BEUDAMED
    FDA Adverse Event Other Summary report: N

    FIXODENT FEX

    MDR report key: 1392801 · Received May 20, 2009

    Report

    Report Number
    MW5011193
    Event Type
    Other
    Date Received
    May 20, 2009
    Product Code
    KOL
    Report Source
    Voluntary report
    Reporter Location
    MD, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    BLOOD TEST COME BACK NEGATIVE. BUT MY HAND IS STILL TINGLING AND MY LEGS DO THE SAME. HAVE SUGAR TEST AND CAME BACK NEGATIVE. THIS IS IN CASE I HAVE TROUBLE LATER. DOSE: DENTURE CREAM. FREQUENCY: DAILY. ROUTE: ORAL. DATES OF USE: 2000 - 2009. EVENT ABATED AFTER USE STOPPED: NO.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 FIXODENT FEX NONE KOL

    Patients

    Seq Age Sex Outcome Treatment
    1