Serious Event

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Serious Event

Serious Adverse Events (SAEs) are adverse events that result in death, are life-threatening, require or prolong hospitalization, cause persistent or significant disability/incapacity, or are congenital anomalies/birth defects. Each serious event is categorized by term, organ system, assessment type, and source vocabulary to provide standardized reporting across clinical trials.

Serious Event path is as follows:

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

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

Serious Event

Ignite Creation Date: 2025-12-24 @ 5:57 PM

Ignite Modification Date: 2025-12-25 @ 3:20 PM

NCT ID: NCT04732468

Term: Diverticulitis

Organ System: Infections and infestations

Assessment Type: SYSTEMATIC_ASSESSMENT

Source Vocabulary: None

Notes: None

Study: NCT04732468

Study Brief: COVID-19 Oral and Subcutaneous Vaccination Using a 2nd Generation (E1/E2B/E3-Deleted) Adenovirus Platform in Healthy Volunteers in USA

Serious Event Stats (If Any):

Serious Event Stats

Group ID	# Events	# Affected	# At Risk	View

EG000	None	0	4	View
EG001	None	1	10	View
EG002	None	0	10	View
EG003	None	0	4	View
EG004	None	0	4	View
EG005	None	0	10	View
EG006	None	0	10	View
EG007	None	0	4	View
EG008	None	0	4	View
EG009	None	0	10	View
EG010	None	0	10	View
EG011	None	0	4	View
EG012	None	0	4	View
EG013	None	0	10	View
EG014	None	0	10	View
EG015	None	0	4	View
EG016	None	0	4	View
EG017	None	0	10	View
EG018	None	0	10	View
EG019	None	0	4	View
EG020	None	0	4	View
EG021	None	0	10	View
EG022	None	0	10	View
EG023	None	0	4	View
EG024	None	None	4	View
EG025	None	None	10	View
EG026	None	None	10	View
EG027	None	None	4	View