MCKESSON

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2008-04-15 for MCKESSON manufactured by .

Event Text Entries

[18601973] Our hospital uses an electronic medication record manufactured by mckesson. There have been numerous occasions of medications being missed completely or delayed because of this program. Frequently the system will advise that there are no medications due at a particular time, but, then, later advise that there are late medications that were actually due at that time. There have been frequent occurrences of medications being "dropped" off the electronic mar resulting in the pt not receiving doses for several days or even the entire hospitalization. I could go on and on about the problems with this system, but there seems to be no resources for us to compare electronic medication dispensing programs and no monitoring or mandatory reporting of adverse events for these systems that are widely used throughout our healthcare system. There is also no "in house" quality monitoring of this system.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report NumberMW5006274
MDR Report Key1029670
Date Received2008-04-15
Date of Report2008-04-15
Date Added to Maude2008-04-22
Event Key0
Report Source CodeVoluntary report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA0
Event Location0
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameMCKESSON
Generic NameHORIZON ADMINRX
Product CodeNZH
Date Received2008-04-15
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Implant FlagN
Date RemovedB
Device Sequence No1
Device Event Key998473
Manufacturer AddressONE POST ST SAN FRANCISCO CA 94104 US


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2008-04-15

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