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From the 6/11/2021 release of VAERS data:

Found 29,871 cases where Vaccine targets COVID-19 (COVID19) and Serious



Case Details

This is page 12 out of 2,988

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VAERS ID: 910649 (history)  
Form: Version 2.0  
Age: 36.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2020-12-17
Onset:2020-12-17
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK5730 / UNK LA / -

Administered by: Unknown       Purchased by: ?
Symptoms: Blood pressure increased, Dizziness, Dyspnoea, Headache, Hypertension, Malaise, Nervousness, Pyrexia
SMQs:, Anaphylactic reaction (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Hypertension (narrow), Cardiomyopathy (broad), Vestibular disorders (broad), 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? Yes
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 202012; Test Name: blood pressure; Result Unstructured Data: Test Result:It was 160''s over 105; Test Date: 202012; Test Name: blood pressure; Result Unstructured Data: Test Result:not come down/ still really high; Test Date: 20201218; Test Name: blood pressure; Result Unstructured Data: Test Result:Her blood pressure was high; Test Date: 20201219; Test Name: blood pressure; Result Unstructured Data: Test Result:138/90; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:156/100; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:her blood pressure was up; Test Date: 20201220; Test Name: blood pressure; Result Unstructured Data: Test Result:had been high all day; Test Date: 20201218; Test Name: Body temperature; Result Unstructured Data: Test Result:low grade fever; Comments: night; Test Date: 202012; Test Name: heart rate; Result Unstructured Data: Test Result:in the low 100''s, around 105; Test Date: 20201218; Test Name: heart rate; Result Unstructured Data: Test Result:in the 100''s
CDC Split Type: USPFIZER INC2020510499

Write-up: low grade fever; Her blood pressure was high/ still really high/ blood pressure was up; headache; Fifteen to twenty minutes after she received the vaccine she became light headed and dizzy/ light headedness and dizziness; This is a spontaneous report from a contactable nurse (patient). A 36-year-old female patient received BNT162B2 (Lot#: EK5730) via an unspecified route of administration on 17Dec2020 afternoon at single dose in the left arm for COVID-19 immunization. Caller was unable to confirm the manufacturer of the vaccine that she received. It is not written on the card, and she didn''t see the vial. The patient medical history was not reported. Concomitant medications included oral contraception pill, but the name was unknown. Fifteen to twenty minutes after she received the vaccine on 17Dec2020 she became light headed and dizzy. She had to catch her breath. She couldn''t shake it off. The light headedness and dizziness lasted at that intensity for 10 minutes, but it never went away. They encouraged her to be admitted in the emergency room (ER). She would say that the seriousness of being light headed and dizzy was disabling. Caller didn''t remember the exact numbers for her blood pressure. It was 160''s over 105. Her heart rate was in the low 100''s, around 105. She stayed at the first monitoring station in the vaccine area for 2 hours. They were taking her blood pressure every five minutes. She was given diphenhydramine hydrochloride (BENADRYL) there and lots of water. After 3 hours and she was not improving they called a "code medic" that got the medical director and nursing supervisor to come. They encouraged her to go to the ER for continual monitoring. She stayed in the ER for4 hours and was given meds to help with the blood pressure. She was discharged from the ER home. She was nervous because of all this stemming from the vaccine. She had a low grade fever on 18Dec2020 (Friday) night. Caller stated her work had already reported her reaction. Occupational safety and the medical director are aware. Caller does not have reference number to provide. On 18Dec2020 (Friday) she was not overly concerned because it was the next day. Her blood pressure was high and her heart rate was in the 100''s. They monitored her for a couple of hours and she was given a diphenhydramine hydrochloride (BENADRYL). She went to the emergency room (ER) for a few more hours and received additional treatment. They sent her home to be monitored at home. She has been taking her blood pressure every day since and it had not come down. It was still really high. She called her primary care doctor. He was wanting her to start blood pressure for medication it. She was concerned about starting it with the assumption that it was related to the vaccine. She would like to know the right thing to do. It seems safe to take the medicine, but it was unknown that whether it was going to mask the blood pressure and something else be going on. On 18Dec2020 she still had a headache and didn''t feel well, but she thought she needed to give it some time. She had been anticipating not to feel well on 18Dec2020 (Friday). On 19Dec2020 she felt better considering she didn''t have a headache. On 19Dec2020 (Saturday) her blood pressure was 138/90 and she felt good. Then on 20Dec2020 she had the bad headache and her blood pressure was up. On 20Dec2020 (Sunday) she had a bad headache and her blood pressure was 156/100. She came to work today and her blood pressure had been high all day. She still had a headache and the light headedness continued. The outcome of the event low grade fever was unknown, of other remain events was not recovered.; Sender''s Comments: A causal association between BNT162B2 and the event dizziness cannot be excluded based on a compatible temporal relation. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to RAs, Ethics Committees, and Investigators, as appropriate.


