FDA Adverse Event Other Summary report: N

EPIC

MDR report key: 16940781 · Received May 15, 2023

Report

Report Number
MW5117571
Event Type
Other
Date Received
May 15, 2023
Report Date
May 15, 2023
Manufacturer
EPIC SYSTEMS CORPORATION
Product Code
OUG
Report Source
Voluntary report
Reporter Occupation
UNKNOWN
Health Professional
*

Narratives

Description of Event or Problem · 0

(B)(6) HAS BEEN AN UPSTICK IN EVENTS WHERE MEDICATIONS ARE SCHEDULED 24-48 HOURS LATER THAN THEY ARE INTENDED TO START IN EPIC. THIS IS BEING DONE WITH THE USE OF THE OPTION TO "START TOMORROW" WHEN ORDERS ARE PLACED BY PROVIDERS OF ALL LEVELS OF EXPERIENCE AND TENURE AT OUR FACILITY, BUT HAS ALSO OCCURRED WHEN CHOOSING DIFFERENT TIMING SUCH AS BID. THIS HAS AFFECTED THE TIMING OF MEDICATIONS COVERING A WIDE RANGE OF INDICATIONS, INCLUDING BUT NOT LIMITED TO INHALED RESPIRATORY TREATMENTS, SEIZURE PROPHYLAXIS, ANTIBIOTICS, AND STRESS DOSE STEROIDS. OUR PHARMACISTS HAVE BEEN ABLE TO CATCH A FEW WHILE VERIFYING MEDICATIONS, BUT SOME HAVE SLIPPED THROUGH THE CRACKS. (B)(6).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
818384 EPIC MEDICAL DEVICE DATA SYSTEM OUG EPIC SYSTEMS CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Unknown