BEUDAMED
    FDA Adverse Event Injury Summary report: N

    FEMTOLASIK

    MDR report key: 19711631 · Received July 10, 2024

    Report

    Report Number
    MW5157128
    Event Type
    Injury
    Date Received
    July 10, 2024
    Date of Event
    January 10, 2023
    Report Date
    July 9, 2024
    Manufacturer
    UNK
    Product Code
    OTL
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    FI
    Reporter Occupation
    OTHER CAREGIVERS
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    I HAD LASER EYE SURGERY (FEMTOLASIK) AND NOW MY EYES ARE SO DRY THAT I HAVE EVEN BEEN CONSIDERING SUICIDE. I HAVE PAIN IN MY EYES AND I DONT KNOW HOW TO LIVE MY LIFE. THIS SUMMER I HAD TO START DEPRESSION MEDICATION. LASER EYE SURGERY RUINED MY LIFE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    362042 FEMTOLASIK FEMTOSECOND LASER SYSTEM FOR REFRACTIVE CORRECTION OTL UNK

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Other| S