BEUDAMED
    FDA Adverse Event Death Summary report: N

    ABBOTT PAIN MGR

    MDR report key: 518221 · Received December 18, 2003

    Report

    Report Number
    2921482-2003-00633
    Event Type
    Death
    Date Received
    December 18, 2003
    Date of Event
    November 13, 2003
    Report Date
    November 21, 2003
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    MEA
    Removal / Correction Number
    NA
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    KY, US
    Reporter Occupation
    RISK MANAGER

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ABBOTT PAIN MGR * MEA ABBOTT LABORATORIES NA NA

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death MORPHINE MANUFACTURED BY ABBOTT.