Received Dec 16, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLU3 | INFLUENZA (SEASONAL) (FLULAVAL) | GLAXOSMITHKLINE BIOLOGICALS | UNK | UNK | — |
Flulaval vial broke while administering and broke on employees finger; Flulaval vial broke while administering and broke on employees finger; Flulaval vial broke while administering and broke on employees finger; Flulaval vial broke while administering and broke on employees finger; This non-serious case was reported by a consumer via interactive digital media and described the occurrence of occupational exposure via skin contact with product in a patient who received Flu Seasonal TIV Quebec (Flulaval) for prophylaxis. This case was associated with a product complaint. On an unknown date, the patient received Flulaval. On an unknown date, an unknown time after receiving Flulaval, the patient experienced occupational exposure via skin contact with product (Verbatim: Flulaval vial broke while administering and broke on employees finger), device breakage (Verbatim: Flulaval vial broke while administering and broke on employees finger), product leakage (Verbatim: Flulaval vial broke while administering and broke on employees finger) and pharmaceutical product complaint (Verbatim: Flulaval vial broke while administering and broke on employees finger). The outcome of the occupational exposure via skin contact with product, device breakage, product leakage and pharmaceutical product complaint were not applicable. It was unknown if the reporter considered the device breakage to be related to Flulaval and Flulaval Pre-Filled Syringe Device. It was unknown if the company considered the device breakage to be related to Flulaval and Flulaval Pre-Filled Syringe Device. This report is made by GSK without prejudice and does not imply any admission or liability for the incident or its consequences. Additional Information: GSK Receipt Date: 11-DEC-2025 This case was reported by a patient via interactive digital media. The Flulaval vial broke while administering and broke on employees finger. The batch number was not provided and unable to contact the reporter.