BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EYE GLASSES

    MDR report key: 5064219 · Received September 1, 2015

    Report

    Report Number
    MW5056044
    Event Type
    Injury
    Date Received
    September 1, 2015
    Date of Event
    August 21, 2009
    Report Date
    September 1, 2015
    Product Code
    HQG
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I WAS PRESCRIBED EYE GLASSES TO CORRECT A SMALL DEGREE OF MYOPIA. UNLIKE DRUG PRESCRIPTIONS, NO WARNING LABEL WAS INCLUDED WITH THIS PRESCRIPTION. I LATER FOUND OUT THAT THE EYE GLASSES LIMIT PERIPHERAL VISION AND ARE KNOWN TO ACTUALLY WORSEN THE SYMPTOMS OF MYOPIA OVER TIME. I HAVE STOPPED WEARING MY EYE GLASSES AND BEGUN TO LIMIT ACTIVITIES WHICH HARM MY VISION SUCH AS COMPUTER USAGE AND MY VISION HAS SLOWLY BEGUN TO RETURN TO WHAT IT ONCE WAS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    579208 EYE GLASSES EYE GLASSES HQG

    Patients

    Seq Age Sex Outcome Treatment
    1 18 YR