BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK SURGERY

    MDR report key: 2820721 · Received October 25, 2012

    Report

    Report Number
    MW5027405
    Event Type
    Injury
    Date Received
    October 25, 2012
    Date of Event
    September 1, 2012
    Report Date
    October 25, 2012
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    CHRONIC DRY EYES. HAD LASIK SURGERY APPROXIMATELY 6 YEARS AGO TO BOTH EYES. CURRENTLY REQUIRING RESTASIS TREATMENT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 56 YR Disability RESTASIS - TO BOTH EYES B.I.D.