이상반응 보고

VAERS ID 2569881
성별 여성
나이 92세
주 코드 IL
제약회사 PFIZER\BIONTECH
로트 번호 GH9694
예방접종 횟수 1
접종일 2022-11-29
발병일 2022-12-02
상태 입원 사망
증상
  • 호흡곤란(Dyspnoea)
  • 쌕쌕거림(Wheezing)
  • 흉부 엑스레이 이상(Chest X-ray abnormal)
  • 발성 장애(Dysphonia)
  • 소변 분석(Urine analysis)
  • 부종(Oedema)
  • 생산적인 기침(Productive cough)
  • 헤모글로빈 감소(Haemoglobin decreased)
  • 빈혈증(Anaemia)
  • 폐렴(Pneumonia)
  • 호흡곤란(Respiratory distress)
  • 죽음(Death)
  • 전반적인 신체 건강 악화(General physical health deterioration)

이환 중 질병

only chronic issues.

지병

chronic pulmonary obstructive disease, HTN, chronic congestive heart failure, renal insufficiency

기타 의료

furosemide, iron sulfate, formoterol, montelukast, pantoprazole, budesonide, metoprolol, tramadol, calcium, enalapril

이전 예방접종

알레르기

codeine cyclobenzaprine

임상 검사

CXR: 12/08/2022 negative; Serum and UA labs: 12/22/2022 new onset anemia with hemoglobin 8.
2 with recent at baseline of 11.
4.
12/28/2022 CXR with multifocal pneumonia.

증상 상세

She received the Pfizer Bivalent inoculation on 11/29/2022, and at that time, was clinically stable with her acute issues with no recent exacerbations.
By 12/01/2022, she with productive cough, hoarseness, wheezing with shortness of breath.
this progressed over the next several days.
negative CXR, yet increasing respiratory distress/cough and edema.
she did not respond with any resolution of symptoms with steroids, diuretics, antibiotics.
she progressive worsening until sent to hospital on 12/28/2022 where had CXR with multifocal pneumonia and she expired on 12/29/2022.