BEUDAMED
    FDA Adverse Event Injury Summary report: N

    LASIK SURGERY

    MDR report key: 1812314 · Received August 17, 2010

    Report

    Report Number
    MW5017165
    Event Type
    Injury
    Date Received
    August 17, 2010
    Date of Event
    September 27, 1999
    Report Date
    August 17, 2010
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    TN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    SEVERE DRY EYES AND DEBILITATING PAIN AFTER LASIK SURGERY. DIAGNOSIS OR REASON FOR USE: TO IMPROVE NEAR-SIGHTEDNESS.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Other| R