BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK

    MDR report key: 1950680 · Received December 29, 2010

    Report

    Report Number
    MW5018781
    Event Type
    Injury
    Date Received
    December 29, 2010
    Date of Event
    October 14, 2010
    Report Date
    December 29, 2010
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    ID, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD LASIK IN (B)(6) 2010, AND IT HAS BEEN THE WORSE THING I HAVE EVER DONE! I HAVE DRY EYES AND DEPRESSION AND BACK ANXIETY AND I WAS NEVER TOLD THE SIDE EFFECTS OR WHAT BAD COULD HAPPEN LIKE RETINAL DETACHMENT DUE TO THE RING THEY USE FOR SUCTION! WHY DIDN'T YOU GUYS DO ANYTHING SOON ABOUT LASIK A LONG TIME AGO WHEN PEOPLE WERE HAVING PROBLEMS THEN? JUST DO SOMETHING ABOUT IT! I HAVE BAD ANXIETY ATTACKS AND DEPRESSION DUE TO IT NOW! LASIK! I DO NOT APPROVE OF IT!

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASIK LASIK LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 27 YR