VAERS ID: 910723 (history)  
Form: Version 2.0  
Age: 61.0  
Sex: Female  
Location: New Jersey  
Vaccinated:2020-12-26
Onset:2020-12-26
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA MODERNA / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Chest X-ray normal, Chest discomfort, Cough, Neutrophil percentage increased, Throat clearing
SMQs:, Anaphylactic reaction (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? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Albuterol 90 mcg/ Aerosol 2 puffs 4 times day Famotidine 20mg po daily Prednisone 20mg po 2 times day Diphenhydramine 25 mg po Q 6 hrs prn
Current Illness: UTI 11/28/2020
Preexisting Conditions: Hx Asthma Hx Uterine Sarcoma
Allergies: MRI Dye, NSAIDs
Diagnostic Lab Data: 12/26 CXR: Negative, no pneumonia, edema or pneumothorax Lab work: Neutrophils 83.6
CDC Split Type:

Write-up: 10 minutes after the vaccination, she began clearing her throat, within 30 minutes began coughing, which led to chest tightness. Was evaluated in the ER and admitted for observation. Given: Prednisone 40mg po, Benadryl 25mg po Duoneb x 3 and Pepcid 20mg


VAERS ID: 910750 (history)  
Form: Version 2.0  
Age: 76.0  
Sex: Male  
Location: Oregon  
Vaccinated:2020-12-22
Onset:2020-12-25
   Days after vaccination:3
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EJ1685 / 1 LA / IM

Administered by: Senior Living       Purchased by: ?
Symptoms: Angiogram cerebral normal, Arteriogram carotid normal, Blood cholesterol normal, Blood creatinine normal, Blood potassium normal, Blood sodium decreased, Blood triglycerides normal, Blood urea normal, Creatinine renal clearance decreased, Drooling, Dysarthria, Haematocrit normal, Haemoglobin normal, High density lipoprotein decreased, Hypertensive urgency, International normalised ratio normal, Magnetic resonance imaging brain normal, Platelet count normal, Posture abnormal, Unresponsive to stimuli, Wheelchair user, White blood cell count normal
SMQs:, Rhabdomyolysis/myopathy (broad), Acute renal failure (broad), Dyslipidaemia (narrow), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Dyskinesia (broad), Dystonia (broad), Parkinson-like events (broad), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hyponatraemia/SIADH (narrow), Hypertension (narrow), Conditions associated with central nervous system haemorrhages and cerebrovascular accidents (broad), Lipodystrophy (broad), Hypotonic-hyporesponsive episode (broad), Chronic kidney disease (broad), Tumour lysis syndrome (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? Yes
Hospitalized? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Tylenol 325mg - 2 tablets Famotidine 20mg - 1 tablet BID Fenofibrate 160mg - 1 tablet daily Vitamin D 2000iu - 1 tablet daily Hydralazine 25mg - 1 tablet TID Amlodipine Besylate 5mg - 1 tablet BID Atorvastatin 40mg - 1 tablet HS Donepezil
Current Illness: none noted
Preexisting Conditions: hypertension associated with Stage 3 chronic kidney disease due to type II diabetes hemiparesis - R dominant side vascular dementia w/out behavioral disturbance hx of stroke with residual deficit -2005 - R medial thamamus -2018 - L basal ganglia paroxysmal atrial fibrillation type II diabetes dysphagia as late effect of stroke sleep apnea hyperlipidemia
Allergies: Aspirin, Ibuprofen, Losartan, Simvastatin, ACE inhibitors, Penicillins
Diagnostic Lab Data: MRI brain - no acute infarct CTA Head/Neck scan - failed to show a new area of ischemia Labs - no infection noted, WBC unrevealing, creatinine clearance 56.5 ml/min (based on SCr of 1.22mg/dL) - at baseline, sodium 134, potassium 4.8, BUN 13, PT INR 1.1, HGB 17.0, platelets 287, hematocrit 51.0, chol 167, trig 131, HDL 35
CDC Split Type:

