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Administered by: Other Purchased by: ?
Life Threatening? No
Write-up: Fever; Painful arm; Fatigue; This is a spontaneous report from a contactable consumer received from the Regulatory Authority Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106050933276410-H3S8Y, Safety Report Unique Identifier GB-MHRA-ADR 25425350. A 30-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, solution for injection, lot number and expiry date were not reported), via an unspecified route of administration on 04Jun2021 (at the age of 30 years old) as 1st dose, single for COVID-19 immunization. Medical history included lactation decreased from an unknown date and unknown if ongoing and suspected COVID-19 (unsure when symptoms stopped) from 26Feb2020 to an unknown date. The patient had not had a COVID-19 test. Patient is not enrolled in clinical trial. Patient is not pregnant. Patient is not currently breastfeeding. The patient''s concomitant medications were not reported. The patient experienced painful arm, fatigue on 04Jun2021 and fever on 05Jun2021. The reporter assessed all events as serious (medically significant). Patient has not tested positive for COVID-19 since having the vaccine. The outcome of the events was not recovered. No follow-up attempts are possible; information about batch/lot number cannot be obtained. No further information is expected.
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