Reporte zur Charge UT7035LA

Symptomtext

a nurse has administered Fluzone Quadrivalent to an elderly patient instead of Flublok with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from a healthcare professional via Medical Information (MI) (Reference number- 00410287) on 29-Dec-2020. This case involves a 73-year-old male patient who had administered INFLUENZA QUADRIVAL A-B VACCINE [FLUZONE QUADRIVALENT] instead of QUADRIVALENT RECOMBINANT VACCINE [FLUBLOK QIV] by nurse on 21-Dec-2020 (lot UT7035LA, expiration date: 30-Jun-2021) via intramuscular route in the left deltoid for prophylactic vaccination (wrong product administered). The patient's medical history, past medical treatment(s), vaccination(s), Concomitant medication and family history were not provided. This was an actual medication error case due to the event wrong product administered (latency: on the same day). At the time of reporting, no adverse event was reported. Disclaimer: 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 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.