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From the 10/15/2021 release of VAERS data:

Found 5 cases where Symptom is Breast feeding and Vaccination Date from '2015-01-01' to '2020-11-30'

Table

   
AgeCountPercent
< 3 Years360%
17-44 Years120%
Unknown120%
TOTAL5100%



Case Details

VAERS ID: 566066 (history)  
Form: Version 1.0  
Age:   
Sex: Female  
Location: Unknown  
Vaccinated:2015-01-17
Onset:0000-00-00
Submitted: 2015-01-27
Entered: 2015-01-27
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. - / UNK UN / SC

Administered by: Other       Purchased by: Other
Symptoms: Breast feeding, 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: No other medications
Current Illness: Unknown
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: WAES1501USA010196

Write-up: This spontaneous report as received from a medical assistant refers to a female patient of unknown age. On 17-JAN-2015 (reported as about 1 week ago) the patient was vaccinated with M-M-R II, 0.5 ml, subcutaneous. Concomitant medication was not reported. The patient who was breastfeeding was administered with M-M-R II. No adverse effects reported. The outcome of the event was unknown. The reporter considered the event to be not related to M-M-R II. Additional information is not expected.


VAERS ID: 703512 (history)  
Form: Version 2.0  
Age: 0.0  
Sex: Female  
Location: Michigan  
Vaccinated:2017-05-24
Onset:2017-05-26
   Days after vaccination:2
Submitted: 0000-00-00
Entered: 2017-07-12
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
HEP: HEP B (RECOMBIVAX HB) / MERCK & CO. INC. N002922 / 1 LL / IM

Administered by: Private       Purchased by: ?
Symptoms: Breast feeding, Cardiac arrest, Cyanosis, Hypotonia, Intensive care, Laboratory test, Nervous system disorder, Respiratory arrest
SMQs:, Torsade de pointes/QT prolongation (broad), Anaphylactic reaction (narrow), Peripheral neuropathy (broad), Arrhythmia related investigations, signs and symptoms (broad), Shock-associated circulatory or cardiac conditions (excl torsade de pointes) (narrow), Acute central respiratory depression (narrow), Guillain-Barre syndrome (broad), Cardiomyopathy (broad), Hypotonic-hyporesponsive episode (broad), Generalised convulsive seizures following immunisation (broad), Hypersensitivity (broad), Respiratory failure (narrow)

Life Threatening? Yes
Birth Defect? No
Died? No
Permanent Disability? Yes
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? Yes
Hospitalized? Yes, 52 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications: vitamin D infant drops
Current Illness: none
Preexisting Conditions: none
Allergies: none
Diagnostic Lab Data: Tests were all preformed at Hospital 5/26/17
CDC Split Type:

Write-up: Patient had gone into cardiac arrest two days later, mom was breastfeeding and baby went blue and stopped breathing, treated in intensive care unit for over 1 month, outcome with poor tone with neurological impairment.


VAERS ID: 886793 (history)  
Form: Version 2.0  
Age: 0.17  
Sex: Male  
Location: Virginia  
Vaccinated:2020-07-23
Onset:2020-07-23
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2020-09-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
RV1: ROTAVIRUS (ROTARIX) / GLAXOSMITHKLINE BIOLOGICALS - / 1 MO / PO

Administered by: Military       Purchased by: ?
Symptoms: Breast feeding, Diarrhoea, Diet refusal, Pain, Screaming
SMQs:, Pseudomembranous colitis (broad), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (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: Vitamin D, infant tylenol
Current Illness: None
Preexisting Conditions: None
Allergies: Unknown
Diagnostic Lab Data:
CDC Split Type:

Write-up: Screaming in pain for multiple hours straight for several days after, refusing to breastfeed for almost 7 hours, diarrhea for more than 10 days


VAERS ID: 1000876 (history)  
Form: Version 2.0  
Age: 30.0  
Sex: Female  
Location: North Carolina  
Vaccinated:2017-08-21
Onset:2017-09-08
   Days after vaccination:18
Submitted: 0000-00-00
Entered: 2021-02-04
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
MMR: MEASLES + MUMPS + RUBELLA (MMR II) / MERCK & CO. INC. N002337 / 3 RA / SC

Administered by: Private       Purchased by: ?
Symptoms: Antinuclear antibody negative, Arthralgia, Blood uric acid normal, Breast feeding, Differential white blood cell count normal, Fatigue, Full blood count normal, Glomerular filtration rate normal, Joint stiffness, Loss of personal independence in daily activities, Metabolic function test normal, Red blood cell sedimentation rate normal, Rheumatoid factor negative, X-ray limb normal
SMQs:, Dementia (broad), 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: Hydromorphone 2mg, Colace stool softener 50mg, Iron 27mg
Current Illness: C-section performed 8/18/2017 - recovering from surgery
Preexisting Conditions: n/a
Allergies: none
Diagnostic Lab Data: X-rays (writs, hands, knees) and blood work (glomerular filtration rate estimate, CMP, uric acid, sed rate, rheumatoid factor, cbc, with differential, aniti ab ana reflex cascade). All tests came back within normal limits.
CDC Split Type:

