BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASER DEVICE USED FOR TURP PROCEDURE

    MDR report key: 399319 · Received June 7, 2002

    Report

    Report Number
    MW1025290
    Event Type
    Injury
    Date Received
    June 7, 2002
    Date of Event
    January 20, 2000
    Report Date
    June 7, 2002
    Manufacturer
    *
    Product Code
    LNK
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    RPTR HAD A PROCEDURE CALLED A TURP TO REDUCE THE SIZE OF PROSTATE. AFTER SURGERY PT EXPERIENCED A GREAT DEAL OF PAIN. THE PAIN HAS BEEN CONSTANT (24 HRS A DAY) FOR THE PAST TWO YEARS. PT HAS GONE TO DOZENS OF DRS AND TO CLINIC TRYING TO FIND OUT WHAT WENT WRONG WITH THE PROCEDURE. TO DATE, PT HAS HAD NO RELIEF NOR ANY EXPLANATION OF WHAT THE PROBLEM MIGHT BE. PT NOW LIVES DAY TO DAY ON DRUGS, PAIN KILLERS, NERVE BLOCKERS, SLEEPING PILLS. IF THERE IS ANYONE ELSE THAT HAS REPORTED A SIMILAR PROBLEM, PT WANTS TO KNOW SO THEY CAN FIND OUT IF THEY HAVE DISCOVERED WHAT THE PROBLEM AND SOLUTION MIGHT BE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASER DEVICE USED FOR TURP PROCEDURE * LNK * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 68 YR Required Intervention| S