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 @ 4:25 AM
Ignite Modification Date:
2025-12-26 @ 3:28 AM
NCT ID:
NCT01673620
Group ID:
EG000
Title:
Montelukast 10 mg/Loratadine 10 mg
Description:
Participants receive montelukast 10 mg/loratadine 10 mg combination tablets once daily for 2 weeks
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
47
Other Number Affected:
3
Other Number At Risk:
47
Study:
NCT01673620
Results Section:
NCT01673620
Adverse Events Module:
NCT01673620