이상반응 보고

VAERS ID 1464906
성별 여성
나이
주 코드 FR
제약회사 PFIZER\BIONTECH
로트 번호
예방접종 횟수 1
접종일 2021-06-01
발병일 2021-06-14
상태
증상
  • 호흡곤란(Dyspnoea)
  • 편두통(Migraine)
  • 변태(Metamorphopsia)
  • 월경 불규칙(Menstruation irregular)
  • 임신의 신체 증상 장애(Somatic symptom disorder of pregnancy)

이환 중 질병

지병

Medical History/Concurrent Conditions: Asthma; Disorder gastrointestinal; Glaucoma; Lactation decreased

기타 의료

이전 예방접종

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임상 검사

증상 상세

False pregnancy; Irregular periods; Difficulty breathing; Distorted vision; Migraine NOS; This is a spontaneous report from a contactable consumer or other non hcp received from the Regulatory Authority.
The regulatory authority report number is GB-MHRA-WEBCOVID-202106242211312540-TZC50.
Safety Report Unique Identifier GB-MHRA-ADR 25539284.
A 29-year-old female non patient received first dose of BNT162B2 (PFIZER-BIONTECH COVID-19 VACCINE, Solution for injection, Batch/lot number and expiry date: not reported) via an unspecified route of administration on 01Jun2021 as single dose for COVID-19 immunisation.
Medical history included gastrointestinal disorder, suppressed lactation, glaucoma, asthma.
Patient has not had symptoms associated with COVID-19 and not had a COVID-19 test.
Patient is not enrolled in clinical trial.
Patient is not currently breastfeeding.
Patient has not tested positive for COVID-19 since having the vaccine.
The patient's concomitant medications were not reported.
On 14Jun2021, the patient experienced false pregnancy, irregular periods, difficulty breathing, distorted vision, migraine nos.
The events were reported as serious, medically significant.
Pregnancy tests have come back positive and negative on and off with no usual period and no unprotected sexual activity.
The outcome of the events was reported as not recovered.
No follow-up attempts are possible; Information about lot/batch number cannot be obtained.