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 @ 5:29 PM
Ignite Modification Date:
2025-12-25 @ 3:03 PM
NCT ID:
NCT02080468
Group ID:
EG000
Title:
Lomitapide & EE/Norgestimate - Taken Together
Description:
2 single oral doses of lomitapide (20 mg) (Day 1 \& Day 22)
21 single oral doses of EE/Norgestimate(Day 8 through day 28)
lomitapide: 20 mg
EE/norgestimate: 1x0.035-mg EE/0.25-mg norgestimate tablet
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
16
Other Number Affected:
8
Other Number At Risk:
16
Study:
NCT02080468
Results Section:
NCT02080468
Adverse Events Module:
NCT02080468