VAERS 2627006
SANOFI PASTEUR · HIB (ACTHIB) · Charge UJ677AAA
- Staat
- MO
- Alter
- -
- Geschlecht
- U
- Eingang
- 05.05.2023
- Impfdatum
- -
- Beginn
- -
- Tage bis Beginn
- -
- Dosis
- UNK
- Route/Site
- OT / -
Symptomtext
administered ACTHIB vaccine that was expired to a patient with no reported adverse event; Initial information received on 02-May-2023 regarding an unsolicited valid non-serious case received from a physician. This case involves a patient of unknown age and gender who was administered HIB (PRP/T) vaccine [ACT-HIB] that was expired with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s), concomitants and family history were not provided. On an unknown date, HIB (PRP/T) vaccine [ACT-HIB] vaccine Powder and solvent for solution for injection (batch/lot number: UJ677AAA; expiry date: 07-Apr-2023; strength, dose, route: unknown) that was expired was administered to a patient in unknown administration site for prophylactic vaccination (immunization) with no reported adverse event (expired product administered) (latency: same day) Action taken: Not applicable. At time of reporting, the outcome was Unknown for the 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 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
- -