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This is VAERS ID 1449508

History of Changes from the VAERS Wayback Machine

First Appeared on 7/9/2021

VAERS ID: 1449508
VAERS Form:2
Age:
Sex:Female
Location:Tennessee
Vaccinated:0000-00-00
Onset:2021-06-01
Submitted:0000-00-00
Entered:2021-07-06
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / UNK - / -

Administered by: Unknown      Purchased by: ??
Symptoms: Abortion spontaneous, Maternal exposure during pregnancy

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? Yes, days:     Extended hospital stay? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data:
CDC 'Split Type': USPFIZER INC2021748887

Write-up: A patient had a second trimester fetal loss right after getting the Covid vaccine.; A patient had a second trimester fetal loss right after getting the Covid vaccine.; This is a spontaneous report from a contactable physician. An adult female patient of an unknown age received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) at an unknown dose on an unknown date via an unknown route for Covid-19 immunization. Medical history and concomitant drug were not provided. Medical history and concomitant drug were not provided. It was unknown if the patient received any other vaccines within 4 weeks prior to the COVID vaccine. Patient had 32 weeks gestation period. Patient had a "second trimester" (as reported) fetal loss right after getting the Covid vaccine. The event onset date was Jun2021. Treatment received for the event. It was unknown if the patient diagnosed with COVID-19 prior to vaccination, and unknown if the patient been tested for COVID-19 since the vaccination. The report was assessed as serious with seriousness criteria of hospitalization. Information on lot/batch number has been requested.; Sender''s Comments: Based on available information, a possible contributory role of bnt162b2 cannot be excluded for the reported events miscarriage. 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.

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