Write-up: Patient began having joint stiffness and pain 3 weeks following vaccination. By ~6 weeks following vaccination, stiffness and pain escalated to the point that she struggles to perform daily tasks. (Hold a pencil, get in and out of a chair, go up and down stairs, put on daughter''s clothing, etc.) Primary joints affected were hands (predominantly right), ankles, and knees. Occasional pain through wrist. Pain continued for 14 months, flaring more significantly during hormonal changes seemingly relate to breastfeeding. During these periods, patient experienced significant fatigue and was unable to perform daily activities. Chiropractic care, nutritional supplements, and dietary changes with the intent to decrease inflammation had positive impact on severity. Patient continues to need lifestyle measures to manage symptoms. There is no other medical explanation for patient''s symptoms, so this is a probable reaction to MMR


VAERS ID: 877550 (history)  
Form: Version 2.0  
Age: 0.17  
Sex: Female  
Location: Foreign  
Vaccinated:2020-05-01
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2020-07-30
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
6VAX-F: DTAP+IPV+HEPB+HIB (NO BRAND NAME) / UNKNOWN MANUFACTURER UNKNOWN / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Allergy test negative, Breast feeding, Eye swelling, Rash, Restlessness, Urticaria
SMQs:, Anaphylactic reaction (broad), Angioedema (narrow), Anticholinergic syndrome (broad), Dementia (broad), Akathisia (broad), Noninfectious encephalopathy/delirium (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? Yes, 1 days
   Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions: Comments: None
Allergies:
Diagnostic Lab Data:
CDC Split Type: GRMSPVaccineP2006GRC00556

Write-up: the girl presented urticaria all over her body with rash and swelling in the eyes; the girl presented urticaria all over her body with rash and swelling in the eyes; the girl presented urticaria all over her body with rash and swelling in the eyes; The first day of urticaria the child was restless; This spontaneous report was received from a physician and refers to a 2-month-old female patient. The patient underwent allergic blood tests (RAST), which were negative. Her diet was mixed, breastfeeding and cow''s milk. No information regarding the patient''s concomitant medications, drug allergies and reactions was provided. In May 2020 (reported as approximately one month ago), the patient was vaccinated with diphtheria toxoid (+) hepatitis b virus vaccine rhbsag (yeast) (+) hib conj vaccine (ompc) (+) pertussis acellular 5-component vaccine (+) poliovirus vaccine inactivated (vero) (+) tetanus toxoid (VAXELIS) (exact dose, route of administration, lot # and expiration date were not provided) for prophylaxis. On an unknown date in 2020 (reported as ten days after the vaccination), the patient presented urticaria all over her body with rash and swelling in the eyes, which characteristically lasted for four days. The first day of urticaria the patient was restless. The outcome of urticaria, restlessness, rash and eye swelling was reported as fully recovered. The causality assessment between the events and the suspect therapy was reported as unknown. Follow-up information was received by MSD affiliates on 14-JUL-2020 and forwarded to MCM on 15-JUL-2020 from a physician. The case upgrades to serious. On an unspecified date, the patient experienced urticaria, restlessness, rash and eye swelling and was hospitalized for one day for precautionary reasons. On an unspecified date, the patient underwent allergic blood tests (RAST) which were negative. Action taken with Vaxelis was unknown. No further information is expected.; Reporter''s Comments: The causality assessment between the events and the suspect therapy was reported as unknown.; Sender''s Comments: The events Eye swelling, Urticaria, Rash and Restlessness were assessed as serious (Hospitalization). The events Eye swelling and Urticaria are unlisted as per Reference Safety Information (Vaxelis SmPC) and are listed as per Reference Safety Information (Vaxelis USPI). The events Rash and Restlessness are listed as per Reference Safety Information (Vaxelis USPI and SmPC). Due to the lack of information, the causal relationship between Vaxelis and the event Eye swelling cannot be excluded and was assessed as related. Considering the current knowledge of the vaccine, the causal relationship between Vaxelis and the events Urticaria, Rash and Restlessness were assessed as related.


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Link To This Search Result:

https://medalerts.org/vaersdb/findfield.php?TABLE=ON&GROUP1=AGE&EVENTS=ON&SYMPTOMS=Breast+feeding+%2810006247%29&VAX_YEAR_LOW=2015&VAX_YEAR_HIGH=2020&VAX_MONTH_HIGH=11

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