MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-02-04 for EPIC SYSTEM manufactured by Epic.
[5498615]
Issue with epic system in which dose is cleared upon order verification. This specifically occurs when pharmacists change the product that the dose clears. This is a problem with the latest version of epic and has affected other hospitals as well. Epic knows about the issue but the fix is taking a long time. We first notified them in xxxxxxx and they already knew about it. Epic suggested a temporary fix but that created a lot more problems so we couldn't implement it. There have been several cases at our hospital where pharmacists didn't realize the dose disappeared and verified the order. The nurse then receives and order without a dose. Access number:(b)(4).
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5040626 |
MDR Report Key | 4494815 |
Date Received | 2015-02-04 |
Date of Report | 2014-11-07 |
Date Added to Maude | 2015-02-11 |
Event Key | 0 |
Report Source Code | Voluntary report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 0 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | EPIC SYSTEM |
Generic Name | ELECTRONIC MEDICAL RECORDS |
Product Code | NSX |
Date Received | 2015-02-04 |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EPIC |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-02-04 |