BEUDAMED
    FDA Adverse Event Injury Summary report: N

    *

    MDR report key: 461718 · Received May 22, 2003

    Report

    Report Number
    MW1028468
    Event Type
    Injury
    Date Received
    May 22, 2003
    Date of Event
    May 5, 2003
    Report Date
    May 22, 2003
    Manufacturer
    *
    Product Code
    LPL
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NC, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    PT WAS SAID TO HAVE BOUGHT THE CONTACT LENSES AT A CONVENIENCE STORE AND WAS TOLD THEY WERE COSMETIC LENSES. PT DEVELOPED PAIN IN 05/2003 IN THE EYES. THE LEFT EYE WAS MORE PAINFUL. PT WENT TO THE EMERGENCY ROOM OF A LOCAL HOSPITAL WHERE THEY WERE REFERRED TO THE OPHTHALMOLOGIST. PT WAS FIRST SEEN IN 05/2003 AND WAS DIAGNOSED WITH SEVERE CORNEAL ABRASION OF THE LEFT EYE AND WITH CORNEAL BURNS OF THE RIGHT EYE. PT WAS TREATED WITH TRIMETHOPRIN, ERYTHROMYCIN OINTMENT AND 5% HOMATROPIN. PT WAS SEEN TWO DAYS LATER AND THE THIRD DAY FOR FOLLOW UP. PT HAS NOT BEEN SEEN SINCE THE LAST VISIT. THE CASE WAS REPORTED TO THE COUNTY HEALTH OFFICER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 * CONTACT LENS LPL * * *

    Patients

    Seq Age Sex Outcome Treatment
    1 34 YR Required Intervention