Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-25 @ 1:47 AM
Ignite Modification Date:
2025-12-26 @ 12:05 AM
NCT ID:
NCT02874794
Group ID:
EG001
Title:
Double Blind Phase Sacubitril/Valsartan
Description:
Minimum dose: 24/26mg, BID, oral, tablet. Maximum dose:
97/103mg, BID, oral, tablet. All patients began on Dose Level 1 (24/26mg) and were titrated every two weeks to target Dose level 3 (97/103mg).
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
17
Serious Number At Risk:
231
Other Number Affected:
43
Other Number At Risk:
231
Study:
NCT02874794
Results Section:
NCT02874794
Adverse Events Module:
NCT02874794