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 @ 11:57 PM
Ignite Modification Date:
2025-12-25 @ 9:54 PM
NCT ID:
NCT00729651
Group ID:
EG000
Title:
Fosamax Plus D
Description:
Once weekly Fosamax plus D tablet \[Alendronate sodium 70 mg/Cholecalciferol 5600 IU\] + once daily calcium formulation \[500 mg/day\]), 16 weeks and patients who received drugs at least once after randomization and was analyzed according to the actually administered study drugs
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
7
Serious Number At Risk:
171
Other Number Affected:
60
Other Number At Risk:
171
Study:
NCT00729651
Results Section:
NCT00729651
Adverse Events Module:
NCT00729651