Received Apr 17, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| YF | YELLOW FEVER (YF-VAX) | SANOFI PASTEUR | UNK | — | OT |
expired YF-Vax was administered with no reported adverse event; Initial information received on 10-Apr-2025 regarding an unsolicited valid non-serious case received from a nurse. This case involves a 21 years old female patient to whom expired yellow fever vaccine [YF-VAX] 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 08-Apr-2025, the patient was administered an expired dose of suspect yellow fever vaccine (Solution for injection) (expiry date: 31-Mar-2025) strength; lot number not reported) via unknown route in unknown administration site for Immunisation with no reported adverse event (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.