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 @ 2:40 AM
Ignite Modification Date:
2025-12-26 @ 1:18 AM
NCT ID:
NCT03449134
Group ID:
EG002
Title:
Gefapixant 45 mg BID
Description:
Participants received a gefapixant 45 mg tablet and placebo tablet to match gefapixant 15 mg BID during the 12-week main study period and 40-week extension period.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
13
Serious Number At Risk:
243
Other Number Affected:
179
Other Number At Risk:
243
Study:
NCT03449134
Results Section:
NCT03449134
Adverse Events Module:
NCT03449134