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:
2025-12-26 @ 10:16 PM
Ignite Modification Date:
2025-12-26 @ 10:16 PM
NCT ID:
NCT01614912
Group ID:
EG000
Title:
SM-13496 (Lurasidone HCl) 40-mg or 80-mg Group
Description:
SM-13496 40 mg or 80 mg was orally administered for 26 weeks to the participants who completed the prior study (D1001056), in which, SM-13496 (40 mg or 80 mg) or placebo was administered for 6 weeks.
Deaths Number Affected:
1
Deaths Number At Risk:
None
Serious Number Affected:
31
Serious Number At Risk:
282
Other Number Affected:
184
Other Number At Risk:
282
Study:
NCT01614912
Results Section:
NCT01614912
Adverse Events Module:
NCT01614912