BEUDAMED
    FDA Adverse Event Injury Summary report: N

    RENU

    MDR report key: 712444 · Received May 8, 2006

    Report

    Report Number
    MW1039058
    Event Type
    Injury
    Date Received
    May 8, 2006
    Date of Event
    November 1, 2005
    Report Date
    May 8, 2006
    Manufacturer
    BAUSCH AND LOMB
    Product Code
    LPN
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MN, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    I HAD AN EYE ULCER THAT WAS RECURRING. I HAD IT TWICE IN NOVEMBER AND ONCE IN JANUARY, FEBRUARY AND MARCH. I USED CONTACTS AND BAUSCH AND LOMB CONTACT SOLUTION. I WAS GIVEN ZYMAR AND LOTEMAX IN NOVEMBER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 RENU * LPN BAUSCH AND LOMB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 28 YR Disability