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 @ 2:16 AM
Ignite Modification Date:
2025-12-26 @ 12:46 AM
NCT ID:
NCT00642460
Group ID:
EG000
Title:
All Tocilizumab (Part I, Part II and Part III)
Description:
Tocilizumab either 8 mg/kg (participants ≥ 30 kg) or 12 mg/kg (participants \<30 kg) iv every 2 weeks for 12 weeks in Part I, every 2 weeks for 92 weeks in Part II and every 2 weeks for 156 weeks in Part III.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
48
Serious Number At Risk:
112
Other Number Affected:
112
Other Number At Risk:
112
Study:
NCT00642460
Results Section:
NCT00642460
Adverse Events Module:
NCT00642460