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Report #2842492

Received May 23, 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
NY
Recovered
Unknown
Vaccinated
—
Onset
—
Days to onset
—
Hospital days
—

Vaccines (2)

TypeNameManufacturerDoseLotRoute / Site
VARCELVARICELLA (VARIVAX)MERCK & CO. INC.UNKZ003766OT
VARCELVARICELLA (VARIVAX)MERCK & CO. INC.UNK——

Symptoms (2)

No adverse eventProduct storage error

Symptom narrative

A pharmacist called and reported that an improperly stored dose of VARIVAX was administered to a patient. The caller did not have any other additional information to add to further clarify the details, including patient demographics or the dates of a; No adverse event; This spontaneous report was received from a/an Pharmacist and refers to a(n) 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 an unknown date, the patient started therapy with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), (lot #Z003766, expiration date: 30-Jan-2027) administered by Unknown route. The patient started therapy with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX), for the treatment of Prophylaxis. On an unknown date, the patient experienced A pharmacist called and reported that an improperly stored dose of VARIVAX was administered to a patient. The caller did not have any other additional information to add to further clarify the details, including patient demographics or the dates of a. On an unknown date, the patient experienced No adverse event. At the reporting time, the outcome of A pharmacist called and reported that an improperly stored dose of VARIVAX was administered to a patient. The caller did not have any other additional information to add to further clarify the details, including patient demographics or the dates of a and No adverse event was unknown. The action taken with Varicella Virus Vaccine Live (Oka-Merck) was reported as not applicable. The case ws determined to be non-valid due to lack of patient's identifiers.