BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MECTA

    MDR report key: 746446 · Received October 5, 2005

    Report

    Report Number
    MW1036827
    Event Type
    Injury
    Date Received
    October 5, 2005
    Date of Event
    August 1, 2005
    Report Date
    October 4, 2005
    Manufacturer
    MECTA CORPORATION,
    Product Code
    GXC
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TX
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    RECEIVED SIX ELETRO SHOCKS WHICH WERE DISCONTINUED DUE TO EXTREME HIGH BLOOD PRESSURE. HAVE MANY PHYSICAL PROBLEMS AFTER THESE TREATMENTS, INCLUDING; PANIC ATTACKS, SEVERE HEADACHES, WEAKNESS ON RIGHT SIDE OF BODY, EXTREME INSOMNIA, CHEST PAINS, BLURRY VISION, NAUSEA, AND MAJOR MEMORY LOSS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MECTA PSYCHIATRIC ELECTROSHOCK GXC MECTA CORPORATION, SPECTRUM *

    Patients

    Seq Age Sex Outcome Treatment
    1 38 YR Other| R| S