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 @ 7:52 PM
Ignite Modification Date:
2025-12-25 @ 5:28 PM
NCT ID:
NCT01423604
Group ID:
EG000
Title:
Ruxolitinib (Safety Run-In)
Description:
Subjects received capecitabine 2000 mg/m\^2 daily (taken as 1000 mg/m2 twice daily \[BID\]) + ruxolitinib 15 mg BID
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
5
Serious Number At Risk:
9
Other Number Affected:
9
Other Number At Risk:
9
Study:
NCT01423604
Results Section:
NCT01423604
Adverse Events Module:
NCT01423604