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 @ 10:59 AM
Ignite Modification Date:
2025-12-26 @ 10:59 AM
NCT ID:
NCT02318706
Group ID:
EG002
Title:
DS-5565 20 mg (10 mg BID)
Description:
Participants who received an oral dose of DS-5565 20 mg (10 mg BID).
During the titration period, DS-5565 was administered orally at a daily dose of 10 mg (5 mg BID) for 1 week.
During the fixed-dose period, a daily dose of 20 mg (10 mg BID) was administered orally for 13 weeks.
Deaths Number Affected:
2
Deaths Number At Risk:
None
Serious Number Affected:
8
Serious Number At Risk:
165
Other Number Affected:
62
Other Number At Risk:
165
Study:
NCT02318706
Results Section:
NCT02318706
Adverse Events Module:
NCT02318706