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 @ 9:08 PM
Ignite Modification Date:
2025-12-25 @ 6:59 PM
NCT ID:
NCT01430104
Group ID:
EG000
Title:
600 mg Aspara-CA + 1 µg Alfarol + 20 µg Teriparatide
Description:
Aspara-CA (600 milligrams \[mg\]) and Alfarol (1.0 microgram \[µg\]) were administered orally once daily after the Teriparatide dose during the 28-day Treatment Period and the 7-day Follow-up Period. Teriparatide (20 µg) was administered subcutaneously once daily for the 28-day Treatment Period.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
29
Other Number Affected:
5
Other Number At Risk:
29
Study:
NCT01430104
Results Section:
NCT01430104
Adverse Events Module:
NCT01430104