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Keywords
Diabetes Mellitus, Type 2 ×
- Clinical Trial (22)
- Adverse event (22)
- Clinical Trial, Phase I (16)
- Contraceptives, Oral, Combined (11)
- Drug-Related Side Effects and Adverse Reactions (9)
- Pharmacokinetics (8)
- Placebos (5)
- Liver (5)
- Signs and Symptoms (4)
- On-Study Form (4)
- End of Study (4)
- Double-Blind Method (4)
- Endocrinology (3)
- Medical Records (3)
- Women (2)
- Cross-Over Studies (2)
- Concomitant Medication (2)
- Diagnostic Imaging (2)
- Enzymes (2)
- Follow-Up Studies (2)
- Hypoglycemia (2)
- Laboratories (2)
- Liver Diseases (2)
- Pregnancy (1)
- Pregnancy Outcome (1)
- Randomized Controlled Trial (1)
- Biopsy (1)
- Blood Glucose (1)
- Heat Stroke (1)
- Simvastatin (1)
- Stroke (1)
- Abortion, Spontaneous (1)
- Cause of Death (1)
- Chemistry (1)
- Vital Signs (1)
- Chest Pain (1)
- Child (1)
- Pre-Study Form (1)
- Electrocardiogram (ECG) (1)
- Chest X- ray (1)
- Coronary Disease (1)
- Death (1)
- Demography (1)
- Diagnosis (1)
- Disease (1)
- Alcohol Drinking (1)
- Drug Tolerance (1)
- Echocardiography (1)
- Eligibility Determination (1)
- Heart Failure (1)
- Hepatitis (1)
- Hospitalization (1)
- Hyperglycemia (1)
- Hypoglycemic Agents (1)
- Myocardial Infarction (1)
- Myocardial Revascularization (1)
- Pancreatitis (1)
- Parasites (1)
Table of contents
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22 Search results.
Itemgroups: Administrative, Adverse Events, Adverse Events/ Serious Adverse Events - Section 1, Adverse Events/ Serious Adverse Events - Section 2 (Seriousness), Adverse Events/ Serious Adverse Events - Section 3 (Demography Data), Adverse Events/ Serious Adverse Events - Section 4, Adverse Events/ Serious Adverse Events - Section 5, Adverse Events/ Serious Adverse Events - Section 6 (Medical Conditions), Adverse Events/ Serious Adverse Events - Section 7 (Other RELEVANT Risk Factors) , Adverse Events/ Serious Adverse Events - Section 8 (RELEVANT Concomitant Medications) , Adverse Events/ Serious Adverse Events - Section 9 (Details of Investigational Product(s)) , Adverse Events/ Serious Adverse Events - Section 10 (Details of RELEVANT ASSESSMENTS) , Adverse Events/ Serious Adverse Events - Section 11 (Narrative Remarks), Prior and Concomitant Medications/Non-drug Therapies , Prior and Concomitant Medications/Non-drug Therapies
Itemgroups: Administrative data, Death, Cause of Death, Classification of Primary Cause of Death, Non-cardiovascular death, Cardiovascular death, Place of Death, Other data, Circumstances of Death, Narrative
Itemgroups: Administrative data, Acute Myocardial Infraction/Hospitalized Angina or Chest Pain, Clinical Presentation, Electrocardiographic Details, Cardiac Enzymes/Markers, CK-MB, Troponin I, Troponin T, Treatment Given for Acute MI/Hospitalized Angina/Chest Pain Event, Other Investigations Undertaken in View of this Event, Final Clinical Diagnosis, Narrative
Itemgroups: Administrative data, Coronary Revascularization, Percutaneous coronary intervention, Coronary artery bypass graft procedure, Specify other coronary revascularization procedure, AE Details, Enzyme Value Data, CK-MB, Troponin I, Troponin T
Itemgroups: Administrative data, Stroke / TIA, Neurological Signs / Symptoms, Neurological Signs / Symptoms Tendencies, Diagnostic Investigations - CT Brain Scan, Diagnostic Investigations - MRI Brain Scan, Diagnostic Investigations - Cerebral Angiography, Diagnostic Investigations - Lumbar Puncture, Final Clinical Diagnosis, Narrative
Itemgroups: Administrative data, Hospitalization for Heart Failure, Clinical Symptoms of Heart Failure, Investigative Evidence of Structural or Functional Heart Disease, Chest X-Ray, Echocardiography, Left ventricular systolic dysfunction / impairment, Significant valvular heart disease, BNP (B-type natriuretic peptide) or NT-proBNP (N-terminal proBNP), Peak BNP/NT-proBNP value + the laboratory upper reference limit, BNP, NT-proBNP, Other Investigations, Treatment, Description of Event
Itemgroups: Administrative data, Liver Events Assessment, Liver Events, Alcohol Intake, Liver Disease Medical Conditions, Drug Related Liver Disease Conditions, Other Medical Conditions
Itemgroups: Administrative data, Liver Biopsy pt 1, Liver Biopsy pt 2, Liver Biopsy pt 3
Itemgroups: Administrative data, (Serious) Hypoglycaemic Events, Serious Adverse Events, Injection Site Reaction, Pancreatitis, Symptoms of Gastrointestinal Illness Associated with Pancreatitis, Pain in the Epigastrium, Pain in the Periumbical Region, Pain in the Right Upper Quadrant, Pain in the Left Upper Quadrant, Pain in the Left Lower Quadrant, Pain in the Right Lower Quadrant, Pain in the Right Flank, Pain in the Left Flank, Pain in the Back, Other Symptoms, Nausea, Vomiting, Fever, Biochemistry, Alkaline phosphatase, Total bilirubin, Direct bilirubin, Creatinine, Other lab test, Diagnostic Studies - Pancreatitis, Abdominal CT Scan, MRI, New Thyroid Nodules, Bidimensional Measurement, Thyroid Nodules AE Details, Thyroid function tests, Free T4, T4, TSH, Free T3, T3 Uptake
Itemgroups: Administrative data, Study Termination
Itemgroups: Administrative data, Section 1, Section 2 - Seriousness, Section 3 - Demography Data, Section 4 - Adverse event after Investigational product withdrawal, Section 5 - Possible Causes of SAE, Section 6 - Relevant Medical Conditions, Section 7 - Relevant Risk Factors, Section 8 - Relevant Concomitant Medications, Section 9 - Details of Investigational Product, Section 10 - Relevant Assessment, Section 11 - Narrative Remarks
Itemgroups: Administrative data, Adverse Events