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 @ 2:45 AM
Ignite Modification Date:
2025-12-26 @ 1:24 AM
NCT ID:
NCT00677833
Group ID:
EG002
Title:
Cohort 2: Azithromycin + Chloroquine
Description:
Azithromycin/Chloroquine administered orally once daily for 3 days as a combination tablet (300 milligrams \[mg\] Azithromycin and 100 mg Chloroquine or 150 mg Azithromycin and 50 mg Chloroquine) on Days 0, 1, 2. The combination tablets were administered on the basis of body weight approximately 30 milligram/kilogram (mg/kg) Azithromycin + approximately 10 mg base/kg Chloroquine base. Cohort 2 included participants between \>=6 months of age to \<=59 months of age.
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
124
Other Number Affected:
103
Other Number At Risk:
124
Study:
NCT00677833
Results Section:
NCT00677833
Adverse Events Module:
NCT00677833