Received Sep 18, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| MEN | MENINGOCOCCAL (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | U8493A A | OT |
| UNK | VACCINE NOT SPECIFIED (NO BRAND NAME) | UNKNOWN MANUFACTURER | UNK | — | OT |
No adverse event; Was supposed to receive MMR instead using correct diluent, was reconstitued with Menquadfi; Wrong product administered; This spontaneous report was received from an Other-health professional and refers to a 65-year-old male patient. The patient's medical history, concurrent conditions, concomitant therapies, drug reactions or allergies were not reported. On 05-Aug-2025, the patient was vaccinated with a dose of Measles, Mumps, and Rubella (M-M-R) vaccine (manufacturer unknown) (lot #, expiration date, strength, dose number, anatomical location not provided); which was supposed to be reconstituted with sterile diluent; however, it was reconstituted with Meningococcal vaccine A/C/Y/W conj (tet tox) (MENQUADFI) Solution for injection (lot #U8493A A, expiration date: 31-May-2028) (wrong diluent used), and was administered intramuscular as prophylactic vaccination. The patient was not supposed to get Meningococcal vaccine A/C/Y/W conj (tet tox) (MENQUADFI) at all (wrong product administered). No reported adverse events.; Sender's Comments: Priority : 5 , Is case serious : No , Index user : Index date : 2025-09-03 , MNSC number : , CLIC number : , ESTAR number : , IRMS number : GS / 2025SA229864 , Central date : 2025-09-03 , Classification : DMC, Attachment description : Post Marketing Basic , Safety case number :