Received Oct 17, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUN3 | INFLUENZA (SEASONAL) (FLUMIST) | MEDIMMUNE VACCINES, INC. | UNK | — | — |
RASH; 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, via unknown on an unknown date. The patient received 1 dose(s). On an unknown date, the patient experienced rash (preferred term: Rash). The outcome of the event(s) of rash 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): rash. The reporter considered that there was a reasonable possibility of a causal relationship between Flumist and the following event(s): rash. 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;Insufficient Information Manufacturer Name:ASTRAZENECA Labeled for single use:No Non-significant correction on 16-Oct-2025: correction product start date. Narrative updated. Non-significant correction on 17-Oct-2025: Nullflavor removed for telephone and fax, Narrative amended.