Write-up: Patient was found slumped over in wheelchair, drooling and unable to respond/follow simple instructions; sent to ED for evaluation. CT scans and MRI NEGATIVE for new/recent stroke; resident slurred speech likely due to hypertensive urgency


VAERS ID: 910822 (history)  
Form: Version 2.0  
Age: 42.0  
Sex: Female  
Location: Mississippi  
Vaccinated:2020-12-22
Onset:2020-12-23
   Days after vaccination:1
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA 011J20A / 1 RA / IM

Administered by: Private       Purchased by: ?
Symptoms: Angioedema, Enlarged uvula, Hypersensitivity, Lip oedema, Lip swelling, Nasal congestion, Oedema mouth, Palatal oedema, Paraesthesia oral, Sneezing, Throat tightness, Tongue oedema
SMQs:, Anaphylactic reaction (narrow), Angioedema (narrow), Oropharyngeal allergic conditions (narrow), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre 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? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: AMLODIPINE, HYDROCHLOROTHIAZIDE, CAMRESE, ICAR-C, LEXAPRO, ACZONE, RETIN A MICRO PUMP
Current Illness: NONE
Preexisting Conditions: ANEMIA
Allergies: NORCO, SPIRONOLACTONE
Diagnostic Lab Data:
CDC Split Type:

Write-up: SNEEZING, STUFFY NOSE, LIP SWELLING, TINGLING MOUTH, THROAT CLOSING, UVULA SWOLLEN 1. Allergic reaction (Allergy, unspecified, initial encounter) . Pt. received Moderna COVID vaccine the morning of 12/22/20 and developed angioedema reaction the afternoon of 12/23 Vaccine is only new medication reported by pt. - denies any new products, foods, etc History of hives with spironolactone 2.5 months ago; taking HCTZ now - unknown if reaction is related to this med rather than vaccine? Due to severity of her reaction and uncertainty if all attributable to vaccine versus some other culprit I would recommend Epi pen at time of discharge Has received IM epinephrine, racemic epi neb, Solu-Medrol, Benadryl, Pepcid in the ED Continue with Benadryl 25mg IV q6h, Pepcid 20mg IV q12h, and Solu-Medrol 40mg IV q6h 2. Angioedema (Angioneurotic edema, initial encounter) . Arrived to the ED with R. side lip, tongue, and uvula and oral cavity edema Airway patent, room air O2 sats WNL - monitor throughout the night for any worsening of angioedema or airway involvement Treatment as above


VAERS ID: 910948 (history)  
Form: Version 2.0  
Age: 46.0  
Sex: Female  
Location: Texas  
Vaccinated:2020-12-23
Onset:2020-12-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0140 / 1 LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Dyspnoea, Erythema
SMQs:, Anaphylactic reaction (narrow), Acute central respiratory depression (broad), Pulmonary hypertension (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? Yes
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness: None known
Preexisting Conditions: Asthma
Allergies: Green beans, cinnamon, shrimp, coconut, egg, iodine, latex, naproxen, oseltamivir, sesame seed, guaifenesin
Diagnostic Lab Data:
CDC Split Type:

Write-up: Difficulty breathing 5 minutes after receiving first dose of Covid-19 vaccine by Pfizer/BioNTech, small erythematous spots to bilateral arms.


VAERS ID: 910959 (history)  
Form: Version 2.0  
Age: 33.0  
Sex: Male  
Location: California  
Vaccinated:2020-12-23
Onset:2020-12-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK#5730 / UNK LA / IM

