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 @ 2:44 AM
Ignite Modification Date: 2025-12-26 @ 1:23 AM
NCT ID: NCT04804033
Term: Nephrolithiasis
Organ System: Renal and urinary disorders
Assessment Type: NON_SYSTEMATIC_ASSESSMENT
Source Vocabulary: MedDRA27.0
Notes: None
Study: NCT04804033
Study Brief: A Study to Evaluate the Efficacy and Safety of Oral Zavegepant in Migraine Prevention
Serious Event Stats (If Any):

Serious Event Stats

Group ID # Events # Affected # At Risk View
EG000 None 0 173 View
EG001 None 0 175 View
EG002 None 0 348 View
EG003 None 0 86 View
EG004 None 0 88 View
EG005 None 0 174 View
EG006 None 1 155 View
EG007 None 0 143 View
EG008 None 0 154 View
EG009 None 0 162 View
EG010 None 0 47 View
EG011 None 0 48 View
EG012 None 0 70 View