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 @ 6:42 PM
Ignite Modification Date:
2025-12-25 @ 4:13 PM
NCT ID:
NCT04668157
Group ID:
EG001
Title:
TAK-536 0.1 mg/kg - 0.8 mg/kg
Description:
TAK-536 0.1 mg/kg (not exceeding 2.5 mg/day), granules, orally, once daily, before or after breakfast on Day 1 for up to 52 weeks in Treatment Period. The dose was titrated to the highest dose of 0.8 mg/kg (not exceeding 20 mg/day) as needed and based on body weight.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
4
Serious Number At Risk:
9
Other Number Affected:
9
Other Number At Risk:
9
Study:
NCT04668157
Results Section:
NCT04668157
Adverse Events Module:
NCT04668157