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Life Threatening? No
Write-up: This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106041729083630-5LEA9. Safety Report Unique Identifier is GB-MHRA-ADR 25422523.A 32-years-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), first dose via an unspecified route of administration on 02Jun2021 (Lot number was not reported) as single dose for COVID-19 immunisation. Medical history included hypothyroidism, Lactation decreased. Hypothyroidism, Patient has not had symptoms associated with COVID-19, 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 nausea on 04Jun2021 with outcome of not recovered, tiredness on 03Jun2021 with outcome of not recovered.Additional Information: Patient has not tested positive for COVID-19 since having the vaccine. Case was reported as serious and seriousness criteria was medically significant. No follow-up attempts are possible; information about lot/batch number cannot be obtained. No further information is expected.
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