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 @ 4:03 PM
Ignite Modification Date:
2025-12-25 @ 2:05 PM
NCT ID:
NCT02517866
Group ID:
EG002
Title:
After Week 6 Azilsartan Medoxomil 80 mg
Description:
Azilsartan medoxomil 80 mg, tablets, orally, once, daily, for Week 6 up to Week 12.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
97
Other Number Affected:
0
Other Number At Risk:
97
Study:
NCT02517866
Results Section:
NCT02517866
Adverse Events Module:
NCT02517866