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This is VAERS ID 1733056

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History of Changes from the VAERS Wayback Machine

First Appeared on 10/15/2021

VAERS ID: 1733056
VAERS Form:2
Age:
Sex:Female
Location:Foreign
Vaccinated:2021-09-13
Onset:2021-09-13
Submitted:0000-00-00
Entered:2021-09-24
Vaccin­ation / Manu­facturer Lot / Dose Site / Route
COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH FF2153 / 1 - / -

Administered by: Other      Purchased by: ??
Symptoms: Syncope

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:
CDC 'Split Type': GBPFIZER INC202101205393

Write-up: Faint; This is a spontaneous report from a contactable other healthcare professional. This is a report received from the Regulatory Authority. Regulatory authority report number GB-MHRA-WEBCOVID-202109131300149790-KQEYK, Safety Report Unique Identifier GB-MHRA-ADR 25931691. A female patient of unspecified age received first dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FF2153), via an unspecified route of administration on 13Sep2021 at single dose for COVID-19 immunisation. The patient''s medical history and concomitant medications were not reported. Patient has not had symptoms associated with COVID-19. Not had a COVID-19 test. Patient is not enrolled in clinical trial. On 13Sep2021, the patient was fainted 2 minutes after vaccination. This report was not related to possible blood clots or low platelet counts. Patient has not tested positive for COVID-19 since having the vaccine. The clinical outcome of the event fainted was recovered on 13Sep2021. No follow-up attempts are needed. No further information is expected.

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