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Administered by: Other Purchased by: ?
Life Threatening? No
Write-up: Fainting; This is a spontaneous report from a contactable pharmacist received from the Agency Regulatory Authority. The regulatory authority report number is GB-MHRA-WEBCOVID-202106041350201580-SAP3P, Safety Report Unique Identifier GB-MHRA-ADR 25420610. A male patient of an unspecified age received the first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE) via an unspecified route of administration on 04Jun2021 (Lot Number: EY5456) as single dose for COVID-19 immunisation. The patient medical history was not reported. Patient had not symptoms associated with COVID-19 or had not a COVID-19 test. The patient''s concomitant medications were not reported. The patient experienced fainting on 04Jun2021. Event outcome was recovered on 04Jun2021. No follow-up attempts are possible. No further information is expected.
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