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Report #2900459

Received Jun 17, 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
50 yrs
State
PA
Recovered
Unknown
Vaccinated
Jun 16, 2026
Onset
Jun 16, 2026
Days to onset
0
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HEPHEP B (ENGERIX-B)GLAXOSMITHKLINE BIOLOGICALSUNKD2D49

Symptoms (1)

Underdose

Symptom narrative

Pediatric dose administered to adult patient; Pediatric dose administered to adult patient; This non-serious case was reported by a nurse via call center representative and described the occurrence of adult use of a child product in a 50-year-old female patient who received HBV (Engerix B pediatric) suspension for injection in pre-filled syringe (batch number D2D49 with expiry date 24-SEP-2027) for prophylaxis. On 16-JUN-2026, the patient received Engerix B pediatric. On 16-JUN-2026, an unknown time after receiving Engerix B pediatric, the patient experienced adult use of a child product (Verbatim: Pediatric dose administered to adult patient) and underdose (Verbatim: Pediatric dose administered to adult patient). The outcome of the 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: 16-JUN-2026 The batch number was not provided upon follow up with the reporter.