Received Oct 21, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUN3 | INFLUENZA (SEASONAL) (FLUMIST) | MEDIMMUNE VACCINES, INC. | UNK | — | — |
NASOPHARYNGITIS; A spontaneous report has been received from a consumer. The report concerns a male patient (age not provided). No medical history was reported. No concomitant products were reported. The patient received Flumist, via unknown on an unknown date. The patient received 1 dose(s). No malfunction has been reported for the Accuspray Single Dose device. On an unknown date, the patient experienced nasopharyngitis (preferred term: Nasopharyngitis). The outcome of the event(s) of nasopharyngitis was unknown. The event was considered non-serious. The reporter considered that there was a reasonable possibility of a causal relationship between Accuspray Single Dose and the following event(s): nasopharyngitis. The reporter considered that there was a reasonable possibility of a causal relationship between Flumist and the following event(s): nasopharyngitis. Device Information: Combination Product Report: Yes Product As Reported: Flumist Brand Name: FLUMIST Product Role:Suspect Device Problem code:Adverse Event Without Identified Device or Use Problem Manufacturer Name:ASTRAZENECA Labeled for single use:No Corrected report on 18-Oct-2025: Patient County set as NASK, Potential SAE and Device malfunction updated as NO. Operator of device updated. Non-Significant correction on 21-Oct-2025: Null flavor removed for telephone and fax, Narrative amended.