Received Oct 9, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| HIBV | HIB (ACTHIB) | SANOFI PASTEUR | 4 | UK151AA | OT / LL |
inadvertently administered expired ACT-HIB to a patient, with no reported adverse event; Initial information received on 08-Oct-2025 regarding an unsolicited valid non-serious case received from a other health professional. This case involves a 18 months old male patient who inadvertently administered expired HIB (PRP/T) VACCINE [ACT-HIB] with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included Hepatitis a vaccine for Immunisation; and Varicella zoster vaccine (Varicella vaccine) for Immunisation. On 08-Oct-2025, the patient inadvertently administered expired a dose 4 of 0.5 ml dose of suspect HIB (PRP/T) VACCINE Powder and solvent for solution for injection (lot UK151AA, Expiry date: 30-Sep-2025) via intramuscular route in the left thigh as Immunization (expired product administered; Latency: same day). Action taken was not applicable. 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.
Hepatitis A; Varicella vaccine