BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 5532287 · Received March 24, 2016

    Report

    Report Number
    MW5061298
    Event Type
    Injury
    Date Received
    March 24, 2016
    Date of Event
    March 7, 2016
    Report Date
    March 24, 2016
    Manufacturer
    FERRING
    Product Code
    MOZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    VA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    WAS GIVEN A SERIES OF SHOTS TO IMPROVE MY MOBILITY AND PAIN AND HAD TO PAY A LARGE CO-PAY AND AS A RESULT OF TAKING EUFLEXXA I HAVE MORE PAIN AND CAN HARDLY MOVE ONE OF MY LEGS. I WORK AND IT HAS REALLY BECOME A PROBLEM FOR ME WITH THE PAIN AND MOBILITY. I HAVE HAD OTHER TREATMENTS AND THEY WORKED AS THEY WERE SUPPOSED TO AND HAD SO MUCH MORE PAIN CONTROL. THE EUFLEXXA ACTUALLY INCREASED MY PAIN.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    180248 EUFLEXXA EUFLEXXA MOZ FERRING 6309501100

    Patients

    Seq Age Sex Outcome Treatment
    1 67 YR Disability