Received Oct 30, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUN4 | INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) | MEDIMMUNE VACCINES, INC. | UNK | YF3413 | — |
NURSE REPORTED THERE WAS 40 MINUTES BETWEEN SPRAY 1 OF FLUMIST AND SPRAY 2 AS THE PATIENT INITIALLY REFUSED SPRAY 2. PATIENT DID RECEIVE BOTH SPRAY 1 AND SPRAY 2 OF FLUMIST.; A spontaneous report has been received from a other health professional. The report concerns a male child patient (age 10 years). No medical history was reported. No concomitant products were reported. The patient received Flumist Quadrivalent (batch number(s) YF3413) (expiration date(s) 08-DEC-2025), via unknown on 16-SEP-2025. The patient received 1 dose(s). On an unknown date, the patient experienced nurse reported there was 40 minutes between spray 1 of flumist and spray 2 as the patient initially refused spray 2. patient did receive both spray 1 and spray 2 of flumist. (preferred term: Incorrect dose administered). The outcome of the event(s) of nurse reported there was 40 minutes between spray 1 of flumist and spray 2 as the patient initially refused spray 2. patient did receive both spray 1 and spray 2 of flumist. was unknown. The event was considered non-serious. The reporter did not consider that there was a reasonable possibility of a causal relationship between Accuspray Single Dose and the following event(s): nurse reported there was 40 minutes between spray 1 of flumist and spray 2 as the patient initially refused spray 2. patient did receive both spray 1 and spray 2 of flumist.. The reporter did not consider that there was a reasonable possibility of a causal relationship between Flumist Quadrivalent and the following event(s): nurse reported there was 40 minutes between spray 1 of flumist and spray 2 as the patient initially refused spray 2. patient did receive both spray 1 and spray 2 of flumist.. Device Information: Combination Product Report: Yes Product As Reported: Flumist Quadrivalent Brand Name: FLUMIST QUADRIVALENT Product Role:Suspect Manufacturer Name:ASTRAZENECA Labeled for single use:No