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 @ 11:56 PM
Ignite Modification Date:
2025-12-25 @ 9:53 PM
NCT ID:
NCT02729051
Group ID:
EG001
Title:
FF/VI 100/25 + UMEC 62.5
Description:
Participants received FF/VI, 100 mcg/25 mcg via ELLIPTA DPI once daily in morning and UMEC 62.5 mcg inhalation powder via ELLIPTA DPI, once daily in the morning. Participants also received albuterol/salbutamol as a rescue medication when needed during the treatment period.
Deaths Number Affected:
5
Deaths Number At Risk:
None
Serious Number Affected:
60
Serious Number At Risk:
528
Other Number Affected:
125
Other Number At Risk:
528
Study:
NCT02729051
Results Section:
NCT02729051
Adverse Events Module:
NCT02729051