BEUDAMED
    FDA Adverse Event Injury Summary report: N

    NA

    MDR report key: 1633058 · Received March 13, 2010

    Report

    Report Number
    MW5015143
    Event Type
    Injury
    Date Received
    March 13, 2010
    Date of Event
    January 15, 2009
    Report Date
    March 13, 2010
    Manufacturer
    NA
    Product Code
    LZS
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    CA, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    HAD LASIK EYE SURGERY. WAS NOT AWARE OF THE REAL IMPACT OF DRY EYE SYNDROME. AFTER 6, DOCTOR SAID I WOULD RECOVER TO 'PRE LASIK CONDITION'. IT'S BEEN OVER A YEAR. MY EYES ARE VERY, VERY SLIGHTLY BETTER. I'M BUYING (B) (6) OF DROPS AND LUBE A YEAR TO KEEP MY EYES MOIST. EVERY HOUR I'M PUTTING IN A DROP BECAUSE OF THE PAIN. DOCTOR HAS NO RESPONSE TO CORRECT THIS AND DOES NOT TAKE ACCOUNTABILITY. WE NEED TO MAKE THIS MORE AWARE AND FIND CAUSE.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 30 YR Required Intervention