BEUDAMED
    FDA Adverse Event Injury Summary report: N

    THIN VISC

    MDR report key: 243704 · Received October 7, 1999

    Report

    Report Number
    MW1017294
    Event Type
    Injury
    Date Received
    October 7, 1999
    Date of Event
    September 15, 1999
    Report Date
    October 7, 1999
    Manufacturer
    WYETH LABORATORIES, INC. DIV. OF WYETH-AYERST PHARMACEUTICALS
    Product Code
    MOZ
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    PT HAS HAD SEVERE JOINT PAIN IN RT KNEE AFTER 3-INJECTION SERIES WAS COMPLETED. HAS HAD NO ADD'L SWELLING OR EFFUSIONS. HAS BEEN TREATED WITH PAIN MEDICATIONS ONLY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THIN VISC Implant HYALURONIC ACID, INTRAARTICULAR MOZ WYETH LABORATORIES, INC. DIV. OF WYETH-AYERST PHARMACEUTICALS NA 0008914902

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR