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Keywords
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- Clinical Trial (5)
- Clinical Trial, Phase I (5)
- Diabetes Mellitus, Type 2 (5)
- Pharmacokinetics (4)
- Drug-Related Side Effects and Adverse Reactions (4)
- Adverse event (4)
- Contraceptives, Oral, Combined (4)
- Laboratories (2)
- Placebos (1)
- Women (1)
- Biopsy (1)
- Cross-Over Studies (1)
- Chest Pain (1)
- Treatment Form (1)
- End of Study (1)
- Electrocardiogram (ECG) (1)
- Chest X- ray (1)
- Coronary Disease (1)
- Double-Blind Method (1)
- Echocardiography (1)
- Enzymes (1)
- Heart Failure (1)
- Hepatitis (1)
- Hypoglycemia (1)
- Injections, Intramuscular (1)
- Liver (1)
- Liver Diseases (1)
- Myocardial Infarction (1)
- Pancreatitis (1)
- Parasites (1)
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5 Search results.
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, 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, Liver Biopsy pt 1, Liver Biopsy pt 2, Liver Biopsy pt 3
Itemgroups: Administrative data, Injection Site Reaction, Local reaction symptoms, Subjects with a severe injection site reaction or a severe systemic allergic reaction must have three 1mL serum samples obtained for immunogenicity testing.
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