Received May 30, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUN4 | INFLUENZA (SEASONAL) (FLUMIST QUADRIVALENT) | MEDIMMUNE VACCINES, INC. | UNK | Unknown | — |
On 15Dec2024 patient received dose of FluMist that expired on 09Dec2024; C: Nurse at HCP office administered expired dose of FluMist; A spontaneous report has been received from a other health professional. The report concerns a female patient born in 1990. No medical history was reported. No concomitant products were reported. The patient received Flumist, Influenza Virus Vaccine Polyvalent, Q/Laiv (batch number(s) Unknown) (expiration date(s) 09-DEC-2024), via unspecified route, on 15-DEC-2024. The patient received 1 dose(s). On an unknown date, the patient experienced on 15dec2024 patient received dose of flumist that expired on 09dec2024 (preferred term: Expired product administered) and c: nurse at hcp office administered expired dose of flumist (preferred term: Wrong technique in product usage process). At the time of reporting, the event c: nurse at hcp office administered expired dose of flumist was ongoing. The outcome of the event(s) of on 15dec2024 patient received dose of flumist that expired on 09dec2024 was unknown. The events were considered non-serious. This case was marked as suppressed due to Misuse/Product use issues with no associated AE. Device Information: Combination Product Report: Yes Product As Reported: Flumist, Influenza Virus Vaccine Polyvalent, Q/Laiv Brand Name: FLUMIST, INFLUENZA VIRUS VACCINE POLYVALENT, Q/LAIV Product Role:Suspect Manufacturer Name:ASTRAZENECA Labeled for single use:No Corrected report the event inappropriate schedule of drug administration deleted as it was already coded in the event expired product administered and Flumist was re coded correctly. Narrative was updated., case suppressed due to Misuse/Product use issues with no associated AE. Case corrected in response to data correction request DCR-011041-A