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 @ 12:44 PM
Ignite Modification Date:
2025-12-25 @ 12:13 PM
NCT ID:
NCT02913261
Group ID:
EG000
Title:
Ruxolitinib (Rux)
Description:
These patients were administered Ruxolitinib orally twice per day (b.i.d) at a dose of 10 mg bid, as two 5-mg tablets. Ruxolitinib was taken without regards to food.
Deaths Number Affected:
89
Deaths Number At Risk:
None
Serious Number Affected:
101
Serious Number At Risk:
152
Other Number Affected:
144
Other Number At Risk:
152
Study:
NCT02913261
Results Section:
NCT02913261
Adverse Events Module:
NCT02913261