdominal pain upper,
Chills,
Headache,
Pneumonia,
Red blood cell count,
Tremor,
X-ray SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Eosinophilic pneumonia (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: amlodipine; lorazepam; CRESTOR; levothyroxine Current Illness: None known Preexisting Conditions: None known Allergies: Diagnostic Lab Data: blood work (RBC), x-rays CDC Split Type:
Write-up: Headache, shaking/shivers, stomach aches, went to ER on 9/18, had blood work done treated for pneumonia (with Z-pack) and for RBC. |
|
| VAERS ID: |
664346 (history) |
| Form: |
Version 1.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-10-15 |
| Onset: | 2016-10-16 |
| Days after vaccination: | 1 |
| Submitted: |
2016-11-05 |
| Days after onset: | 20 |
| Entered: |
2016-11-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI678AE / 1 |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Bursitis,
Pain in extremity,
Tenderness SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: None Preexisting Conditions: No allergies; Unknown medical conditions Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt. has been experiencing pain and tenderness in her left arm since receiving her influenza vaccine. Pt. described the pain as being like bursitis. |
|
| VAERS ID: |
669470 (history) |
| Form: |
Version 1.0 |
| Age: |
1.42 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-10-19 |
| Onset: | 2016-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
2016-10-26 |
| Days after onset: | 7 |
| Entered: |
2016-11-08 |
| Days after submission: | 13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U5599AC / UNK |
UN / UN |
Administered by: Public Purchased by: Other Symptoms: Injection site reaction,
Injection site swelling,
Injection site warmth,
Pyrexia,
Rash macular SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: POLY-VI-SOL Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Fever, swollen, warm thigh (anteriorly) with blotchy red macular rash-significant increase in size of thigh; No systemic rash. |
|
| VAERS ID: |
666942 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2016-11-17 |
| Entered: |
2016-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / UN |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / UNK |
UN / UN |
Administered by: Other Purchased by: Unknown Symptoms: Malaise,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2016532711
Write-up: This is a spontaneous report from a contactable physician communicated to a Pfizer sales representative who reported for himself. This elderly male patient received on an unknown date a single dose of PREVNAR 13 and influenza vaccine (manufacturer unknown), both for immunization. Concomitant medications and medical history were not reported. On an unspecified date the patient felt sick and arm was sore. Outcome of the event arm was sore was recovered on an unspecified date after 12 hours. Outcome of the event felt sick was unknown. |
|
| VAERS ID: |
667128 (history) |
| Form: |
Version 1.0 |
| Age: |
6.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-11-09 |
| Onset: | 2016-11-10 |
| Days after vaccination: | 1 |
| Submitted: |
2016-11-17 |
| Days after onset: | 7 |
| Entered: |
2016-11-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI678AD / UNK |
RA / UN |
Administered by: Private Purchased by: Public Symptoms: Erythema,
Local reaction,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Asthma Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Large localized reaction - several centimeters in diameter - redness and swelling. |
|
| VAERS ID: |
668067 (history) |
| Form: |
Version 1.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-09-27 |
| Onset: | 2016-09-27 |
| Days after vaccination: | 0 |
| Submitted: |
2016-11-22 |
| Days after onset: | 56 |
| Entered: |
2016-11-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
3CG9P / UNK |
UN / IM |
Administered by: Other Purchased by: Other Symptoms: Chills,
Influenza like illness,
Injection site erythema,
Injection site pain,
Malaise,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Sertraline; Levothyroxine; Amlodipine; Losartan/HCTZ Current Illness: None Preexisting Conditions: Hypertension; hypothyroidism Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Had pain and redness at site of immunization. Had flu like symptoms (chills, fever, malaise for 3 days after immunization. |
|
| VAERS ID: |
668119 (history) |
| Form: |
Version 1.0 |
| Age: |
42.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-11-07 |
| Onset: | 2016-11-13 |
| Days after vaccination: | 6 |
| Submitted: |
2016-11-16 |
| Days after onset: | 3 |
| Entered: |
2016-11-23 |
| Days after submission: | 7 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
WT56908 / 1 |
RA / UN |
Administered by: Other Purchased by: Other Symptoms: Alanine aminotransferase increased,
Aspartate aminotransferase increased,
C-reactive protein increased,
Dyspnoea,
Electrocardiogram PR interval,
Electrocardiogram abnormal,
Electrocardiogram repolarisation abnormality,
Pericarditis,
Pleuritic pain,
Red blood cell sedimentation rate increased,
Troponin normal,
White blood cell count increased SMQs:, Torsade de pointes/QT prolongation (broad), Liver related investigations, signs and symptoms (narrow), Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Arrhythmia related investigations, signs and symptoms (narrow), Conduction defects (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Chronic kidney disease (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: EPZICOM; Rilpivirine; Dolutegravir; KLONOPIN; MARINOL; WELLBUTRIN SR; Hydroxyzine mirtazapine; Prazosin; LATUDA; Aspirin, PRN Current Illness: None Preexisting Conditions: Hx: HIV; Ulcerative Colitis; Psychiatric, Hx MVA-pedestrian with traumatic injury; lumbar radicalopathy Allergies: Diagnostic Lab Data: 11/3/16, Elevated WBC, 14.5; Elevated Sedrate at 33; CRP was 39.5; AST, 53; ALT, 86; Neg, Troponin; Neg, CXR; EKG: Mild tachycardia, early repolarization, evid PR Depression (diffuse) CDC Split Type:
Write-up: Nov 13 ER visit for <24hr duration acute most pleuritic pain with SOB. No hypoxia, afebrile. Dx: Pericardial Inflammation. Tx: Torodal IM- home with anti-inflammatory meds. |
|
| VAERS ID: |
668650 (history) |
| Form: |
Version 1.0 |
| Age: |
57.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-11-28 |
| Onset: | 2016-11-29 |
| Days after vaccination: | 1 |
| Submitted: |
2016-11-29 |
| Days after onset: | 0 |
| Entered: |
2016-11-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI643AE / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
M022086 / 1 |
RA / SC |
Administered by: Public Purchased by: Public Symptoms: Skin reaction SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Iron Current Illness: None Preexisting Conditions: Early COPD - quit smoking approximately 1 yr ago; Hyperlipidemia Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt given a PNEUMOVAX in (R) upper arm an FLUZONE QUADRIVALVENT in (L) deltoid on 11/28/16 at 8:42 A. Pt came in the morning to show underpart of (R) upper arm slightly red and swollen. No redness at injection site. |
|
| VAERS ID: |
668677 (history) |
| Form: |
Version 1.0 |
| Age: |
33.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2016-11-17 |
| Onset: | 2016-11-18 |
| Days after vaccination: | 1 |
| Submitted: |
2016-11-25 |
| Days after onset: | 7 |
| Entered: |
2016-11-29 |
| Days after submission: | 4 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
WT57208 / 2 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Inflammation,
Mobility decreased,
Pain in extremity SMQs:, Parkinson-like events (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Gabapentin; clonazepam; sertraline Current Illness: No Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient has inflammation and pain up and down arm and in shoulder. Patient has significant decrease in range of motion in arm. |
|
| VAERS ID: |
669329 (history) |
| Form: |
Version 1.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
2016-12-02 |
| Entered: |
2016-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
UN / SYR |
Administered by: Other Purchased by: Unknown Symptoms: Gastrointestinal disorder,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2016SA214131
Write-up: Initial unsolicited report received from a physician via other company (Pfizer) (manufacturer report number- 2016517225) on 21 November 2016. This case involves a female patient (age not reported) who was vaccinated with a dose of INFLUENZA VACCINE (FLU SHOT) (batch number, dose in series, dose, route and site of administration was not reported) on an unspecified date. The patient''s medical history and concomitant medications were not reported. On an unspecified date, following the vaccination, the patient had experienced fever and Gastro-intestinal disorder. Relevant laboratory data and corrective treatment was not reported. The outcome of event was not reported. List of documents held by sender: none. |
|
| VAERS ID: |
671888 (history) |
| Form: |
Version 1.0 |
| Age: |
13.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-12-06 |
| Onset: | 2016-12-07 |
| Days after vaccination: | 1 |
| Submitted: |
2016-12-07 |
| Days after onset: | 0 |
| Entered: |
2016-12-13 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI684AB / 7+ |
LA / IM |
| HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. |
M016193 / 3 |
RA / IM |
Administered by: Private Purchased by: Other Symptoms: Blindness transient,
Dizziness,
Head injury,
Headache,
Vision blurred SMQs:, Anticholinergic syndrome (broad), Embolic and thrombotic events, arterial (narrow), Accidents and injuries (narrow), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: No illness Preexisting Conditions: Entoptic phenomenon; no other dxs; no allergies Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Received vaccine 12/6/16 no adverse symptoms or events until 12/7/16 at 0515 while pt in shower. Pt began to feel lightheaded, dizzy, (+) blurred vision. About 30 sec couldn''t see. No LOC. Hit head (right side). Frontal H/A rates 2/10. Negative for N/V. |
|
| VAERS ID: |
673675 (history) |
| Form: |
Version 1.0 |
| Age: |
49.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2015-09-18 |
| Onset: | 2015-11-01 |
| Days after vaccination: | 44 |
| Submitted: |
2016-12-20 |
| Days after onset: | 415 |
| Entered: |
2016-12-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
59CK3 / UNK |
- / IM |
Administered by: Private Purchased by: Unknown Symptoms: Arthralgia,
Headache,
Hypoaesthesia,
Muscle mass,
Myalgia,
Paraesthesia,
Vision blurred SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Glaucoma (broad), Lens disorders (broad), Eosinophilic pneumonia (broad), Retinal disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: LUE and LLE intermittent numbness, difficulty focusing L eye, numbness L half of face, lumps in muscles, pain/tingling R forehead, diffuse muscle pain and joint pain. |
|
| VAERS ID: |
676288 (history) |
| Form: |
Version 1.0 |
| Age: |
28.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-12-16 |
| Onset: | 2016-12-18 |
| Days after vaccination: | 2 |
| Submitted: |
2017-01-02 |
| Days after onset: | 15 |
| Entered: |
2017-01-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
WT54006 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Pruritus,
Rash generalised SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient got flu shot on 12/16/16, 48 hours later she started feeling itchy, 60hrs later shot developed rash all over (not at site of injection). Went to clinic, started Rx for Prednisone on 12/22/16. Completed Prednisone on 12/28/16, still symptomatic. Also taking BENADRYL. |
|
| VAERS ID: |
678545 (history) |
| Form: |
Version 1.0 |
| Age: |
85.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-01-10 |
| Onset: | 2017-01-13 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-01-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI740AA / 1 |
LA / UN |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
M88543 / 1 |
RA / UN |
Administered by: Other Purchased by: Private Symptoms: Injection site erythema,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient had a reaction to the vaccine that developed approximately 3 days after receiving it. Redness and warmth developed on the outside and back of her right arm. This reaction did no occur at the injection site. |
|
| VAERS ID: |
679909 (history) |
| Form: |
Version 1.0 |
| Age: |
44.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-12-23 |
| Onset: | 2016-12-24 |
| Days after vaccination: | 1 |
| Submitted: |
2017-01-28 |
| Days after onset: | 35 |
| Entered: |
2017-01-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1620261 / 2 |
UN / UN |
Administered by: Unknown Purchased by: Private Symptoms: Abdominal pain,
Cholecystectomy,
Cholecystitis SMQs:, Acute pancreatitis (broad), Retroperitoneal fibrosis (broad), Infectious biliary disorders (narrow), Gallbladder related disorders (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: none Allergies: Diagnostic Lab Data: Gallbladder Inflammation, had to be removed CDC Split Type:
Write-up: Intense abdominal pain. |
|
| VAERS ID: |
680901 (history) |
| Form: |
Version 1.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2016-12-28 |
| Onset: | 2016-12-29 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-02-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
1620301 / 7+ |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
M037533 / 1 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Fatigue,
Injection site reaction,
Injection site urticaria,
Malaise,
Rash macular SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: CELEXA Current Illness: None Preexisting Conditions: Allergy, sulfa Allergies: Diagnostic Lab Data: No itching. Hives very tender CDC Split Type:
Write-up: 24 hrs after vaccine administered developed general malaise and fatigue. 48 hrs after vaccine, blotchy hives scattered over (L) upper arm. Applied ice pack PRN and took ZYRTEC qd. Symptoms started to improve on day 5 then fully resolved on day 7 after vaccine. |
|
| VAERS ID: |
681738 (history) |
| Form: |
Version 1.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-01-30 |
| Onset: | 2017-02-01 |
| Days after vaccination: | 2 |
| Submitted: |
2017-02-07 |
| Days after onset: | 6 |
| Entered: |
2017-02-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
A2Z34 / UNK |
LA / IM |
Administered by: Other Purchased by: Private Symptoms: Diarrhoea,
Paraesthesia,
Vaccination complication SMQs:, Peripheral neuropathy (broad), Pseudomembranous colitis (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Noninfectious diarrhoea (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Coronary artery disease Preexisting Conditions: Sulfur Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Began with feet tingling progresses all over, diarrhea and progressively getting worse. Called Friday 2/03/17 to say she was on route to the hospital. Her primary care physician advised for her to go to the ER. He believed she was having an adverse reaction to her vaccination. |
|
| VAERS ID: |
685233 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-01-25 |
| Onset: | 0000-00-00 |
| Submitted: |
2017-01-29 |
| Entered: |
2017-03-07 |
| Days after submission: | 37 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI722AA / 1 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Rash,
Skin warm,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: COPD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient''s arm became warm with hives/rash. |
|
| VAERS ID: |
712804 (history) |
| Form: |
Version 2.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-09-14 |
| Onset: | 2017-09-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-09-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI845AA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Swelling face SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: None reported Allergies: Biaxin Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced some facial swelling to the left side of her face along the jawline, where her jawline meets her ear. Patient came back to the pharmacy to purchase some Benadryl as she was advised to do by her doctor''s office. |
|
| VAERS ID: |
713872 (history) |
| Form: |
Version 1.0 |
| Age: |
77.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-09-12 |
| Onset: | 2017-09-13 |
| Days after vaccination: | 1 |
| Submitted: |
2017-09-14 |
| Days after onset: | 1 |
| Entered: |
2017-09-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
179002 / 1 |
RA / UN |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
U5770AA / 1 |
LA / UN |
Administered by: Other Purchased by: Unknown Symptoms: Injection site erythema,
Injection site haemorrhage,
Injection site swelling SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: No Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Swollen/red bicep and arm not at inject site. Patient stated arm is much larger than other arm and bleed a lot at time of injection. |
|
| VAERS ID: |
714302 (history) |
| Form: |
Version 2.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-09-22 |
| Onset: | 2017-09-23 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-09-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
XT31908 / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
N013541 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Dyspnoea,
Headache,
Injected limb mobility decreased,
Injection site pain,
Malaise,
Musculoskeletal stiffness,
Pain SMQs:, Anaphylactic reaction (broad), Dystonia (broad), Parkinson-like events (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Cardiomyopathy (broad), Arthritis (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNKNOWN Current Illness: UNKNOWN Preexisting Conditions: UNKNOWN Allergies: NO KNOWN DRUG ALLERGIES Diagnostic Lab Data: UNKNOWN CDC Split Type:
Write-up: Patient called on 9/23/17 to report adverse events to pharmacist. Complaint of stiff neck, sore arms at injection site and cannot move her arms. She received AFLURIA 2017-2018 single dose syringe injection in left deltoid muscle and PNEMOVAX 23 in right deltoid muscle. Not feeling well, shortness of breath, terrible pain and headache. When asked on a scale of 1-10, how bad the pain was, she said 9-10. Pharmacist strongly recommended that she immediately go to the emergency room/hospital. Unknown if patient actually went to the ER or not. |
|
| VAERS ID: |
714905 (history) |
| Form: |
Version 2.0 |
| Age: |
54.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-09-26 |
| Onset: | 2017-09-26 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-09-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
Z55C4 / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Immediate post-injection reaction,
Injection site erythema,
Injection site swelling,
Malaise SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: valacyclovir 500, one tablet once daily. Current Illness: none Preexisting Conditions: none Allergies: NKDA Diagnostic Lab Data: CDC Split Type:
Write-up: Immediately after delivering dose, patients arm became swollen and red, about 1" circumference around the injection site. There were no systemic signs of allergic reaction/anaphylaxis, no disorientation or difficulty breathing, or swelling any other areas of the body that were noticeable to me. I asked her to stay in the store for 15 minutes, and swelling went down slightly, she then left with her mother to run an errand down the street, then cam back about 30 minutes later for me to check on her; again swelling was reduced to about 1/2" circumference and redness was minimal. I called again the morning of 9/27/2017- she states she is feeling slightly under the weather but that the swelling in her arm is less than it was last night. |
|
| VAERS ID: |
715266 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-09-28 |
| Onset: | 2017-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-09-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI811AB / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Dizziness,
Throat tightness,
Tremor SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad), Hypersensitivity (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: none Preexisting Conditions: hyperlipidemia and GERD Allergies: Shellfish, no drug allergies Diagnostic Lab Data: none CDC Split Type:
Write-up: Patient departed the clinic to drive home and became dizzy and shakey. Patient felt as though her throat was closing. |
|
| VAERS ID: |
716298 (history) |
| Form: |
Version 1.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-01 |
| Onset: | 0000-00-00 |
| Submitted: |
2017-10-03 |
| Entered: |
2017-10-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
1790002 / 2 |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Extra dose administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Same vaccine (FLUAD) administered twice within two weeks of each other. No adverse events reported yet. |
|
| VAERS ID: |
718104 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-10-02 |
| Onset: | 2017-10-03 |
| Days after vaccination: | 1 |
| Submitted: |
2017-10-04 |
| Days after onset: | 1 |
| Entered: |
2017-10-05 |
| Days after submission: | 1 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
AF543 / UNK |
RA / UN |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI864AA / 3 |
RA / UN |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
954G2 / 2 |
LA / UN |
| MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
N013863 / UNK |
LA / SC |
Administered by: Public Purchased by: Public Symptoms: Erythema,
Injection site rash,
Pruritus,
Pyrexia,
Rash,
Swelling,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: NAS; Undescended (L) tests; IUGR Allergies: Diagnostic Lab Data: None ordered CDC Split Type:
Write-up: Vaccines given on 10-2-17 (L) deltoid: Hep A - (L) arm; MMRV - RN. (R) deltoid: KINRIX and FLUZONE - RN. Seen in office 10-4-17 with rash on (Rt) deltoid, (Lt) arm and (L) forehead - reddened, localized swelling and itching. Fever/vomiting in less than 24 hours. Unknown if vaccine related. |
|
| VAERS ID: |
719441 (history) |
| Form: |
Version 2.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-10-08 |
| Onset: | 2017-10-09 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
195218 / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Influenza SMQs:, Infective pneumonia (broad), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: no Current Illness: no Preexisting Conditions: no Allergies: no Diagnostic Lab Data: no CDC Split Type: no
Write-up: 10 hours after injection I developed full blown influenza. |
|
| VAERS ID: |
720649 (history) |
| Form: |
Version 1.0 |
| Age: |
7.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-10-06 |
| Onset: | 2017-10-07 |
| Days after vaccination: | 1 |
| Submitted: |
2017-10-16 |
| Days after onset: | 9 |
| Entered: |
2017-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
4E532 / UNK |
LA / SYR |
Administered by: Public Purchased by: Unknown Symptoms: Injection site reaction,
Rash erythematous SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pt. developed red raised rash around injection site. |
|
| VAERS ID: |
720808 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-05 |
| Onset: | 2017-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
XF32908 / UNK |
RA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
NO13541 / UNK |
RA / IM |
Administered by: Work Purchased by: ? Symptoms: Injected limb mobility decreased,
Injection site erythema,
Injection site pain,
Injection site swelling,
Pain in extremity SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: BLOOD PRESSURE MEDICATION, THYROID MEDICATION Current Illness: NONE Preexisting Conditions: HEART DISEASE; STENT PLACEMENT Allergies: SULFA DRUGS Diagnostic Lab Data: CDC Split Type:
Write-up: Patient received a flu shot and PNEUMOVAX 23 in left deltoin, 1 inch apart on Thursday Oct. 5, 2017. That same evening her arm was sore so patient iced it and took ibuprofen for pain. Next day, upper right arm was more swollen. She continued with ice and ibuprofen. On Saturday Oct. 7, 2017 patient could not move her arm, whole circumference of upper right arm, below injection site was very red, and swollen and sore. Patient went to urgent care on 10/7/17 where she was advised to use topical hydrocortisone cream and allergy tablets. She was not given any antibiotics. On Wednesday Oct. 11, 2017 I saw the patient''s arm. The swelling and soreness was gone. I followed up by phone conversation with the patient on 10/12/17 and the patient did not report swelling and felt better. |
|
| VAERS ID: |
721284 (history) |
| Form: |
Version 2.0 |
| Age: |
46.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-16 |
| Onset: | 2017-10-18 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U1826AD / UNK |
LA / IM |
Administered by: Other Purchased by: ? Symptoms: Body temperature increased,
Contusion,
Erythema,
Pain,
Skin mass,
Skin warm SMQs:, Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Neuroleptic malignant syndrome (broad), Accidents and injuries (narrow), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: allergic to berries Diagnostic Lab Data: CDC Split Type:
Write-up: Pain, redness, knot under skin, warmth, bruise and temp 100.7. |
|
| VAERS ID: |
721690 (history) |
| Form: |
Version 2.0 |
| Age: |
66.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-01 |
| Onset: | 2017-10-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI887AA / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Arthralgia,
Chills,
Headache,
Hypersomnia,
Myalgia,
Pyrexia SMQs:, Rhabdomyolysis/myopathy (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Eosinophilic pneumonia (broad), Depression (excl suicide and self injury) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Simvastatin, Levothyroxine, Aspirin Current Illness: No Preexisting Conditions: NO Allergies: Amoxicillin, Dilaudid Diagnostic Lab Data: CDC Split Type:
Write-up: Patient reports at 4:00 pm she developed a fever of 101 degrees, chills, sever joint and muscle aches, and a head ache. She slept for 12 hours and symptoms have fully resolved a this time. |
|
| VAERS ID: |
721762 (history) |
| Form: |
Version 2.0 |
| Age: |
61.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-10-01 |
| Onset: | 2017-10-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
XF33008 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Pityriasis rosea SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Januvia, lisinopril, metformin, atorvastatin Current Illness: Preexisting Conditions: Allergies: No known allergies Diagnostic Lab Data: Unknown CDC Split Type:
Write-up: Pityriasis rosea. |
|
| VAERS ID: |
722094 (history) |
| Form: |
Version 2.0 |
| Age: |
39.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-05 |
