Symptomtext
excursion was due to the door being ajar. The temperature of the refrigerator reached 41.0-62.0 degrees Fahrenheit with no adverse event; Initial information received on 03-Jan-2023 regarding an unsolicited valid serious case received from a other health professional. This case involves an event of product storage error of MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE [MENQUADFI], DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE [ADACEL] and DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE [PENTACEL] (excursion was due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event). On 30-Dec-2022, it was reported DIPHTHERIA/TETANUS/5 HYBRID AC PERTUSSIS/IPV(MRC5)/HIB(PRP/T) VACCINE (lot UJ680ABA), DIPHTHERIA-2/TETANUS/5 AC PERTUSSIS VACCINE (lot U7561AA) and MENINGOCOCCAL A-C-Y-W135 (T CONJ) VACCINE lot (U7576AD) (strength, formulation, dose, route and expiry date: unknown) to be used for immunization was exposed to excursion due to the door being ajar. the temperature of the refrigerator reached 41.0-62.0 degrees fahrenheit with no adverse event (product storage error) (unknown latency). Action taken: not applicable. It was not reported if the patient received a corrective treatment for the events. Outcome: 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 the guidelines. 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.