FDA Adverse Event Injury Summary report: N

MILLENIUM

MDR report key: 1658771 · Received April 8, 2010

Report

Report Number
MW5015530
Event Type
Injury
Date Received
April 8, 2010
Date of Event
November 30, 2006
Report Date
April 8, 2010
Manufacturer
CERNER CORPORATION
Product Code
NSX
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
PA, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

THIS INCIDENT TYPIFIES INNUMERABLE SIMILAR INCIDENTS WHEREBY A MEDICATION THAT IS ORDERED DAILY AT TWO DISTINCT DOSES TO BE ADMINISTERED DAILY AT TWO DISTINCT TIMES IS INVARIABLY INCORRECTLY SCHEDULED BY THE MILLENNIUM CPOE DEVICE. THE DEVICE SCHEDULES BOTH DOSES TO BE ADMINISTERED AT THE SAME TIME, THE EARLIEST TIME. THIS CAUSES AN EXCESSIVE DOSE OF MEDICATION TO BE ADMINISTERED AT ONCE, OR ALTERNATIVELY, CAUSING THE SECOND DOSE OF MEDICATION TO BE SKIPPED BY THE NURSE AND DISCARDED AS BEING DUPLICATE. FOR INSTANCE, VENLAFAXINE WAS ORDERED AS 150 MG DAILY AT 9AM AND 75 MG DAILY AT 2PM. THE NURSE TASK LIST SHOWED 225MG TO BE ADMINISTERED AT 9AM. THE E-MAR DISPLAYED THE CORRECT DESCRIPTION IN THE MEDICATION COLUMN, BUT IT WAS NOT SCHEDULED AT THE CORRECT TIME ON THE TIME LINE. THIS DEFECT AND INTERNAL INCONSISTENCY ENDANGERS ALL PTS WHO ARE TO RECEIVE MEDICATIONS OF TWO DISTINCT DOSES AT TWO DISTINCT TIMES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MILLENIUM CPOE, POWER CHART NSX CERNER CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 63 YR Life Threatening