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Report #2894011

Received Apr 24, 2026

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
CA
Recovered
Unknown
Vaccinated
Mar 17, 2026
Onset
Mar 13, 2026
Days to onset
Hospital days

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
HEPHEP B (ENGERIX-B)GLAXOSMITHKLINE BIOLOGICALS2
HEPHEP B (ENGERIX-B)GLAXOSMITHKLINE BIOLOGICALSUNK

Symptoms (1)

Underdose

Symptom narrative

Administration of second pediatric dose; Administration of second pediatric dose; Second dose early; Administration of first pediatric dose; Administration of first pediatric dose; This non-serious case was reported by a other health professional via call center representative and described the occurrence of adult use of a child product in a 42-year-old female patient who received HBV (Engerix B pediatric) for prophylaxis. Co-suspect products included HBV (Engerix B pediatric) (batch number LG749, expiry date 13-SEP-2026) for prophylaxis. On 17-MAR-2026, the patient received the 2nd dose of Engerix B pediatric. On 13-MAR-2026, the patient received the 1st dose of Engerix B pediatric. On 13-MAR-2026, not applicable after receiving Engerix B pediatric, 14 days after receiving Engerix B pediatric and 18 days after starting Engerix B pediatric, the patient experienced adult use of a child product (Verbatim: Administration of first pediatric dose) and underdose (Verbatim: Administration of first pediatric dose). On 17-MAR-2026, the patient experienced adult use of a child product (Verbatim: Administration of second pediatric dose), underdose (Verbatim: Administration of second pediatric dose) and drug dose administration interval too short (Verbatim: Second dose early). The outcome of the adult use of a child product, underdose, drug dose administration interval too short, adult use of a child product and underdose were 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: 14-APR-2026 The reporter reported about the administration after a 42-year-old patient received 2 pediatric doses on 13-MAR-2026 and 17-MAR-2026. The batch number was not provided upon follow- up with the reporter.