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 @ 10:20 PM
Ignite Modification Date:
2025-12-25 @ 7:53 PM
NCT ID:
NCT02784535
Group ID:
EG002
Title:
Atomoxetine
Description:
Double blind Atomoxetine 18 mg or Atomoxetine 10 mg.
Depending upon the dose the participant qualified as Atomoxetine Responders. Subjects received atomoxetine capsules 18 mg or 10 mg three times a day.
The dose stratification was not done
Majority of the subjects received 18 mg of Atomoxetine three times a day .
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
2
Serious Number At Risk:
40
Other Number Affected:
13
Other Number At Risk:
40
Study:
NCT02784535
Results Section:
NCT02784535
Adverse Events Module:
NCT02784535