BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DENTAL AMALGAM

    MDR report key: 6215441 · Received December 30, 2016

    Report

    Report Number
    MW5066996
    Event Type
    Injury
    Date Received
    December 30, 2016
    Date of Event
    August 2, 2002
    Report Date
    December 22, 2016
    Manufacturer
    UNKNOWN
    Product Code
    OIV
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    (B)(4). AFTER SUFFERING FOR YEARS WITH EXTREME FATIGUE AND ANXIETY/PANIC ATTACKS, SHYNESS AND VERY RED ITCHY HANDS, I HAD MY AMALGAM FILLINGS REMOVED WITHOUT PRECAUTIONS BY A DENTIST WHO DID NOT BELIEVE IN MERCURY TOXICITY AND DID NOT GIVE ME AN OXYGEN MASK. I BREATHED IN A LOT OF VAPOR AND DUST DURING THE REMOVAL OF 15 AMALGAM FILLINGS AND SHORTLY AFTER THAT, I SUFFERED MY FIRST MIGRAINE HEADACHE AND HAVE BEEN SUFFERING SEVERE MIGRAINES EVER SINCE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    865584 DENTAL AMALGAM OIV UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 50.000 YR Other| R