Other Event

Other Event

Other Adverse Events are non-serious adverse events that exceed a specific frequency threshold (typically 5% within any study arm). These events are reported to provide comprehensive safety information about all noteworthy adverse occurrences during clinical trials. Each other event is categorized by term, organ system, assessment type, and source vocabulary for standardized reporting.

Other Event path is as follows:

Study -> Results Section -> Adverse Events Module -> Other Event

Study -> Results Section -> Adverse Events Module -> Other Event -> Other Event Stats

Other Event


Ignite Creation Date: 2025-12-25 @ 12:56 AM
Ignite Modification Date: 2025-12-25 @ 11:10 PM
NCT ID: NCT03861767
Term: Time of prescription of study drug until 90 days after surgery
Organ System: Skin and subcutaneous tissue disorders
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: None
Notes: Adverse Events were monitored/assessed without regard to the specific Adverse Event Term
Study: NCT03861767
Study Brief: REMAP Trial for Optimizing Surgical Outcomes at UPMC
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG007 0 0 26 View
EG000 1 1 39 View
EG001 0 0 20 View
EG002 0 0 5 View
EG003 0 0 39 View
EG004 0 0 19 View
EG005 0 0 8 View
EG006 0 0 40 View
EG008 None None 0 View
EG009 0 0 106 View