BEUDAMED
    FDA Adverse Event Other Summary report: N

    HYALGAN

    MDR report key: 386912 · Received March 13, 2002

    Report

    Report Number
    MW1024584
    Event Type
    Other
    Date Received
    March 13, 2002
    Date of Event
    October 10, 2001
    Report Date
    March 12, 2002
    Manufacturer
    *
    Product Code
    MOZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    PT WITH DJD RIGHT KNEE WITH SYNOVITIS - UNDERWENT HYALGAN INJECTIONS IN 2001, THEN 8 DAYS LATER, 1 WEEK X 3. IMMEDIATE SWELLING NOTED AFTER 2ND SHOT. ASPIRATION OF CLEAR SYNOVIAL FLUID 6 DAYS LATER. 2ND ASPIRATION 5 DAYS LATER (CLEAR SEROUS). MRI: DJD - MENISCAL TEAR. PT PRESENTLY DOING WELL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 HYALGAN INTRA-ARTICULAR INJECTION MOZ * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 79 YR Other