| Onset: | 2017-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-10-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
XF33008 / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Chest discomfort,
Dizziness,
Dysphagia,
Dyspnoea,
Electrocardiogram normal,
Eyelid margin crusting,
Fibrin D dimer normal,
Hypertension,
Metabolic function test normal,
Ocular hyperaemia,
Troponin I normal SMQs:, Anaphylactic reaction (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Glaucoma (broad), Hypertension (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Periorbital and eyelid disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: When I was very young, perhaps four, I reacted with a high fever and hallucinations to the TDAP (so my mother recalls). I do not Other Medications: none Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: On 10/5/17, I received the following tests: -EKG 12-LEAD -BASIC METABOLIC PANEL -D-DIMER -TROPONIN I All came back negative for any adverse heart conditions. CDC Split Type:
Write-up: About 2 1/2 hours after the shot, I began having discomfort in my chest. I first thought it was heartburn (which I don''t typically experience, in fact, haven''t outside of pregnancy.) However, the feeling did not ease up. I went down to ask the school nurse if it could be a side effect of the shot, but as I walked, I began to get lightheaded. She checked my blood pressure and found it to be unusually high (180/90), but it lowered on a subsequent check to about 150/90 (still atypically high for me.) She suggested I get checked out. I went to the emergency room where they ran a series of tests that all came back negative (see below). All told, my symptoms included: -Tightness/discomfort in my chest - lasted about 8 hours -Difficulty swallowing (like a lump in my throat) - lasted about 8 hours -Shortness of breath - lasted about 8 hours -Redness in the eyes - lasted about 8 hours -My right eye was crusted shut two mornings later. Just that one morning. Two days after the shot, all symptoms had cleared up without treatment. |
|
| VAERS ID: |
724451 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-11-01 |
| Onset: | 2017-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
XF32908 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Immediate post-injection reaction,
Injection site induration,
Injection site swelling,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: cetirizine Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling underneath the skin about 1/2 inch in diameter- skin became hard and swollen immediately after giving the shot, even circumference around injection site. |
|
| VAERS ID: |
724792 (history) |
| Form: |
Version 1.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-17 |
| Onset: | 2017-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
2017-10-17 |
| Days after onset: | 0 |
| Entered: |
2017-11-02 |
| Days after submission: | 16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
G294R / UNK |
LA / UN |
Administered by: Public Purchased by: Unknown Symptoms: Dysgeusia,
Paraesthesia oral SMQs:, Taste and smell disorders (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine given Lt. deltoid-after approx 7 minutes she commented that she could taste the vaccine-5 minutes later said her tongue felt fuzzy-checked no enlargement-no other symptoms. |
|
| VAERS ID: |
725070 (history) |
| Form: |
Version 1.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-12 |
| Onset: | 2017-10-13 |
| Days after vaccination: | 1 |
| Submitted: |
2017-11-02 |
| Days after onset: | 20 |
| Entered: |
2017-11-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
255C4 / UNK |
LA / UN |
Administered by: Other Purchased by: Other Symptoms: Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Sore arm for two months, hasn''t had a flu shot since then~Influenza (Seasonal) (no brand name)~UN~0.00~Patient Other Medications: Current Illness: None Preexisting Conditions: None that knows of Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient reported this year her arm was so sore she believes it was bursitis. She had to have physical therapy to loosen up arm. (She said 10 yrs ago it was sore for 2 months). Did not report this on consent form as a previous reaction. Hasn''t had a flu shot for 10 years. |
|
| VAERS ID: |
725778 (history) |
| Form: |
Version 2.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-09 |
| Onset: | 2017-10-13 |
| Days after vaccination: | 4 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
- / UNK |
- / - |
Administered by: Private Purchased by: ? Symptoms: Asthenia,
Headache,
Malaise,
Nausea,
Rash,
Tremor SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: onset of rash Preexisting Conditions: fibromyalgia, arthritis Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Headache, nausea, weakness, shakiness from about 4-5 days after immunization. Immunization date is estimated, as vaccination was administered at primary care office "about a month ago." Malaise persists and nausea is improved but persists. Since flu vaccination pt had 3 visits with different providers at primary care. Pt was told the rash was "not hives." Rash persists & she will go to dermatology today. Upon my request that practice submit a VAERS report, I learned there is no documentation of any adverse events, rash began before the vaccine was administered and other symptoms are not documented. |
|
| VAERS ID: |
726254 (history) |
| Form: |
Version 2.0 |
| Age: |
63.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-10-10 |
| Onset: | 2017-10-12 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
C559A / N/A |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Erythema SMQs:, Anaphylactic reaction (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Did receive cortisone shot 2 days after Current Illness: unknown Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none CDC Split Type:
Write-up: Patient stated that a couple of days after he received the FLUARIX vaccine his face got bright bright red like a hot flash. This would come and go and lasted for approximately a week before it went away. Patient stated they had also received a cortisone shot within a few days of receiving FLUARIX. Patient stated they went in to see their doctor and the doctor thought it was most likely due to the flu vaccine. No treatment needed. Symptoms cleared up completely after approximately a week. Patient stated they had never had a reaction like this to the flu vaccine. |
|
| VAERS ID: |
726570 (history) |
| Form: |
Version 2.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-26 |
| Onset: | 2017-11-01 |
| Days after vaccination: | 6 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
572KT / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Loss of personal independence in daily activities,
Nausea,
Pain,
Pain in extremity,
Sleep disorder SMQs:, Acute pancreatitis (broad), Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: ranitidine; ADVIL Current Illness: none Preexisting Conditions: none Allergies: sulfa antibiotics Diagnostic Lab Data: none as of yet. CDC Split Type:
Write-up: Patient reported normal arm soreness the immediate days following vaccination. However the soreness developed into sharp pains when moving her arm. She gets a nauseating feeling during the pain. The pain is so bad that she has a hard time sleep on that arm during the night for it wakes her up. This developed within a week of getting the shot and has not abated. The patient does state it is starting to interfere with daily life. Patient does plan on following up this week with her primary care doctor. |
|
| VAERS ID: |
726796 (history) |
| Form: |
Version 2.0 |
| Age: |
27.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-05 |
| Onset: | 2017-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9M3F7 / 1 |
LA / SYR |
Administered by: Work Purchased by: ? Symptoms: Injection site pain,
Mobility decreased SMQs:, Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Paxil & birth control Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Arm soreness at site of injection. Over a month later the arm is still sore. Can''t lift objects above head or across body. |
|
| VAERS ID: |
726797 (history) |
| Form: |
Version 2.0 |
| Age: |
37.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-05 |
| Onset: | 2017-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9M3F7 / 1 |
RA / SYR |
Administered by: Work Purchased by: ? Symptoms: Injected limb mobility decreased,
Injection site pain,
Insomnia,
Loss of personal independence in daily activities,
Muscular weakness,
Pain SMQs:, Rhabdomyolysis/myopathy (broad), Peripheral neuropathy (broad), Dementia (broad), Guillain-Barre syndrome (broad), Noninfectious encephalopathy/delirium (broad), Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Allegra D; Birth Control (generic for Ortho-tri-cyclin; Woman''s Multi-vitamin; Wellbutrin Current Illness: None Preexisting Conditions: None Allergies: Ciprofloxacilin & Clindamycin Benzolyl Diagnostic Lab Data: Physical Therapy started 11/13 and scheduled 2 days/week for a few weeks to see if it will help. MRI scheduled for 12/12/17 if still in pain. CDC Split Type:
Write-up: I have gotten the flu shot for years and usually have arm pain for a day or two after and then it subsides. This time the pain started in the afternoon of the shot and got so bad I couldn''t lift my arm. The pain did not go away within a few days and has proceeded to get worse 6 weeks later. My arm is weak, the pain is causing trouble sleeping for the past few weeks. I can''t lift my arm without pain and activities have been limited (including getting dressed and driving). The pain is in my upper arm that I got the shot in and started the afternoon of the shot. Pain is sometimes in muscle and others closer to the shoulder. I tried Aleve, Advil, Tylenol, etc but none helped. Went to my Primary care who recommended starting with physical therapy. If it''s not better I am scheduled for an MRI on 12/12. PMC said that the injection could have been too high in either the joint or bursa, but not 100%. |
|
| VAERS ID: |
726806 (history) |
| Form: |
Version 2.0 |
| Age: |
71.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-19 |
| Onset: | 2017-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI882AA / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Chills,
Fatigue,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No meds Current Illness: None Preexisting Conditions: None Allergies: Epinephrine = syncope Diagnostic Lab Data: None CDC Split Type:
Write-up: Seen at Doctor''s office on 10/26/17. Has had daily fevers since 10/19/17 as high as 102. Denies any other symptoms other than chills and fatigue. |
|
| VAERS ID: |
726941 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-05 |
| Onset: | 2017-10-06 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9M3F7 / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Arthralgia,
Drug administered at inappropriate site,
Joint range of motion decreased,
Limb discomfort,
Pain,
Pain in extremity,
Periarthritis,
Sleep disorder SMQs:, Drug abuse and dependence (broad), Arthritis (narrow), Tendinopathies and ligament disorders (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: WELLBUTRIN Current Illness: no illnesses Preexisting Conditions: M.S. (asymptomatic) Allergies: AMOXIL, sulfa drugs, MACROBID Diagnostic Lab Data: P.T. assessment reveals possible bursa damage from needle improperly inserted.; ortho appt on 11/28 for further details; Testing is ongoing and ortho visit pending, future MRI possible CDC Split Type:
Write-up: Vaccine was administered higher on my arm than usual; first 24 hours/through the night arm was heavy and sore and continued through the next day. Pain settled deep into the shoulder joint. Range of motion restricted and painful--most acutely upon external rotation. Initial assessment by primary physician (10/19/17) dx as "frozen shoulder" and referred to Orthopedist (pending 11/28/17) and physical therapy (11/6; 11/10; 11/16). Two prescriptions of prednisone (20 mgx3; 8 days taper); nightly ice compress. Pain lessens when taking prednisone but otherwise can be excruciating; sleep interrupted by not being able to move without pain. |
|
| VAERS ID: |
727107 (history) |
| Form: |
Version 2.0 |
| Age: |
79.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-31 |
| Onset: | 2017-11-04 |
| Days after vaccination: | 4 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
179401 / N/A |
LA / SC |
Administered by: Pharmacy Purchased by: ? Symptoms: Erythema,
Swelling SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: n/a Current Illness: n/a Preexisting Conditions: HTN Allergies: n/a Diagnostic Lab Data: n/a CDC Split Type:
Write-up: She had redness, swelling, and a nurse at the local health center thought maybe a cellulitis. |
|
| VAERS ID: |
727416 (history) |
| Form: |
Version 2.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-19 |
| Onset: | 2017-10-20 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UI829AA / UNK |
RA / IM |
Administered by: Work Purchased by: ? Symptoms: Pain in extremity,
Sleep disorder SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Mild thalassemia Allergies: Amoxicillin Diagnostic Lab Data: None so far. CDC Split Type:
Write-up: Patient had initial soreness in arm, originally thought it was the normal soreness associated with a flu shot. Over the next few weeks has progressively gotten worse. According to patient PCP thought there was some swelling and bruising underneath in the arm muscle, but no bruising or obvious swelling could be observed by just looking at arm. Patient reported still being sore and having difficulty with arm towards end of work day and pain/soreness has affected her sleep. |
|
| VAERS ID: |
728805 (history) |
| Form: |
Version 2.0 |
| Age: |
66.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-11-14 |
| Onset: | 2017-11-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / 1 |
RA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Blood test,
Injection site reaction,
Periarthritis,
X-ray SMQs:, Arthritis (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: choline, 8 mg aspirin (1), Occuvite, multi-vitamin, acidophilus,lysine Current Illness: none Preexisting Conditions: I have ''frozen shoulder'' in my right shoulder (site of vaccination), torn rotator cuff in left shoulder as a result of a fall I September of 2017 Allergies: none known Diagnostic Lab Data: x-ray, blood test performed 11/18/2017 CDC Split Type:
Write-up: Frozen shoulder in right shoulder - site of flu shot. |
|
| VAERS ID: |
729044 (history) |
| Form: |
Version 1.0 |
| Age: |
38.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-19 |
| Onset: | 0000-00-00 |
| Submitted: |
2017-12-01 |
| Entered: |
2017-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
195234 / 1 |
LA / SYR |
Administered by: Other Purchased by: Public Symptoms: Injected limb mobility decreased SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Physician Assessment CDC Split Type:
Write-up: Patient reports decreased arm mobility following flu shot resulting in a need for doctor visit and Physical therapy. |
|
| VAERS ID: |
729098 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-10-10 |
| Onset: | 2017-10-10 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
5GC54 / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Drug administered at inappropriate site,
Injection site pain SMQs:, Drug abuse and dependence (broad), Extravasation events (injections, infusions and implants) (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: none Allergies: Sulfa Diagnostic Lab Data: unknown CDC Split Type:
Write-up: Patient reported pain in shoulder almost immediately after injection. She stated that she felt that the injection was given to high in the deltoid, nearly in the joint. She has seen her physician multiple times, has been given a cortisone injection and is currently still in physical therapy for this. She reported this to me today, 12/1/17, as she felt we should know for educational purposes. |
|
| VAERS ID: |
731264 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-12-13 |
| Onset: | 2017-12-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-12-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUVIRIN) / NOVARTIS VACCINES AND DIAGNOSTICS |
- / 1 |
RA / SYR |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Private Purchased by: ? Symptoms: Fatigue,
Feeling abnormal,
Injection site swelling,
Insomnia,
Myalgia,
Pain,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Dementia (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: DIOVAN, CELEXA, vitamin D, LANTUS, glimiperide Current Illness: Preexisting Conditions: Sleep apnea, diabetes, high BP, high cholesterol Allergies: Penicillin, sulpha Diagnostic Lab Data: CDC Split Type:
Write-up: The night of having the shot my arm was throbbing severely, couldn''t even sleep it hurt so much. Very swollen around the injection site also. After a few days the pain was gone but I have not felt right since having it. Very foggy brained and not feeling all there. And so run down and exhausted I cannot wake up. It has been a week now since having it and still feeling the same. A lot of all body muscle pain also. |
|
| VAERS ID: |
732030 (history) |
| Form: |
Version 2.0 |
| Age: |
78.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-11-14 |
| Onset: | 2017-11-28 |
| Days after vaccination: | 14 |
| Submitted: |
0000-00-00 |
| Entered: |
2017-12-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI882AA / UNK |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Musculoskeletal pain SMQs:, Rhabdomyolysis/myopathy (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Gabapentin, metformin, levothyroxine, aspirin Current Illness: none Preexisting Conditions: hypothyroid, elevated blood pressure, endophthalmitis, osteopenia Allergies: shellfish allergy Diagnostic Lab Data: CDC Split Type:
Write-up: Pt tolerated vaccine well, later complains of shoulder pain for last 6 weeks since vaccine. |
|
| VAERS ID: |
735079 (history) |
| Form: |
Version 2.0 |
| Age: |
4.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-01-07 |
| Onset: | 2018-01-08 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-01-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (AFLURIA) / CSL LIMITED |
- / UNK |
RA / SYR |
Administered by: Private Purchased by: ? Symptoms: Cold urticaria,
Cough,
Pyrexia,
Urticaria SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None and no family history Diagnostic Lab Data: None. Dr recommends allergist given we are on to week 3 CDC Split Type:
Write-up: Hives on hands and feet triggered when she went outside in cold 24 hours later. Continued on and off for several days, not severe but noticeable for a child who hadn''t been sick for 3 years straight. Would go away on own. Into third week and she developed a cough and got hives again and also fevers. |
|
| VAERS ID: |
735322 (history) |
| Form: |
Version 2.0 |
| Age: |
48.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-09-21 |
| Onset: | 2017-09-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-01-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U5913A / UNK |
LA / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
R70448 / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site pain,
Injection site pruritus,
Insomnia SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: TOPAMAX; ADVIL; PROAIR; SYMBICORT; FLONASE Current Illness: Acute URI 8/12/2017 Preexisting Conditions: Asthma; leiomyoma of uterus; sinusitis; nodule (R) lung Allergies: Morphine; DEMEROL; PERCOCET; PHENERGAN Diagnostic Lab Data: None - pt. refused follow up assessment CDC Split Type:
Write-up: Pt reports: "I received my flu and pneumonia shots on my left arm, it was excruciating that same day, and has been hurting ever since. Some days don''t bother me much at all, but in general it is bothersome all the time. Some days it is just itchy, some days just hurts, sometimes so badly cannot sleep on that side. Says can still feel exactly where the injections were given". Denies redness or swelling at sites. |
|
| VAERS ID: |
735957 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2017-12-07 |
| Onset: | 2017-12-10 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-02-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT5954LA / UNK |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Angiotensin converting enzyme,
Antibody test negative,
Asthenia,
Balance disorder,
CSF test normal,
Cerebral venous thrombosis,
Cervical radiculopathy,
Coagulation test,
Computerised tomogram head abnormal,
Confusional state,
Culture negative,
Diplopia,
Disturbance in attention,
Haematology test normal,
Headache,
Injection site pain,
Loss of personal independence in daily activities,
Lumbar puncture,
Mental status changes,
Musculoskeletal stiffness,
Nausea,
Noninfective encephalitis,
Nuclear magnetic resonance imaging,
Pain,
Pain in extremity,
Polymerase chain reaction,
Scan with contrast,
Serology negative,
Speech disorder,
Subdural effusion,
VIth nerve paralysis,
Venogram,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Ischaemic central nervous system vascular conditions (narrow), Dementia (broad), Embolic and thrombotic events, venous (narrow), Dystonia (broad), Parkinson-like events (broad), Thrombophlebitis (broad), Psychosis and psychotic disorders (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (narrow), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Extravasation events (injections, infusions and implants) (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad), Vestibular disorders (broad), Ocular motility disorders (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 7 days
Extended hospital stay? No Previous Vaccinations: Other Medications: COLESTID; B complex vitamins, Vitamin D, Vitamin C Current Illness: None Preexisting Conditions: Familial hyperlipidemia Allergies: Pravastatin (felt ill) Diagnostic Lab Data: CT studies of the brain with and without contrast 12/25, 12/27, 12/28 and 12/29. MRI studies with and without contrast 12/25,12/29, 12/30 and 1/18. MRI venogram 12/26. Lumbar puncture 12/27. Multiple studies including cultures, PCR and antibody studies for wide variety of infectious agents (all negative), hypercoagulability studies, CSF ACE determination (normal), multiple hematologic, serum studies, all unremarkable. No etiologic agent for these events found except for proceeding immunization. No prior history of thromboembolic episodes for this patient or his family. CDC Split Type:
Write-up: 12/7/2017 received immunization. 12/10/2017 noted right arm immunization site extremely sore and developed severe headache, nausea, vomiting, stiff neck, pain radiating down into right shoulder and arm especially with head movement. 12/13/2017 developed diplopia with worsening of all symptoms. Around 12/23 experiencing global weakness, mental status changes, confusion, difficulties of concentration, speech and balance. Completely incapacitated by 12/25 when he presented to the emergency department. CT of brain completed with evidence of acute right cortical vein thrombosis. Transferred emergently to another Hospital. He underwent intensive workup confirming right posterior, parietal and frontal cortical vein thrombosis with associated subarachnoid and subdural inflammation with effusions. Left complete sixth cranial nerve palsy. Evidence of right cervical neuralgia. Hospitalized 12/25-12/31/2017. Symptoms slowly improving except for a sixth nerve palsy which is unchanged. |
|
| VAERS ID: |
736004 (history) |
| Form: |
Version 2.0 |
| Age: |
44.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2017-11-20 |
| Onset: | 2017-11-20 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-02-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
195223 / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Pain,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: mulit-vitamin Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: None as of yet as I would have to pay out of pocket for any tests. CDC Split Type:
Write-up: Severe to moderate pain in left arm depending on movement. |
|
| VAERS ID: |
736562 (history) |
| Form: |
Version 1.0 |
| Age: |
4.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-01-22 |
| Onset: | 2018-01-23 |
| Days after vaccination: | 1 |
| Submitted: |
2018-02-02 |
| Days after onset: | 10 |
| Entered: |
2018-02-07 |
| Days after submission: | 5 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT5954JA / 4 |
LA / UN |
Administered by: Private Purchased by: Public Symptoms: Asthma,
Condition aggravated,
Injection site erythema,
Injection site pain,
Injection site swelling,
Pyrexia,
Respiratory symptom SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Swelling of leg~Influenza (Seasonal) (no brand name)~1~0.00~Patient Other Medications: FLOVENT; PROAIR inhalers Current Illness: Developed cough and fever that night Preexisting Conditions: Had similar reaction to flu vaccine in 2017 Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Swelling of entire upper arm, with redness, tenderness and fever. Started evening of vaccine administration. Seen in office 2 days later, difficult to tell whether cellulitis or severe local reaction. Then developed respiratory symptoms triggering his asthma. |
|
| VAERS ID: |
739320 (history) |
| Form: |
Version 2.0 |
| Age: |
1.25 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-02-02 |
| Onset: | 2018-02-02 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-03-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPVHIB: DTAP + IPV + HIB (PENTACEL) / SANOFI PASTEUR |
C5230AA / 4 |
- / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT5949KA / 2 |
- / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
S58703 / 4 |
- / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect product formulation administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/A Current Illness: None Preexisting Conditions: None Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type:
Write-up: The PENTACEL was incorrectly mixed prior to administration. Two vials of diluent were combined and administered. The vial with the powder Hib was not used. |
|
| VAERS ID: |
772111 (history) |
| Form: |
Version 2.0 |
| Age: |
48.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-09-13 |
| Onset: | 2018-09-14 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-09-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
UN / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Back pain,
Muscle spasms SMQs:, Retroperitoneal fibrosis (broad), Dystonia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type:
Write-up: Back Spasms, Locked up in lower back where it was very painful to move. |
|
| VAERS ID: |
774681 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-09-28 |
