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|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||- / UNK||- / -|
Administered by: Other Purchased by: ??
Symptoms: Abortion spontaneous
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Diagnostic Lab Data:
CDC 'Split Type': AUPFIZER INC2021678384
Write-up: Abortion spontaneous; This is a spontaneous report from a contactable healthcare professional via the regulatory authority. The regulatory authority report number is 561521. A 31-year-old female patient received bnt162b2 (COMIRNATY), via an unspecified route of administration on an unspecified date (Batch/Lot number was not reported) at single dose for covid-19 immunisation. The patient was pregnant at the time of vaccination. The patient''s medical history and concomitant medications were not reported. On an unknown date, the patient experienced abortion spontaneous. The outcome of the event was unknown. No follow-up attempts are possible; information about lot/batch number cannot be obtained.
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