BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRANSCRANIAL MAGNETIC STIMULATION

    MDR report key: 15041947 · Received July 18, 2022

    Report

    Report Number
    MW5110902
    Event Type
    Injury
    Date Received
    July 18, 2022
    Date of Event
    April 9, 2021
    Report Date
    July 14, 2022
    Manufacturer
    UNKNOWN
    Product Code
    OBP
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    WA, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I HAVE SUSTAINED LONG TERM, POTENTIALLY PERMANENT DAMAGE FROM TRANSCRANIAL MAGNETIC STIMULATION (TMS), WHICH WAS REPORTED TO ME BY DOCTORS AND PRACTITIONERS TO BE COMPLETELY SAFE. EVER SINCE I HAD TMS, I'VE HAD BEATING, DEBILITATING HEADACHES, DEPERSONALIZATION AND IDIOPATHIC NEUROLOGICAL DYSFUNCTION, EYE PAIN AND DRYNESS, MADDENING SCALP TENSION, THE POPPING UP OF NEW EYE FLOATERS AND INCREASED ANXIETY/DEPRESSION. I THINK ABOUT TAKING MY OWN LIFE MULTIPLE TIMES DAILY AS A DIRECT RESULT OF THE DAMAGE I SUSTAINED FROM TMS. I FEEL BETRAYED BY THE MEDICAL SYSTEM AS I DID MY DUE DILIGENCE ON RESEARCH AND FOUND NO REPORTING OF THE LIFE SHATTERING DAMAGE THAT WAS DONE TO ME. IT HAS BEEN OVER 15 MONTHS SINCE MY LAST TMS TREATMENT AND MY SYMPTOMS HAVE BEEN ONLY WORSENING. I HAVE NOTHING LEFT TO LIVE FOR AFTER TMS. THE NEUROLOGIST INSISTED THAT TMS WAS SAFE AND THEREFORE DIDN'T PUT MUCH INTO THIS TEST. FDA SAFETY REPORT ID # (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1112323 TRANSCRANIAL MAGNETIC STIMULATION TRANSCRANIAL MAGNETIC STIMULATOR OBP UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Male Life Threatening| S| H| R BILLBERRY| DIAZEPAM| VITAMIN B1