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:
2025-12-25 @ 3:45 AM
Ignite Modification Date:
2025-12-26 @ 2:32 AM
NCT ID:
NCT00949702
Group ID:
EG000
Title:
Vemurafenib 960 mg
Description:
Patients received vemurafenib 960 mg (four 240 mg tablets) bid (bis in die, twice daily) orally until disease progression, unacceptable toxicity, withdrawal of consent, or another reason as determined by the investigator.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
67
Serious Number At Risk:
132
Other Number Affected:
131
Other Number At Risk:
132
Study:
NCT00949702
Results Section:
NCT00949702
Adverse Events Module:
NCT00949702