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From the 11/12/2021 release of VAERS data:

This is VAERS ID 1067790

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Case Details

VAERS ID: 1067790 (history)  
Form: Version 2.0  
Age:   
Sex: Female  
Location: Foreign  
Vaccinated:0000-00-00
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-03-03
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Foetal death
SMQs:, Termination of pregnancy and risk of abortion (narrow)

Life Threatening? No
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:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC Split Type: ILPFIZER INC2021208688

Write-up: A woman in week 20 or 24 was vaccinated and the next day the fetus died; This is a spontaneous report from a contactable physician who reported similar events for two patients. This is the first of two reports. A pregnant female patient (in week 20 or 24 of pregnancy) received bnt162b2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on an unspecified date at single dose for covid-19 immunisation. The patient medical history and concomitant medications were not reported. The patient was vaccinated and the next day the fetus died on an unspecified date. The reporter did not think there was a connection but due to the proximity to the vaccine she reported. Information about batch/lot number as been requested.; Sender''s Comments: Based on the information provided by the reporter, it appears unlikely that subject product, BNT162B2 vaccine, contributed to the event of fetal death. There is very limited information provided in this report. This case will be reassessed upon receipt of follow-up information. 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.,Linked Report(s) : IL-PFIZER INC-2021209291 same reporter/vaccine/event different patient; Reported Cause(s) of Death: fetal death


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