BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HBOT

    MDR report key: 5035582 · Received August 23, 2015

    Report

    Report Number
    MW5055765
    Event Type
    Injury
    Date Received
    August 23, 2015
    Date of Event
    August 19, 2015
    Report Date
    August 23, 2015
    Product Code
    CBF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    MY PARENTS, UNFORTUNATELY FERVENT BELIEVERS IN ALTERNATIVE MEDICINE WOO, COERCED ME INTO DOING HBOT THERAPY AND NOW MY LEG MUSCLES ARE SO SORE THAT IT KEEPS ME FROM SLEEP. I AM UNAWARE OF ALL THE MEDICATIONS I'M ON (AT LEAST 10) BECAUSE MY MOTHER IS A CONTROL FREAK AND WON'T EVEN REMIND ME WHAT MEDICATIONS I'VE BEEN PRESCRIBED. SHE JUST GIVES THEM ALL TO ME EACH NIGHT IN A TINY ZIPLOCK BAG. CYMBALTA IS THE ONLY ONE I CAN THINK OF OFF THE TOP OF MY HEAD.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    557068 HBOT NONE CBF

    Patients

    Seq Age Sex Outcome Treatment
    1 25 YR