Received Apr 16, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLU3 | INFLUENZA (SEASONAL) (FLUZONE) | SANOFI PASTEUR | UNK | — | — |
received one too many flu vaccines/Upon discussion caller confirmed product was FLUZONE, with no reproted adverse event; Initial information received on 31-Mar-2026 regarding an unsolicited valid non-serious case received from a Physician. This case involves a patient of unknown age and unknown gender who received too many Influenza Usp Trival A-B Subvirion No Preservative Vaccine [Fluzone] with no reported adverse event The patient's past medical history, medical treatment(s), vaccination(s), family history were not provided. The patient received too many Influenza Usp Trival A-B Subvirion No Preservative Vaccine, Suspension for injection of unknown strength (batch/expiry: unknown) via unknown route in an unknown administration site for prophylactic vaccination (Immunisation) with no reported adverse event (Extra dose administered) (latency: unknown). Information regarding batch number corresponding to the one at time of event occurrence is requested. Action taken: Not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Comments: NONE