Symptomtext
expired vaccine was administered to a patient with no adverse event; Initial information received on 31-May-2022 regarding an unsolicited valid non-serious case received via other health professional. This case involves a 15 months old male patient who experienced expired vaccine was administered to a patient with no adverse event while receiving vaccine hib (prp/t) vaccine (Act-Hib). The patient's past medical history, medical treatment(s), vaccination(s) and family history were not provided. Concomitant medications included pneumococcal vaccine conj 13v (crm197) (Prevnar 13). On 31-May-2022, the patient received a dose of suspect hib (prp/t) vaccine at a dose of 0.5 ml with lot UJ513AB and expiry date: 29-May-2022 (expired product administered) via intramuscular route in left thigh for Immunization. Action taken: not applicable. 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 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.