Received Oct 10, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLU3 | INFLUENZA (SEASONAL) (FLUBLOK) | SANOFI PASTEUR | UNK | — | OT |
local reactions at vaccination arm/site experienced following Flublok administration were a little intense; Initial information received on 04-Oct-2025 regarding an unsolicited valid non-serious case received from a consumer/non-hcp(non-healthcare professional). This case involves Adult female patient who had local reactions at vaccination arm/site, were a little intense after receiving Influenza Trivalent Recombinant Vaccine [Flublok]. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received an unknown dose of suspect Influenza Trivalent Recombinant Vaccine, Solution for injection (lot number, expiry date and strength not reported) via unknown route in unknown administration site for prophylactic vaccination (Immunisation). Information on the batch number was requested corresponding to the one at time of event occurrence. On an unknown date, the patient developed local reactions at vaccination arm/site, were a little intense (vaccination site reaction) (latency unknown) following the administration of Influenza Trivalent Recombinant Vaccine. Action taken was not applicable. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was Recovered / Resolved on an unknown date for the event.