BEUDAMED
    FDA Adverse Event Death Summary report: N

    SPECTRUM IQ IV PUMP

    MDR report key: 11920846 · Received June 1, 2021

    Report

    Report Number
    MW5101641
    Event Type
    Death
    Date Received
    June 1, 2021
    Date of Event
    April 27, 2021
    Report Date
    May 27, 2021
    Manufacturer
    BAXTER HEALTHCARE CORPORATION
    Product Code
    FRN
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PR, US
    Reporter Occupation
    PHARMACIST

    Narratives

    Description of Event or Problem · 1

    DILTIAZEM 125 MG/100 ML 0.9%NS AT 5 ML/HR WAS ADMINISTERED IN A 1HR AND 30MIN PERIOD OF TIME INSTEAD OF 20 HOURS, POSSIBLY DUE TO MISTAKE IN IV LINE SWITCHING. FDA SAFETY REPORT ID#: (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    807566 SPECTRUM IQ IV PUMP PUMP, INFUSION FRN BAXTER HEALTHCARE CORPORATION

    Patients

    Seq Age Sex Outcome Treatment
    1 81 YR Death