MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2015-06-25 for MCKESSON PARAGON CPOE SOFTWARE USING FDB DATABASE manufactured by Mckesson.
[6047269]
I have reported this before. Inappropriate choices for medications ordering. Mckesson paragon cpoe software using fdb database. I have reported to mckesson and they say it's an issue with fdb. Will upload the screenshot. Digoxin oral ordering. Suggests only weight based dosing. Even further down the list it does even not offer digoxin 0. 125 mg or digoxin 0. 25 mg. (b)(6).
Patient Sequence No: 1, Text Type: D, B5
Report Number | MW5043422 |
MDR Report Key | 4884222 |
Date Received | 2015-06-25 |
Date of Report | 2015-04-02 |
Date Added to Maude | 2015-07-06 |
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 | MCKESSON PARAGON CPOE SOFTWARE USING FDB DATABASE |
Generic Name | MCKESSON PARAGON CPOE SOFTWARE USING FDB DATABASE |
Product Code | NSX |
Date Received | 2015-06-25 |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MCKESSON |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2015-06-25 |