VAERS 1429462
SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ225ABA
- Staat
- CA
- Alter
- 1,3
- Geschlecht
- F
- Eingang
- 26.06.2021
- Impfdatum
- 27.04.2021
- Beginn
- 27.04.2021
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / -
Symptomtext
The Patient received a dose of ACTHIB that was 4 days expired with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from the other health professional via medical information (Reference number- 00650269) and transmitted to Sanofi on 21-Jun-2021. This case involves a one-year-old female patient who received a 0.5 mL dose of suspect HIB (PRP/T) VACCINE [ACT-HIB] [total, once, lot number: UJ225ABA, expiry date: 23-APR-2021, other dosing details were not reported] on 27-Apr-2021 for prophylactic vaccination that was 4 days expired (expired product administered). Medical history, medical treatment, vaccination, family history and concomitant medication were not reported. It was a case of actual medication error de to expired vaccine used. At the time of report, reporter was requesting clinical guidance If does it need to be re-administered. At the time of report, no adverse event was reported. At the time of reporting, event outcome was unknown for event. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the guidelines. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Weitere VAERSDATA-Felder
- Praegender Schweregrund
- Expired product administered
- Hospital-Tage
- -
- Labordaten
- -
- Aktuelle Erkrankungen
- -
- Vorgeschichte
- -
- Andere Medikamente
- -
- Allergien
- -
- Vorherige Impfungen
- -