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Report #2871364

Received Nov 7, 2025

A note on interpretation. VAERS reports are unverified and may be incomplete or coincidental. A report does not establish that a vaccine caused an event, and counts should not be used to calculate incidence or infer causation. Full disclaimer

Overview

Sex
Female
Age
Age unknown
State
CO
Recovered
Unknown
Vaccinated
Sep 29, 2025
Onset
Sep 29, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HEPABHEP A + HEP B (TWINRIX)GLAXOSMITHKLINE BIOLOGICALSUNKP2443—

Symptoms (2)

Inappropriate schedule of product administrationWrong product administered

Symptom narrative

A 63 years old female patient received a dose of Havrix an 5 months later a dose of Twinrix.; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of drug dose administration interval too short in a 63-year-old female patient who received HAB (Twinrix) (batch number P2443, expiry date 18-SEP-2027) for prophylaxis. Previously administered products included Havrix (1st dose received on 14th April 2025). On 29-SEP-2025, the patient received Twinrix. On 29-SEP-2025, an unknown time after receiving Twinrix, the patient experienced drug dose administration interval too short (Verbatim: A 63 years old female patient received a dose of Havrix an 5 months later a dose of Twinrix.). The outcome of the drug dose administration interval too short was not applicable. 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: 22-OCT-2025 The patient received Havrix on 4/14/2025 and then the next HepA dose was a dose of Twinrix on 9/29/2025. The reporter asked what was the dosing schedule to follow.