BEUDAMED
    FDA Adverse Event Injury Summary report: N

    TRANSCRANIAL MAGNETIC STIMULATION

    MDR report key: 20324036 · Received September 26, 2024

    Report

    Report Number
    MW5160248
    Event Type
    Injury
    Date Received
    September 26, 2024
    Date of Event
    July 22, 2024
    Report Date
    September 23, 2024
    Manufacturer
    UNK
    Product Code
    QCI
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NV, US
    Reporter Occupation
    PATIENT
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I RECEIVED A TREATMENT FOR TMS (TRANSCRANIAL MAGNETIC STIMULATION), FOR A TOTAL OF 4-5 SESSIONS. I HAVE HAD NON STOP MIGRAINES AND DAILY HEADACHES AND DO NOT FEEL RIGHT. THEY DISMISSED ME AS CRAZY. I WAS PERFECTLY FINE BEFORE TMS, NOW I HAVE BEEN SUFFERING EVERYDAY SINCE THE FIRST SESSION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    46296 TRANSCRANIAL MAGNETIC STIMULATION TRANSCRANIAL MAGNETIC STIMULATION SYSTEM FOR OBSESSIVE-COMPULSIVE DISORDER QCI UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 26 YR Female Required Intervention