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 @ 9:19 PM
Ignite Modification Date:
2025-12-25 @ 7:06 PM
NCT ID:
NCT01976104
Group ID:
EG003
Title:
40 mg Avatrombopag (Higher Baseline Platelet Count)
Description:
Participants with a baseline platelet count of greater than or equal to 40 to less than 50 x 10\^9/L took two 20 mg tablets (40 mg total) avatrombopag (2nd generation) orally, once daily with a meal on Days 1 through 5.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
1
Serious Number At Risk:
57
Other Number Affected:
14
Other Number At Risk:
57
Study:
NCT01976104
Results Section:
NCT01976104
Adverse Events Module:
NCT01976104