| Onset: | 2018-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-09-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT6310MA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Blindness,
Cardiac monitoring,
Dizziness,
Dyspnoea,
Feeling hot,
Pain,
Pharyngeal oedema SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Oropharyngeal allergic conditions (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Glaucoma (broad), Optic nerve disorders (broad), Cardiomyopathy (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: XOPENEX; ADVAIR; hydroxyzine; ZYRTEC; clonidine; escitalopram Current Illness: Fever 7 days prior to immunization Preexisting Conditions: Allergies; Asthma; Anxiety Allergies: Shellfish; sulfa; CECLOR; erythromycin Diagnostic Lab Data: Blood pressure; Cardiac monitor; Oxygenation levels were taken CDC Split Type:
Write-up: Approximately a few minutes after immunization, patient started feeling really hot, dizziness, prickly pain from head to toe, then things went black (she could not see anything but remained conscious) and had trouble breathing due to throat swelling. EPI-PEN was administered and EMT arrived and advised patient to go to Emergency room for further care and observation. Patient was given prednisone in emergency room and was observed. Patient was discharged with additional doses of prednisone for the next few days. Provider treating patient in ER. |
|
| VAERS ID: |
775453 (history) |
| Form: |
Version 2.0 |
| Age: |
29.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-02 |
| Onset: | 2018-10-02 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9455T / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Abdominal discomfort,
Blood glucose increased,
Dizziness,
Posture abnormal,
Visual impairment SMQs:, Hyperglycaemia/new onset diabetes mellitus (narrow), Anticholinergic syndrome (broad), Dystonia (broad), Gastrointestinal perforation, ulcer, haemorrhage, obstruction non-specific findings/procedures (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Glaucoma (broad), Optic nerve disorders (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: Unknown Preexisting Conditions: Unknown Allergies: Unknown Diagnostic Lab Data: Transported to Medical Center ED. Test and results are unknown to this reporter. CDC Split Type:
Write-up: On 10/2/18 at approximately 1:30 PM, I administered a flu vaccine per protocol to patient at employee/spouse clinic. Since it was her first flu vaccine, I asked her to stay for a 15 minute observation in the event of any untoward reaction to the vaccine. After 10 minutes elapsed, patient complained of dizziness, lightheadedness and visual disturbances. She was fully oriented, heart rate was palpable and approximately 70, she answered questions appropriately and was not experiencing difficulty breathing. Her eyes closed and she had difficulty sitting up and supporting her head. 911 was called for assistance. I moved her to a supine position which helped somewhat, but she still complained of the above symptoms although they were less severe. In addition, she started complaining of lower abdominal discomfort. Vital signs before EMTs arrived were 86/54, 78 and 20. After EMTs arrived, her vital signs continued to be on the low side. Blood glucose was 129. The decision was made to transport her to the ER for further evaluation. Her husband had been called and arrived to accompany her in the ambulance which departed at approximately 2PM. |
|
| VAERS ID: |
777134 (history) |
| Form: |
Version 2.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-08 |
| Onset: | 2018-10-08 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
2544611A / N/A |
LA / IM |
| VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS |
ZN22Z / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site cellulitis,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: fluoxetine; ibuprofen; lisinopril; SPIRIVA; SYMBICORT; VENTOLIN Current Illness: Preexisting Conditions: Pulmonary emphysema; Sciatica; Tobacco user; Chronic CHF; Depression; Benign hypertension Allergies: codeine; iodine; penicillins Diagnostic Lab Data: CDC Split Type:
Write-up: Fever of 99.9 on 10/10, cellulitis of upper arm around injection site - advised BENADRYL PRN and given prescription for antibiotic. |
|
| VAERS ID: |
778871 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-16 |
| Onset: | 2018-10-16 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UJ030AA / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Immediate post-injection reaction,
Injection site bruising,
Injection site swelling,
Myalgia,
Neck pain,
Pain in extremity SMQs:, Rhabdomyolysis/myopathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Instant black and blue bruise and swelling at injection site that increased in size over 10 min. Pain and soreness radiating up arm throughout shoulder and neck within minutes as well as pain radiating down left leg, described as "muscle soreness and aches". I asked patient to wait in the store for about 40 min following vaccine, checking up every 10 min. Called her primary care physician that she was supposed to see that day for a flu shot but decided to come to pharmacy instead. Spoke w nurse/MD who advised me that patient was ok to go home and should just be aware if symptoms don''t subside. Counseled patient that she should see her MD if the pain/aches did not get better or got worse throughout the night. Checked up on patient at home 1.5 hours after vaccine and she seemed to be feeling okay, leg was still achy but arm and neck getting better. Advised her to ice arm to decrease swelling. |
|
| VAERS ID: |
779457 (history) |
| Form: |
Version 2.0 |
| Age: |
74.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-10-15 |
| Onset: | 2018-10-17 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Nasopharyngitis,
Oropharyngeal pain SMQs:, Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: metformin; multivitamin Current Illness: None Preexisting Conditions: Sleep Apnea; Type two Diabetes; Mild case - CT lymphoma Allergies: None that i know of. Diagnostic Lab Data: None CDC Split Type:
Write-up: I can''t provide the detail on the vaccine (above) administered except it was the one for seniors. Patient 74 year old Male. After my normal visit with my Primary Care Doctor. On Monday morning October 15th? I had both blood work done and this years Senior -Inactivated Influenza Vaccine administered by nurse. Within two days I have now come down with both a sore throat which has morphed into a full blown cold (my assumption) with associated symptoms. I am reporting this because of the paper work given to be by my provider (VACCINE INFORMATION STATEMENT) regarding the shot administered. I fully understand it may have nothing to do with the vaccine but thought I would report it to you. Thank you, Sent to both Doctor and to (VAERS). |
|
| VAERS ID: |
779604 (history) |
| Form: |
Version 2.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-11 |
| Onset: | 2018-10-11 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Contusion,
Fatigue,
Pain in extremity,
Rash,
Skin discolouration,
Throat irritation SMQs:, Anaphylactic reaction (broad), Haemorrhage terms (excl laboratory terms) (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Accidents and injuries (narrow), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: CALCIUM 250MG Current Illness: NONE Preexisting Conditions: NONE Allergies: ALLERGIES TO DUST/RAGWEED/CAT Diagnostic Lab Data: CDC Split Type:
Write-up: MY REACTIONS WERE SORE LT ARM WITHIN 2 HOURS BLACK AND BLUE THAT EVENING ALONG WITH RASH ON LT ARM TO ELBOW APPEARING AROUND 10PM. I HAD SCRATCHY THROAT AND FATIGUE. RASH LASTED UNTIL 10/16 EVENING. BRUISE STILL APPARENT (10/18) 2INCHES IN DIAMETER. |
|
| VAERS ID: |
781634 (history) |
| Form: |
Version 2.0 |
| Age: |
3.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-11 |
| Onset: | 2018-10-12 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-10-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ025AC / 5 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Rash papular SMQs:, Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: I do not remember what vaccine it was but she once had a reaction that almost looked like a chemical burn on her leg. Other Medications: Daily multi vitamin Current Illness: cold within the month of vaccination Preexisting Conditions: asthma Allergies: none Diagnostic Lab Data: none CDC Split Type:
Write-up: Pt got a rash on her arm. It was bumpy and red at times. It seemed to flare up when she got hot. Eventually, it spread to her chest and back as well. It was treated with benedryl cream and tablets at first, and later with zyrtec and an ointment that the doctor prescribed. It is finally clearing up and nearly gone. |
|
| VAERS ID: |
783046 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
UN / SC |
Administered by: Unknown Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2018SA284662
Write-up: Initial information received on 10-Oct-2018 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves patient who experienced administered the vaccine to a patient SQ instead of IM, while he/she received vaccine FLUZONE QUADRIVALENT. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE lot number not reported via subcutaneous route. It was a case of actual medication error due to vaccine administered at inappropriate site. The patient outcome is reported as Not Applicable for administered the vaccine to a patient SQ instead of IM. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
784616 (history) |
| Form: |
Version 2.0 |
| Age: |
12.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-01 |
| Onset: | 2018-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ041AB / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Pruritus,
Rhinorrhoea,
Throat irritation SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Secundum ASD defect - repaired 6-2011 Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: C/O itchy hands/feet/neck at 3 mins after vaccine given - VS remained stable throughout 45 mins of observation - Did have throat clearing and runny nose at 1610 -given BENADRYL at 1605 = symptoms resolved by 1640 |
|
| VAERS ID: |
785703 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-09 |
| Onset: | 2018-11-10 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: SYNTHROID, lisinopril, hydrochlorothiazide Current Illness: none Preexisting Conditions: COPD Allergies: none Diagnostic Lab Data: none CDC Split Type:
Write-up: Patient requested pneumonia vaccine, but without verifying the paperwork she filled I gave her FLUARIX vaccine. |
|
| VAERS ID: |
786446 (history) |
| Form: |
Version 2.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-09 |
| Onset: | 2018-10-09 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
252671 / 1 |
RA / IM |
Administered by: School Purchased by: ? Symptoms: Injection site pain,
Pain in extremity SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: Uknown Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Pain during administration. Over the next week post-vaccination the pain continued to increase into shoulder. The following week, the patient experienced a great deal of pain in right shoulder and arm making it difficult to do certain tasks. She has been seen by urgent care who prescribed prednisolone. She followed up with her PCP and now has a future appointment with orthopedics for continued pain. |
|
| VAERS ID: |
786722 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-03 |
| Onset: | 2018-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
- / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site pain,
Mobility decreased,
Sleep disorder SMQs:, Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Red rash at injection site 2016 Other Medications: ZOLOFT; SYNTHROID; calcium; bio-flex; fish oil; CBD oil Current Illness: None Preexisting Conditions: Hypothyroidism; Dysthymia Allergies: sulfa by hx Diagnostic Lab Data: None CDC Split Type:
Write-up: Severe pain in upper left arm. (On scale 1-20, it was a 20), lasting 48 hours. Extremely painful to the point of almost going to the emergency room at local hospital. After first 48 hours pain remained, however ranges from 0 to 10. During the initial 24 hours, it required immobilizing my arm. Ibuprofen was ineffective. In addition, following the first 24 hours, I was not able to raise my arm beyond shoulder height for the next 48 hours. Pain continues to be present intermittently, daytime or while sleeping it reaches a level to awaken me. Treatment includes Ibuprofen and topical application of CBD. Sought mendial attention from PCP, OD. |
|
| VAERS ID: |
786980 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-16 |
| Onset: | 2018-11-16 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
YF39908 / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Anxiety,
Dysphonia,
Rash,
Rash erythematous,
Throat irritation SMQs:, Anaphylactic reaction (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: B-12, Ferrous sulfate, Vit C, Vit D, Multi vit, Asprin, ESTRACE cream, Melatonin, Gabapentin, Mg, atorvastatin, Glipizide ER, JANUVIA Current Illness: unknown Preexisting Conditions: Diabetes II, hyperlipidemia, Hx of CVA, Vit D deficiency, B-12 deficiency, hypomagnesemia Allergies: FLAGYL, IV iron infusion, nortriptyline, sulfa, metformin Diagnostic Lab Data: None CDC Split Type:
Write-up: Six hours after vaccine she had rapid onset hoarseness, scratchy throat, erythematous rash on chest, and anxiety. |
|
| VAERS ID: |
787279 (history) |
| Form: |
Version 2.0 |
| Age: |
7.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-19 |
| Onset: | 2018-11-19 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
B4J3H / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Extra dose administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Sodium Fluoride Current Illness: None Preexisting Conditions: None Allergies: NKDA Diagnostic Lab Data: None CDC Split Type:
Write-up: Patient was already vaccinated for Influenza on 9/26/18, second one was given in error. Patient had no adverse reaction to first or second vaccine. |
|
| VAERS ID: |
787498 (history) |
| Form: |
Version 2.0 |
| Age: |
54.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-11-21 |
| Onset: | 2018-11-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
YF44409 / 1 |
- / - |
Administered by: Pharmacy Purchased by: ? Symptoms: Immediate post-injection reaction,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: none Preexisting Conditions: Post kidney transplant Allergies: none Diagnostic Lab Data: none as of filing report. CDC Split Type:
Write-up: Upon administration of the vaccine, pt developed significant localized swelling at administration site. Approximately the size of a marble. Pt reported no other side effects. |
|
| VAERS ID: |
787524 (history) |
| Form: |
Version 2.0 |
| Age: |
32.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-09 |
| Onset: | 2018-10-09 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
252671 / 1 |
AR / IM |
Administered by: School Purchased by: ? Symptoms: Joint range of motion decreased,
Pain in extremity,
X-ray SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: Unknown Allergies: N/A Diagnostic Lab Data: X-ray CDC Split Type:
Write-up: In patient''s words "My arm started hurting after the shot, but the pain continued to get much worse and then the pain plateaued at about 1.5 weeks. My range of motion has been extremely limited the last 6 weeks and it has been difficult to perform even the most simple task. I have received care from my primary care physician, x-rays, orthopedic, and am scheduled for physical therapy and a future MRI." |
|
| VAERS ID: |
788908 (history) |
| Form: |
Version 2.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-10-18 |
| Onset: | 2018-10-21 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-11-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
250793 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Rash generalised SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Multivitamin; B12; Ferrous sulfate Current Illness: None Preexisting Conditions: COPD Allergies: Penicillin; codeine; peanuts Diagnostic Lab Data: CDC Split Type:
Write-up: Rash on arms, legs, back and stomach beginning 3 days after vaccination. Patient received 2 rounds of MEDROL dose-pak, but after completion both times the rash returned. |
|
| VAERS ID: |
789195 (history) |
| Form: |
Version 2.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-03 |
| Onset: | 2018-11-05 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
2XF7E / 1 |
LA / IM |
Administered by: Military Purchased by: ? Symptoms: Rosacea SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: CLARITIN D Current Illness: N/A Preexisting Conditions: N/A Allergies: Possible egg allergy- has to be denatured Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Patient fount out two days later that she had a rosacea all over her body. No other symptoms reported. |
|
| VAERS ID: |
789595 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-11-26 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-12-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UJ043AB / UNK |
RA / IM |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2018SA328851
Write-up: Initial information received on 28-Nov-2018 regarding an unsolicited valid non-serious case received from a nurse. This case involves a 70 years old male patient who was vaccinated with a 0.5 ml dose of FLUZONE HIGH DOSE (Batch number: UJ043AB, expiration date: 22-May-2019, route: intramuscular and site of administration was right deltoid) on 26-Nov-2018. The patients medical history and concomitant medications were not reported. It was an actual medication error due to incorrect product storage. Nurse states that she accidentally gave a FLUZONE HIGH DOSE injection to a patient after a temperature excursion/no AE. No adverse event reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holders compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. List of documents held by sender: none. |
|
| VAERS ID: |
792132 (history) |
| Form: |
Version 2.0 |
| Age: |
14.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-12-14 |
| Onset: | 2018-12-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-12-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ087AB / 4 |
LA / IM |
| HPV9: HPV (GARDASIL 9) / MERCK & CO. INC. |
R017457 / 2 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Blood pressure decreased,
Dizziness,
Headache,
Pain,
Pallor,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Dizzy after HPV #1 7-12-17 - HPV 9 by Merck Co - 12 yr old Other Medications: None Current Illness: Preexisting Conditions: Allergies: amoxicillin Diagnostic Lab Data: CDC Split Type:
Write-up: Pt pale - dizzy - faint - at 5 mins after vaccine received - started to vomit several mins after that - severe vomiting and HA x 10 mins - decreased BP also - recovered after 30 mins after vaccine given - H/A and soreness persisted into next day. HA = headache. |
|
| VAERS ID: |
792161 (history) |
| Form: |
Version 2.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-12-14 |
| Onset: | 2018-12-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-12-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9455T / N/A |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
R007722 / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site erythema,
Injection site urticaria,
Pain in extremity,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Extravasation events (injections, infusions and implants) (broad), Hypersensitivity (narrow), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: PROVENTIL HFA, LEVORA, WELLBUTRIN XL, Methylphenidate Current Illness: common cold, no fever Preexisting Conditions: Asthma, Dysmenorrhea, ADHD, Depressive D/O Allergies: Prednisone Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Red area developed around injection site in the right arm several hours after receiving the PCV23 vaccine and became the size of a half dollar per patient''s mother. Hives also developed in upper right arm after several hours and gradually spread to the lower arm. Right arm described as very sore. Patient denied fever, denied shortness of breath, and denied throat swelling/closing. The vaccines were given on 12/14/2018 and adverse reaction was reported to us by the patient''s mother on 12/17/2018. Patient''s PCP, NP was informed immediately. NP recommended cold compresses, ibuprofen as needed for discomfort, and to follow-up with an office visit if redness persists/worsens or if pt. develops a fever. Explained that the symptoms would improve slowly. NP also informed staff to do VAERS report. |
|
| VAERS ID: |
793416 (history) |
| Form: |
Version 2.0 |
| Age: |
36.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-11-19 |
| Onset: | 2018-11-20 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2018-12-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
U6263CA / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Blood test normal,
Injected limb mobility decreased,
Injection site pain,
Rotator cuff syndrome,
X-ray normal SMQs:, Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Budesonide Nasal rinse bid, sprinolactone 100mg qhs, tartazone cream Qhs, Combivent QD, Albuterol PRN, Bupinrophine 2mg QD. Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: They did an xray and some bloodwork nothing else yet CDC Split Type:
Write-up: When Vacine was administered, I remember thinking it was given too high in the arm, and the administrator stated it was VERY hard to push in. About 17 hours after receiving shot I awoke to significant pain in the left shoulder, where I received the shot. Over the next day or so the pain continued but also seemed to worsen whenever I tried to use that arm-as in reaching across, over my head or behind me. After about a week and a half I went to the doctors- he told me just to watch it and take Aleve instead of ibuprofen. After another several days I called back as pain is not lessening-he recommended I go to muscle- skeletal doctor-as well as have x-ray and blood work done (both showed nothing). I was seen at ortho about 3 weeks to a month after administration of shot. That doctor said it was a probable rotator-cuff injury and to even double or triple my aleve intake as well as start PT. (First appointment with PT tomorrow 12/27/18.) In the mean time I followed up with my PCP. (The first doctor I saw was at my PCP''s office but not her.) My regular PCP- prescribed an oral steroid as my pain had not improved or lessened taking aleve or Ibuprofen. My understanding is PT and steroids and if the pain continues then we will do an MRI of the soft tissue. I have been unable to effectively use my left arm related to pain for over one month currently. |
|
| VAERS ID: |
793858 (history) |
| Form: |
Version 1.0 |
| Age: |
2.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2018-12-24 |
| Onset: | 2018-12-27 |
| Days after vaccination: | 3 |
| Submitted: |
2018-12-28 |
| Days after onset: | 1 |
| Entered: |
2018-12-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAP: DTAP (INFANRIX) / GLAXOSMITHKLINE BIOLOGICALS |
T79X3 / 4 |
RL / IM |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
TM925 / 2 |
LL / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
3KT7B / 2 |
LL / IM |
Administered by: Private Purchased by: Public Symptoms: Injection site rash SMQs:, Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Sodium Fluride Current Illness: None Preexisting Conditions: None Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: (R) thigh, half dollar size rash. No fever, no behavior changes. 12/27/18. |
|
| VAERS ID: |
794728 (history) |
| Form: |
Version 2.0 |
| Age: |
66.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2018-08-29 |
| Onset: | 2018-09-15 |
| Days after vaccination: | 17 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-01-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UI997AB / 1 |
LA / IM |
| VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS |
524S7 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Neuralgic amyotrophy,
Radiculitis brachial SMQs:, Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: HYPERTENSION Allergies: PENICILLIN Diagnostic Lab Data: CDC Split Type:
Write-up: BRACHIAL NEURITIS, PARSONAGE-TURNER SYNDROME. |
|
| VAERS ID: |
799166 (history) |
| Form: |
Version 2.0 |
| Age: |
76.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-01-24 |
| Onset: | 2019-01-26 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-01-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UJ052AB / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Chills,
Hyperhidrosis,
Pain SMQs:, Neuroleptic malignant syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: Essential hypertension Allergies: Sulfa drugs, sertraline, voltaren, amiloride, hydroxychloroquin. Diagnostic Lab Data: None presently CDC Split Type:
Write-up: 2 days after vaccination patient experiencing chills and sweats without fever, diffuse pain. No trouble at injection site, no respiratory symptoms. Reported to pharmacy today; directed patient to reach out to primary care doctor, waiting to hear back from them. |
|
| VAERS ID: |
810773 (history) |
| Form: |
Version 2.0 |
| Age: |
59.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-03-23 |
| Onset: | 2019-03-24 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-04-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
YF37606 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: GLUCERNA, VITAMIN B, MULTIVITAMIN Current Illness: NONE Preexisting Conditions: DIABETES Allergies: CODIENE, SEA FOOD Diagnostic Lab Data: N/A CDC Split Type:
Write-up: PATIENT REPORTS THAT HIS ARM STILL HURTS (REPORTED TO PHARMACIST ON 4/19/19) AFTER GETTING THE FLU SHOT. PATIENT RECEIVED THE FLU SHOT ON 03/23/2019 |
|
| VAERS ID: |
835754 (history) |
| Form: |
Version 2.0 |
| Age: |
81.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-09-18 |
| Onset: | 2019-09-18 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-09-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA3: INFLUENZA (SEASONAL) (FLUAD) / NOVARTIS VACCINES AND DIAGNOSTICS |
260388 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site bruising,
Injection site pain,
Injection site warmth SMQs:, Haemorrhage terms (excl laboratory terms) (narrow), Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: carvedilol, lisinopril (due to stent) Current Illness: Has stent Preexisting Conditions: stent Allergies: no known allergies Diagnostic Lab Data: none CDC Split Type:
