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Report #2874155

Received Nov 21, 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
AR
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HEPAHEP A (HAVRIX)GLAXOSMITHKLINE BIOLOGICALS24T93R—

Symptoms (1)

Inappropriate schedule of product administration

Symptom narrative

the administration of Havrix after only 2 months after the initial dose was given; 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 78-year-old female patient who received HAV (Havrix) (batch number 4T93R, expiry date 07-NOV-2026) for prophylaxis. Concomitant products included HEPATITIS A VACCINE INACT (HAVRIX). On an unknown date, the patient received the 2nd dose of Havrix. On an unknown date, an unknown time after receiving Havrix, the patient experienced drug dose administration interval too short (Verbatim: the administration of Havrix after only 2 months after the initial dose was given). 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: 18-NOV-2025 The Vaccine Administration Facility was the same as Primary Reporter. The batch number was not provided upon follow- up with the reporter

Other medications

HAVRIX