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:
2025-12-26 @ 11:09 AM
Ignite Modification Date:
2025-12-26 @ 11:09 AM
NCT ID:
NCT01510912
Group ID:
EG000
Title:
Diclofenac 35 mg Capsules
Description:
Participants were administered Diclofenac 35 mg capsules two times daily and could either be uptitrated to three times daily or remain at two times daily. Participants who were uptitrated to three times daily were allowed to downtitrate to two times daily either temporarily or permanently. Participants could change regimens between two and three times daily as often as needed, with the approval of the investigator.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
42
Serious Number At Risk:
601
Other Number Affected:
191
Other Number At Risk:
601
Study:
NCT01510912
Results Section:
NCT01510912
Adverse Events Module:
NCT01510912