Write-up: No pain or abnormalities upon administration. Pharmacist covered with bandage. The next day the patient noticed a bruse underneath the bandage. It was a little achy and slightly warm. It didn''t bother her otherwise had no pain or sensation. Kept moving her arm. Has no pain/sensation like a normal bruise. Bowling didn''t irritate it. Just has a visual bruise and it feels a little bit warm. Patient has tried icing but it didn''t change the size. It is however turning yellow (healing) and starting to get slightly smaller. As long as it continues to get smaller, no further medical action is necessary. If patient develops a fever, or experiences pain/tenderness advised her to be checked out. |
|
| VAERS ID: |
839525 (history) |
| Form: |
Version 1.0 |
| Age: |
61.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-10-02 |
| Onset: | 2019-10-03 |
| Days after vaccination: | 1 |
| Submitted: |
2019-10-07 |
| Days after onset: | 4 |
| Entered: |
2019-10-09 |
| Days after submission: | 2 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
2DB5X / UNK |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
R002354 / UNK |
LA / IM |
Administered by: Public Purchased by: Public Symptoms: Fatigue,
Full blood count,
Injection site erythema,
Malaise,
Pain in extremity,
White blood cell count increased SMQs:, Neuroleptic malignant syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: 0 Preexisting Conditions: Aspirin - allergy, Allergies: Diagnostic Lab Data: CBC on 10/3/19: WBC 17.0, CDC Split Type:
Write-up: Pt returned the day after immunizations with feelings of fatigue + malaise, soreness in L arm. Labs drawn. Pt returned the following day to review lab results, L arm with clear demarcated erythema along L deltoid, no significant swelling or heat. Pt afebrile the whole duration. |
|
| VAERS ID: |
839950 (history) |
| Form: |
Version 2.0 |
| Age: |
76.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-10-09 |
| Onset: | 2019-10-10 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
QFAA1919 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Rash,
Skin irritation SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Tamsulosin 0.4mg daily Current Illness: None Preexisting Conditions: Allergies: Hydrocodone Diagnostic Lab Data: CDC Split Type:
Write-up: A day after the patient received the vaccine, they noticed irritation and a light rash not localized to the injection site. Patient consulted their doctor who suggested the events could be related to the immunization. |
|
| VAERS ID: |
840828 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Influenza like illness SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2019438279
Write-up: Experienced flu like symptoms for 2 days from receiving Prevnar 13 and flu together; This is a spontaneous report from a contactable Pharmacist, via a sales representative, who reported similar events for three patients. This is the first of three reports. This Pharmacist reported for a patient that: A patient of unspecified age and gender received pneumococcal 13-val conj vac (dipht crm197 protein) (PREVNAR 13), at single dose and influenza vaccine (FLU) both via an unspecified route of administration on the same unspecified date for immunisation. The patient medical history and concomitant medications were not reported. The patient experienced flu like symptoms for 2 days on an unspecified date with outcome of recovered. No follow-up attempts are possible. No further information is expected, information about batch number cannot be obtained.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2019438282 same reporter, same product, same event, and different patient;US-PFIZER INC-2019438281 same reporter, same product, same event, and different patient |
|
| VAERS ID: |
840829 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Influenza like illness SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2019438281
Write-up: flu like symptoms; This is a spontaneous report from a contactable pharmacist received via a Pfizer sales representative. This pharmacist reported similar events for three patients. This is the second of three reports. A patient of unspecified age and gender received pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) (PREVNAR 13, lot number and expiry date unknown) and influenza vaccine (FLU), both via an unspecified route of administration on an unspecified date at a single dose for immunization. The patient''s medical history and concomitant medications were not reported. The pharmacist reported that the patient experienced side effects from receiving pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) and flu together on an unspecified date. The patient experienced flu like symptoms for 2 days. The outcome of the event was unknown. No follow up attempts are possible, information on the lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2019438279 same reporter, same product, same event, and different patient;US-PFIZER INC-2019438282 same reporter, same product, same event, and different patient |
|
| VAERS ID: |
840830 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
- / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Influenza like illness SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USPFIZER INC2019438282
Write-up: flu like symptoms; This is a spontaneous report from a contactable pharmacist received via a Pfizer sales representative. This pharmacist reported similar events for three patients. This is the third of three reports. A patient of unspecified age and gender received pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) (PREVNAR 13, lot number and expiry date unknown), and influenza vaccine (FLU), both via an unspecified route of administration on an unspecified date at a single dose for immunization. The patient''s medical history and concomitant medications were not reported. The pharmacist reported that the patient experienced side effects from receiving pneumococcal 13-valent conjugated vaccine (diphtheria crm197 protein) and flu together on an unspecified date. The patient experienced flu like symptoms for 2 days. The outcome of the event was unknown. No follow up attempts are possible, information on the lot/batch number cannot be obtained. No further information is expected.; Sender''s Comments: Linked Report(s) : US-PFIZER INC-2019438281 same reporter, same product, same event, and different patient;US-PFIZER INC-2019438279 same reporter, same product, same event, and different patient |
|
| VAERS ID: |
841068 (history) |
| Form: |
Version 2.0 |
| Age: |
24.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Expired product administered,
Exposure during pregnancy,
No adverse event SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2019SA278118
Write-up: expired dose of Fluzone was given to a 24 year old pregnant patient, no AE; expired dose of Fluzone was given to a 24 year old pregnant patient, no AE; Initial information received on 04-Oct-2019 regarding an unsolicited valid non-serious case received from a nurse. This case involves a 24 years old female patient who received expired dose of vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] (lot number not reported, that expired in June) via unknown route in unknown administration site on an unknown date, while she was pregnant. Data regarding this pregnancy were received prospectively, i.e. before pregnancy outcome was known. The vaccination occurred at unknown gestation period. The date of last menstrual period was not reported. The estimated due date was not reported. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. It was an actual medication error case due to expired vaccine used. It was also a case of vaccine exposure during pregnancy. At the time of report, no adverse event was reported. Additionally, at time of reporting, the outcome of the pregnancy was unknown. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. Information on the batch number was requested. List of documents held by sender: none. |
|
| VAERS ID: |
841069 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT6261JA / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Expired product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2019SA278130
Write-up: expired Fluzone Quadrivalent was inadvertently administered to a patient/no AE; Initial information received on 04-Oct-2019 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a patient who received an expired dos of vaccine INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT]. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B VACCINE lot UT6261JA (Expiration Date: 30-Jun-2019). It was of actual medication error case due to expired vaccine used It was unknown whether adverse event was noticed or not. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
842438 (history) |
| Form: |
Version 1.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-10-03 |
| Onset: | 2019-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
2019-10-07 |
| Days after onset: | 4 |
| Entered: |
2019-10-21 |
| Days after submission: | 14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
2DB5X / UNK |
RA / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
BE554 / 1 |
RA / IM |
| HPV4: HPV (GARDASIL) / MERCK & CO. INC. |
1614897 / 2 |
LA / IM |
Administered by: Private Purchased by: Public Symptoms: Presyncope SMQs:, Anticholinergic syndrome (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: 0 Preexisting Conditions: 0 Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: vasovagal reaction to HPV vaccine (#2) |
|
| VAERS ID: |
843834 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
- / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Extra dose administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2019SA292196
Write-up: a consumer received 2 Fluzone High Dose vaccines in one day/No AE; Initial information received on 18-Oct-2019 regarding an unsolicited valid non-serious case received from other health professional. This case involves patient of an unknown demographics who received two doses of vaccine INFLUENZA USP TRIVAL A-B HIGH DOSE SUBVIRION VACCINE [FLUZONE HIGH DOSE] lot number not reported via unknown route in unknown administration site on an unknown date. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. It was a case of actual medication error due to extra dose administered. It was given in a nursing home. Pharmacist do have a note saying that some guy was given two doses of Fluzone High-Dose vaccine in the same day. At the time of report no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. Information on the batch number was requested. |
|
| VAERS ID: |
844694 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-10-28 |
| Onset: | 2019-10-29 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-10-31 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
261199 / 1 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
S025133 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Erythema,
Fluid retention,
Headache,
Pain in extremity,
Peripheral swelling,
Pyrexia SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Omeprazole DR 20mg daily Breo Ellipta 200-25 1 puff daily Montelukast 10mg daily Current Illness: N/A Preexisting Conditions: Heartburn, Athsma Allergies: Bactrim, Celexa, Citalopram Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced extreme redness and swelling to outer and inner arm. Inner arm had a sack-like fluid buildup, possibly in lymph system, but was mostly reduced by the time they reported it to this Rph. Very painful, red, sore, came with excessive fever and headache. Patient will be reporting to MD''s office in case cellulitis is suspected and/or antibiotics recommended. Patient experienced this within 12 hours after administration of vaccine by the following morning. |
|
| VAERS ID: |
845758 (history) |
| Form: |
Version 2.0 |
| Age: |
40.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-11-01 |
| Onset: | 2019-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
3FS25 / 1 |
LA / IM |
Administered by: Work Purchased by: ? Symptoms: Dizziness,
Feeling abnormal,
Vision blurred SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Glaucoma (broad), Lens disorders (broad), Retinal disorders (broad), Vestibular disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: Vertigo - 2 years Allergies: unknown Diagnostic Lab Data: n/a CDC Split Type:
Write-up: Patient had never had a flu shot before, was not allergic to eggs, was feeling well today and had never had Gillian-Barre Syndrome. He received his shot and sat with my for 15 min. Reported feeling fine and left. Following the above incident, he returned to the room stating ?I think I?m having a reaction, I feel like I?m tripping on acid, I feel off, my vision is blurry and I feel dizzy?. I cleared the room, one employee choose not to leave, patient said it was fine. Employee who did not leave reported that he was a first responder and wanted to stay in case I needed anything. BP was 132/82, pulse was regular. Pupils were equal, round and reactive. Lung and heart sounds WNL. No other symptoms. Patient sat with me for a bit, then said he was going back to his office. I requested that he let someone nearby know how he is feeling and let them check in on him, he said he would. He returned to the room during the clinic and said he was a bit better. Following the completion of the clinic, I checked in with him. Reported still having difficulty with his vision and felt off, but was OK, ?I do have an issue with vertigo, cutting caffeine out has helped. I still feel like I?m looking through things and not at them? Reported being in treatment for 2 years for this issue, unable to find a cause. I requested that he notify his PCP today and report the reaction, as well as not driving himself if he continued to have difficulty seeing. Also recommended future vaccinations be administered at his medical home for observation following. |
|
| VAERS ID: |
846521 (history) |
| Form: |
Version 2.0 |
| Age: |
77.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-10-07 |
| Onset: | 2019-10-07 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-11-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
UJ245AA / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Joint range of motion decreased,
Pain in extremity SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: n/a CDC Split Type:
Write-up: For a month the patient has experienced limited range of motion in her left arm, along with soreness. She has tried icing and stretching with little results. Patient says the pain has decreased by about 50% since the shot but still has limited motions in activities such as yoga. Patient is following up with her primary car physician. |
|
| VAERS ID: |
847494 (history) |
| Form: |
Version 2.0 |
| Age: |
50.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-11-12 |
| Onset: | 2019-11-12 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-11-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7AR35 / 1 |
RA / IM |
Administered by: Work Purchased by: ? Symptoms: Dizziness,
Ear discomfort,
Injection site pruritus,
Paranasal sinus discomfort,
Pruritus,
Respiratory tract congestion SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: unknown Current Illness: unknown Preexisting Conditions: unknown Allergies: unknown Diagnostic Lab Data: unknown CDC Split Type:
Write-up: experienced: some localized itching at the site of the injection, but no hives, followed by more generalized itching (still no hives). Then I started to feel really congested and could feel quickly worsening sinus pressure, which put pressure in my ears, thus making me feel a little dizzy. But that was where things maxed out and it got better from there. I took a Zyrtec and Aleve and am mostly back to normal. Not sure if it was a reaction to the vaccine itself or something I was exposed to in the process. I do have some environmental allergies and sensitivities, so perhaps that was a factor. |
|
| VAERS ID: |
848262 (history) |
| Form: |
Version 1.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-11-13 |
| Onset: | 2019-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
2019-11-15 |
| Days after onset: | 2 |
| Entered: |
2019-11-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
QFAA1939 / 2 |
LA / IM |
| PPV: PNEUMO (PNEUMOVAX) / MERCK & CO. INC. |
R016640 / 2 |
LA / IM |
Administered by: Other Purchased by: Other Symptoms: Chills,
Hyperhidrosis,
Pain in extremity,
Skin warm SMQs:, Neuroleptic malignant syndrome (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? Yes
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: None Preexisting Conditions: Penicillin Allergy Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: 11/13 - Received vaccine, very sore arm 11/14 - Chills + sweats all day 11/15 - Reduces spread from delt down to elbow warm to touch; MD prescribed Keflex 250 mg QD x 5 days |
|
| VAERS ID: |
848967 (history) |
| Form: |
Version 2.0 |
| Age: |
58.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-09-26 |
| Onset: | 2019-10-17 |
| Days after vaccination: | 21 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
2DB5X / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Guillain-Barre syndrome,
Immunoglobulin therapy SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 10 days
Extended hospital stay? No Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: Parkinson''s disease, DM, CAD Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 3 weeks after flu vaccine admitted to the Medical Center Emergency Dept with symptoms consistent with Guillain Barre syndrome. Neurological consult felt consistent with GBS. Treated with 5 days IVIG, transfered to accute rehab on 11/5/19 |
|
| VAERS ID: |
850454 (history) |
| Form: |
Version 2.0 |
| Age: |
9.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-10-31 |
| Onset: | 2019-10-31 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-12-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ231AB / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Fall,
Head injury,
Headache,
Syncope,
Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Patient experienced a syncopal event about 5 minutes after influenza vaccination. She fell backwards and hit her head. C/o headache at the back of her head. Vomited about 10-15 minutes after the fall. |
|
| VAERS ID: |
854781 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2019-12-12 |
| Onset: | 2019-12-12 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2019-12-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE) / SANOFI PASTEUR |
49281-0405-65 / 1 |
LA / SYR |
Administered by: Pharmacy Purchased by: ? Symptoms: Chills,
Feeling cold,
Pyrexia,
Vomiting SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: L-Thyroxine Tab 125mg Sertraline Hcl Tab 25mg CBD Softgel 20mg Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type:
Write-up: Started with being chilled to the bone like I''ve never experience before, shivering wearing two undergarments, two sweaters plus a blanket and sitting in front of a gas-fired fireplace. First vomit occurred approximately 3:30 pm Second vomit occurred approximately 4:15 pm Fever 101.6 deg Called pharmacy for consultation and was advised to contact my immediate healthcare provider if my temperature rose above 101 deg. My temp rose to 101.7 and decided to wait and see if it got any higher, which it didn''t. I had a fever that lasted 36 hours, then I was fine again. |
|
| VAERS ID: |
857408 (history) |
| Form: |
Version 2.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-01-14 |
| Onset: | 2020-01-17 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-01-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
5RS7Z / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Erythema,
Swelling,
Vaccine positive rechallenge SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Flu vaccine- received in December 2018 Other Medications: Cyclobenzaprine, Flovent, Proair, Triamterene/HCTZ, Indomethacin, Colchicine Current Illness: None recorded Preexisting Conditions: Hypertension, Gout, Obstructive sleep apnea Allergies: Ace inhibitors, Atenolol, Codeine, Flonase, Percocet, Pneumonia vaccine Diagnostic Lab Data: CDC Split Type:
Write-up: Sx- redness, swelling . Was treated supportively w/ ice packs. Pt. had same reaction with last year''s Flu vaccine administration. |
|
| VAERS ID: |
857473 (history) |
| Form: |
Version 1.0 |
| Age: |
11.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-01-20 |
| Onset: | 0000-00-00 |
| Submitted: |
2020-01-21 |
| Entered: |
2020-01-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUN4: INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) / MEDIMMUNE VACCINES, INC. |
LJ2265 / 1 |
NS / IN |
Administered by: Private Purchased by: Public Symptoms: Expired product administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: anxiety autism spectrum disorder Allergies: Diagnostic Lab Data: None CDC Split Type:
Write-up: Administered expired vaccine. No adverse effects noted per parent. |
|
| VAERS ID: |
860888 (history) |
| Form: |
Version 2.0 |
| Age: |
5.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2020-02-05 |
| Onset: | 2020-02-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-02-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (KINRIX) / GLAXOSMITHKLINE BIOLOGICALS |
HB7L7 / UNK |
LL / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
5RS77 / UNK |
LL / IM |
| MMRV: MEASLES + MUMPS + RUBELLA + VARICELLA (PROQUAD) / MERCK & CO. INC. |
S022104 / UNK |
RA / SC |
Administered by: Private Purchased by: ? Symptoms: Hallucination,
Moaning,
Pyrexia,
Tremor,
Vertigo SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Parkinson-like events (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Flinstone Multivitamin Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: none symptoms resolved when mom reported. CDC Split Type:
Write-up: Mother reported patient had fever (unsure how high, no working Thermometer) with hallucinations (everything in room spinning, moving fast, flashing, hands shaking, moaning in sleep. The night following vaccinations |
|
| VAERS ID: |
863691 (history) |
| Form: |
Version 2.0 |
| Age: |
12.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2019-09-23 |
| Onset: | 2019-09-24 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-03-02 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
2277M / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Axillary pain,
Joint range of motion decreased,
Malaise,
Rash,
Respiratory tract congestion,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypersensitivity (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type:
Write-up: Day after the vaccine developed some pain in left axilla, left anterior shoulder, and left chest. No redness, warmth. Afebrile. Did have slight decrease in ROM. General malaise, congestion, developed emesis two days afterwards. Also had rash in left armpit. Pain resolved within 2 days and had no further issues. Unclear if vaccine related. |
|
| VAERS ID: |
881048 (history) |
| Form: |
Version 2.0 |
| Age: |
93.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-08-27 |
| Onset: | 2020-08-27 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-08-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ444AA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Asthenia,
Dizziness SMQs:, Anticholinergic syndrome (broad), Guillain-Barre syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Eliquis 2.5mg, Calcitriol 0.25mcg, Pravastatin, Losartan, Carvedilol Current Illness: NO Preexisting Conditions: Hypertension Allergies: NO Diagnostic Lab Data: CDC Split Type:
Write-up: Patient felt dizzy after maybe about 5-10minutes of receiving Fluzone HD, as pt was walking out of the store. He had to lay down on the floor as he was feeling weak.He was attended by an EMT, and was taken to hospital. |
|
| VAERS ID: |
882336 (history) |
| Form: |
Version 2.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-05 |
| Onset: | 2020-09-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-09-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
AFLURIA PFS 202 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Conjunctivitis,
Eye discharge,
Eye irritation,
Eye swelling,
Eyelid margin crusting,
Ocular hyperaemia SMQs:, Severe cutaneous adverse reactions (broad), Anaphylactic reaction (broad), Angioedema (narrow), Glaucoma (broad), Corneal disorders (broad), Conjunctival disorders (narrow), Periorbital and eyelid disorders (narrow), Ocular infections (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atenolol 25mg Aspirin .81mg Hydrochlorothiazide 25mg Current Illness: none Preexisting Conditions: resistant hypertension Allergies: epinephrine Diagnostic Lab Data: none CDC Split Type:
Write-up: Pinkeye. Swollen right and left eye. Both red and burning, draining. Right eye stuck shut and crusty upon awakening the next morning. Continued to be swollen and red. |
|
| VAERS ID: |
883724 (history) |
| Form: |
Version 2.0 |
| Age: |
5.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-09-11 |
| Onset: | 2020-09-12 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-09-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPIPV: DTAP + IPV (QUADRACEL) / SANOFI PASTEUR |
C5688AA / UNK |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
3X2KX / UNK |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site erythema,
Injection site pruritus,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: none Preexisting Conditions: Autism Spectrum Allergies: seasonal Diagnostic Lab Data: none CDC Split Type:
Write-up: Large Amount Swelling & Redness on Left Arm at Immunization site-9/12/20, About 800pm, Earlier in the day, complaints of Left shoulder itching. Advised cool compress, Antihistamine, Tylenol |
|
| VAERS ID: |
885601 (history) |
| Form: |
Version 2.0 |
| Age: |
26.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-22 |
| Onset: | 2020-09-23 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-09-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
P100247696 / N/A |
LA / IM |
Administered by: Military Purchased by: ? Symptoms: Axillary pain,
Injection site erythema,
Injection site induration,
Injection site mass,
Injection site swelling,
Skin warm SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Redness, swelling around injection site with hard lump. Pain in armpit. Hot to touch. Diameter about 3 inches. Started to improve 24 Sept 2020 in the afternoon. |
|
| VAERS ID: |
886246 (history) |
| Form: |
Version 2.0 |
| Age: |
15.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-28 |
| Onset: | 2020-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-09-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT7011MA / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Blood glucose increased,
Headache,
Nausea,
Syncope,
Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (narrow), Arrhythmia related investigations, signs and symptoms (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Multivitamin Current Illness: None Preexisting Conditions: Migraine Allergies: None Diagnostic Lab Data: Blood Glucose = 126 CDC Split Type:
Write-up: Vasovagal syncope, prolonged recovery with nausea, vomiting, headache X4 hours |
