Reporte zur Charge UI196AB

Symptomtext

bad reaction; Initial information was received on 16-Jul-2021 regarding an unsolicited valid non-serious case from a consumer/non-hcp (healthcare professional). This case involves a male patient who experienced bad reaction (adverse event) after receiving vaccine INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED [FLUZONE QUADRIVALENT MULTIDOSE]. The patient's medical history, past medical treatments, past vaccinations, concomitant medication and family history were not provided. In 2014, the patient received a dose of suspect INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED (lot UI196AB and expiry date: 30-Jun-2015) via unknown route at an unknown administration site for prophylactic vaccination. On an unknown date, the patient developed a non-serious bad reaction (adverse reaction) (unknown latency) following the administration of INFLUENZA QUADRIVAL A-B MULTIDOSE VACCINE PRESERVED. It was reported that "reporter would like to know the ingredients in FLULAVAL 2014 MDV? Please see Event Field for additional information. Additional Description of event Adverse events : Caller would like to know the ingredients in FLULAVAL 2014 MDV? Caller would like to know what went into his body. Advised caller to visit website which is a institute of health website." Laboratory data was not reported. It was not reported if the patient received a corrective treatment for the event. At time of reporting, the outcome was unknown for the event.