BEUDAMED
    FDA Adverse Event Injury Summary report: N

    MYCHART

    MDR report key: 4834775 · Received June 4, 2015

    Report

    Report Number
    MW5042999
    Event Type
    Injury
    Date Received
    June 4, 2015
    Date of Event
    May 12, 2015
    Report Date
    June 4, 2015
    Manufacturer
    EPIC
    Product Code
    MMH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    PA, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Description of Event or Problem · 1

    WHEN ENTERING A WEIGHT FOR DOSING MEDICATION, THE DEVICE DOES NOT SPECIFY THE UNITS IE KG FOR WEIGHT ENTRY. INNUMERABLE HEALTH CARE PROFESSIONALS ENTERED THE WEIGHT IN POUNDS RESULTING IN POTENTIAL OVERDOSES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    363694 MYCHART CPOE/EHR MMH EPIC

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR Life Threatening