Received Jun 7, 2025
| Type | Name | Manufacturer | Dose | Lot | Route / Site |
|---|---|---|---|---|---|
| RAB | RABIES (IMOVAX) | SANOFI PASTEUR | UNK | — | OT |
imovax was told to take her booster shot on Day 7 and 21 but she took it on Day 9 with no reported adverse event; Initial information received on 05-Jun-2025 regarding an unsolicited valid non-serious case received from a patient. This case involves an unknown age female patient who was on RABIES (HDC) VACCINE [IMOVAX RABIES] was told to take her booster shot on day 7 and 21 but she took it on day 9 with no reported adverse event. The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. On an unknown date, the patient received a Booster dose of suspect RABIES (HDC) VACCINE Powder and solvent for suspension for injection (strength, dose, batch and expiry date unknown) via unknown route in unknown administration site for Immunization was told to take her booster shot on day 7 and 21 but she took it on day 9 with no reported adverse event (inappropriate schedule of product administration) (same day latency). Information on batch number and expiry date corresponding to the one at time of event occurrence was requested. 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.