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Report #2899403

Received Jun 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
Unknown
Age
Age unknown
State
WI
Recovered
Unknown
Vaccinated
Onset
Days to onset
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNK

Symptoms (1)

Product preparation issue

Symptom narrative

The two vials of Arexvy were not mixed before administration/ Arexvy was not mixed with both vials before given to patient; The two vials of Arexvy were not mixed before administration; This non-serious case was reported by a nurse via sales rep and described the occurrence of inappropriate preparation of medication in a patient who received RSVPreF3 adjuvanted (Arexvy) suspension for injection for prophylaxis. On an unknown date, the patient received Arexvy. On an unknown date, an unknown time after receiving Arexvy, the patient experienced inappropriate preparation of medication (Verbatim: The two vials of Arexvy were not mixed before administration/ Arexvy was not mixed with both vials before given to patient) and inappropriate dose of vaccine administered (Verbatim: The two vials of Arexvy were not mixed before administration). The outcome of the inappropriate preparation of medication and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 03-JUN-2026 The batch number was not provided upon follow up with the reporter.