BEUDAMED
    FDA Adverse Event Other Summary report: N

    PUREVISION CONTACT LENSES BY B & L

    MDR report key: 355019 · Received October 6, 2001

    Report

    Report Number
    MW1023019
    Event Type
    Other
    Date Received
    October 6, 2001
    Date of Event
    May 1, 2001
    Report Date
    October 5, 2001
    Manufacturer
    BAUSCH & LOMB
    Product Code
    LPM
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    NJ, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT WAS REFIT FROM ACUVUE TO PUREVISION IN 2000 AND DEVELOPED ALLERGIC REACTION IN BOTH EYES 10 MONTHS LATER. (RESOLVED BY DISCONTINUING CONTACT LENS WEAR. REFIT TO ACUVUE CONTACT LENS WITH REACTION.)

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    45178 PUREVISION CONTACT LENSES BY B & L CONTACT LENSES LPM BAUSCH & LOMB * *

    Patients

    Seq Age Sex Outcome Treatment
    1 47 YR Other