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This is VAERS ID 1090242

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History of Changes from the VAERS Wayback Machine

First Appeared on 7/2/2021

VAERS ID: 1090242
VAERS Form:2
Age:
Sex:Female
Location:Foreign
Vaccinated:2020-12-29
Onset:0000-00-00
Submitted:0000-00-00
Entered:2021-03-11
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH - / 1 - / -

Administered by: Other      Purchased by: ??
Symptoms: Abortion spontaneous, Pregnancy test, Product supply issue, Inappropriate schedule of product administration

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? Yes
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Hospitalized? No
Previous Vaccinations:
Other Medications:
Current Illness:
Preexisting Conditions:
Allergies:
Diagnostic Lab Data: Test Date: 20210105; Test Name: pregnancy test; Test Result: Positive
CDC 'Split Type': DEPFIZER INC2021009218

Write-up: I suffered an early miscarriage; The next appointment at the vaccination center was in mid-Apr2021/ continue to be vaccinated after an elapsed vaccination interval of more than 42 days; The next appointment at the vaccination center was in mid-Apr2021/ continue to be vaccinated after an elapsed vaccination interval of more than 42 days; This is a spontaneous report based on information received by Pfizer from Biontech [manufacturer control number: 5308], license party for Comirnaty. A contactable physician (patient) reported that a female patient of unspecified age received the first dose of BNT162B2 (COMIRNATY, lot number and expiry date unknown) via an unspecified route of administration on 29Dec2020 at single dose for Covid-19 immunization. Medical history and concomitant medications were not reported. The patient said she was a doctor in a clinic and had received the first vaccination with vaccine Comirnaty on 29Dec2020. In the course of the procedure, it turned out that she was pregnant, which was why she canceled the second vaccination appointment at the clinic. She had taken a pregnancy test on 05Jan2021, which showed positive. Her second vaccination would be on 19Jan2021. She did not know she was pregnant before she received the vaccine. In the meantime, she suffered an early miscarriage in 2021 and inquired at the clinic about the possibility of a second vaccination. Unfortunately, from now on only with another vaccine (Astra Zeneca). The next appointment at the vaccination center was in mid-Apr2021. She was asking how she should continue to be vaccinated after an elapsed vaccination interval of more than 42 days. Again 2 times or is there any data on "mixing" different vaccines. Nature of Pregnancy was early pregnancy. The outcome of the event early miscarriage was recovered, of other events was unknown. Information on the lot/batch number has been requested. Follow-up (15Feb2021): New information received from the same contactable physician (patient) included: case upgraded to serious, reaction data (removed event she was pregnant, added event early miscarriage, The next appointment at the vaccination center was in mid-Apr2021/ continue to be vaccinated after an elapsed vaccination interval of more than 42 days, outcome and event details). Information on the lot/batch number has been requested.; Sender''s Comments: Based on temporal association and known product profile of BNT162B2 (COMIRNATY, lot number and expiry date unknown), the contributory role of the product cannot be totally excluded. This case will be reassessed should additional information becomes available. 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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