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 @ 4:40 PM
Ignite Modification Date:
2025-12-25 @ 2:29 PM
NCT ID:
NCT01761266
Group ID:
EG001
Title:
Sorafenib
Description:
Participants received sorafenib 400 mg tablets, orally, twice daily (BID) in continuous 28-day treatment cycles up to documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent.
Deaths Number Affected:
402
Deaths Number At Risk:
None
Serious Number Affected:
149
Serious Number At Risk:
475
Other Number Affected:
469
Other Number At Risk:
475
Study:
NCT01761266
Results Section:
NCT01761266
Adverse Events Module:
NCT01761266