Received Oct 10, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| FLUX | INFLUENZA (SEASONAL) (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | — |
| MMR | MEASLES + MUMPS + RUBELLA (MMR II) | MERCK & CO. INC. | UNK | Z004961 | — |
No additional AE/PQC.; a patient who was administered a dose of MMR-II that was inadvertently reconstituted with a prefilled syringe containing a flu vaccine (unspecified) instead of sterile diluent; Caller reported AE on behalf of a patient who was administered a dose of MMR-II that was inadvertently reconstituted with a prefilled syringe containing a flu vaccine (unspecified) instead of sterile diluent on 10/03/2025. No symptoms reported. Obtai; This spontaneous report was received from a Nurse and refers to a 32-year-old patient of unknown gender. The patient's pertinent medical history, concurrent conditions, concomitant medications, and previous drug reactions or allergies were not reported. On 03-Oct-2025, the patient was vaccinated with Measles, Mumps, and Rubella (Wistar RA 27-3) Virus Vaccine, Live (M-M-R II), lot #Z004961. The lot number has been verified as valid, with an expiration date of 24-Feb-2027. The vaccine was administered at a dose of 0.5 mL for prophylaxis (route of administration and anatomical site of injection were not provided). The vaccine was inadvertently reconstituted with a prefilled syringe containing an influenza vaccine (reported as "flu vaccine," trade name unspecified) instead of the sterile diluent (dose description, indication, lot # and expiration date was not provided) (Wrong vaccine administered, vaccine incorrect diluent used). No symptoms were reported (no adverse event).; Reporter's Comments: Keywords: OCL