BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK SURGERY

    MDR report key: 1950873 · Received December 31, 2010

    Report

    Report Number
    MW5018832
    Event Type
    Injury
    Date Received
    December 31, 2010
    Date of Event
    September 1, 2008
    Report Date
    December 31, 2010
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    FIVE YEARS POST LASIK SURGERY BEGAN PROGRESSIVE AND SEVERE NIGHT VISION, I DO NOT DRIVE AT NIGHT EXCEPT IN A WELL LIT CITY. HAD BILATERAL LASIK 2002, AT THE TIME NO PROBLEMS. I RECEIVE ANNUAL EYE EXAMS. LAST EXAM (B)(6) 2010. (B)(6).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LASIK SURGERY NONE LZS

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Other