Symptomtext
Pentacel and Acthib on the same day in error due to the wrongfully pulling the ActHib vaccine. with no reported adverse event; Pentacel and Acthib on the same day in error due to the wrongfully pulling the ActHib vaccine. with no reported adverse event; Initial information regarding an unsolicited valid non-serious case was received from other health care professional via physician. (Reference number- 00647951) and transmitted to Sanofi on 18-Jun-2021. This case involves a 1 year old female patient administered DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (Lot number: U6899AB and expiry date: 17-amy-2022) and 0.50ml dose of HIB (PRP/T) VACCINE [ACT-HIB] standard once (Lot number: UJ398AAA and expiry date: 06-Aug-2021) via intramuscular route in left thigh for prophylactic vaccination on 18-Jun-2021 on the same day in error due to the wrongfully pulling the ACT-HIB vaccine (wrong product administered and extra dose administered) Relevant medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included PNEUMOCOCCAL VACCINE CONJ 13V (CRM197) (PREVNAR 13) and MEASLES VACCINE, MUMPS VACCINE, RUBELLA VACCINE (MEASLES, MUMPS AND RUBELLA VACCINE) for prophylactic vaccination. It was a case of an actual medication error due to wrong vaccine administered and extra dose administered (latency same day). At the time of report, no adverse event was reported. At the time of reporting, the outcome of both events were unknown. 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