BEUDAMED
    FDA Adverse Event Injury Summary report: N

    BAUSCH & LOMB

    MDR report key: 1100646 · Received August 6, 2008

    Report

    Report Number
    MW5007920
    Event Type
    Injury
    Date Received
    August 6, 2008
    Date of Event
    August 1, 1953
    Report Date
    August 6, 2008
    Product Code
    LPN
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    AL, US
    Reporter Occupation
    PATIENT

    Narratives

    Description of Event or Problem · 1

    EYES SWELLED AND TURNED RED AFTER USE OF PRODUCT BAUSCH & LOMB NU. ROUTE: OTIC. DATES OF USE: 2008. EVENT ABATED AFTER USE STOPPED: YES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BAUSCH & LOMB CONTACT SOLUTION LPN

    Patients

    Seq Age Sex Outcome Treatment
    1 Other BAUSCH & LOMB CONTACT SOLUTION