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Report #2841512

Received May 19, 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
Male
Age
54 yrs
State
OH
Recovered
Unknown
Vaccinated
May 9, 2025
Onset
May 9, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HEPAHEP A (HAVRIX)GLAXOSMITHKLINE BIOLOGICALSUNK2345bLA

Symptoms (2)

Inappropriate schedule of product administrationNo adverse event

Symptom narrative

The first dose had been given on February 7, 2025, and the second dose had been given on May 9, 2025, six months earlier; This non-serious case was reported by a other health professional via sales rep and described the occurrence of drug dose administration interval too short in a 54-year-old male patient who received HAV (Havrix adult) (batch number 2345b, expiry date 02-FEB-2026) for prophylaxis. Concurrent medical conditions included fatty liver, hypertension and sleep disorder. Concomitant products included Hepatitis a vaccine inact (Havrix) and amitriptyline. On 09-MAY-2025, the patient received Havrix adult (left deltoid). On 09-MAY-2025, an unknown time after receiving Havrix adult, the patient experienced drug dose administration interval too short (Verbatim: The first dose had been given on February 7, 2025, and the second dose had been given on May 9, 2025, six months earlier). The outcome of the drug dose administration interval too short was not applicable. Additional Information: GSK Receipt Date: 09-MAY-2025 The first dose had been given on 7th February 2025, and the second dose had been given on 9th May 2025, six months earlier, which led to Drug dose administration interval too short. No symptoms had been recorded.

Current illness

Fatty liver; Hypertension; Sleep disorder

Other medications

Havrix; Amitriptyline