Report #2854172

Received Aug 14, 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: VA
Recovered: Unknown
Vaccinated: Jun 18, 2025
Onset: Jun 18, 2025
Days to onset: 0
Hospital days: —

Vaccines (2)

Type	Name	Manufacturer	Dose	Lot	Route / Site
VARCEL	VARICELLA (VARIVAX)	MERCK & CO. INC.	UNK	Y019318	—
VARCEL	VARICELLA (VARIVAX)	MERCK & CO. INC.	UNK	—	—

Symptoms (2)

No adverse eventProduct storage error

Symptom narrative

No symptoms or side effects were reported by HCP.; HCP reporting that a patient received a dose of improperly stored VARIVAX; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history was not reported. The patient's concurrent conditions were not reported. Concomitant therapies were not reported. On 18-JUN-2025, the patient was vaccinated with improperly stored dose of Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), Injection (lot #Y019318 was valid, expiration date: 21-NOV-2026, 0.5 mL, route of administration and anatomical location were not provided) with sterile diluent (MERCK STERILE DILUENT) for prophylaxis (Product storage error). Temperature excursion of 52.2 F was reported. No symptoms or side effects were reported (No adverse event). No product quality complaint (PQC).