BEUDAMED
    FDA Adverse Event Other Summary report: N

    LASIK

    MDR report key: 1840194 · Received September 16, 2010

    Report

    Report Number
    MW5017461
    Event Type
    Other
    Date Received
    September 16, 2010
    Date of Event
    March 20, 2001
    Report Date
    September 16, 2010
    Product Code
    LZS
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD LASIK DONE BACK IN 2001 AT THE (B)(6) CLINIC IN (B)(6). WHAT AN AWFUL MISTAKE THAT WAS. I HAD A CORNEAL FLAP COMPLICATION RIGHT AFTER THE SURGERY THE NEXT DAY WITH MY LEFT EYE, AND THEY HAD TO FIX MY FLAP PUTTING A PROTECTIVE BANDAGE OVER IT. MY VISION SEEMED GREAT AFTER THAT FOR ABOUT EIGHT YEARS. UNTIL JUST THIS YEAR, I AM SUFFERING WITH AWFUL NIGHT GLARE, HALOS, AND 20/40 VISION IN MY LEFT EYE. HOWEVER, MY RIGHT EYE IS 20/20 VISION. I DON'T MEAN TO COMPLAIN BUT I HAVE A PAIR OF GLASSES NOW AND I CAN'T WEAR THEM ALL THE TIME BECAUSE I GET HEADACHES WHEN I WEAR THEM AND SOMETIMES WHEN I DON'T WEAR THEM. I JUST DON'T UNDERSTAND, AND I DO NOT WANT ANYONE TO EXPERIENCE WHAT I AM GOING THROUGH. IT'S NOT FUN AND I WOULD HAVE BEEN BETTER OFF NOT GETTING THE PROCEDURE DONE AT ALL.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR