Received Apr 10, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| UNK | VACCINE NOT SPECIFIED (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
| VARCEL | VARICELLA (VARIVAX) | MERCK & CO. INC. | UNK | Y002061 | — |
No Additional AE; HCP called to report one patient received VARIVAX after improperly stored. Np side effects or symptoms reported. No additional information provided. No Additional AE/ No PQC.; This spontaneous report was received from the nurse regarding 22-year-old male patient. The patient's medical history, concurrent conditions and concomitant therapies were not reported. On 09-Apr-2025, the patient was vaccinated with Varicella Virus Vaccine Live (Oka-Merck) (VARIVAX) lyophilisate and solvent for solution for injection 0.5 mL, lot#Y002061 (expiration date: 09-JAN-2026), along with sterile diluent (MERCK STERILE DILUENT) (lot number and expiration date not reported) as prophylaxis after being improperly stored (product storage error). Np side effects or symptoms were reported. No additional information was provided. No additional adverse event (AE) was reported.