BEUDAMED
    FDA Adverse Event Injury Summary report: N

    ECT MACHINE

    MDR report key: 18667940 · Received February 7, 2024

    Report

    Report Number
    MW5151178
    Event Type
    Injury
    Date Received
    February 7, 2024
    Date of Event
    February 4, 2024
    Report Date
    February 5, 2024
    Manufacturer
    UNK
    Product Code
    QGH
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I AM REPORTING THIS DATE BUT RECEIVED THE TREATMENT OVER A PERIOD PRIOR TO THIS. I HAD OVER 50 BILATERAL ECT TREATMENTS OVER A PERIOD OF TIME AND RECEIVING THEM TIMES PER WEEK. I WAS LEFT WITH SEVER BRAIN DAMAGE MEMORY LOSS AND LOSS OF FUNCTION. MY FAMILY RECORDS THIS AS BEGINNING SHORTLY AFTER I INITIALLY STARTED TREATMENT BUT WERE TOLD IT WAS TEMPORARY AND GOES AWAY. I HAVE ENTIRE YEARS OF MY LIFE SURROUNDING PRIOR TO AND SINCE THAT ARE JUST MISSING. I WASN'T ABLE TO EVEN KNOW HOW BADLY I WAS AFFECTED UNTIL A FEW WEEKS AGO WHEN DISCOVERED SOME OLD JOURNALS I HAD KEPT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1365042 ECT MACHINE ELECTROCONVULSIVE THERAPY DEVICE FOR CATATONIA, MAJOR DEPRESSIVE DISORDER, AND B QGH UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 46 YR Female Other| R| S