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 @ 1:51 PM
Ignite Modification Date: 2025-12-25 @ 12:42 PM
NCT ID: NCT04426695
Term: COVID-19
Organ System: Infections and infestations
Assessment Type: SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA (24.0)
Notes: None
Study: NCT04426695
Study Brief: Safety, Tolerability, and Efficacy of Anti-Spike (S) SARS-CoV-2 Monoclonal Antibodies for Hospitalized Adult Patients With COVID-19
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 1 1 18 View
EG001 1 1 18 View
EG002 1 1 20 View
EG003 7 7 198 View
EG004 0 0 202 View
EG005 6 6 197 View
EG006 6 6 204 View
EG007 4 4 206 View
EG008 7 7 205 View
EG009 4 4 51 View
EG010 7 7 56 View
EG011 10 8 54 View
EG012 2 2 12 View
EG013 1 1 12 View
EG014 2 2 11 View
EG015 10 10 247 View
EG016 5 5 246 View
EG017 9 8 246 View