Received Aug 26, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| DTPPVHBHPB | DTAP+IPV+HIB+HEPB (VAXELIS) | MSP VACCINE COMPANY | 1 | U7536AA | LL |
No adverse event experienced; Patient received an expired dose of VAXELIS/ No side effects or symptoms reported.; This non-serious, spontaneous, safety report with reference number: 02818204/ 02818200 was received by partner on 06-JUN-2025 and forwarded to agency on 09-JUN-2025 from a medical assistant. Due to the nature of the event, the causality between Vaxelis and the event of " Patient received an expired dose of VAXELIS/ No side effects or symptoms reported." were not applicable. Further information is expected. FOLLOW-UP INFORMAWTION was received on 24-JUN-2025 from a medical assistant. Due to the nature of the event, the causality between Vaxelis and the event of "Patient received an expired dose of VAXELIS/ No side effects or symptoms reported, and no adverse event" were not applicable. Further information is not expected.
Prophylaxis
ROTATEQ; PREVENAR