|
| VAERS ID: |
886636 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-29 |
| Onset: | 2020-09-29 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
RA / UN |
Administered by: Pharmacy Purchased by: ? Symptoms: Fatigue,
Headache,
Nausea SMQs:, Acute pancreatitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Vit D 3, Escitalopram, thyroxine Current Illness: none Preexisting Conditions: hypothyroidism, vitiligo , depression Allergies: penicillin Diagnostic Lab Data: none yet CDC Split Type:
Write-up: Fatigue, Severe headache, Nausea |
|
| VAERS ID: |
888143 (history) |
| Form: |
Version 2.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-23 |
| Onset: | 2020-10-01 |
| Days after vaccination: | 8 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
49281-0420-50 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Herpes zoster,
Pain,
Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Opportunistic infections (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 1959 Smallpox Vaccine- developed Cowpox Other Medications: Preservation vitamins Flovent inhaler Singular Pepcid 81 mg aspirin Omeprazole Current Illness: Allergies Preexisting Conditions: Allergies Rheumatoid Arthritis Fibromyalgia Allergies: Penicillin Tree Nuts Macrodantin Mold spores Sulfa Seasonal grasses Latex. Pollens Bee sting. Cats Diagnostic Lab Data: Doctors visit on 10/05/2020. No tests needed. CDC Split Type:
Write-up: 8 days after flu shot (10/01/2020) came down with Shingles. Confirmed by doctor visit 4 days later (on 10/05/2020) and began medication for rash (Valacyclovir) and pain (Gabapenten) |
|
| VAERS ID: |
888629 (history) |
| Form: |
Version 2.0 |
| Age: |
20.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-08 |
| Onset: | 2020-10-08 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
279836 / 1 |
LA / IM |
Administered by: School Purchased by: ? Symptoms: Dizziness,
Lip injury,
Loss of consciousness,
Tooth fracture SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: N/A Preexisting Conditions: NO Allergies: NO Diagnostic Lab Data: CDC Split Type:
Write-up: PATIENT RECEIVED FLUCELVAX. SHE WAS CHECKING OUT OF FLU CLINIC AND SHE PASSED OUT, CUT HER LOWER LIP WITH HER FRONT TEETH AND CHIPPED HER UPPER FRONT RIGHT TOOTH. SHE QUICKLY REGAINED CONSCIOUSNESS BUT CONTINUED TO FEEL FAINT. SHE WAS TRANSPORTED TO THE HOSPITAL FOR FOLLOW UP. |
|
| VAERS ID: |
890009 (history) |
| Form: |
Version 2.0 |
| Age: |
47.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-14 |
| Onset: | 2020-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT6681KA / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Expired product administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Multivitamin Tart cherry extract Fish oil Albuterol sulfate flonase allergy relief CoQ10 Current Illness: Preexisting Conditions: asthma Allergies: no known drug allergies Diagnostic Lab Data: NA CDC Split Type:
Write-up: Expired vaccine administered. Vaccine expiration date was 6/30/2020., vaccine administered on 10/14/2020. Patient denied negative reaction after administration, no signs/symptoms of a reaction. Per recommendation of a website, repeat vaccine should be administered. Based on that recommendation the visit provider will contact the patient to disuss/ arrange repeat clinic visit for a second vaccine.. What should we do if a dose of expired vaccine is given to a patient? The dose should be repeated. If the expired dose is a live virus vaccine, you should wait at least 4 weeks after the previous (expired) dose was given before repeating it. If the expired dose is not a live vaccine, the dose should be repeated as soon as possible. If you prefer, you can perform serologic testing to check for immunity for certain vaccinations (e.g., measles, mumps, rubella, varicella, and hepatitis A). |
|
| VAERS ID: |
890078 (history) |
| Form: |
Version 2.0 |
| Age: |
69.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-05 |
| Onset: | 2020-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
279818 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site pain,
Pain SMQs:, Extravasation events (injections, infusions and implants) (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: penicillin Diagnostic Lab Data: CDC Split Type:
Write-up: patient has had pain for 10 days at injection site and radiating around her back shoulder med |
|
| VAERS ID: |
890884 (history) |
| Form: |
Version 2.0 |
| Age: |
7.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-17 |
| Onset: | 2020-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U7012BA / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Peripheral swelling,
Pyrexia,
Skin warm SMQs:, Cardiac failure (broad), Angioedema (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: multivitamin Current Illness: none Preexisting Conditions: none Allergies: none Diagnostic Lab Data: None CDC Split Type:
Write-up: The following morning after receiving vaccine, left arm became swollen and warm to touch. Fevers T-101.8/102.6 Advised cool compresses, antihistamine, Tylenol or Ibuprofen increasing fluid intake |
|
| VAERS ID: |
891141 (history) |
| Form: |
Version 2.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-01 |
| Onset: | 2020-10-15 |
| Days after vaccination: | 14 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ5181AB / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Arthritis,
Body temperature increased,
Condition aggravated,
Influenza,
Pain of skin,
Pericarditis,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Chronic kidney disease (broad), Arthritis (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), Immune-mediated/autoimmune disorders (broad), Noninfectious myocarditis/pericarditis (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: albuterol sulfate (HFA Aerosol Inhaler) albuteroL 90 mcg/actuation Inhale 2 puffs into the lungs every 6 hours as needed for Wheezing. Use with spacer Dispense: 1 Inhaler ? diclofenac sodium (Gel) VOLTAREN 1 % Apply 4 g topically 4 times d Current Illness: none Preexisting Conditions: Attention deficit hyperactivity disorder (ADHD) Edit Overview Unprioritized ??Change Dx Resolve Overview ritalin since 2003 ???????? Worked well but stopped for HTN ???????? ?? Depression Create Overview Unprioritized ??Change Dx Resolve HTN (hypertension) Edit Overview Unprioritized ??Change Dx Resolve S/P Lapidus and 2nd toe weil osteotomy 11/7/2016 ange Dx Resolve Claw toe, acquired Create Overview Unprioritized ??Change Dx Resolve Osteopenia Allergies: Chlorhexidine Gluconate Hives, Itching High 10/27/2016 Past Updates... Adverse Reactions/Drug Intolerances Betadine [Povidone-iodine (with Soap)] Diagnostic Lab Data: none CDC Split Type:
Write-up: I had a violent reaction to my high-dose flu shot last thurs 3pm. By around 9pm, uncontrollable shaking, skin hurt, wherever I have arthritis became enflamed. I started taking Advil but even with that I had temp of 101 but became normal the next day. The worst was that it triggered my pericarditis very badly - the worst in many, many years. So painful I had to sleep sitting up. I have been treating with Advil and much, much better. Flu symptoms now gone. |
|
| VAERS ID: |
891731 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-08 |
| Onset: | 2020-10-08 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
QFAA2019 / UNK |
- / IM |
Administered by: Unknown Purchased by: ? Symptoms: Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: hypertension, depression, hyperlipidemia Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: received flublok 10/8/2020 and within 20 minutes developed diffuse hives |
|
| VAERS ID: |
891784 (history) |
| Form: |
Version 2.0 |
| Age: |
3.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-16 |
| Onset: | 2020-10-17 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U7012BA / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Injection site erythema,
Injection site swelling SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: vitamin D; miralax, BeneFiber. Current Illness: Preexisting Conditions: Allergies: None Known Diagnostic Lab Data: NONE CDC Split Type:
Write-up: SWELLING and redness oF Right arm, initially at The injection site with progression to Below Elbow. Not Streaking, Doubt cellulitis Not a systemic allergic reaction |
|
| VAERS ID: |
892308 (history) |
| Form: |
Version 2.0 |
| Age: |
82.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-30 |
| Onset: | 2020-10-01 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
279815 / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Pain in extremity,
Paraesthesia SMQs:, Peripheral neuropathy (broad), Guillain-Barre syndrome (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Ever since getting the vaccine the patient''s arm and hand hurt and is tingling |
|
| VAERS ID: |
893196 (history) |
| Form: |
Version 2.0 |
| Age: |
36.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-10 |
| Onset: | 2020-10-10 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Mobility decreased,
Pain,
Pain in extremity SMQs:, Parkinson-like events (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Birth Control - Orsythia Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: After an in person appointment with my NP, the NP believes it is reaction of my muscle and not an injury to the bursa. CDC Split Type:
Write-up: Starting within an hour of vaccination, I had major soreness in upper arm and had difficulty lifting arm. This is normal for me for the 2 days after vaccination but my pain is still consistent on 10/28 - 18 days after the injection. Pain moving, pushing, pulling, lifting, twisting across upper arm directly below tip of shoulder bone that affects everything I do. I tried taking the NP recommended does of 600mg 3x a day of ibuprofen for 5 days and did not feel any change besides a slight dulling of the pain. Today, 10/28, I began the NP prescribed Prednisone which I will take for 5 days. I had no pain before this injection. |
|
| VAERS ID: |
895446 (history) |
| Form: |
Version 2.0 |
| Age: |
77.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-19 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ546AA / 1 |
RA / OT |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product distribution issue SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2020SA297931
Write-up: Shipment had been in transit to long with no AE; Initial information regarding an unsolicited valid Non-serious case was received from a pharmacist via The Agency (Reference number- 00325402) and transmitted to Sanofi on 21-Oct-2020. It was reported that a 77-year old female patient who received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT (lot number: UJ546AA, expiry date: 06/30/2021, Route: Via intramuscular in the right arm) which received delay shipment (Product distribution issue) on 19-oct-2020 and vaccine will administrated as soon as they received for prophylactic vaccination. The patient''s medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. It was an actual medication error case due to product shipment delay. At the time of reporting, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
895454 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-11-08 |
| Onset: | 2020-11-09 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
70461-0120-03 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Accident,
Arthralgia,
Chills,
Condition aggravated,
Fatigue,
Gait disturbance,
No reaction on previous exposure to drug,
Pain SMQs:, Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Accidents and injuries (narrow), Arthritis (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: None Preexisting Conditions: None Allergies: demerol Diagnostic Lab Data: None CDC Split Type:
Write-up: Around 3:00 AM I woke up shivering. The shivering was severe although I didn''t feel all that cold. It was borderline uncontrollable and it was difficult to walk (and I had an accident on the way to the bathroom). I have never had a similar reaction to a flu vaccination before, though I have received them yearly for decades. In addition, the usual level of arthritic pain I have in my shoulders and hips was exacerbated. I fell asleep in perhaps two hours after putting a heating pad on my chest and on one especially sore shoulder, and I was still shivering when I drifted off. I am fatigued and achey today, but feel much better than I did during the night, and not shivering. |
|
| VAERS ID: |
896285 (history) |
| Form: |
Version 2.0 |
| Age: |
69.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-28 |
| Onset: | 2020-11-12 |
| Days after vaccination: | 15 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
279821 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site pain,
Mobility decreased,
Muscle spasms SMQs:, Dystonia (broad), Parkinson-like events (broad), Extravasation events (injections, infusions and implants) (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: KIDDNEY TRANSPLANT (NO DATE), CHRONIC PAIN. Allergies: NKA Diagnostic Lab Data: nothing so far CDC Split Type:
Write-up: 2 weeks after vaccination patient is complaining of severe pain in the injection site, (like someone punched him), limited mobility, muscle cramp. No bruising, no swelling, no lump. He did not have any symptoms after injection, usual injection site pain next day after inoculation, nothing major. Then about 2 weeks later it started, it has been hurting him for about 3 days now. I advised to call his doctor, use ice or warm compress, Arnica gel on painful area. |
|
| VAERS ID: |
896629 (history) |
| Form: |
Version 2.0 |
| Age: |
28.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-30 |
| Onset: | 2020-10-30 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ533AA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Mobility decreased,
Myalgia SMQs:, Rhabdomyolysis/myopathy (broad), Parkinson-like events (broad), Eosinophilic pneumonia (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: patient complained of severe muscle pain and difficulty moving arm for more than a week after shot. Patient refused to see medical doctor to evaluate |
|
| VAERS ID: |
896746 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2020-10-19 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-16 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ546AA / UNK |
RA / OT |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product distribution issue SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2020SA297615
Write-up: Shipment had been in transit to long with no AE; Initial information regarding an unsolicited valid Non-serious case was received from a pharmacist. (Reference number-00325689) and transmitted to Sanofi on 21-Oct-2020. It was reported that a 68-year old patient (gender not reported) who received INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT (lot number: UJ546AA, expiry date: 06/30/2021, Route: Via intramuscular in the right arm) which received delay shipment (Product distribution issue) on 19-oct-2020 and vaccine will administrated as soon as they received for prophylactic vaccination. The patient''s medical history, past medical treatment, vaccination, concomitant medication and family history were not provided. It was an actual medication error case due to product shipment delay. At the time of reporting, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
897367 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-07 |
| Onset: | 2020-10-08 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Bursitis,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: Went to MD, is doing physical therapy. CDC Split Type:
Write-up: Caused arm Pain and inflammation in Bursa of Shoulder |
|
| VAERS ID: |
898038 (history) |
| Form: |
Version 2.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-11-17 |
| Onset: | 2020-11-19 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
2FS5G / 2 |
RA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
C5631AA / 1 |
- / IM |
| VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS |
2737P / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Erythema,
Peripheral swelling,
Rash SMQs:, Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Left arm red & swollen. Red area about 4 inches long, 2-3 wide. Rash all chest and breasts to top of belly |
|
| VAERS ID: |
898129 (history) |
| Form: |
Version 2.0 |
| Age: |
66.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-11-10 |
| Onset: | 2020-11-15 |
| Days after vaccination: | 5 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-23 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Guillain-Barre syndrome SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 8 days
Extended hospital stay? No Previous Vaccinations: Other Medications: enalapril/HCTZ, famotidine, naproxen, sildenafil, Current Illness: none Preexisting Conditions: hypertension, GERD Allergies: none Diagnostic Lab Data: CDC Split Type:
Write-up: Guillain-Barre |
|
| VAERS ID: |
899201 (history) |
| Form: |
Version 2.0 |
| Age: |
83.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-10-19 |
| Onset: | 2020-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ546AA / UNK |
LA / OT |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2020SA298606
Write-up: the shipment had been in transit to long with no AE; FLUZONE HIGH DOSE QUADRIVLAENT administered after the vaccine was in transit to long with no AE; Initial information received on 21-Oct-2020 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 83 years old female patient who received a 0.7 mL dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (lot number: UJ546AA, expiry date: 30-Jun-2021) via intramuscular route in the left arm on an 19-Oct-2020 for prophylactic vaccination. It was also reported that shipment had been in transit to long (product storage error and product distribution issue). The patient''s medical history, past medical treatments, vaccinations and family history were not provided. No concomitant medication was given to the patient. It was an actual medication error due incorrect product storage. It was a case of product shipment delay. At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
899202 (history) |
| Form: |
Version 2.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-19 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ546AA / UNK |
LA / OT |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product distribution issue,
Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2020SA298655
Write-up: The patient was administered the vaccine which was in transit to long/no AE; The vaccine was in transit to long/no AE; Initial information regarding an unsolicited valid non-serious case was received from a pharmacist via The Agency (Reference number- 00325681) and transmitted to Sanofi on 21-Oct-2020.. This case involves a 71 year old male patient who was administered 0.7 ml INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (lot UJ546AA, expiry date: 30-Jun-2021) via intramuscular route in the left arm for prophylactic vaccination on 19-Oct-2020 (product storage error and product distribution issue) Medical history, medical treatment(s), vaccination(s), concomitant medications and family history were not provided. It was a case of an actual medication error due to incorrect product storage. It was also a case of product shipment delay. At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
899452 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ546AA / UNK |
LA / OT |
Administered by: Unknown Purchased by: ? Symptoms: No adverse event,
Product distribution issue,
Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2020SA298725
Write-up: the shipment had been in transit to long with no AE; FLUZONE HIGH DOSE QUADRIVLAENT administered after the vaccine was in transit to long with no AE; Initial information received on 21-Oct-2020 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 80 years old male patient who received a 0.7 mL dose of INFLUENZA QUADRIVAL A-B HIGH DOSE HV VACCINE [FLUZONE HIGH-DOSE QUADRIVALENT] (lot number: UJ546AA, expiry date: 30-Jun-2021) via intramuscular route and left arm site on an unknown date for prophylactic vaccination which was administered after the vaccine in the shipment had been in transit to long (product storage error and product distribution issue). The patient''s medical history, past medical treatments, vaccinations and family history were not provided. No concomitant medication was given to the patient. It was an actual medication error due incorrect product storage. It was a case of product shipment delay. At the time of report, no adverse event was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
901726 (history) |
| Form: |
Version 2.0 |
| Age: |
60.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-12-09 |
| Onset: | 2020-12-11 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-12-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
237PS / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Arthralgia,
Joint swelling,
Pain,
Pruritus,
Skin warm SMQs:, Anaphylactic reaction (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Hypersensitivity (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient woke up on day 2 with a swollen shoulder that was warm, itchy, and painful. Pain was radiating. She was counseled to apply ice to the site, and to contact her primary care provider. |
|
| VAERS ID: |
902154 (history) |
| Form: |
Version 2.0 |
| Age: |
21.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-11-13 |
| Onset: | 2020-11-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2020-12-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U7045DA / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Amnesia,
Fatigue,
Seizure,
Tremor,
Unresponsive to stimuli,
Urinary incontinence SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Dementia (broad), Convulsions (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: No prescriptions, over-the-counter medications, dietary supplements, or herbal remedies being taken at the time of vaccination. Current Illness: No other illnesses at the time of vaccination and up to one month prior. Preexisting Conditions: No chronic or long-standing health conditions. Allergies: No allergies to medications, food, or other products. Diagnostic Lab Data: No medical tests and laboratory results related to the adverse event. CDC Split Type:
Write-up: After his flu shot on 11/13, he was being driven home by his brother and he started seizing. He was shaking and unresponsive and urinated in the car seat. Brother pulled the car over and shook patient who came around. He was very tired afterward, and did not remember the event. He also had a seizure after a series of immunizations as a young child, but not sure which shot caused it that time. Mom thinks flu vaccine was one of the shots given that day. We will no longer give him flu shots. |
|
| VAERS ID: |
918422 (history) |
| Form: |
Version 2.0 |
| Age: |
80.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2020-10-22 |
| Onset: | 2020-10-22 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-01-04 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
- / - |
Administered by: Private Purchased by: ? Symptoms: Pruritus,
Skin discolouration SMQs:, Anaphylactic reaction (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 4/11/2001 Influenza Other Medications: see medical record Current Illness: See medical record Preexisting Conditions: See medical record Allergies: Penicillin, Influenza, Gatifloxacin Diagnostic Lab Data: CDC Split Type:
Write-up: See medical record note dated 12/31/20. Itching, discoloration of both arms. |
|
| VAERS ID: |
979781 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-01-25 |
| Onset: | 2021-01-25 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-01-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Asthma SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Eosinophilic pneumonia (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: 6 hours after receiving fluzone high dose vaccination had a 2 to 3 hours asthma attack. Patient recovered after the 2 to 3 hours. |
|
| VAERS ID: |
1062880 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-02-26 |
| Onset: | 2021-02-26 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-03-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
279834 / UNK |
- / - |
| VARZOS: ZOSTER (SHINGRIX) / GLAXOSMITHKLINE BIOLOGICALS |
- / 1 |
RA / IM |
Administered by: Work Purchased by: ? Symptoms: No adverse event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Fluoxetine, Amlodipine Current Illness: Cough Preexisting Conditions: Hypertension, depression, insomnia Allergies: No known allergies Diagnostic Lab Data: CDC Split Type:
Write-up: No adverse reaction reported by patient. Patient under the age of 50, as recommended/ required for first dose of Zoster. |
|
| VAERS ID: |
1400131 (history) |
| Form: |
Version 2.0 |
| Age: |
0.58 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2021-06-15 |
| Onset: | 2021-06-15 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-06-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
P100251769 / 2 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect dose administered,
Product administered to patient of inappropriate age,
Wrong product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: no Preexisting Conditions: no Allergies: none Diagnostic Lab Data: CDC Split Type:
Write-up: Wrong Flu vaccine was for 3 years and up, this child is 7 mo old. 0.5 ml administered not 0.25 ml |
|
| VAERS ID: |
1715584 (history) |
| Form: |
Version 2.0 |
| Age: |
87.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-20 |
| Onset: | 2021-09-20 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Back pain,
Facial pain,
Flushing,
Headache,
Pain in extremity SMQs:, Anaphylactic reaction (broad), Retroperitoneal fibrosis (broad), Glaucoma (broad), Hypersensitivity (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Atenolol, Losartan/Hydrochlorothiazide, and Simvastatin Calcium, Centrum Silver 55 Plus, OsteoBiflex, Baby Aspirin Current Illness: None Preexisting Conditions: Pre-Diabetes, Hypercholesterolemia, Hypertension Allergies: Carbocaine, ACE Inhibitors (cough), Procardia XL, Prazosin Clams and Swordfish Diagnostic Lab Data: N/A CDC Split Type:
Write-up: A few minutes after receiving the Fluad Quad 65+ vaccine, the patient had pain in her legs, back, and face. Her face felt flushed and she had a headache. It only lasted about 5-7 minutes and then she felt ok. The patient was monitored for 1 hour and she was given water. |
|
| VAERS ID: |
1750142 (history) |
| Form: |
Version 2.0 |
| Age: |
29.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Vaccine was given SubQ instead of IM |
|
| VAERS ID: |
1750144 (history) |
| Form: |
Version 2.0 |
| Age: |
