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Report #2854868

Received Aug 20, 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
AZ
Recovered
Unknown
Vaccinated
Aug 14, 2025
Onset
Aug 14, 2025
Days to onset
0
Hospital days
—

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
VARZOSZOSTER (SHINGRIX)GLAXOSMITHKLINE BIOLOGICALS25Y4TL—

Symptoms (1)

Inappropriate schedule of product administration

Symptom narrative

received a dose of Shingrix more than one year later from the first dose; This non-serious case was reported by a pharmacist via call center representative and described the occurrence of drug dose administration interval too long in a adult female patient who received Herpes zoster (Shingrix) (batch number 5Y4TL, expiry date 31-JAN-2027) for prophylaxis. Previously administered products included Shingrix (received first dose in March 2024). On 14-AUG-2025, the patient received the 2nd dose of Shingrix. On 14-AUG-2025, an unknown time after receiving Shingrix, the patient experienced drug dose administration interval too long (Verbatim: received a dose of Shingrix more than one year later from the first dose). The outcome of the drug dose administration interval too long was not applicable. Additional Information: GSK Receipt Date: 14-AUG-2025 The patient received the second dose of Shingrix later than the recommended interval, which led to lengthening of vaccine schedule. The reporter asked that the patient need to restart the series.