Administered by: Private       Purchased by: ?
Symptoms: Alanine aminotransferase increased, Angiogram cerebral normal, Arteriogram carotid normal, Aspartate aminotransferase increased, Blood albumin normal, Blood alkaline phosphatase normal, Blood bilirubin normal, Blood chloride normal, Blood creatinine normal, Blood glucose normal, Blood potassium decreased, Blood sodium decreased, Blood urea normal, Carbon dioxide decreased, Computerised tomogram head normal, Confusional state, Electroencephalogram normal, Eosinophil count normal, Haematocrit decreased, Haemoglobin decreased, Head discomfort, Hypoaesthesia, Hypokalaemia, Language disorder, Magnetic resonance imaging brain normal, Mean cell haemoglobin concentration normal, Mean cell volume normal, Mean platelet volume decreased, Migraine, Peripheral coldness, Platelet count normal, Red blood cell count decreased, Salivary hypersecretion, Troponin I normal, White blood cell count normal
SMQs:, Liver related investigations, signs and symptoms (narrow), Haematopoietic erythropenia (narrow), Peripheral neuropathy (broad), Haemorrhage laboratory terms (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Dementia (broad), Oropharyngeal conditions (excl neoplasms, infections and allergies) (narrow), Guillain-Barre syndrome (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Hyponatraemia/SIADH (narrow), Chronic kidney disease (broad), Myelodysplastic syndrome (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Hypoglycaemia (broad), Hypokalaemia (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? Yes, 2 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: No
Current Illness: No
Preexisting Conditions: No
Allergies: No known allergies
Diagnostic Lab Data: CMP: Recent Labs 12/23/20 1525 12/23/20 1650 NA 135* -- K 3.3* -- CL 101 -- CO2 20.3 -- GLUCOSE 124 106 BUN 11.0 -- CREATININE 1.1 -- ALBUMIN 3.8 -- ALKPHOS 67 -- ALT 37 -- AST 41* -- BILITOT 0.4 -- ? ? CBC: Recent Labs 12/23/20 1525 WBC 10.00 EOSABS 0.2 RBC 4.51 HGB 13.5 HCT 39.1 MCV 86.7 MCHC 34.6 PLT 343 MPV 7.1* ? Results from last 7 days Lab Units 12/23/20 1525 TROPONIN I ng/mL <0.017 ? Results from last 7 days Lab Units 12/23/20 1525 TROPONIN I ng/mL <0.017? ? Lab Results Component Value Date ? HGB 13.5 12/23/2020 ? ? ? Lab Results Component Value Date ? HGB 13.5 12/23/2020 ? ?
CDC Split Type:

Write-up: 33 y.o.?male?with no significant past medical history except for obesity who has been working as a nurse in the emergency room department in our hospital and today he received COVID-19 vaccine and 30 minutes later patient started having increased saliva, cold hands and feet, left-sided pressure-like headache and some numbness in his legs at the same time he suddenly started talking only in first language and lost his ability to speak in second language. ?He understand second language but replying first language stating that he is talking in second language. ?On exam he was alert oriented confused by people not understanding his second language stating that his numbness and cold feeling in the hands and feet have improved. ?Initially patient received 10 mg of Decadron for possible allergic reaction he had a head CT scan that was negative and his labs were remarkable only for hypokalemia. ?Patient had no prior history of any neurological symptoms he was advised admission to the hospital for observation ? ? Patient symptoms resolved next day,he is alert oriented able to communicate in second language he had a head MRI and head neck MRA that came back negative and had an EEG that showed no seizure activities. Patient was seen in neurology consultation who felt that patient most likely had an episode of migraine headache. Patient is going to be discharged home and to have a follow-up with his primary care physician next week ?


VAERS ID: 910996 (history)  
Form: Version 2.0  
Age: 64.0  
Sex: Female  
Location: California  
Vaccinated:2020-12-24
Onset:2020-12-24
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Asthma, Chest discomfort, Condition aggravated, Dizziness, Malaise, Palpitations, Supraventricular tachycardia
SMQs:, Anaphylactic reaction (broad), Asthma/bronchospasm (narrow), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Supraventricular tachyarrhythmias (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), 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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Advair Diskus 500 mcg-50 mcg inhalation powder 1 inhal, inhalation, BID amLODIPine 5 mg oral tablet 5 mg = 1 tab, PO, daily calcium carbonate 1 tab, PO, daily cyclobenzaprine 10 mg oral tablet 10 mg = 1 tab, PRN, PO, QHS Euthyrox 112 mcg (0
Current Illness: Asthma exacerbation, started oral steroids 12/21
Preexisting Conditions: Asthma, hypertension, dyslipidemia, hypothyroidism, appendectomy, history of uterine fibroids status post endometrial ablation
Allergies: Tape-Blisters sulfa drugs-Hives Toradol-Itching Vicodin-Rash
Diagnostic Lab Data:
CDC Split Type:

Write-up: Patient reports taking Pfizer Covid vaccine and 2 hours after that she reports feeling not well. She recorded that one of the side effects was heart arrhythmias and hence she had her coworker checked her rhythm and she reported that her heart rate was in 180s and hence she was brought to the emergency department for further evaluation. She reports at the time she had palpitations and felt mild lightheadedness and dizziness. She was found to be in SVT with heart rate in the range of 1 80-220 and she received 1 dose of 6 mg Adenoscan after which she converted to normal sinus rhythm. At the time of my evaluation she is in normal sinus rhythm with heart rate in the range of 90-100. She denies any further palpitations. She reports she had chest tightness for the last 3 days which was assumed to be secondary to asthma and for which she was prescribed prednisone. Currently with the prednisone she does not feel any further chest tightness. She denies any chest pain shortness of breath, fever or chills. She reports remote history of arrhythmia following her foot surgery in the past however does not recall what arrhythmia she had at that time.


