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 @ 1:57 PM
Ignite Modification Date:
2025-12-25 @ 12:45 PM
NCT ID:
NCT00586495
Group ID:
EG000
Title:
Sorafenib (Nexavar, BAY43-9006)
Description:
Sorafenib 200 mg tablets (400 mg \[2 x 200 mg tablets\] twice daily \[bid\] or 400 mg once daily \[od\] or 400 mg every other day \[qod\]) administered orally
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
34
Serious Number At Risk:
95
Other Number Affected:
95
Other Number At Risk:
95
Study:
NCT00586495
Results Section:
NCT00586495
Adverse Events Module:
NCT00586495