Other Event

Other Event

Other Adverse Events are non-serious adverse events that exceed a specific frequency threshold (typically 5% within any study arm). These events are reported to provide comprehensive safety information about all noteworthy adverse occurrences during clinical trials. Each other event is categorized by term, organ system, assessment type, and source vocabulary for standardized reporting.

Other Event path is as follows:

Study -> Results Section -> Adverse Events Module -> Other Event

Study -> Results Section -> Adverse Events Module -> Other Event -> Other Event Stats

Other Event


Ignite Creation Date: 2025-12-25 @ 4:05 AM
Ignite Modification Date: 2025-12-26 @ 3:01 AM
NCT ID: NCT00943202
Term: Decreased activity
Organ System: General disorders
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA (13.0)
Notes: Solicited from participants aged 36 months to 17 years only.
Study: NCT00943202
Study Brief: Sanofi Pasteur, TIV + H1N1, Pediatric Population
Other Event Stats (If Any):

Other Event Stats

Group ID # Events # Affected # At Risk View
EG003 26 21 104 View
EG000 35 27 98 View
EG001 44 21 100 View
EG002 40 26 98 View