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Report #2842973

Received May 28, 2025

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
NM
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
RSVRSV (AREXVY)GLAXOSMITHKLINE BIOLOGICALSUNK——
VARZOSZOSTER (SHINGRIX)GLAXOSMITHKLINE BIOLOGICALSUNK——

Symptoms (2)

RashRash vesicular

Symptom narrative

blustery rash on hands and feet with severe pain; blustery rash on hands and feet with severe pain; This non-serious case was reported by a consumer via sales rep and described the occurrence of rash in a patient who received Herpes zoster (Shingrix) for prophylaxis. Co-suspect products included RSVPreF3 adjuvanted (Arexvy) for prophylaxis. On an unknown date, the patient received Shingrix and Arexvy. On an unknown date, an unknown time after receiving Shingrix and Arexvy, the patient experienced rash (Verbatim: blustery rash on hands and feet with severe pain) and pain (Verbatim: blustery rash on hands and feet with severe pain). The outcome of the rash was unknown and the outcome of the pain was not reported. It was unknown if the reporter considered the rash and pain to be related to Shingrix and Arexvy. It was unknown if the company considered the rash and pain to be related to Shingrix and Arexvy. Additional Information: GSK Receipt Date: 21-MAY-2025 The patient was vaccinated with Shingrix and Arexvy at the pharmacy in the same day. The patient later developed a blustery rash on hands and feet with severe pain.; Sender's Comments: US-GSK-US2025063431:same reporter