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From the 3/29/2024 release of VAERS data:

Found 7 cases where Symptom is Breast feeding and Vaccination Date from '2015-01-01' to '2020-11-30'

Government Disclaimer on use of this data

Table

   
AgeCountPercent
< 6 Months457.14%
30-39 Years114.29%
Unknown228.57%
TOTAL7100%



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), Noninfectious myocarditis/pericarditis (broad)

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:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 996693 (history)  
Form: Version 2.0  
Age: 0.08  
Sex: Female  
Location: Foreign  
Vaccinated:2018-11-20
Onset:2018-11-20
   Days after vaccination:0
Submitted: 0000-00-00
Entered: 2021-02-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
DTP: DTP (NO BRAND NAME) / UNKNOWN MANUFACTURER 20917002A / UNK - / OT
HEP: HEP B (FOREIGN) / MERCK & CO. INC. - / UNK - / OT
HIBV: HIB (ACTHIB) / SANOFI PASTEUR - / UNK - / OT
PNC10: PNEUMO (SYNFLORIX) / GLAXOSMITHKLINE BIOLOGICALS - / UNK - / OT

Administered by: Other       Purchased by: ?
Symptoms: Abdominal pain, Agitation, Apathy, Breast feeding, Constipation, Crying, Decreased appetite, Diarrhoea, Febrile convulsion, Hyperaesthesia, Insomnia, Muscle strain, Poor feeding infant, Product administered to patient of inappropriate age, Pyrexia, Somnolence, Vaccination site erythema, Vaccination site oedema, Vaccination site swelling, Vomiting
SMQs:, Acute pancreatitis (broad), Neuroleptic malignant syndrome (broad), Anticholinergic syndrome (narrow), Retroperitoneal fibrosis (broad), Dementia (broad), Convulsions (narrow), Pseudomembranous colitis (broad), Psychosis and psychotic disorders (broad), Noninfectious encephalitis (broad), Noninfectious encephalopathy/delirium (broad), Noninfectious meningitis (broad), Accidents and injuries (narrow), Gastrointestinal nonspecific symptoms and therapeutic procedures (narrow), Hostility/aggression (broad), Depression (excl suicide and self injury) (broad), Neonatal disorders (narrow), Generalised convulsive seizures following immunisation (narrow), Noninfectious diarrhoea (narrow), Tendinopathies and ligament disorders (broad), Medication errors (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:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type:

Write-up:


VAERS ID: 2306778 (history)  
Form: Version 2.0  
Age:   
Sex: Male  
Location: Foreign  
Vaccinated:2018-01-12
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2022-06-02
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
TDAP: TDAP (NO BRAND NAME) / UNKNOWN MANUFACTURER UNK / UNK - / SYR
UNK: VACCINE NOT SPECIFIED (NO BRAND NAME) / UNKNOWN MANUFACTURER UNK / UNK - / SYR

Administered by: Unknown       Purchased by: ?
Symptoms: Breast feeding, Foetal exposure during pregnancy
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (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
Extended hospital stay? Yes
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: BRGLAXOSMITHKLINEBR2022GS

Write-up: developed other health conditions or complications and was hospitalized because of that; Fetal exposure during pregnancy, second trimester; This retrospective pregnancy case was reported by a other health professional via licensee and described the occurrence of hospitalization in a male infant exposed to DTPa (Reduced antigen) (dTpa vaccine) in utero. The mother received the product for prophylaxis. Co-suspect product exposures included INFLUENZA VIRUS VACCINE INACTIVATED (VAXIGRIP SANOFI (FLU VACCINE)). On 12th January 2018, the mother received dTpa vaccine (intramuscular) and VAXIGRIP SANOFI (FLU VACCINE) (intramuscular). The mother''s last menstrual period was on an unknown date and estimated date of delivery was on an unknown date. The infant was exposed to dTpa vaccine at an unknown time during the pregnancy. The infant was born via unknown delivery. The infant was diagnosed with hospitalization (serious criteria hospitalization) and fetal exposure during pregnancy, second trimester. On an unknown date, the outcome of the hospitalization and fetal exposure during pregnancy, second trimester were unknown. It was unknown if the reporter considered the hospitalization to be related to dTpa vaccine. See case BR2022GSK086821 for details regarding the mother case. Additional Information: GSK Receipt Date: 20-MAY-2022 Reporter''s Comment: The pharmacovigilance document by Sanofi, containing information on a severe adverse event report after using an adsorbent vaccine against diphtheria, tetanus, and (acellular) pertussis (dTpa vaccine). The mother gave birth on male baby 49 cm tall and normal head circumference. The patient survived his first 28 days of life. The baby was on exclusive breastfeeding (no formula) during the hospitalization period, more than once a day. The baby developed other health conditions or complications between his 29th day and 1 year of life, and was hospitalized because of that.; Sender''s Comments: BR-GLAXOSMITHKLINE-BR2022GSK086821:Mother case


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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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