BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EUFLEXXA

    MDR report key: 6080973 · Received November 2, 2016

    Report

    Report Number
    MW5065838
    Event Type
    Injury
    Date Received
    November 2, 2016
    Date of Event
    September 27, 2016
    Report Date
    November 2, 2016
    Manufacturer
    FERRING
    Product Code
    MOZ
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    KY, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    AFTER THE FIRST INJECTION ((B)(6)2016) IN BOTH KNEES WAS GIVEN OVER NEXT FEW HOURS STARTED HAVING A VERY INTENSE HOT, BURNING PAIN IN BOTH KNEES- PAIN LASTED ABUT 24 HOURS. SECOND INFECTION ((B)(6)) IN BOTH KNEES, PAIN WAS MORE INTENSE (IN BOTH KNEES) AND LASTED FOR 6 DAYS. I DECIDED WITH THE DOCTOR NOT TO GET THE THIRD INJECTION N THE SERIES BECAUSE OF THESE EFFECTS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    726013 EUFLEXXA EUFLEXXA MOZ FERRING

    Patients

    Seq Age Sex Outcome Treatment
    1 60 YR CELEBREX| NEURONTIN| TOPIMAX