VAERS 2673858
SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ787AA
- Staat
- MI
- Alter
- 1,0
- Geschlecht
- F
- Eingang
- 21.08.2023
- Impfdatum
- 14.08.2023
- Beginn
- 14.08.2023
- Tage bis Beginn
- 0,0
- Dosis
- UNK
- Route/Site
- OT / LL
Symptomtext
expired ACT HIB vaccine was administered with no reported adverse event; Initial information received on 15-Aug-2023 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 12 months old female patient for whom expired HIB (PRP/T) vaccine [ACT-HIB] vaccine was administered with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 14-Aug-2023, the patient received an expired dose of 0.5 ml (Frequency = once) suspect HIB (PRP/T) VACCINE powder and solvent for solution for injection (lot: UJ787AA) via intramuscular route in the left thigh for Immunisation with no reported adverse event (expired product administered) (latency: same day). Action taken: not applicable. At time of reporting, the outcome was Unknown. 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 Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. 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
- -