BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 7024673 · Received November 13, 2017

    Report

    Report Number
    MW5073259
    Event Type
    Injury
    Date Received
    November 13, 2017
    Date of Event
    November 1, 2017
    Report Date
    November 7, 2017
    Manufacturer
    FERRING PHARMACEUTICALS
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    PLEASE SEND ME AN EMAIL ADDRESS, AS I WOULD LIKE TO SEND YOU PICTURES OF MY REACTION TO A EUFLEXXA SHOT. I HAD ONE SHOT OF EUFLEXXA LAST WEDNESDAY, AND MY KNEE BROKE OUT IN 3 AREAS AROUND THE INJECTION. I HAD BURNING AND ITCHING OVER THE PAST WEEK. AFTER TAKING BENADRYL FOR SEVERAL DAYS, THERE WAS NOT MUCH IMPROVEMENT. "HAVE YOU SEEN THIS HAPPEN BEFORE, WHAT DO YOU SUGGEST." THANK YOU. DATE THE PERSON FIRST STARTED TAKING OR USING THE PRODUCT: (B)(6) 2017. DATE THE PERSON STOPPED TAKING OR USING THE PRODUCT: (B)(6) 2017. "DID THE PROBLEM STOP AFTER THE PERSON REDUCED THE DOES OR STOPPED TAKING OR USING THE PRODUCT: YES." KNEE OSTEOARTHRITIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    806163 EUFLEXXA EUFLEXXA MOZ FERRING PHARMACEUTICALS

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR