Received Jun 13, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| VARCEL | VARICELLA (VARIVAX) | MERCK & CO. INC. | UNK | Y017063 | — |
No symptoms reported; Nurse called to report TE for VARIVAX and reports the VARIVAX was inadvertently administered; This spontaneous report was received from a nurse and refers to a patient of unknown age and gender. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 19-May-2025, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) for prophylaxis (lot #Y017063 was verified to be a valid number, expiration date: 11-Oct-2026) (dose, scheme, route of administration, formulation and injection site were not reported) reconstituted with sterile diluent (BAXTER STERILE DILUENT) (dose, frequency, route of administration, expiration date and lot # were not reported). The vaccine underwent a temperature excursion of -11.5 Celsius degree for 24 minutes (product storage error). No symptoms were reported (no adverse event).
Sterile diluent