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|History of Changes from the VAERS Wayback Machine|
|Vaccination / Manufacturer||Lot / Dose||Site / Route|
|COVID19: COVID19 (COVID19 (PFIZER-BIONTECH)) / PFIZER/BIONTECH||FE3380 / 2||- / -|
Administered by: Other Purchased by: ??
Life Threatening? No
Birth Defect? No
Permanent Disability? No
Office Visit (V2.0)? No
ER or Office Visit (V1.0)? No
ER or ED Visit (V2.0)? No
Other Medications: Pfizer, Inc. EUA 027034
Preexisting Conditions: Medical History/Concurrent Conditions: Anxiety
Diagnostic Lab Data:
CDC 'Split Type': GBPFIZER INC202101224690
Write-up: Painful periods/ awful period pains; This is a spontaneous report from a contactable consumer, the patient. This is a report received from the Regulatory Agency (RA). Regulatory authority report number GB-MHRA-WEBCOVID-202109160755429710-VTWGO, Safety Report Unique Identifier GB-MHRA-ADR 25950286. A 29-year-old female patient received the second dose of BNT162b2 (PFIZER-BIONTECH COVID-19 mRNA VACCINE; Lot Number: FE3380) via an unspecified route of administration on 19Aug2021, as a single dose for COVID-19 immunisation. Medical history included anxiety. The patient did not have symptoms associated with COVID-19. The patient was not enrolled in clinical trial. The patient was not pregnant and was not breastfeeding. Concomitant medication included propranolol (MANUFACTURER UNKNOWN) for anxiety for a day on 19Aug2021. On 11Sep2021, 23 days after vaccination, the patient experienced painful periods/ period on time but the most awful period pains that woke her up; the event painful periods was reported as serious for being medically significant. The patient took painkillers and hot water bottle but did nothing to help. The patient did not have a COVID-19 test. The patient had not tested positive for COVID-19 since having the vaccine. The clinical outcome of the event painful periods/ awful period pains was resolving at the time of this report. No follow-up attempts are needed. No further information is expected.
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