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: 2025-12-25 @ 12:41 AM
Ignite Modification Date: 2025-12-25 @ 10:52 PM
NCT ID: NCT01307267
Term: Enterocolitis
Organ System: Gastrointestinal disorders
Assessment Type: NON_SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA 21.1
Notes: None
Study: NCT01307267
Study Brief: A Study Of PF-05082566 As A Single Agent And In Combination With Rituximab
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 0 0 4 View
EG001 0 0 3 View
EG002 0 0 6 View
EG003 0 0 4 View
EG004 0 0 3 View
EG005 0 0 42 View
EG006 0 0 3 View
EG007 0 0 4 View
EG008 1 1 31 View
EG009 0 0 5 View
EG010 0 0 6 View
EG011 0 0 11 View
EG012 0 0 3 View
EG013 0 0 3 View
EG014 0 0 4 View
EG015 0 0 3 View
EG016 0 0 3 View
EG017 0 0 3 View
EG018 0 0 4 View
EG019 0 0 32 View
EG020 0 0 3 View
EG021 0 0 5 View
EG022 0 0 4 View