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Life Threatening? No
Write-up: Sickness; Stiffness; This is a spontaneous report from a contactable consumer received from the Regulatory Agency (RA). The regulatory authority report number is GB-MHRA-WEBCOVID-202106050922139490-LKBP3. Safety Report Unique Identifier GB-MHRA-ADR 25425331. A 34-year-old female patient received BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE), via an unspecified route of administration on 03Jun2021 (at the age of 34 years) (Batch/Lot number was not reported) as 1ST DOSE, SINGLE for covid-19 immunisation. Medical history included lactation decreased Patient has not had symptoms associated with COVID-19. 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 sickness and stiffness on 03Jun2021. The events were assessed a serious (medically significant). Lab data includes COVID-19 virus test: Negative COVID-19 test on 04Jun2021. Patient has not tested positive for COVID-19 since having the vaccine. The outcome of the event sickness was recovered on 04Jun2021 and stiffness was recovered on 05Jul2021. No follow-up attempts are possible, information about the batch number cannot be obtained.
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