Received Dec 29, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUN3 | INFLUENZA (SEASONAL) (FLUMIST) | MEDIMMUNE VACCINES, INC. | UNK | Unknown | — |
Heavy nosebleed; A spontaneous report has been received from a consumer. The report concerns a female patient (age not provided). No medical history was reported. No concomitant products were reported. The patient received Flumist (batch number(s) Unknown), via unknown on an unknown date. The patient received 1 dose(s). It is unknown who administered Flumist to the patient. On an unknown date, the patient experienced heavy nosebleed (preferred term: Epistaxis). It is unknown if any action was taken with Flumist (flumist, influenza virus vaccine polyvalent, q/laiv). The outcome of the event(s) of heavy nosebleed was unknown. The event was considered non-serious. Device Information: Combination Product Report: Yes Product As Reported: Flumist Brand Name: FLUMIST Product Role: Suspect Manufacturer Name: ASTRAZENECA Labeled for single use: No Non significant correction on 22-Oct-2025: Null flavor was added. Narrative amended.