Received Aug 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| DTPPVHBHPB | DTAP+IPV+HIB+HEPB (VAXELIS) | MSP VACCINE COMPANY | UNK | U7374BA | RL |
No adverse event; Which an expired dose of VAXELIS was administered to a patient; This non-serious spontaneous safety report with reference number 02814911 was received by partner on 02-JUN-2025 and forwarded on 02-JUN-2025 from a healthcare professional. This case is non-valid as no patient identifiers were not provided at the time of reporting. Due to the nature of the event, the causality between Vaxelis and the event of "Which an expired dose of VAXELIS was administered to a patient" was not applicable. Further information is expected. SIGNFICANT FOLLOW-UP INFORMATION was received from a nurse on 06-JUN-2025. Patient identifiers were provided, and the case is now valid. Due to the nature of the event, the causality between Vaxelis and the events of "expired dose of VAXELIS was administered to a patient" and "No adverse event" were not applicable. Further information is not expected.
Prophylaxis
PREVNAR 20; ROTATEQ