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Report #2886697

Received Feb 24, 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
HI
Recovered
Unknown
Vaccinated
Feb 3, 2026
Onset
Feb 3, 2026
Days to onset
0
Hospital days

Vaccines (1)

TypeNameManufacturerDoseLotRoute / Site
VARCELVARICELLA (VARIVAX)MERCK & CO. INC.UNKY017062

Symptoms (2)

No adverse eventProduct storage error

Symptom narrative

No additional AE/no PQC reported; Customer called to report TE. Vaccines were administered to patients. Symptoms were not reported. Permission to contact was granted. AE was filled in case #s 02952625; 02952673; 02952674; 02952675; 02952676; 02952677; 02952678; 02952679; 02952680; 02; This spontaneous report was received from a medical assistant and refers to a patient of unknown age and gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, and previous drug reactions or allergies were not reported. On 03-Feb-2026, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), lot #Y017062 has been verified to be a valid lot number, expiration date: 11-Oct-2026, administered for prophylaxis (dose, route of administration and anatomical site of injection were not reported). The vaccine was reconstituted with sterile diluent solution for injection (Hollister-Stier STERILE DILUENT), (lot # and expiration date were not reported). The reconstituted vaccine underwent a temperature excursion, being exposed to temperatures between -14°C and -10°C (reported as -13.6°C) for a duration of 2 hours, 5 minutes, and 0 seconds (Improper storage of product in use). No additional adverse event was reported (no adverse event).

Other medications

MERCK STERILE DILUENT