BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SYNVISC

    MDR report key: 1970003 · Received January 13, 2011

    Report

    Report Number
    MW5019091
    Event Type
    Injury
    Date Received
    January 13, 2011
    Date of Event
    December 1, 2010
    Report Date
    January 15, 2011
    Product Code
    MOZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    ON (B)(6) 2010, MY ORTHOPEDIST INJECTED SYNVISC INTO MY RIGHT KNEE TO IMPROVE MY WALKING. IMMEDIATELY, I FELT PAIN IN MY KNEECAP AND HAD DIFFICULTY IN WALKING FOR THE NEXT 3 WEEKS. AFTER A MONTH, I HAD SIGNIFICANT IMPROVEMENT AND, AT PRESENT, AM DOING BETTER. FREQUENCY 1 X 6 MOS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SYNVISC SYNVISC MOZ

    Patients

    Seq Age Sex Outcome Treatment
    1 83 YR Other