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Report #2881134

Received Jan 8, 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
WI
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
HIBVHIB (HIBERIX)GLAXOSMITHKLINE BIOLOGICALSUNK7JF7—

Symptoms (1)

Product preparation issue

Symptom narrative

diluent only was administered; diluent only was administered; This non-serious case was reported by a nurse via call center representative and described the occurrence of inappropriate preparation of medication in a female patient who received Hib (Hiberix) (batch number 7JF7, expiry date 15-JUL-2026) for prophylaxis. On an unknown date, the patient received Hiberix. On an unknown date, an unknown time after receiving Hiberix, the patient experienced inappropriate preparation of medication (Verbatim: diluent only was administered) and inappropriate dose of vaccine administered (Verbatim: diluent only was administered). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 06-JAN-2026 Nurse reported Hiberix was maladministered to a patient possibly only diluent was administered. This case is one of the three linked cases, reported by the same reporter.; Sender's Comments: US-GSK-US2026001197:Same reporter US-GSK-US2026001207:Same reporter