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Report #2840781

Received May 13, 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
Female
Age
Age unknown
State
—
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
VARZOSZOSTER (SHINGRIX)GLAXOSMITHKLINE BIOLOGICALS1UNK—

Symptoms (2)

NauseaVomiting

Symptom narrative

patient developed nausea; vomiting; This non-serious case was reported by a consumer via sales rep and described the occurrence of nausea in a 55-year-old female patient who received Herpes zoster (Shingrix) for prophylaxis. On an unknown date, the patient received the 1st dose of Shingrix. On an unknown date, several hours after receiving Shingrix, the patient experienced nausea (Verbatim: patient developed nausea) and vomiting (Verbatim: vomiting). Shingrix was discontinued. The outcome of the nausea and vomiting were not reported. It was unknown if the reporter considered the nausea and vomiting to be related to Shingrix. It was unknown if the company considered the nausea and vomiting to be related to Shingrix. Additional Information: GSK Receipt Date: 09-MAY-2025 The reporter reported that the patient took the 1 dose of the Shingrix. Within a few hours the patient developed nausea and vomiting. Her side effects were so severe that her doctor decided not to give her dose 2 of the series.