VAERS ID: 911025 (history)  
Form: Version 2.0  
Age: 43.0  
Sex: Female  
Location: California  
Vaccinated:2020-12-20
Onset:2020-12-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Private       Purchased by: ?
Symptoms: Chest X-ray abnormal, Chills, Cough, Diarrhoea, Headache, Hypotension, Laboratory test normal, Lung opacity, Myalgia, Occupational exposure to SARS-CoV-2, Pyrexia, SARS-CoV-2 test positive, Tachypnoea
SMQs:, Rhabdomyolysis/myopathy (broad), Anaphylactic reaction (narrow), Asthma/bronchospasm (broad), Interstitial lung disease (narrow), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (broad), Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Cardiomyopathy (broad), Eosinophilic pneumonia (broad), Noninfectious diarrhoea (narrow), Respiratory failure (broad), Tendinopathies and ligament disorders (broad), Drug reaction with eosinophilia and systemic symptoms syndrome (broad), Infective pneumonia (broad), Dehydration (broad), Hypokalaemia (broad), Opportunistic infections (broad), COVID-19 (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, ? days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: amLODIPine 10 mg PO daily ascorbic acid 250 mg PO dailyJardiance 25 mg oral tablet 25 mg = 1 tab, PO, daily Jardiance 25 mg PO daily losartan 100 mg PO daily metformin 1000 mg PO BID Omega-3 1 cap PO daily simvastatin 20 mg oral tablet PO Q
Current Illness: none
Preexisting Conditions: Type 2 diabetes, hypertension
Allergies: Lactose-diarrhea
Diagnostic Lab Data: 12/26 SARS-CoV-2 PCR positive In the emergency department the patient was mildly hypotensive 97/54, low-grade fever 37.4, tachypneic, saturating 90% on room air, labs showed no leukocytosis, normocytic anemia, hyponatremia and hypochloremia, chest x-ray showed bilateral groundglass opacities.
CDC Split Type:

Write-up: Patient presents to the emergency department 12/26 complaining of dry cough associated with fever and chills and headache associated with myalgia and diarrhea for 1 week duration. She had Covid vaccine 12/20 and the symptoms started the same night, she denied any sick contacts at home however she works at the Covid unit and reports constant exposure to sick Covid patients.


VAERS ID: 911035 (history)  
Form: Version 2.0  
Age: 47.0  
Sex: Female  
Location: Alabama  
Vaccinated:2020-12-22
Onset:2020-12-22
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-28
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (MODERNA)) / MODERNA - / UNK - / IM

Administered by: Private       Purchased by: ?
Symptoms: Angiogram cerebral normal, Arteriogram carotid normal, Blindness, Cerebrovascular accident, Computerised tomogram head normal, Electrocardiogram normal, Eye irritation, Frustration tolerance decreased, Full blood count normal, Incoherent, Loss of consciousness, Metabolic function test normal, Migraine, Panic reaction, Posture abnormal, Posturing, Seizure, Transient ischaemic attack
SMQs:, Torsade de pointes/QT prolongation (broad), Hyperglycaemia/new onset diabetes mellitus (broad), Neuroleptic malignant syndrome (broad), Systemic lupus erythematosus (broad), Anticholinergic syndrome (broad), Arrhythmia related investigations, signs and symptoms (broad), Ischaemic central nervous system vascular conditions (narrow), Haemorrhagic central nervous system vascular conditions (narrow), Convulsions (narrow), Embolic and thrombotic events, arterial (narrow), Embolic and thrombotic events, vessel type unspecified and mixed arterial and venous (narrow), Dystonia (broad), Psychosis and psychotic disorders (narrow), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Glaucoma (broad), Optic nerve disorders (broad), Corneal disorders (broad), Retinal disorders (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? Yes
Hospitalized? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: Vitamin D weekly Fluoxetine Daily
Current Illness:
Preexisting Conditions: Depression
Allergies: No known food or medication allergies Seasonal Allergies ~ 5-6 years
Diagnostic Lab Data: CTA- head/ neck- normal CT Scan head unremarkable EKG- sinus rhythm without ischemic changes CBC/CMP fully unremarkable
CDC Split Type:

