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VAERS ID 2404172
성별 알 수 없음
나이 65세
주 코드 AZ
제약회사 MODERNA
로트 번호 058A222A
예방접종 횟수
접종일 2022-07-14
발병일 2022-07-14
상태
증상
  • 부작용 없음(No adverse event)
  • 제품 보관 오류(Product storage error)
  • 유통기한이 지난 제품이 관리됨(Expired product administered)

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임상 검사

증상 상세

Vaccine was stored in refrigerator on 04-Jun-2022 and administered vaccine on 14-Jul-2022; No adverse event; Patient administered the vaccine after the 30 day by used; This spontaneous case was reported by an other health care professional and describes the occurrence of EXPIRED PRODUCT ADMINISTERED (Patient administered the vaccine after the 30 day by used), PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 04-Jun-2022 and administered vaccine on 14-Jul-2022) and NO ADVERSE EVENT (No adverse event) in a 65-year-old patient of an unknown gender who received mRNA-1273 (Moderna COVID-19 Vaccine) (batch no.
058A22-2A) for COVID-19 prophylaxis.
No Medical History information was reported.
On 14-Jul-2022, the patient received dose of mRNA-1273 (Moderna COVID-19 Vaccine) (unknown route) 1 dosage form.
On 14-Jul-2022, the patient experienced EXPIRED PRODUCT ADMINISTERED (Patient administered the vaccine after the 30 day by used).
On an unknown date, the patient experienced PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 04-Jun-2022 and administered vaccine on 14-Jul-2022) and NO ADVERSE EVENT (No adverse event).
At the time of the report, EXPIRED PRODUCT ADMINISTERED (Patient administered the vaccine after the 30 day by used), PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 04-Jun-2022 and administered vaccine on 14-Jul-2022) and NO ADVERSE EVENT (No adverse event) outcome was unknown.
For mRNA-1273 (Moderna COVID-19 Vaccine) (Unknown), the reporter considered NO ADVERSE EVENT (No adverse event) to be not related.
No further causality assessments were provided for EXPIRED PRODUCT ADMINISTERED (Patient administered the vaccine after the 30 day by used) and PRODUCT STORAGE ERROR (Vaccine was stored in refrigerator on 04-Jun-2022 and administered vaccine on 14-Jul-2022).
No concomitant product use was reported.
Reportedly, Patient received half dose.
Vial did not undergo any temperature excursions.
No treatment information was provided.