BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK EYE SURGERY

    MDR report key: 939358 · Received November 4, 2007

    Report

    Report Number
    MW5004321
    Event Type
    Injury
    Date Received
    November 4, 2007
    Date of Event
    February 12, 2007
    Report Date
    November 4, 2007
    Product Code
    HQF
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD LASIK SURGERY. SINCE THAT DATE, I HAVE NOT SEEN CLEARLY. MY VISION IS BLURRED. I CAN NOT DRIVE AT NIGHT AND MY EYE IS CONTINUALLY DRY. RIGHT NOW I AM TO PUT 12-20 DROPS A DAY OF ONE MEDICATION/2 DROPS A DAY OF ANOTHER MEDICATION AND A THIRD GEL FOR NIGHT TIME. MY EYE IS GETTING WORSE WITH ALL THESE SYMPTOMS. I HAD ONLY MY LEFT EYE DONE. THIS WAS A VANITY ISSUE TO START WITH NOW IT'S JUST A MATTER OF SEEING WITHOUT GLARE, DRYNESS AND BLUR.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 54 YR Disability