Write-up: Approximately 7 hours after receiving the vaccine patient who is a L&D Nurse return to work in her area. She describes that after finishing with a C-section she felt burning in both of her eyes (she thought this feels like an allergic reaction, but I am not sweating and haven''t rubbed my eyes). She went to the restroom to get a cloth to wash her eyes; afterwards she reports her vision went totally black in both eyes. She reports feeling frustrated that no one came to help and some panic in trying to figure out how to get out of the restroom. She did make it out of the bathroom. Her Staff reports she postured and turned arms inward, head going to one side and passed out. They also report ~ 10 minutes of incoherent conversation and stating "I got the vaccine, maybe I was given the wrong thing and now I''m blind". Upon waking, patient vision fully restored and patient does not remember incoherent conversation. Differential diagnosis- TIA vs. CVA $g seizure disorder$g$g$g complex migraine


VAERS ID: 911462 (history)  
Form: Version 2.0  
Age: 62.0  
Sex: Female  
Location: Oklahoma  
Vaccinated:2020-12-18
Onset:2020-12-18
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-12-29
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EK5730 / 1 - / OT

Administered by: Unknown       Purchased by: ?
Symptoms: Dyspnoea, Pain in extremity
SMQs:, Anaphylactic reaction (broad), Acute central respiratory depression (broad), Pulmonary hypertension (broad), Cardiomyopathy (broad), Tendinopathies and ligament disorders (broad)

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? No
Previous Vaccinations:
Other Medications: ; HCTZ; ; ; ; ; ; ; ZYRTEC [CETIRIZINE HYDROCHLORIDE]; ; VITAMINS [ASCORBIC ACID;ERGOCALCIFEROL;NICOTINAMIDE;RETINOL;RIBOFLAVIN;THIAMINE HYDROCHLORIDE];
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Allergy; Asthma; Blood cholesterol abnormal; Blood pressure high; Diabetes; Post procedural pain; Reflux gastritis; Rosacea; Sciatica; Shingles; Sinus congestion; Swelling
Allergies:
Diagnostic Lab Data:
CDC Split Type: USPFIZER INC2020508893

Write-up: she is better but still not good; not to be able to breath; sore right arm; This is a spontaneous report from a contactable nurse (patient herself). A 62-year-old female patient received bnt162b2 (BNT162B2, lot EK5730), intramuscular on 18Dec2020 at single dose for immunisation. Medical history included asthma (hospitalized on Jan2020 and has not had any issues since that time, referring to her asthma) diabetes, high blood pressure, swelling, sciatica, blood cholesterol abnormal, rosacea, reflux, allergies, sinus congestion, shingles and post carpal tunnel surgery. Concomitant medications included lisinopril, hydrochlorothiazide, gabapentin, rosuvastatin, metformin, glipizide, doxycycline, sucralfate, cetirizine hydrochloride (ZYRTEC), pseudoephedrine, ascorbic acid, ergocalciferol, nicotinamide, retinol, riboflavin, thiamine hydrochloride (VITAMINS) and tramadol. The patient reported that she not to be able to breath (seriousness criteria-life threatening) on 22Dec2020. She woke up this morning and could not breathe and there was no reason for her to not be able to breath. She thought she may have had a reaction to the COVID vaccine. It was the only thing she could think of that might have caused her not to be able to breathe this morning. As treatment for not to be able to breath, she used Budesonide and Levosalbutamol in her nebulizer. She had sore right arm on 18Dec2020. She informed that she had done everything she can and she was better but still not good. She planned to take the second dose of the COVID Vaccine because she thought it was more important to be protected. She suspected that the vaccine was related to the events sore right arm and could not breathe. The outcome of the event not to be able to breath was recovering; for sore right arm was recovered on unknown date in Dec2020; for she is better but still not good was unknown.; Sender''s Comments: Severe allergic reaction including anaphylaxis is the known risk factor; a possible causal association between administration of BNT162B2 and the onset of not being able to breath cannot be excluded, considering the plausible temporal relationship and the known adverse event profile of the suspect product. The impact of this report on the benefit/risk profile of the Pfizer product is evaluated as part of Pfizer procedures for safety evaluation, including the review and analysis of aggregate data for adverse events. Any safety concern identified as part of this review, as well as any appropriate action in response, will be promptly notified to Regulatory Authorities, Ethics Committees and Investigators, as appropriate.


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