FDA Adverse Event Malfunction Summary report: N

HNA MILLENNIUM POWER ORDERS

MDR report key: 358222 · Received October 22, 2001

Report

Report Number
1931259-2001-00002
Event Type
Malfunction
Date Received
October 22, 2001
Date of Event
October 3, 2001
Report Date
October 19, 2001
Manufacturer
CERNER CORPORATION
Product Code
MMH
Removal / Correction Number
NA
Report Source
Manufacturer report
Reporter Location
MO, US
Reporter Occupation
OTHER

Narratives

Description of Event or Problem · 1

PLEASE SEE INITIAL REPORT.

Description of Event or Problem · 1

A USER ENTERED AN ORDER DURING THE ORDER ENTRY PROCESS, WITH A FREQUENCY OF EVERY 8 HOURS AND THEN USED THE AD HOC SCHEDULING FEATURE TO MODIFY THE DEFAULTED ADMINISTRATION TIMES FOR THAT FREQUENCY. AFTER THIS WAS DONE, THE USER CHANGED THE FREQUENCY OF THE ORDER TO A 12-HOUR FREQUENCY WITHOUT MODIFYING THE AD HOC ADMINISTRATIONS TIMES. THE SOFTWARE DID NOT CLEAR THE PREVIOUSLY ENTERED AD HOC ADMINISTRATION TIMES TO ADJUST TO THE DEFAULT TIMES FOR THE NEW FREQUENCY. THIS RESULTED IN A PATIENT RECEIVING A MEDICATIONS 3 TIMES A DAY AS OPPOSED TO 2 TIMES A DAY. THE DRUG WAS CARBAMAZEPENE. THIS INCORRECT ORDER FREQUENCY WAS REPEATED FOR 3 DAYS, ULTIMATELY RESULTING IN THE PATIENT RECEIVING OF TOTAL OF 3 EXTRA DOSES OVER A 3-DAY PERIOD (1 EXTRA DOSE PER DAY). ON THE FOURTH DAY, THE NURSE CARING FOR THE PATIENT NOTICED THE INCONSISTENCY IN THE ORDER AND CONDUCTED A FURTHER INVESTIGATION WITH THE PHARMACIST. THE PATIENT WAS DISCHARGED ON TIME; NO EXTENDED STAY WAS NECESSARY AS A RESULT OF THE OVERMEDICATION. THE PATIENT'S CARBAMAZEPENE LEVELS WERE CHECKED DURING A FOLLOW-UP VISIT THAT OCCURRED 5 DAYS AFTER DISCHARGE, AND WERE NOTED AS NORMAL AT THAT TIME.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
47565 HNA MILLENNIUM POWER ORDERS SOFTWARE MMH CERNER CORPORATION RELEASE 500 NA

Patients

Seq Age Sex Outcome Treatment
1 53 YR Other