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:
2025-12-24 @ 1:30 PM
Ignite Modification Date:
2025-12-25 @ 12:32 PM
NCT ID:
NCT02663895
Group ID:
EG000
Title:
Oral Treprostinil
Description:
Treprostinil 0.125 mg TID, increased by 0.125 mg TID every 3 to 4 days as tolerated for 12-month period of time.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
12
Other Number Affected:
11
Other Number At Risk:
12
Study:
NCT02663895
Results Section:
NCT02663895
Adverse Events Module:
NCT02663895