61.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Administered SubQ instead of IM |
|
| VAERS ID: |
1750148 (history) |
| Form: |
Version 2.0 |
| Age: |
31.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Given SubQ instead of IM |
|
| VAERS ID: |
1750151 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750321 (history) |
| Form: |
Version 2.0 |
| Age: |
32.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered vaccine SubQ instead of IM. |
|
| VAERS ID: |
1750325 (history) |
| Form: |
Version 2.0 |
| Age: |
39.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered vaccine SubQ instead of IM. |
|
| VAERS ID: |
1750332 (history) |
| Form: |
Version 2.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM |
|
| VAERS ID: |
1750340 (history) |
| Form: |
Version 2.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750343 (history) |
| Form: |
Version 2.0 |
| Age: |
64.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750347 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750351 (history) |
| Form: |
Version 2.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750355 (history) |
| Form: |
Version 2.0 |
| Age: |
46.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750358 (history) |
| Form: |
Version 2.0 |
| Age: |
52.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered injection SubQ instead of IM. |
|
| VAERS ID: |
1750367 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
312846 / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM. |
|
| VAERS ID: |
1750369 (history) |
| Form: |
Version 2.0 |
| Age: |
49.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM |
|
| VAERS ID: |
1750370 (history) |
| Form: |
Version 2.0 |
| Age: |
53.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-09-28 |
| Onset: | 2021-09-28 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-09-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
X2K7D / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Incorrect route of product administration SMQs:, Drug abuse and dependence (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: RN administered SubQ instead of IM |
|
| VAERS ID: |
1825556 (history) |
| Form: |
Version 2.0 |
| Age: |
56.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2021-10-25 |
| Onset: | 2021-10-26 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
MODERNA BOOSTER / 3 |
LA / SYR |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
- / UNK |
- / - |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
NO CLUE WHAT VE / 1 |
RA / - |
Administered by: Pharmacy Purchased by: ? Symptoms: Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Metoprolo 25 mgs Chlorthalidone .25 mgs Diltiazem ER 120 MG CoQ10 Asprin .81 mgs Current Illness: None Preexisting Conditions: none Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Was told I could get the Moderna Booster and Flu shot together. within 24 hours I had a fever of 104. Sat in cool bath for 90 minutes and took Tylenol to get it down to 100. Stayed around 100 for the remainder of the evening. I do not know which seasonal flu shot was given, so I just picked the top one. |
|
| VAERS ID: |
1833023 (history) |
| Form: |
Version 2.0 |
| Age: |
80.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-10-29 |
| Onset: | 2021-10-29 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
- / 1 |
RA / SYR |
Administered by: Private Purchased by: ? Symptoms: Asthenia,
Delirium,
Diplegia,
Disorientation,
Fatigue,
Hypersomnia,
Mobility decreased,
Monoplegia,
Urinary incontinence SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (narrow), Noninfectious meningitis (broad), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Depression (excl suicide and self injury) (broad), Tendinopathies and ligament disorders (broad), Hypoglycaemia (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: High blood pressure medication, Vitamins Current Illness: None Preexisting Conditions: High blood pressure, CLL Disease Allergies: Pollen, Hay Diagnostic Lab Data: CDC Split Type:
Write-up: Extreme fatigue, slept for hours, paralyzed in arm and legs, extreme weakness, couldn''t get up to use the bathroom, could hold urine, urine ran down legs. Felt delerious. Couldn''t tell where she was. Had to use clothes to soak up the urine. Tried to call doctor. Couldn''t reach him. Fortunately, son came by 24 hours and was able to help. Very frightening, very upsetting experience. |
|
| VAERS ID: |
1846220 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-10-26 |
| Onset: | 2021-11-01 |
| Days after vaccination: | 6 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-05 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FF2587 / 3 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Cough,
Dyspnoea,
Extra dose administered,
Respiratory tract congestion SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Pfizer COVID Vaccine # 2 Other Medications: Xeralto Sivastatin Prednisone Wixela Sertraline Calcium with D Current Illness: Polymyositis Pulmonary fibrosis diagnosed after 2nd Pfizer Covid shot in January 2021 Preexisting Conditions: Polymyositis Pulmonary Emboli Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Following both my second COVID vaccine in January 2021 and my booster in October 2021 I developed severe congestion, cough and shortness of breath. It appears to have exacerbated my auto immune both times. The first episode required a trip to the ER for shortness of breath. |
|
| VAERS ID: |
1848739 (history) |
| Form: |
Version 2.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-10-29 |
| Onset: | 2021-10-30 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UJ775AB / UNK |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Muscle swelling,
Oedema peripheral,
Tenderness SMQs:, Cardiac failure (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: AMOXICILLIN Diagnostic Lab Data: CDC Split Type:
Write-up: Patient reported right shoulder, pectoral muscle and arm pit swelling overnight with visible signs upon waking. Tender to the touch at point of swelling (not at injection site). Patient reported to the pharmacy Monday morning and said it was improved, still a little sore but swelling was down. No fever or other symptoms to report - not even sure it was from the shot but the timing coincided within 12 hours of administration and patient did not knowingly experience any other events that would have precipitated the reaction. |
|
| VAERS ID: |
1888119 (history) |
| Form: |
Version 2.0 |
| Age: |
70.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-10-14 |
| Onset: | 2021-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-20 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ760AA / N/A |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Arthralgia,
Injected limb mobility decreased,
Pain in extremity SMQs:, Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: levothyroxine, losartan, zolpidem, atorvastatin, estradiol cream Current Illness: unknown Preexisting Conditions: hypothyroidism, hypertension, hypercholesterolemia Allergies: None known Diagnostic Lab Data: Xray and ultrasound have been ordered. CDC Split Type:
Write-up: The patient received Fluzone HD Quad vaccine 0.7ml intramuscularly in right arm on 10/14/21. She reported arm/shoulder pain and having pain difficulty when raising her arm since receiving the vaccine. She reported this to the pharmacy the week of 11/15/21. She contacted her doctor and is having an x-ray and ultrasound performed. Her physician has been notified by the pharmacy and the patient has a follow-up appointment scheduled on December 9th. |
|
| VAERS ID: |
1888790 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2020-09-24 |
| Onset: | 2020-09-24 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
33332-0320-01 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Allergy test negative,
Dysphagia,
Dysphonia,
Eye discharge,
Paraesthesia oral,
Pharyngeal paraesthesia,
Throat tightness SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Multivitamin D3 2000IU Current Illness: None Preexisting Conditions: None Allergies: Penecillin Diagnostic Lab Data: Allergy test showed no evidence of allergy to flu shot on 10/19/21. CDC Split Type:
Write-up: Tightness in throat, trouble swallowing, unusual hoarseness,tingling feeling in mouth and throat, thick yellow discharge from eyes |
|
| VAERS ID: |
1888814 (history) |
| Form: |
Version 2.0 |
| Age: |
58.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-10-19 |
| Onset: | 2021-10-19 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
33332-0321-01 / 1 |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: Dysphagia,
Throat tightness SMQs:, Anaphylactic reaction (broad), Angioedema (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Hypersensitivity (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: 9/24/2020, Flu vaccination Afluria Quad previously reported Other Medications: Mulitvitamin D3 2000 IU Current Illness: None Preexisting Conditions: None Allergies: Penecillin Diagnostic Lab Data: CDC Split Type:
Write-up: Tightness in throat, trouble swallowing 3 hours after injection. Since my experience a year before (9/24/2020) I took diphenhydramine HCI 50 mg (2 Benadryl tablets) and symptoms calmed. Took another 50 mg 4 hours later and became symptom free. |
|
| VAERS ID: |
1932123 (history) |
| Form: |
Version 2.0 |
| Age: |
53.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2021-12-04 |
| Onset: | 2021-12-04 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-12-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / 2 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Lisinopril 10 mg once daily Current Illness: none Preexisting Conditions: none Allergies: NKDA Diagnostic Lab Data: none CDC Split Type:
Write-up: Patient received second influenza dose on 12.4.21 when he had already received a first influenza dose on 9/22/21 - no adverse events reported by patient. |
|
| VAERS ID: |
1935917 (history) |
| Form: |
Version 2.0 |
| Age: |
72.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-12-08 |
| Onset: | 2021-12-08 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2021-12-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
- / - |
Administered by: Private Purchased by: ? Symptoms: Dizziness,
Lymphadenopathy,
Nausea,
Pain in extremity,
Retching,
Vomiting SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Venlafaxine; Losartan; Tramadol; Amlodipine; Cosentyx; Magnesium; Claritin: Probiotic; Voltarin 1% topical gel prn; Acyclovir PRN; Clobeta cream Current Illness: Occipital neuralgia Preexisting Conditions: Occipital neuralgia; htn; psoriatic arthritis; Allergies: Codeine; Plaquenil Diagnostic Lab Data: none CDC Split Type:
Write-up: Initially had arm soreness, underarm enlarged LAD, then later that evening (about 5 hours later), dizziness with nausea, vomiting, dry heaving. |
|
| VAERS ID: |
2010628 (history) |
| Form: |
Version 2.0 |
| Age: |
0.33 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-01-06 |
| Onset: | 2022-01-06 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-01-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| DTAPHEPBIP: DTAP + HEPB + IPV (PEDIARIX) / GLAXOSMITHKLINE BIOLOGICALS |
Z4R9R / 2 |
RL / IM |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
5NF7J / UNK |
RL / IM |
| HIBV: HIB (ACTHIB) / SANOFI PASTEUR |
UJ587AA / 2 |
LL / IM |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
EK6267 / 2 |
LL / IM |
| RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS |
G973H / 2 |
MO / PO |
Administered by: Private Purchased by: ? Symptoms: Product administered to patient of inappropriate age,
Wrong patient SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Vitamin D infant drops Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: None CDC Split Type:
Write-up: Family arrived to office with 2 children (ages 2yr and 4mo) for well child visits. The mom asked for flu vaccine for the 2yr old and nurse misunderstood and thought that request was for the 4mo old. Vaccine given erroneously to the 4mos old patient. Provider has discussed incident with family. |
|
| VAERS ID: |
2024747 (history) |
| Form: |
Version 2.0 |
| Age: |
0.25 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-01-10 |
| Onset: | 2022-01-11 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-01-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
574R7 / 1 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Product administered to patient of inappropriate age SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: formula intolerance, noisy breathing Preexisting Conditions: formula intolerance, noisy breathing Allergies: none Diagnostic Lab Data: none CDC Split Type:
Write-up: none |
|
| VAERS ID: |
2032235 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-01-13 |
| Onset: | 2022-01-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-01-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
9P935 / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: patient came to flu clinic requesting flu vaccine which was administered. Later when entering information into the Immunization Registry staff found that patient previously recieved flu vaccine this season, Oct 2021. |
|
| VAERS ID: |
2035562 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2021-12-09 |
| Onset: | 2021-12-12 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-01-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FH8027 / 3 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ764AC / 7+ |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Atrial fibrillation SMQs:, Supraventricular tachyarrhythmias (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: acetaminophen, amlodipine, atorvastatin, carvedilol, docusate, triamterene-hydrochlorothiazide, valsartan Current Illness: Preexisting Conditions: hypertension, hyperlipidemia, prediabetes, lumbar radiculopathy Allergies: lisinopril, almonds, sea salt Diagnostic Lab Data: CDC Split Type:
Write-up: atrial fibrillation with rapid ventricular response identified at acute office visit on 12/9/21. Transferred to Emergency Department. Treated with IV antiarrhythmics and converted to sinus rhythm. |
|
| VAERS ID: |
2048403 (history) |
| Form: |
Version 2.0 |
| Age: |
35.0 |
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2021-12-11 |
| Onset: | 2022-01-16 |
| Days after vaccination: | 36 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-01-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
- / 3 |
LA / SC |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
- / 1 |
LA / SC |
Administered by: Private Purchased by: ? Symptoms: Bell's palsy,
Facial paralysis,
Facial paresis,
Magnetic resonance imaging head SMQs:, Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious meningitis (broad), Hearing impairment (broad), Immune-mediated/autoimmune disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Levothyroxine: 0.025 mg. OTC Vitamin C supplement Current Illness: Respiratory illness (tested negative for COVID-19.) Preexisting Conditions: Sleep apnea. Asthma. Allergies: Amoxicillin and Wellbutrin. Averse reaction to Valium. Diagnostic Lab Data: Ruled out stroke - Head MRI. CDC Split Type:
Write-up: Bell?s Palsy. Slight drooping on right side of face observed by family within 2 weeks of vaccines. Significant experience of facial weakness/paralysis experienced on 5 weeks later and Bell?s Palsy diagnosed during Emergency Room visit. |
|
| VAERS ID: |
2317423 (history) |
| Form: |
Version 2.0 |
| Age: |
45.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-11-11 |
| Onset: | 2021-11-20 |
| Days after vaccination: | 9 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-06-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
039F21A / UNK |
LA / IM |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
308485 / UNK |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Autopsy,
Death,
Exercise lack of,
Fatigue,
Malaise,
Pulmonary embolism,
Respiratory disorder,
Unresponsive to stimuli SMQs:, Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Embolic and thrombotic events, venous (narrow), Acute central respiratory depression (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hypotonic-hyporesponsive episode (broad), Respiratory failure (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? Yes
Date died: 2021-11-21
Days after onset: 1
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Possibly Topiramate, Sertraline hydrochloride, Clonazepam, Desogestrel; ethinyl estradiol Current Illness: unknown Preexisting Conditions: migraines, anxiety Allergies: unknown Diagnostic Lab Data: autopsy CDC Split Type:
Write-up: Decedent was reportedly feeling unwell with respiratory complaints for several days to week prior to death, progressively became more ?wiped out? and tired, staying in bed most of the time. She was found unresponsive in the bathroom where she was pronounced dead by EMS. Autopsy confirmed bilateral pulmonary thromboemboli as cause of death, with multiple risk factors including obesity (BMI 46.9), recently sedentary, COVID-19 and Influenza vaccinations, and Desogestrel/ethinyl estradiol |
|
| VAERS ID: |
2441009 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-09-12 |
| Onset: | 2022-09-12 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-09-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AS7145B / 1 |
LA / IM |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
346347 / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Back pain,
Chest pain,
Dizziness,
Emotional distress,
Flushing,
Immediate post-injection reaction SMQs:, Anaphylactic reaction (broad), Anticholinergic syndrome (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Depression (excl suicide and self injury) (broad), Vestibular disorders (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Not Known Current Illness: Patient stated that she had chest pain prior to getting the vaccinations. Preexisting Conditions: Unknown, patient stated she is generally healthy. Allergies: No known allergies Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Patient received both vaccinations, exited the vaccination room and then immediately began complaining that she was feeling lightheaded. She was very flushed and appeared to be in distress. She re-entered the vaccination room where she appeared to have significant back pain and continued lightheadedness. She was able to lie down more comfortably on the floor and rested while EMS was contacted. She complained of some chest pain and stated she had chest pain prior to the administrations of the vaccines. EMS arrived within 15 minutes, assessed the patient and transported her to the local hospital. |
|
| VAERS ID: |
2464675 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-09-20 |
| Onset: | 2022-09-21 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-09-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9693 / N/A |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / UNK |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Bell's palsy,
Borrelia test negative SMQs:, Hearing impairment (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: Valtrex zyrtec synthroid zoloft wellbutrin Current Illness: none Preexisting Conditions: hashimoto''s thyroiditis Allergies: guava Diagnostic Lab Data: Lyme negative CDC Split Type:
Write-up: Bell''s Palsy right face 24 hours after vaccination Treated with prednisone and valtrex |
|
| VAERS ID: |
2466693 (history) |
| Form: |
Version 2.0 |
| Age: |
30.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-01 |
| Onset: | 2022-10-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9694 / 4 |
LA / IM |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
UJ903AA / UNK |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Fall,
Tremor SMQs:, Neuroleptic malignant syndrome (broad), Parkinson-like events (broad), Noninfectious encephalopathy/delirium (broad), Accidents and injuries (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: not known Current Illness: not known Preexisting Conditions: not known Allergies: penicillin Diagnostic Lab Data: CDC Split Type:
Write-up: He was sitting after receiving vaccinations (maybe 5 minutes) and then fell over onto floor in a plank position and was slightly shaking. regained consciousness after less than 30 seconds. Taken by ambulance for further treatment/testing |
|
| VAERS ID: |
2473630 (history) |
| Form: |
Version 2.0 |
| Age: |
17.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-10 |
| Onset: | 2022-10-10 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-10 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9697 / 4 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT7681LA / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness,
Feeling hot,
Vomiting SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: Unknown Preexisting Conditions: Unknown Allergies: NKA Diagnostic Lab Data: CDC Split Type:
Write-up: Patient post vaccinations c/o feeling warm and lightheaded, patient vomited x1 with resolution of symptoms. Patient was offered water and was continuously monitored. HR 76 strong/regular 1306 All symptoms resolved |
|
| VAERS ID: |
2476265 (history) |
| Form: |
Version 2.0 |
| Age: |
9.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-03 |
| Onset: | 2022-10-03 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
FL2757 / 2 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
UT7681LA / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Expired product administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: COVID vaccine given 3 days post expiration date. No adverse event occured. PCP, dept of health notified and family notified. Awaiting advice from dept of health on validity of dose and subsequent dosing. |
|
| VAERS ID: |
2477966 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-13 |
| Onset: | 2022-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ872AA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Dyspnoea,
Gait disturbance,
Hypoaesthesia oral,
Spinal pain SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Anticholinergic syndrome (broad), Parkinson-like events (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Arthritis (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Patient was fine immediately after his flu shot, has always tolerated them in the past he said and this was his second year getting the high dose according to our records. He went to go do his shopping and came back a few minutes later out of breath and in distress. He said he almost didn''t make it back he had sudden severe acute pain in his lower spine with numbness and had a hard time walking/breathing. I checked his BP it was 186/107 with pulse of 57, then 159/91 with a pulse of 48. We used a different machine after he had a while to sit and start feeling better/drink some water and it was 168/96 with pulse 51. I called his doctor''s office and let them know what happened. |
|
| VAERS ID: |
2478911 (history) |
| Form: |
Version 2.0 |
| Age: |
52.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-12 |
| Onset: | 2022-10-12 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-14 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
D34TF / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Rash,
Rash erythematous,
Rash papular,
Rash pruritic,
Skin warm,
Urticaria SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: After Moderna booster-lymph swelling left axilla Other Medications: Busperone Pantprozole Current Illness: N/A Preexisting Conditions: Gerd Allergies: N/A Diagnostic Lab Data: Was seen by primary care, started prescription strength topical cream today (10-14-22) Triamcinolone Acetonide Cream USP 0.5% BID CDC Split Type:
Write-up: Red warm rash w raised hives mainly over left side of abdomen but extending to right side as well. Very itchy |
|
| VAERS ID: |
2480380 (history) |
| Form: |
Version 2.0 |
| Age: |
21.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-14 |
| Onset: | 2022-10-14 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AS7164B / 4 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
AS5RM / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Eye movement disorder,
Loss of consciousness,
Malaise,
Pallor,
Posture abnormal,
Vomiting SMQs:, Torsade de pointes/QT prolongation (broad), Acute pancreatitis (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Dystonia (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Ocular motility disorders (narrow), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Unknown Current Illness: N/A Preexisting Conditions: Ehlers Danlos Type 3, Hypothyroidism, Hiatal Hernia, Chronic Depression, Chronic Nausea, Chronic Fatigue Allergies: Peppermint, nickel and gluten Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Patient received Moderna COVID19 Bivalent Updated Booster 12+ 0.5ml in the right deltoid and Fluarix quad 0.5ml in the left deltoid. The patient then asked for some water and for a receptacle to vomit into. The patient lost color, stated she was feeling unwell and shortly thereafter she her head fell back, her eyes rolled back in her head and she lost consciousness. She came to quickly, but again lost consciousness a second time. She did come to again and asked for the pharmacist and technician to contact her mother who was out waiting in the car. 911 was called immediately after she lost consciousness the first time. EMS arrived and evaluated the patient. The patient and her mother decided to not seek further treatment at the hospital. The patient does have a history of passing out after blood draws, but has never passed out after vaccinations. This information was not disclosed to the pharmacy prior to administration. |
|
| VAERS ID: |
2480392 (history) |
| Form: |
Version 2.0 |
| Age: |
47.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-17 |
| Onset: | 2022-10-17 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
053D22A / 4 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
95ZA7 / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness,
Nausea,
Pallor SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Zoloft Current Illness: None Preexisting Conditions: None Allergies: NKA Diagnostic Lab Data: CDC Split Type:
Write-up: Patient received 2 vaccines this morning at around 10:22 a.m. (covid & flu). After receiving the 2nd injection at 10:24, patient started to feel nauseous and lightheaded. Vaccinator quickly reached out for assistance and patient laid down on the cot with a cool cloth. Vitals obtained at 10:30 HR 64; BP 97/65 (within normal range per patient); SAT 99% RA; skin color = pale Patient was offered fruit bar and water as she stated maybe she hadn''t eaten enough at breakfast. She has ever felt this way after attempting to watch a medical procedure on a family member. 10:33 patient sitting up, advised she was feeling better. Repeat B/P 71/43 Patient started to feel lightheaded again and laid back down. Patient was continuously monitored, at 10:46 vitals returned to patients'' normal range of B/P 98/64 ; HR 75; SAT 100% RA for 10+ minutes. Patient was up and walking around at the clinic and advised she was feeling back to normal. Patient advised if anything changed to seek medical attention. |
