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Report #2831540

Received Mar 14, 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
74 yrs
State
TX
Recovered
Unknown
Vaccinated
Mar 11, 2025
Onset
Mar 11, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HEPABHEP A + HEP B (TWINRIX)GLAXOSMITHKLINE BIOLOGICALS2M4B34—

Symptoms (1)

Inappropriate schedule of product administration

Symptom narrative

came back for the 2nd dose in 11/Mar/2025; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of drug dose administration interval too long in a 74-year-old female patient who received HAB (Twinrix) (batch number M4B34, expiry date 28-SEP-2026) for prophylaxis. Previously administered products included Twinrix (the 1st dose of Twinrix was administered to the patient back in September 2024). On 11-MAR-2025, the patient received the 2nd dose of Twinrix. On 11-MAR-2025, an unknown time after receiving Twinrix, the patient experienced drug dose administration interval too long (Verbatim: came back for the 2nd dose in 11/Mar/2025). The outcome of the drug dose administration interval too long 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 : 11-MAR-2025 A pharmacist called to inform that a patient delayed their 2nd dose of Twinrix. The patient received 2nd dose of Twinrix, later than the recommended interval, which led to lengthening of vaccination schedule.