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 @ 3:06 PM
Ignite Modification Date:
2025-12-25 @ 1:27 PM
NCT ID:
NCT00099359
Group ID:
EG001
Title:
ARM B (ZDV + NVP)
Description:
ZDV, given for 6 weeks:
12 mg PO BID if birthweight (BW) \> 2000 grams 8 mg PO BID if BW \< 2000 grams
AND NVP, first dose initiated within 48 hrs of birth, second dose 48 hrs (+ 4 hours) after the first dose, and third dose 96 hours (+ 4 hours) after the second dose :
12 mg PO per dose if BW \> 2000 grams, 8 mg PO per dose if BW \< 2000 grams
Deaths Number Affected:
None
Deaths Number At Risk:
None
Serious Number Affected:
211
Serious Number At Risk:
580
Other Number Affected:
482
Other Number At Risk:
580
Study:
NCT00099359
Results Section:
NCT00099359
Adverse Events Module:
NCT00099359