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Report #2900216

Received Jun 15, 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
OH
Recovered
Unknown
Vaccinated
Jun 8, 2026
Onset
Jun 8, 2026
Days to onset
0
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNK3CA5T

Symptoms (1)

Product preparation issue

Symptom narrative

Possible administration with sterile diluent; Possible administration with sterile diluent; This non-serious case was reported by a other health professional via call center representative and described the occurrence of wrong solution used in drug reconstitution in a patient who received RSVPreF3 adjuvanted (Arexvy) suspension for injection (batch number 3CA5T with expiry date 27-FEB-2027) for prophylaxis. On 08-JUN-2026, the patient received Arexvy. On 08-JUN-2026, an unknown time after receiving Arexvy, the patient experienced wrong solution used in drug reconstitution (Verbatim: Possible administration with sterile diluent) and inappropriate dose of vaccine administered (Verbatim: Possible administration with sterile diluent). The outcome of the wrong solution used in drug reconstitution and inappropriate dose of vaccine administered were not applicable. Additional Information: GSK Receipt Date: 08-JUN-2026 A reporter requested data about the possibility of having had administered Arexvy with sterile water diluent instead of the adjuvant in an unknow patient, with the administration taking place in the last week.