BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VIAGRA

    MDR report key: 1174083 · Received September 23, 2008

    Report

    Report Number
    MW5008397
    Event Type
    Injury
    Date Received
    September 23, 2008
    Date of Event
    August 12, 1996
    Report Date
    September 23, 2008
    Manufacturer
    ENCORE
    Product Code
    LKY
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I WAS OPERATED ON FOR PENILE IMPLANT. ONE WEEK LATER I GOT AN INFECTION WHICH THE SURGEON COULD NOT CLEAR. ABOUT A MONTH LATER I HAD THE PENILE DEVICE REMOVED. I HAVE HAD SOME SUCCESS IN USING A VACUUM TUBE FOR HARDNESS BUT IT IS TOO DIFFICULT TO USE AND EMBARRASSING. THE OPERATING DOCTOR HAD ME TRY VIAGRA BUT DIDN'T EXPECT ANY RESULTS, AND THERE WAS NONE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 VIAGRA ENCORE VACUUM TUBE LKY ENCORE

    Patients

    Seq Age Sex Outcome Treatment
    1 84 YR Disability