|
| VAERS ID: |
2483063 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-19 |
| Onset: | 2022-10-01 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
346354 / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Syringe issue SMQs:, Medication errors (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: n/a Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: when I went to administer the vaccine, the needle malfunctioned and the vaccine leaked down her arm completely. Pt said she did not feel any was injected, I agreed. We discussed and bc she is low risk and only 67 we decided to administer regular flu instead of senior in case any got in to her system. Pt is fine, this is just a formality b/c of the needle malfunction. |
|
| VAERS ID: |
2485636 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-20 |
| Onset: | 2022-10-21 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
QFAA2225 / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Vaccination site erythema,
Vaccination site induration,
Vaccination site paraesthesia SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: patient had a red, tingling hard portion on her arm below the vaccination site. she saw her doctor and they deemed it a normal reaction for a robust immune system |
|
| VAERS ID: |
2488472 (history) |
| Form: |
Version 2.0 |
| Age: |
59.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-24 |
| Onset: | 2022-10-24 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-10-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9702 / 1 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
T9HA2 / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness,
Fatigue SMQs:, Anticholinergic syndrome (broad), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Has experienced dizziness with past vaccines and other procedures involving needles Other Medications: unknown Current Illness: Preexisting Conditions: none reported Allergies: none reported Diagnostic Lab Data: none CDC Split Type:
Write-up: Within 2 minutes of second vaccine (Fluarix) patient asked if she could sit on the floor stating "This sometimes happens to me with needles, I feel dizzy and need to sit" Immediately provided a space to sit on floor and assisted her to sit. She then laid down flat and was monitored for 5 minutes. No s/s of distress noted. After 5 minutes she was allowed to sit for 5 minutes at which time she stated "I feel much better", allowed to stand to determine if dizziness would return and monitored for an additional 15 mins while seated in a chair. Encourage to drink fluids and call provider if any further symptoms of concern. Was able to walk from clinic with no return of symptoms. Called patient on 10/26/22 to assess needs. States she was "a little tired last evening" but feels "fine" today. Denies any return of dizziness. Encourage to drink fluids and call provider if any further symptoms of concern. |
|
| VAERS ID: |
2497804 (history) |
| Form: |
Version 2.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-01 |
| Onset: | 2022-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UT7733AA / UNK |
RA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Extra dose administered,
Pain in extremity SMQs:, Tendinopathies and ligament disorders (broad), Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient requested a flu vaccination and the vaccine checklist was completed with the patient prior to administration. After the vaccinator had administered the influenza vaccine the patient then informed her that she remembered she had already received one. Patient was asked to wait at the clinic which she did for approximately 30 minutes. Staff contact the state health department for any further instruction. Patient was informed that she may have an increased likelihood of symptoms and if so to contact us with any concerns. Patient said she felt fine and left on her own accord. Phone follow up with patient on 11/3. Patient said did feel soreness in her arm but took tylenol and was fine. No further discomfort of symptoms. |
|
| VAERS ID: |
2497877 (history) |
| Form: |
Version 2.0 |
| Age: |
50.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-11-03 |
| Onset: | 2022-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
062F22A / 4 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7TP53 / UNK |
RA / IM |
Administered by: Unknown Purchased by: ? Symptoms: Dizziness,
Hyperhidrosis,
Pallor SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient arrived at clinic today to get a Moderna Bivalent Booster and a Flu vaccine. In between doses he startd to feel light headed and did not say anything initially. After 2nd dose (flu) he let the vaccinator know. Pt was c/o feeling lightheaded, pale and sweaty. Provided patient with PFA, water and a snack. Within just a couple of minutes he was feeling much better. Continued to monitor patient for another few minutes. |
|
| VAERS ID: |
2500630 (history) |
| Form: |
Version 2.0 |
| Age: |
38.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-02 |
| Onset: | 2022-11-02 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-07 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
GF3N2 / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Burning sensation,
Rash erythematous SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: acetaminophen (Tylenol) 325 mg Tablet albuterol 90 mcg/actuation HFA Aerosol Inhaler Current Illness: N/A Preexisting Conditions: Acute frontal sinusitis Asthma Heart palpitations Raynaud disease Allergies: NKDA Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Patient states, "I received my flu shot on Wednesday that night I noticed bumps on my left forearm. Thursday they were red and today have a slight burning sensation. It is also on the left side of my face". |
|
| VAERS ID: |
2507084 (history) |
| Form: |
Version 1.0 |
| Age: |
5.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-28 |
| Onset: | 0000-00-00 |
| Submitted: |
2022-11-01 |
| Entered: |
2022-11-07 |
| Days after submission: | 6 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 1 |
LA / - |
| DTAPIPV: DTAP + IPV (QUADRACEL) / SANOFI PASTEUR |
C6002BA / 1 |
RA / - |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U7684DA / 7+ |
LA / - |
Administered by: Private Purchased by: Public Symptoms: No adverse event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Multivitamin Current Illness: N/A Preexisting Conditions: Soy allergy Allergies: Diagnostic Lab Data: N/A CDC Split Type:
Write-up: No adverse events |
|
| VAERS ID: |
2502040 (history) |
| Form: |
Version 2.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-08 |
| Onset: | 2022-11-08 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9697 / 4 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
7TP53 / UNK |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Anxiety,
Dizziness,
Immediate post-injection reaction,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad), Hypersensitivity (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Pt came to the clinic to get her Flu & Covid Bivalent vaccines. Immediately after the administration of the 1st vaccine (Flu), pt. started to feel lightheaded and nauseous. She was transferred to a wheelchair and then to a cot to lay down. She was offered water/snack and vitals monitored. She advised she felt a bit anxious before coming in for the vaccines. Pt wanted to proceed with her 2nd vaccine (Pfizer Bivalent). That was administered at 1455 with no troubles. Pt was monitored for approximately 25 minutes after her last vaccine, and she advised she was feeling back to normal. Vitals all were within normal limits during the duration. |
|
| VAERS ID: |
2503457 (history) |
| Form: |
Version 2.0 |
| Age: |
14.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-01 |
| Onset: | 2022-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
UJ892AA / N/A |
RA / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Innocent murmur Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient received the vaccine no adverse effect has been reported |
|
| VAERS ID: |
2513004 (history) |
| Form: |
Version 2.0 |
| Age: |
10.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-21 |
| Onset: | 2022-11-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GK1657 / 3 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U7684DA / UNK |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Fall,
Immediate post-injection reaction,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Arrhythmia related investigations, signs and symptoms (broad), Accidents and injuries (narrow), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (narrow), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: None Allergies: NKA Diagnostic Lab Data: CDC Split Type:
Write-up: Patient rcv''d Bivalent Booster with no issues followed by her Flu vaccine. Immediately following she experienced a 30 second syncopal episode. She fell to the floor landing partially on her mom. PE completed with no findings, vitals were monitored and remained within normal limits, patient was provided with water and a snack. Within 5 minutes patient was feeling 100% better. |
|
| VAERS ID: |
2513024 (history) |
| Form: |
Version 2.0 |
| Age: |
26.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-11-21 |
| Onset: | 2022-11-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (NOVAVAX)) / NOVAVAX |
4302MF023 / 2 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UT7701MA / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Dizziness,
Nausea SMQs:, Acute pancreatitis (broad), Anticholinergic syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Vestibular disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: After shot was administered patient felt lightheaded and nauseated. |
|
| VAERS ID: |
2514033 (history) |
| Form: |
Version 2.0 |
| Age: |
37.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-11-22 |
| Onset: | 2022-11-22 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-11-22 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GL0446 / 3 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT7723LA / 1 |
LA / IM |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
2CA18C1 / 2 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Expired product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: none Preexisting Conditions: none Allergies: Aspirin, caffeine Diagnostic Lab Data: CDC Split Type:
Write-up: Patient was given a vaccine that expired on 11/21/2022 on 11/22/2022 due to a vial being presumed non-expired. Error was spotted post-administration. Patient did not report any adverse reactions before leaving the clinic. |
|
| VAERS ID: |
2520831 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-30 |
| Onset: | 2022-11-30 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-12-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
T9HA2 / N/A |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: No adverse event,
Product administered to patient of inappropriate age SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Individual received Fluarix Quad Influenza vaccine that is eligible for those between 6 months to 64 years old. Individual was observed for 15 minutes and did not exhibit any signs/symptoms of acute anaphylaxis. |
|
| VAERS ID: |
2528834 (history) |
| Form: |
Version 2.0 |
| Age: |
47.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-12-09 |
| Onset: | 2022-12-01 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-12-12 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
AS3401B / 2 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Extra dose administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: trazodone, paliperidone, nicotrol, benztropine Current Illness: possible intermittent asthma Preexisting Conditions: n/a Allergies: Nickel, bee sting, grapefruit juice, pollen, cats Diagnostic Lab Data: n/a CDC Split Type:
Write-up: Patient received an unintentional second dose of yearly flu vaccine, having received the other flu shot on 09/28/2022. It was not noticed until after administration when entering the second dose into the VT state IMR. No adverse effects/events reported. |
|
| VAERS ID: |
2543591 (history) |
| Form: |
Version 2.0 |
| Age: |
71.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-09-23 |
| Onset: | 2022-09-26 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2022-12-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UJ904AD / UNK |
- / SYR |
Administered by: Private Purchased by: ? Symptoms: Guillain-Barre syndrome,
Immunoglobulin therapy SMQs:, Peripheral neuropathy (narrow), Guillain-Barre syndrome (narrow), Demyelination (narrow), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 14 days
Extended hospital stay? No Previous Vaccinations: Other Medications: atorvastatin, OTC Magnesium, Zinc spray, Vit. D3, Vit. B12 Current Illness: not ill at the time of the vaccination. Preexisting Conditions: mild emphysema Allergies: only allergic to Bupropion Diagnostic Lab Data: Full dosages of Immunoglobulin Therapy CDC Split Type:
Write-up: Contracted Guillain-Barre Syndrome |
|
| VAERS ID: |
2562321 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-17 |
| Onset: | 2023-01-14 |
| Days after vaccination: | 89 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-01-18 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9693 / 4 |
AR / SYR |
| FLU4: INFLUENZA (SEASONAL) (AFLURIA QUADRIVALENT) / SEQIRUS, INC. |
346361 / N/A |
AR / SYR |
Administered by: Private Purchased by: ? Symptoms: Atrial fibrillation,
Blood test normal,
Condition aggravated SMQs:, Supraventricular tachyarrhythmias (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Other Medications: losartan; Current Illness: None Preexisting Conditions: high blood pressure Allergies: Sulfa Diagnostic Lab Data: Blood panel was taken but everything looked good. CDC Split Type: vsafe
Write-up: On the 14th of January, I had an afib attack. I have prescriptions for this and took one of each. I have had this in the past but have not had many episodes of it. I saw my doctor and I was told to take my blood pressure medication. I have not had another incident since. The issue seems to have resolved as of 01/17/2023. |
|
| VAERS ID: |
2588476 (history) |
| Form: |
Version 2.0 |
| Age: |
38.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-02-27 |
| Onset: | 2023-02-27 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-02-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6743 / 3 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT7723NA / 2 |
LA / IM |
| TDAP: TDAP (BOOSTRIX) / GLAXOSMITHKLINE BIOLOGICALS |
775YF / 1 |
RA / IM |
Administered by: Public Purchased by: ? Symptoms: Extra dose administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: NKA Diagnostic Lab Data: CDC Split Type:
Write-up: Client was given the influenza vaccine without requesting it. She had received the vaccine 5 months previous. She was told she would be unlikely to have adverse affects from the second dose and to let the health department know if she felt any negative affects. Client was satisfied with the explanation. |
|
| VAERS ID: |
2593227 (history) |
| Form: |
Version 2.0 |
| Age: |
2.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-02-27 |
| Onset: | 2023-02-27 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-03-08 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLULAVAL QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
5M2H2 / 1 |
LA / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
U007684 / 1 |
LA / SC |
| PNC13: PNEUMO (PREVNAR13) / PFIZER/WYETH |
FF7357 / 4 |
LL / IM |
| TD: TD ADSORBED (TDVAX) / MASS. PUB HLTH BIOL LAB |
A142A / 4 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/A Current Illness: N/A Preexisting Conditions: N/A Allergies: N/A Diagnostic Lab Data: N/A CDC Split Type:
Write-up: A Tetanus and Diptheria vaccine was given instead of a Vaxelius. |
|
| VAERS ID: |
2614675 (history) |
| Form: |
Version 2.0 |
| Age: |
68.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-10-07 |
| Onset: | 2023-01-26 |
| Days after vaccination: | 111 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-04-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9703 / 5 |
AR / IM |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
- / 1 |
AR / IM |
Administered by: Private Purchased by: ? Symptoms: COVID-19,
Cough,
Ear pain,
Fatigue,
Headache,
Malaise,
Oropharyngeal pain,
Productive cough,
SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: After the Shingles Vaccination, developed redness and swell under the injection site. It was warm to touch and red. It looked li Other Medications: Esomeprazole; Famotidine; Mometasone FUROATE Nasal Spray; Estradiol; Verapamil; Amitiza; Vitamin D3; Multivitamin with Iron; Tums Current Illness: N/A Preexisting Conditions: Acid Reflux; Tachycardia Allergies: Contrast Dye; Fruits with Stones; Assortment of Shellfish Diagnostic Lab Data: 26JAN2023 COVID-19 Test -Positive CDC Split Type: vsafe
Write-up: I had symptoms on the 26th and tested positive on the 27th of January. I had headache and a dry cough. When I decided to test the symptoms worsened, and tested because I had an appointment. I called my PCP and they said to use any over the counter medication for headache relief and isolate for 5 days. Basically, wait to feel better and test after 10 days. I got sicker during isolation and called a on call doctor, and we discussed taking Paxlovid and that''s what I did. I was so sick that during the five days of taking it left a terrible taste. I had more symptoms during that time as well. I had mark malaise, fatigue and a productive cough that was painful in my throat and ears. The headache was quite bad. By the time I finished the Paxlovid, in terms of symptoms they did back off a little. I feel good now. |
|
| VAERS ID: |
2616195 (history) |
| Form: |
Version 2.0 |
| Age: |
62.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-14 |
| Onset: | 2023-02-21 |
| Days after vaccination: | 130 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-04-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ3277 / 5 |
AR / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / 1 |
AR / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: COVID-19,
Chills,
Cough,
Ear discomfort,
Hyperhidrosis,
Impaired work ability,
Insomnia,
Nasal congestion,
Rhinorrhoea,
SARS-CoV-2 test positive,
Throat irritation,
Vomiting SMQs:, Anaphylactic reaction (broad), Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hypoglycaemia (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Omeprazole; Folic Acid; Methotrexate; Vitamin D; Fish Oil; Baby Aspirin Current Illness: No Preexisting Conditions: Arthritis Allergies: Atropine; Ampicillin; Sulfa Diagnostic Lab Data: 21FEB2023 Home COVID2023 - positive CDC Split Type: vsafe
Write-up: I had a stuffy nose that eventually led to a cough. On Tuesday night I threw up, I couldn''t sleep, I had chills, sweating. On Wednesday, I was blowing my nose constantly, I had to fly home, could not get my ears to pop open, I did not go work on Thursday. I took a home COVID-19 test that came back positive. I was taking over the medication, everything seemed to be going away, then the cough came back with a vengeance. I was coughing so hard it was giving me a headache. I tried talking to my doctor, but he was running late, I talked to his nurse who suggested I try Mucinex DM. I took two full bottles. I am still coughing because of a lingering tickle in my throat. |
|
| VAERS ID: |
2620788 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2022-10-17 |
| Onset: | 2023-02-01 |
| Days after vaccination: | 107 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-04-25 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GJ6739 / 5 |
AR / IM |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
Administered by: Private Purchased by: ? Symptoms: Arrhythmia,
Blood test normal,
Cardiac monitoring abnormal,
Chest X-ray normal,
Electrocardiogram normal,
Laboratory test normal,
Palpitations SMQs:, Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Cardiac arrhythmia terms, nonspecific (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: Shingles I had fever, body aches and chills Other Medications: Omeprazole ; Baby Aspirin ; Iron Supplement; Atorvastatin ; Losartan ; Magnesium; Vitamin D Current Illness: N/A Preexisting Conditions: Coronary Artery Disease since 2015 Allergies: N/A Diagnostic Lab Data: Bloodwork, EKG ; Chest X-ray - Nothing CDC Split Type: vsafe
Write-up: I heart palpitations on and off. I went to the ER and they took a whole bunch of test and nothing came up. I wore heart monitor and nothing came up except for heart arrhythmia. I don''t have the date of the tests . I still have heart palutations. I had the flu vaccine on the other other but I cannot remember which arm. |
|
| VAERS ID: |
2629095 (history) |
| Form: |
Version 2.0 |
| Age: |
43.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2022-11-01 |
| Onset: | 2023-05-01 |
| Days after vaccination: | 181 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-05-09 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
GH9693 / 4 |
LA / IM |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: COVID-19,
Cough,
Discharge,
Fatigue,
Oropharyngeal pain,
Pain,
Pyrexia,
Respiratory tract congestion,
SARS-CoV-2 test positive SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Opportunistic infections (broad), COVID-19 (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Hydrochlorothiazide; Sertraline; Zyrtec; Valsartan; Colace; Mucinex D; Melatonin; Potassium; Turmeric; Vitamin C; Pepcid; Meloxicam Current Illness: N/A Preexisting Conditions: Chronic Fatigue; Psoriasis; Hashimoto''s Allergies: Seasonal Allergies Diagnostic Lab Data: 01MAY2023 COVID-19 Test -Positive CDC Split Type: vsafe
Write-up: I tested positive for COVID-19 5/1/23. I had fatigue, body aches, sore throat, congestion, drainage, low grade fever, and a cough. I contacted my doctor and was not prescribed medication, but the nurse suggested that I take a full dose of Mucinex D. I am still dealing with congestion, fatigue, and a cough. |
|
| VAERS ID: |
2684450 (history) |
| Form: |
Version 2.0 |
| Age: |
87.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-09-19 |
| Onset: | 2023-09-20 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-09-21 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
U8084BA / UNK |
- / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Asthenia,
Blood glucose normal,
Chills,
Constipation,
Decreased appetite,
Feeling abnormal SMQs:, Dementia (broad), Guillain-Barre syndrome (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: diabetes hypertension Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient called 9/20/23 around noontime to inform us that she woke up feeling funny this morning. She stated having no appetite, being constipated, and experiencing chills. She did not take her temp so unsure if she had a fever. She did check her blood glucose before eating anything and it was 177. Patient is not experiencing any pain at site of injection. She reported feeling better at the time when she called but still just weak and no appetite. Patient stated she has not had this type of response to vaccines in the past. After she got off the phone with me she was going to also call her PCP office to inform them as well. |
|
| VAERS ID: |
2688277 (history) |
| Form: |
Version 2.0 |
| Age: |
55.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-09-21 |
| Onset: | 2023-09-21 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-09-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
U8058AA / 1 |
RA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Chest pain,
Dizziness,
Electrocardiogram normal,
Feeling abnormal,
Laboratory test normal,
Pain in extremity SMQs:, Anticholinergic syndrome (broad), Dementia (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, ? days
Extended hospital stay? No Previous Vaccinations: Other Medications: gabapentin, amlodipine, omeprazole, simvastatin, Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: after getting flublok, patient did not feel good, chest pain and arm pain , dizziness so he went to ER that night. They did ECG and other tests but all came normal. |
|
| VAERS ID: |
2689160 (history) |
| Form: |
Version 2.0 |
| Age: |
77.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-09-24 |
| Onset: | 2023-09-24 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
VT8094BA / 1 |
LA / IM |
Administered by: Public Purchased by: ? Symptoms: Injection site pain,
Musculoskeletal chest pain,
Neck pain,
Pain,
Pain in extremity SMQs:, Extravasation events (injections, infusions and implants) (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Alfuzosin, atorvastatin, bupropion, buspirone, AREDS, (ketorolac, prednisolone, moxifloxiicin opthamalmic drops),Metoprolol Current Illness: s/p cataract surgery 9/18/2023 Preexisting Conditions: anxiety, high cholesterol, aortic stenosis s/p TAVR (metoprolol is for this not HTN), prostate enlargemntt Allergies: None Diagnostic Lab Data: None CDC Split Type:
Write-up: extreme pain in L shoulder about 15 min after injection radiating to neck and then down arm to fingers and in ribs, , causing patient too think he might be having a heart attack. symptoms passed gradually within 20 minutes with some additional aching pain in legs that was milder and faded gradually |
|
| VAERS ID: |
2689800 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-09-21 |
| Onset: | 2023-09-01 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
| UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / 3 |
- / - |
Administered by: Other Purchased by: ? Symptoms: Chills,
Pyrexia,
Rash SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Comments: No Medical History information was reported. Patient had no known allergies. Allergies: Diagnostic Lab Data: Test Name: Fever; Result Unstructured Data: as high 101.0 CDC Split Type: USMODERNATX, INC.MOD20237
