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From the 11/19/2021 release of VAERS data:

This is VAERS ID 1053462

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Case Details

VAERS ID: 1053462 (history)  
Form: Version 2.0  
Age: 32.0  
Sex: Female  
Location: Foreign  
Vaccinated:2021-01-06
Onset:0000-00-00
Submitted: 0000-00-00
Entered: 2021-02-25
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH EL0141 / UNK - / -

Administered by: Other       Purchased by: ?
Symptoms: Abortion spontaneous, Headache, Human chorionic gonadotropin, Maternal exposure during pregnancy, Pain in extremity, Pregnancy test, SARS-CoV-2 test
SMQs:, Pregnancy, labour and delivery complications and risk factors (excl abortions and stillbirth) (narrow), Termination of pregnancy and risk of abortion (narrow), Tendinopathies and ligament disorders (broad), COVID-19 (broad)

Life Threatening? No
Birth Defect? No
Died? No
Permanent Disability? No
Recovered? No
Office Visit? No
ER Visit? No
ER or Doctor Visit? No
Hospitalized? No
Previous Vaccinations:
Other Medications: FOLIC ACID
Current Illness:
Preexisting Conditions: Medical History/Concurrent Conditions: Folic acid supplementation
Allergies:
Diagnostic Lab Data: Test Name: Blood hcg; Result Unstructured Data: Test Result:Blood hcg showed early miscarriage; Test Name: pregnancy test; Test Result: Positive ; Test Name: COVID-19; Result Unstructured Data: Test Result:No - Negative COVID-19 test
CDC Split Type: GBPFIZER INC2021147303

Write-up: Maternal exposure during pregnancy; Early miscarriage; Headache; Painful arm; This is a spontaneous report from a consumer or other non hcp. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202102100805410190. Safety Report Unique Identifier GB-MHRA-ADR 24731748. A 32-year-old female patient started to receive BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, lot number: EL0141), via an unspecified route of administration, on 06Jan2021 at SINGLE DOSE for covid-19 immunisation. Medical history included folic acid supplementation. Concomitant medication included folic acid for Folic acid supplementation. The patient experienced maternal exposure during pregnancy, early miscarriage, headache and painful arm on an unspecified date. The events were assessed as medically significant by the reporter. The mother reported she became pregnant while taking bnt162b2. Patient was exposed to the medicine first-trimester (1-12 weeks). The patient underwent lab tests and procedures which included Blood hcg: blood hcg showed early miscarriage, pregnancy test: positive and COVID-19: no - negative covid-19 test on unspecified date. Outcome of the event early miscarriage was recovered with sequelae while outcome of the events painful arm and headache was recovered on an unspecified date. Outcome of the remaining event was unknown. No follow-up attempts are possible. No further information is expected.


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