Adverse Events Module

Adverse Events Module

For researchers submitting trial data to ClinicalTrials.gov, the Adverse Events module is one of four mandatory results sections. It requires reporting in three primary categories: All-Cause Mortality: A table tracking all deaths that occurred during the study, regardless of cause. Serious Adverse Events (SAEs): A tabular summary of events resulting in death, life-threatening conditions, hospitalization, or significant disability. Other Adverse Events: A table for non-serious events that exceed a specific frequency threshold, such as 5% within any study arm.

Adverse Events Module path is as follows:

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

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

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

Adverse Events Module


Ignite Creation Date: 2025-12-24 @ 9:58 PM
Ignite Modification Date: 2025-12-25 @ 7:35 PM
NCT ID: NCT04429932
Description: None
Frequency Threshold: 0
Time Frame: 9 days
Study: NCT04429932
Study Brief: A Study to Evaluate Nicotine Uptake and Biomarkers in Adult Smokers Using mybluTM Electronic Cigarettes
Event Groups(If Any):

Event Groups

Title Description Deaths # Affected Deaths # At Risk Serious # Affected Serious # At Risk Other # Affected Other # At Risk View
Product Variant B MyBlu e- igarette variant B (2.4% nicotine) 0 None 0 16 1 16 View
Product Variant A MyBlu e-cigarette variant A (2.4% nicotine) 0 None 0 18 3 18 View
Product Variant C MyBlu e-cigarette variant C (2.4% nicotine) 0 None 0 16 1 16 View
Product Variant D MyBlu e-cigarette variant D (2.4% nicotine) 0 None 0 18 1 18 View
Product Variant E MyBlu e- cigarette variant E (1.2% nicotine) 0 None 0 20 2 20 View
Product Variant F MyBlu e-cigarette variant F (1.2% nicotine) 0 None 0 20 1 20 View
Product Variant G MyBlu e-cigarette variant G (2.4% nicotine) 0 None 0 20 0 20 View
Product Variant H MyBlu e-cigarette variant H (2.4% nicotine) 0 None 0 20 1 20 View
Serious Events(If Any):
Other Events(If Any):

Other Events

Term Type Organ System Vocab View
Headache NON_SYSTEMATIC_ASSESSMENT Nervous system disorders MedDRA® Version 22.0 View
Hypoesthesia NON_SYSTEMATIC_ASSESSMENT Nervous system disorders MedDRA® Version 22.0 View
Migraine NON_SYSTEMATIC_ASSESSMENT Nervous system disorders MedDRA® Version 22.0 View
Dysmenorrhea NON_SYSTEMATIC_ASSESSMENT Reproductive system and breast disorders MedDRA® Version 22.0 View
Oropharyngeal discomfort NON_SYSTEMATIC_ASSESSMENT Respiratory, thoracic and mediastinal disorders MedDRA® Version 22.0 View
Contact dermitits NON_SYSTEMATIC_ASSESSMENT Skin and subcutaneous tissue disorders MedDRA® Version 22.0 View
Constipation NON_SYSTEMATIC_ASSESSMENT Gastrointestinal disorders MedDRA® Version 22.0 View
Diarrhea NON_SYSTEMATIC_ASSESSMENT Gastrointestinal disorders MedDRA® Version 22.0 View