Write-up: Rash; fevers; chills; This spontaneous case was reported by a consumer and describes the occurrence of RASH (Rash), PYREXIA (fevers) and CHILLS (chills) in a 67-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) for COVID-19 prophylaxis. Co-suspect product included non-company product INFLUENZA VACCINE for an unknown indication. No Medical History information was reported. Patient had no known allergies. On 21-Sep-2023, the patient received third dose of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE (unknown route) 1 dosage form. In September 2023, the patient experienced RASH (Rash), PYREXIA (fevers) and CHILLS (chills). The patient was treated with ASPIRIN [ACETYLSALICYLIC ACID] for Rash, Fever and Chills, at an unspecified dose and frequency. On 25-Sep-2023, RASH (Rash) had resolved. At the time of the report, PYREXIA (fevers) and CHILLS (chills) was resolving. DIAGNOSTIC RESULTS (normal ranges are provided in parenthesis if available): On an unknown date, Body temperature: as high 101.0. For mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (Unknown), the reporter did not provide any causality assessments. No concomitant medication was reported. The patient did not receive any other vaccines in the 4 weeks prior to COVID-19 vaccine. Patient reported side effects such as rash and fevers for about 2-3 days and chills. Rash had cleared, and the fever seems to be going away. Fevers were as high 101.0. Patient reported that she was taking Aspirin for the symptoms. |
|
| VAERS ID: |
2694010 (history) |
| Form: |
Version 2.0 |
| Age: |
65.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-10-05 |
| Onset: | 2023-10-05 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / UNK |
- / - |
Administered by: Pharmacy Purchased by: ? Symptoms: Arthralgia,
Chills,
Dizziness,
Fatigue,
Palpitations,
Pyrexia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Cardiomyopathy (broad), Vestibular disorders (broad), Arthritis (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: No Preexisting Conditions: Allergies: No Diagnostic Lab Data: CDC Split Type:
Write-up: Chills, fever, severe joint pain, heart palpitation, fatigue, dizziness |
|
| VAERS ID: |
2695828 (history) |
| Form: |
Version 2.0 |
| Age: |
42.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-10-13 |
| Onset: | 2023-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT804MA / UNK |
RA / - |
| TDAP: TDAP (ADACEL) / SANOFI PASTEUR |
2CA56C1 / UNK |
LA / - |
Administered by: Private Purchased by: ? Symptoms: Unevaluable event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/A- prescribed Advair Diskus after 10/13/23 visit. Current Illness: N/A Preexisting Conditions: Presumed asthma. Allergies: Penicillin. Diagnostic Lab Data: N/A CDC Split Type:
Write-up: N/A |
|
| VAERS ID: |
2698686 (history) |
| Form: |
Version 2.0 |
| Age: |
57.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-10-09 |
| Onset: | 2023-10-01 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-19 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUX: INFLUENZA (SEASONAL) (NO BRAND NAME) / UNKNOWN MANUFACTURER |
- / UNK |
- / - |
| UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER |
3030535 / UNK |
- / - |
Administered by: Other Purchased by: ? Symptoms: Dizziness,
Erythema,
Headache,
Nasopharyngitis,
Peripheral swelling,
Pruritus,
Syncope SMQs:, Torsade de pointes/QT prolongation (broad), Cardiac failure (broad), Anaphylactic reaction (broad), Angioedema (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), Hypotonic-hyporesponsive episode (broad), Hypersensitivity (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USMODERNATX, INC.MOD20237
Write-up: Faint; Dizzy/ Lightheaded like a balloon/ / Feeling like she was going to fall over; headache; swelling on her arm; redness; itchiness; cold; This spontaneous case was reported by a consumer and describes the occurrence of SYNCOPE (Faint) in a 57-year-old female patient who received mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (batch no. 3030535) for COVID-19 prophylaxis. The occurrence of additional non-serious events is detailed below. Co-suspect product included non-company product INFLUENZA VACCINE (FLU VACCINE VII) for an unknown indication. No Medical History information was reported. On 09-Oct-2023, the patient received dose of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (unknown route) 1 dosage form and dose of INFLUENZA VACCINE (FLU VACCINE VII) (unknown route) 1 dosage form. On 10-Oct-2023, the patient experienced SYNCOPE (Faint) (seriousness criterion medically significant) and DIZZINESS (Dizzy/ Lightheaded like a balloon/ / Feeling like she was going to fall over). In October 2023, the patient experienced PERIPHERAL SWELLING (swelling on her arm), ERYTHEMA (redness), PRURITUS (itchiness), NASOPHARYNGITIS (cold) and HEADACHE (headache). The patient was treated with PARACETAMOL (TYLENOL) at an unspecified dose and frequency. At the time of the report, SYNCOPE (Faint), PERIPHERAL SWELLING (swelling on her arm), ERYTHEMA (redness), PRURITUS (itchiness), NASOPHARYNGITIS (cold), DIZZINESS (Dizzy/ Lightheaded like a balloon/ / Feeling like she was going to fall over) and HEADACHE (headache) outcome was unknown. For mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) (Unknown), the reporter did not provide any causality assessments. No concomitant drug was reported. Halfway through the night after receiving the most recent dose of the vaccine she felt dizzy, lightheaded like a balloon, and faint. She went to work, where she felt she got worse. Feeling like she was going to fall over, was dizzy, cold, and had a headache. She also had some swelling on her arm, itchiness, and redness. She called her doctor who recommended ice on her arm, Tylenol, rest, and drinking lots of fluids. She had attempted these treatments. Company comment: This spontaneous case concerns a 57-year-old female patient, with no medical history reported, who experienced the unexpected and serious (medically significant) event of SYNCOPE, halfway through the night after receiving an unspecified dose of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) vaccine, among other non-serious events. Vaccination with influenza vaccine on the same day remains as a confounder for the event. She took paracetamol, rest, and drank fluids as treatment. No further clinical information was available for medical review. She reported having received previous doses of the COVID-19 vaccines without any specifications. The benefit-risk relationship of mRNA-1273.815 (SPIKEVAX 2023-2024 PFS) vaccine is not affected by this report. This case was linked to US-MODERNATX, INC.-MOD-2023-745400 (E2B Linked Report).; Sender''s Comments: US-MODERNATX, INC.-MOD-2023-745400:Spikevax NOS case (Same patient) |
|
| VAERS ID: |
2702316 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 2023-10-13 |
| Onset: | 2023-10-13 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT8040JA / UNK |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Medication error,
No adverse event,
Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2023SA321509
Write-up: Pre-filled syringes were placed in the cooler, reported a temperature below 0?C, Human error: Yes Duration of excursion: 1 hour with no reported adverse event; products been administered post excursion patients with no reported adverse event; Initial information received on 18-Oct-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves 86 patients of unknown age and demographics who were administered Influenza Quadrival A-B vaccine [FLUZONE QUADRIVALENT] post excursion where pre-filled syringes were placed in the cooler, reported a temperature below 0?c, human error: yes duration of excursion: 1 hour with no reported adverse event. The patient''s past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 13-Oct-2023, the patients received an unknown dose of suspect Influenza Quadrival A-B vaccine Suspension for injection of lot UT8040JA and expiry: 30-Jun-2024 via unknown route in unknown administration site for immunization. On an unknown date, it was reported that the pre-filled syringes of Influenza Quadrival A-B vaccine were placed in the cooler, reported a temperature below 0?C, human error: yes duration of excursion: 1 hour with no reported adverse event (product storage error) (unknown latency). On 13-Oct-2023, the patient had been administered Influenza Quadrival A-B vaccine post excursion patients with no reported adverse event (poor quality product administered) (latency: same day). No lab data was reported. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
2703742 (history) |
| Form: |
Version 2.0 |
| Age: |
75.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-10-26 |
| Onset: | 2023-10-27 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-27 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
U8084AB / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Injection site erythema,
Injection site induration,
Injection site swelling,
Injection site warmth SMQs:, Extravasation events (injections, infusions and implants) (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: UNKNOWN. CONFIRMED NO BLOOD THINNERS Current Illness: NONE STATED Preexisting Conditions: NONE STATED Allergies: NO KNOWN ALLERGIES Diagnostic Lab Data: CDC Split Type:
Write-up: PATIENT REPORTED BACK TO PHARMACY THE DAY AFTER VACCINATION AT ~11AM. PATIENTS LEFT UPPER ARM WAS VERY SWOLLEN AND RED FROM THE DELTOID TO THE ELBOW. DOES NOT REPORT PAIN. PATIENT STATES HARDNESS AND WARMNESS IN THE AREA. RECOMMENDED THE PATIENT REPORT TO URGENT CARE OR EMERGENCY ROOM FOR EVALUATION. RECOMMENDED ICING THE AREA IN THE MEANTIME TO REDUCE SWELLING. PATIENT STATES SHE MAY NOT BE ABLE TO SEEK MEDICAL EVALUATION DUE TO TAKING CARE OF A FAMILY MEMBER AT HOME. |
|
| VAERS ID: |
2705189 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU3: INFLUENZA (SEASONAL) (FLUARIX) / GLAXOSMITHKLINE BIOLOGICALS |
UT8040JA / UNK |
- / - |
Administered by: Unknown Purchased by: ? Symptoms: Product storage error SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USGSKUS2023144359
Write-up: Fluarix exposed to below 0 C; This non-serious case was reported by a other health professional via call center representative and described the occurrence of incorrect storage of drug in an unspecified number of patients who received Flu Seasonal TIV Dresden (Fluarix) (batch number UT8040JA, expiry date 30-JUN-2024) for prophylaxis. On an unknown date, the patient received Fluarix. On an unknown date, an unknown time after receiving Fluarix, the patient experienced incorrect storage of drug (Verbatim: Fluarix exposed to below 0 C). The outcome of the incorrect storage of drug was unknown. Additional Information: GSK receipt date: 18-Oct-2023 The reporter mentioned that it might be a sanofi vaccine. The reporter did not see in the batch. Documenting just in case. Consented to follow up via email. Fluarix exposed to below 0 C and was administered to over 86 people at a flu clinic, which led to incorrect storage of drug. |
|
| VAERS ID: |
2705295 (history) |
| Form: |
Version 2.0 |
| Age: |
|
| Sex: |
Unknown |
| Location: |
Vermont |
| Vaccinated: | 0000-00-00 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-10-28 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
- / 1 |
- / OT |
Administered by: Unknown Purchased by: ? Symptoms: Incorrect dose administered,
No adverse event SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type: USSA2023SA326751
Write-up: Fluzone quadrivalent dose was given a patient after not being viable/it was not supported by extended stability information post excursion and vaccine was given to patient with no adverse event; not supported by the extended stability information post excursion with no reported adverse event; Initial information received on 19-Oct-2023 regarding an unsolicited valid non-serious case received from a nurse. This case involves a patient of an unknown age and gender and nurse reported that the Influenza Quadrival A-B Vaccine [Fluzone Quadrivalent] dose was given a patient after not being viable/it was not supported by extended stability information post excursion with no reported adverse event. On an unknown date, the patient received a unknown (dose 1) dose of suspect Influenza Quadrival A-B Vaccine Suspension for injection (strength, expiry date and lot number not reported) via unknown route in unknown administration site as Immunization and dose was given a patient after not being viable/it was not supported by extended stability information post excursion with no adverse event (poor quality product administered) (same day latency); (product storage error) (unknown latency). Information on the batch number was requested. Action taken: not applicable. At time of reporting, the outcome was Unknown for the events. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder''s compliance with the requirements set out in the Directive and Regulatory Authority Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error. |
|
| VAERS ID: |
2708158 (history) |
| Form: |
Version 2.0 |
| Age: |
63.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-11-01 |
| Onset: | 2023-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-11-01 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
U8233AA / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Product administered to patient of inappropriate age SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Patient received a high dose flu vaccine |
|
| VAERS ID: |
2709700 (history) |
| Form: |
Version 2.0 |
| Age: |
6.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-11-03 |
| Onset: | 2023-11-03 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-11-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
HH3252 / 5 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U8230CA / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Underdose,
Wrong patient SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: None Current Illness: None Preexisting Conditions: Juvenile Plantar dermatosis Allergies: None Diagnostic Lab Data: N/A CDC Split Type:
Write-up: Patient and his younger brother were in office for Flu and Covid vaccines. I was assisting a newer M.A. in drawing up/administering. Discussed vaccinating different ages and encouraged drawing separate trays and labeling each with name/age as with Covid vaccine. We prepared two separate trays each labeled for the boys with their separate ages, 5-11 (Patient) and brother (6m-<5yrs.) Brother was going to go first, then did not want to. Brother was crying. Patient said he would go first. I had Brother''s tray and administered the Flu and YOUNG CHILD Covid to Patient who should have gotten the 5-11 dose. I realized my error immediately afterwards as having grabbed the wrong tray. We took a time out, I explained my error to co-worker. I had staff re-draw the 6m-<5yr dose, verified, and we went back in. I apologized to mom and explained what had happened, that Patient got the dose intended for a younger child. Told mom that I will find out from Health Dept. what to do. Mom expressed understanding and will wait to hear what is recommended. Staff administered the imms to Brother with the correct dosing. I apologized to mom again. |
|
| VAERS ID: |
2710314 (history) |
| Form: |
Version 2.0 |
| Age: |
73.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-10-31 |
| Onset: | 2023-11-01 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-11-06 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUA4: INFLUENZA (SEASONAL) (FLUAD QUADRIVALENT) / SEQIRUS, INC. |
- / UNK |
- / - |
Administered by: Other Purchased by: ? Symptoms: Dyspepsia SMQs:, Gastrointestinal nonspecific dysfunction (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: none Current Illness: Preexisting Conditions: none known Allergies: none Diagnostic Lab Data: none CDC Split Type:
Write-up: patient claims to have self diagnosed pancreatitis after developing a burning sensation in her stomach. diagnosed via online research. |
|
| VAERS ID: |
2719006 (history) |
| Form: |
Version 2.0 |
| Age: |
1.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-11-01 |
| Onset: | 2023-11-01 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-11-29 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U8041DA / 1 |
RL / IM |
| HEPA: HEP A (HAVRIX) / GLAXOSMITHKLINE BIOLOGICALS |
Y3ME2 / 1 |
LL / IM |
| MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. |
W019422 / 1 |
LL / IM |
| UNK: VACCINE NOT SPECIFIED (OTHER) / UNKNOWN MANUFACTURER |
X019438 / 3 |
LL / IM |
| VARCEL: VARICELLA (VARIVAX) / MERCK & CO. INC. |
X006982 / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Inappropriate schedule of product administration SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Ferrous Sulfate Luride Current Illness: none Preexisting Conditions: Iron-deficiency anemia Allergies: NKA Diagnostic Lab Data: none CDC Split Type:
Write-up: none noted |
|
| VAERS ID: |
2719542 (history) |
| Form: |
Version 2.0 |
| Age: |
67.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-11-16 |
| Onset: | 0000-00-00 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-11-30 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH |
HG7557 / 5 |
RA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE HIGH-DOSE QUADRIVALENT) / SANOFI PASTEUR |
UT8BA131 / 7+ |
RA / IM |
| PNC20: PNEUMO (PREVNAR20) / PFIZER/WYETH |
GW7964 / UNK |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: No adverse event SMQs:
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: estradiol magnesium oxide Multivitamin 50 Plus propranolol Relpax Vitamin B-2 Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: PCP and Pt made aware. No ill effects Noted. |
|
| VAERS ID: |
2722841 (history) |
| Form: |
Version 2.0 |
| Age: |
24.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2023-12-11 |
| Onset: | 2023-12-11 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-12-11 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
3031632 / 1 |
LA / IM |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
U8058AA / UNK |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Dyspnoea,
Hypoaesthesia,
Loss of consciousness,
Malaise,
Mydriasis,
Pallor SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (broad), Peripheral neuropathy (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypoglycaemia (broad), Sexual dysfunction (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? No
Previous Vaccinations: when he woke up he stated that he had to sit down while at restaurant the last time he got a covid vaccine, no mention of this o Other Medications: Vitamin D Current Illness: unknown Preexisting Conditions: unknown Allergies: n/a Diagnostic Lab Data: CDC Split Type:
Write-up: Approx 7 to 10 min after vaccination I was alerted by someone waiting for their vaccine that patient wasn''t doing well. I went out to see and he looked pale. He was having a hard time breathing, told me his arms felt numb. His pupils were dilated. He was sitting on the floor when I got out there. I immediately tried to get him to lie down and put his feet up on a chair. He passed out, I told Tech to call 911 and I went into phcy to get EpiPen. When I returned he was awake and wondered what had happened. EMTs arrived within 10 minutes, took my version of events and took over. They eventually transported him to the ED |
|
| VAERS ID: |
2726722 (history) |
| Form: |
Version 2.0 |
| Age: |
1.67 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-11-27 |
| Onset: | 2023-11-30 |
| Days after vaccination: | 3 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-12-13 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
U8203GA / 3 |
LL / IM |
Administered by: Private Purchased by: ? Symptoms: Activated partial thromboplastin time,
C-reactive protein,
Ear infection,
Full blood count,
Gait disturbance,
Henoch-Schonlein purpura,
International normalised ratio,
Metabolic function test,
Pain,
Prothrombin time,
Rash,
Red blood cell sedimentation rate,
Urine analysis SMQs:, Anaphylactic reaction (broad), Peripheral neuropathy (broad), Haemorrhage terms (excl laboratory terms) (narrow), Anticholinergic syndrome (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Vasculitis (narrow), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Immune-mediated/autoimmune disorders (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: prescribed Amoxicillin for ear infection at visit on 11/30/22 then dx. with HSP Tylenol Ibuprofen Current Illness: none Preexisting Conditions: none Allergies: NKDA Diagnostic Lab Data: PT, INR, PTT, CMP, CBC done on 11/30/23 UA & BP in office on 12/7/23 ESR, CRP UA in office 12/1/23 CDC Split Type:
Write-up: Mom chatted with our triage nurse on 11/30/23 that starting on Tuesday 11/28 she was having pain and would not walk. Developed a rash on 11/29 on lower abdomen, back & legs. Triage nurse recommended an appt and they were seen on 11/30/23 and they were dx with purpura Henoch (Schonlein) HSP (D69.0) & ear infection. |
|
| VAERS ID: |
2724395 (history) |
| Form: |
Version 2.0 |
| Age: |
40.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-12-12 |
| Onset: | 2023-12-14 |
| Days after vaccination: | 2 |
| Submitted: |
0000-00-00 |
| Entered: |
2023-12-15 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (PFIZER-BIONTECH BIVALENT)) / PFIZER/BIONTECH |
- / 1 |
LA / IM |
| FLU4: INFLUENZA (SEASONAL) (FLUARIX QUADRIVALENT) / GLAXOSMITHKLINE BIOLOGICALS |
- / 1 |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Oedema peripheral SMQs:, Cardiac failure (broad), Angioedema (broad), Haemodynamic oedema, effusions and fluid overload (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Wellbutrin, methylphenidate, omeprazole, NAC Current Illness: none Preexisting Conditions: hyperlipidemia, GERD, ADD Allergies: amoxicillin, penicillin Diagnostic Lab Data: none CDC Split Type:
Write-up: Swelling in left armpit that extends to rib area. |
|
| VAERS ID: |
2729580 (history) |
| Form: |
Version 2.0 |
| Age: |
19.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-12-20 |
| Onset: | 2023-12-20 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2024-01-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
3031416 / 5 |
LA / IM |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
944451 / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Blister,
Blister infected,
Blister rupture,
Immediate post-injection reaction,
Vaccination site rash SMQs:, Severe cutaneous adverse reactions (broad), Hypersensitivity (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: gabapentin, escitalopram, epi pen (PRN allergic reaction) Current Illness: n/a Preexisting Conditions: CRPS, PNES Allergies: cephalosporins, tree nuts Diagnostic Lab Data: CDC Split Type:
Write-up: vaccination area had immediate rash. Blister appeared appx 3 days after date of vaccine. Blister popped c. 12/30/2023 and becameinfected- today is the worst that the infection has been. Primary care has not given any antibiotics as of this reporting |
|
| VAERS ID: |
2739090 (history) |
| Form: |
Version 2.0 |
| Age: |
33.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2023-10-17 |
| Onset: | 2023-10-18 |
| Days after vaccination: | 1 |
| Submitted: |
0000-00-00 |
| Entered: |
2024-01-24 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19-2: COVID19 (COVID19 (MODERNA BIVALENT)) / MODERNA |
AU3835D / 1 |
LA / IM |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
U8058AA / 1 |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Brain fog,
Dizziness,
Fatigue,
Headache,
Tachycardia SMQs:, Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Noninfectious encephalopathy/delirium (broad), Vestibular disorders (broad), Dehydration (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Sertraline 50mg, Progesterone 200mg, Vitamin D, Omega 3, Vitamin B Complex Current Illness: None Preexisting Conditions: Endometriosis, psoriasis Allergies: None Diagnostic Lab Data: CDC Split Type:
Write-up: Symptoms of ME/CFS and/or POTS - dizziness, fatigue, headaches, brain fog, postural tachycardia - all in varying intensities and duration each day. |
|
| VAERS ID: |
2749416 (history) |
| Form: |
Version 2.0 |
| Age: |
62.0 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2021-02-01 |
| Onset: | 2021-02-05 |
| Days after vaccination: | 4 |
| Submitted: |
0000-00-00 |
| Entered: |
2024-02-26 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA |
013L20A / 2 |
LA / IM |
| FLUR4: INFLUENZA (SEASONAL) (FLUBLOK QUADRIVALENT) / PROTEIN SCIENCES CORPORATION |
- / N/A |
LA / IM |
Administered by: Private Purchased by: ? Symptoms: Back pain,
Chest pain,
Fatigue,
Oedema peripheral,
Pain,
Pain in extremity SMQs:, Cardiac failure (broad), Angioedema (broad), Retroperitoneal fibrosis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (broad), Haemodynamic oedema, effusions and fluid overload (narrow), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No Office Visit? Yes
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Naltrexone 4,5mg daily, aspirin 81mg daily, vitamin c, d, b complex, Ketamine troche 10mg prn Current Illness: Complex Regional Pain Syndrome Preexisting Conditions: Complex Regional Pain Syndrome Allergies: plavix, prednisone, sls Diagnostic Lab Data: none CDC Split Type:
Write-up: After second Covid had left arm pain, armpit swelling and fatigue that continue to the present. The fatigue after the Covid began to resolve in September 2021, but returned after the seasonal flu vaccine that was mandatory for work. Since the flu vaccine the symptoms are left arm pain that goes to my back or chest or down my arm at times. Continues intermittent swelling in armpit. Have times hurts to lay on my left arm or raise it. Have continued severe fatigue since these two vaccines. |
|
| VAERS ID: |
2764936 (history) |
| Form: |
Version 2.0 |
| Age: |
0.33 |
| Sex: |
Female |
| Location: |
Vermont |
| Vaccinated: | 2024-05-02 |
| Onset: | 2024-05-02 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2024-05-03 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLU4: INFLUENZA (SEASONAL) (FLUZONE QUADRIVALENT) / SANOFI PASTEUR |
UT8055LA / 1 |
RL / IM |
Administered by: Private Purchased by: ? Symptoms: Wrong product administered SMQs:, Medication errors (narrow)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: N/a Current Illness: None Preexisting Conditions: None Allergies: none Diagnostic Lab Data: None necessary CDC Split Type:
Write-up: Patient inadvertently given Influenza rather than PCV 20 |
|
| VAERS ID: |
2774213 (history) |
| Form: |
Version 2.0 |
| Age: |
18.0 |
| Sex: |
Male |
| Location: |
Vermont |
| Vaccinated: | 2024-01-30 |
| Onset: | 2024-01-30 |
| Days after vaccination: | 0 |
| Submitted: |
0000-00-00 |
| Entered: |
2024-06-17 |
| Vaccination / Manufacturer |
Lot / Dose |
Site / Route |
| FLUC4: INFLUENZA (SEASONAL) (FLUCELVAX QUADRIVALENT) / SEQIRUS, INC. |
374410 / N/A |
LA / IM |
Administered by: Pharmacy Purchased by: ? Symptoms: Rash SMQs:, Anaphylactic reaction (broad), Hypersensitivity (narrow), Drug reaction with eosinophilia and systemic symptoms syndrome (broad)
Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations: Other Medications: Current Illness: Preexisting Conditions: Allergies: Diagnostic Lab Data: CDC Split Type:
Write-up: Systemic: Allergic: Rash Generalized-Mild, Other Vaccines: VaccineTypeBrand: Pfizer 2023-24 12 yr+ syringe (comirtnaty); Manufacturer: Pfizer; LotNumber: hn0478; Route: intramuscular; BodySite: left deltoid; Dose: ; VaxDate: 01/30/2024 |
|