Received Sep 30, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | OT / RA |
adverse reaction 4 inches below the injection site. It was red, inflamed and hard to the touch, 4 inches in diameter patch; adverse reaction 4 inches below the injection site. It was red, inflamed and hard to the touch, 4 inches in diameter patch; adverse reaction 4 inches below the injection site. It was red, inflamed and hard to the touch, 4 inches in diameter patch; Initial information received on 22-Sep-2025 regarding an unsolicited valid non-serious case received from a patient. This case involves a 77 years old female patient who had adverse reaction 4 inches below the injection site. it was red, inflamed and hard to the touch, 4 inches in diameter patch after receiving influenza vaccine The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On 19-Sep-2025, the patient received a dose of suspect influenza vaccine produced by unknown manufacturer (dose, strength, form, route, batch number, expiry date was unknown) in the right upper arm as immunization and that a tuberculin needle was used. No other vaccines were given On 20-SEP-2025 the patient had adverse reaction 4 inches below the injection site. it was red, inflamed and hard to the touch, 4 inches in diameter patch (vaccination site erythema) (vaccination site induration) (vaccination site inflammation) (Latency: 1 day) Action taken was not applicable. The patient was treated with Ibuprofen and ice bag for all the events. At time of reporting, the outcome was Not Recovered / Not Resolved for all the events