Received Mar 28, 2026
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| RAB | RABIES (IMOVAX) | SANOFI PASTEUR | UNK | — | — |
they are using a day 0 to day 7 process but the patient is on day 8, with no reported adverse event; Initial information received on 11-Mar-2026 regarding an unsolicited valid non-serious case received from a pharmacist. This case involves a 28-year-old female patient who had an incorrect immunization rabies vaccine (IMOVAX RABIES), schedule where they were using a day 0 to day 7 process but the patient was on day 8, with no reported adverse event The patient's past medical history, past drugs, vaccination(s), family history, and concomitant medications were not provided. On 10-Mar-2026, the patient was to receive the rabies vaccine (Imovax Rabies) Powder and solvent for suspension for injection as part of an immunization schedule (dose, strength, route: not reported) The pharmacist reported that they were using a day 0 to day 7 immunization process but the patient was on day 8, with no reported adverse event [Routine immunisation schedule incomplete, onset: 10-Mar-2026, latency: same day] (batch: unknown, expiry: unknown). Action taken: Not applicable. This suspected adverse reaction report is submitted and classified as a medication error solely and exclusively to ensure the marketing authorization holder's compliance with the requirements set out in the Directive 2001/83/EC and Module VI of the Good Pharmacovigilance Practices. The classification as a medical error is in no way intended, nor should it be interpreted or construed as an allegation or claim made by the marketing authorization holder that any third party has contributed to or is to be held liable for the occurrence of this medication error.
Comments: NONE