BEUDAMED
    FDA Adverse Event Death Summary report: N

    ABBOTT

    MDR report key: 328784 · Received April 19, 2001

    Report

    Report Number
    328784
    Event Type
    Death
    Date Received
    April 19, 2001
    Date of Event
    April 4, 2001
    Report Date
    April 13, 2001
    Manufacturer
    ABBOTT LABORATORIES
    Product Code
    FRN
    Adverse Event
    Yes
    Report Source
    User Facility report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    PT IN HOSPICE CARE FOR END-STAGE LUNG CANCER ADMITTED WITH DEEP VEIN THROMBOSIS. THE PT WAS ORDERED TO RECEIVE MORPHINE SULFATE 2MG PER HOUR BY CONTINUOUS INFUSION USING AN ABBOTT PLUM - A+ DEVICE. TWEMTY SEVEN MINUTES AFTER INITIATION OF DRIP, PT DISCOVERED TO HAVE RECEIVED AN INADVERTENT OVERDOSE OF 100MG. PT WAS OVERSEDATED BUT BREATHING SPONTANEOUSLY. MEDICAL CONSULTATION WAS OBTAINED IMMEDIATELY. NARCAN WAS ADMINISTERED AND THE PT BECAME ALERT. THE PT EXPIRED THREE HOURS LATER OF RESPIRATORY FAILURE RESULTING FROM THE DISEASE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    17997 ABBOTT PUMP PLUM A+ FRN ABBOTT LABORATORIES 11973 *

    Patients

    Seq Age Sex Outcome Treatment
    1 65 YR Death