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 @ 9:24 PM
Ignite Modification Date:
2025-12-25 @ 7:10 PM
NCT ID:
NCT01996332
Group ID:
EG000
Title:
Erlotinib 150 mg/Day
Description:
Participants received erlotinib 150 mg/day, orally, until progressive disease or unacceptable toxicity.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
566
Serious Number At Risk:
1805
Other Number Affected:
1695
Other Number At Risk:
1797
Study:
NCT01996332
Results Section:
NCT01996332
Adverse Events Module:
NCT01996332