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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||EW4109 / 1||- / -|
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': GBPFIZER INC2021774190
Write-up: Miscarriage of pregnancy; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106211940174840-TURSX, Safety Report Unique Identifier: GB-MHRA-ADR 25514849. This consumer reported information for both mother and baby. This is the maternal report. A female patient of an unspecified age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number: EW4109), via an unspecified route of administration on 18May2021 as dose 1, single for COVID-19 immunization. The patient''s medical history and concomitant medications were not reported. Patient has not had symptoms associated with COVID-19 and not had a COVID-19 test. Patient is not enrolled in clinical trial. The patient experienced miscarriage of pregnancy on an unspecified date. The outcome of the event was not recovered. No follow-up attempts are possible. No further information is expected.
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