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:
2025-12-26 @ 10:57 AM
Ignite Modification Date:
2025-12-26 @ 10:57 AM
NCT ID:
NCT02663908
Group ID:
EG000
Title:
Degarelix 240 mg/80 mg
Description:
Degarelix 240 mg/80 mg: Degarelix at a starting dose of 240 mg administered as two SC depot injections, each containing 120 mg of degarelix; followed by up to 11 maintenance doses of 80 mg degarelix administered as single SC depot injections at monthly (28-day) intervals.
Deaths Number Affected:
11
Deaths Number At Risk:
None
Serious Number Affected:
47
Serious Number At Risk:
275
Other Number Affected:
250
Other Number At Risk:
275
Study:
NCT02663908
Results Section:
NCT02663908
Adverse Events Module:
NCT02663908