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 @ 11:19 PM
Ignite Modification Date:
2025-12-25 @ 9:01 PM
NCT ID:
NCT01822756
Group ID:
EG001
Title:
Cohort B (-1)
Description:
RUX Orally, Twice Daily 5 mg BID; Gemcitabine 1000 mg/m\^2 on Days 1, 8, and 15; nab-paclitaxel 100 mg/m\^2 on Days 1, 8, and 15; + GCSF
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
4
Other Number Affected:
4
Other Number At Risk:
4
Study:
NCT01822756
Results Section:
NCT01822756
Adverse Events Module:
NCT01822756