Received Aug 15, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| HEPA | HEP A (HAVRIX) | GLAXOSMITHKLINE BIOLOGICALS | UNK | HR4RB | — |
Havrix adult dose administered to pediatric patient; Havrix adult dose administered to pediatric patient; This non-serious case was reported by a nurse via call center representative and described the occurrence of adult product administered to child in a 3-year-old male patient who received HAV (Havrix adult) (batch number HR4RB, expiry date 18-DEC-2025) for prophylaxis. On 05-AUG-2025, the patient received Havrix adult. On 05-AUG-2025, an unknown time after receiving Havrix adult, the patient experienced adult product administered to child (Verbatim: Havrix adult dose administered to pediatric patient) and overdose (Verbatim: Havrix adult dose administered to pediatric patient). The outcome of the adult product administered to child and overdose were not applicable. Additional Information: GSK receipt date: 05-AUG-2025 The nurse called to report a pediatric patient of 3 years and 8 months was given an adult dose of the Havrix vaccine which led to adult product administration to child and overdose.