BEUDAMED
    FDA Adverse Event Other Summary report: N

    1221842-1999-00007

    MDR report key: 244969 · Received October 15, 1999

    Report

    Report Number
    1221842-1999-00007
    Event Type
    Other
    Date Received
    October 15, 1999
    Date of Event
    June 4, 1999
    Report Date
    September 18, 1999
    Product Code
    LZS
    Report Source
    Manufacturer report

    Narratives

    Description of Event or Problem · 1

    LASIK EYE SURGERY PERFORMED TO CORRECT MYOPIA AND ASTIGMATISM. RESULTED IN SEVERE HALO, GHOSTING, STARBURST, EYE STRAIN, MUSCLE COORDINATION PROBLEMS, PHOTOSENSITIVITY, SEVERE DRY EYES (I.E., PERMANENT EYE DAMAGE EVEN THOUGH REPORTER HAS VISUAL ACUITY OF 20/20).

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1