Received Feb 24, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | OT |
Type A flu only; Initial information received on 12-Feb-2025 regarding an unsolicited valid non-serious case received from a Patient. This case involves Adult female patient who experienced type a flu only after receiving Influenza Vaccine. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a dose of suspect Influenza vaccine solution for injection produced by unknown manufacturer lot number not reported via unknown route in unknown administration site (strength and expiration date: not provided) for Immunisation. Information regarding batch number and expiration date corresponding to the one at a time of event occurrence was requested. On an unknown date the patient developed type a flu only (influenza) (unknown latency). Action taken- not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Unknown for the event.