HNA MILLENNIUM POWER ORDERS
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
PLEASE SEE INITIAL REPORT.
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 |