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 @ 10:03 PM
Ignite Modification Date:
2025-12-25 @ 7:39 PM
NCT ID:
NCT01101035
Group ID:
EG000
Title:
Febuxostat
Description:
Febuxostat 40 mg (or 80 mg beginning on week 4 if serum uric acid level was ≥6.0 mg/dL), tablets, orally, once daily for up to approximately 82 months.
Deaths Number Affected:
243
Deaths Number At Risk:
None
Serious Number Affected:
1046
Serious Number At Risk:
3098
Other Number Affected:
1450
Other Number At Risk:
3098
Study:
NCT01101035
Results Section:
NCT01101035
Adverse Events Module:
NCT01101035