Eplerenone

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Nume		Eplerenone

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Boli A-Z		Abdominal Obesity-Metabolic Syndrome 1 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 Acquired Immunodeficiency Syndrome Acute Myocardial Infarction Adenoma Adrenal Gland Disease Adrenal Gland Hyperfunction Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency Aldosterone-Producing Adenoma Aneurysm Aortic Aneurysm Aortic Aneurysm, Familial Abdominal, 1 Aortic Disease Apnea, Obstructive Sleep Arrhythmogenic Right Ventricular Cardiomyopathy Arteries, Anomalies of Arteriosclerosis Atrial Fibrillation Atrophic Muscular Disease Autonomic Dysfunction Autonomic Nervous System Disease Back Pain Breast Cancer Breast Disease Camurati-Engelmann Disease Cardiomyopathy, Dilated, 1a Cardiomyopathy, Dilated, 3b Central Serous Chorioretinopathy Chiari Malformation Type Ii Chronic Kidney Failure Color Blindness Color Vision Deficiency Congestive Heart Failure Conn's Syndrome Coronary Artery Anomaly Coronary Heart Disease 1 Degenerative Disc Disease Dextro-Looped Transposition of the Great Arteries Diabetes Insipidus Diabetes Mellitus Diabetes Mellitus, Noninsulin-Dependent Diastolic Heart Failure Dilated Cardiomyopathy Dysautonomia End Stage Renal Failure Fatty Liver Disease Genitourinary Tract Anomalies Gitelman Syndrome Glucose Intolerance Glucose Metabolism Disease Gonadal Disease Gout Heart Disease Herpes Zoster Hyperglycemia Hyperinsulinism Hyperparathyroidism Hypertension, Essential Hypoglycemia Hypokalemia Infertility Influenza Ischemia Ischemic Heart Disease Kidney Disease Lipid Metabolism Disorder Lipodystrophy Lipoid Congenital Adrenal Hyperplasia Liver Disease Macular Degeneration, Age-Related, 1 Microvascular Complications of Diabetes 5 Multiple System Atrophy 1 Muscle Disorders Muscle Tissue Disease Muscular Dystrophy Muscular Dystrophy, Becker Type Muscular Dystrophy, Duchenne and Becker Type Muscular Dystrophy, Duchenne Type Myocardial Infarction Myocarditis Myopathy Myotonia Congenita, Autosomal Recessive Nervous System Disease Neuritis Neuromuscular Disease Neuropathy Oculocerebral Syndrome with Hypopigmentation Overnutrition Parathyroid Gland Disease Paresthesia Paroxysmal Ventricular Fibrillation Pericarditis Peripheral Nervous System Disease Postural Hypotension Primary Hyperparathyroidism Progressive Familial Heart Block Progressive Familial Heart Block, Type Ia Pure Autonomic Failure Radiculopathy Renal Fibrosis Renal Tubular Transport Disease Respiratory System Disease Retinal Disease Retinal Vein Occlusion Retinitis Sex Differentiation Disease Single Ventricular Heart Skin Conditions Skin Disease Sleep Apnea Sleep Disorder Spastic Diplegia Spinal and Bulbar Muscular Atrophy, X-Linked 1 Spinal Disease Systolic Heart Failure Tetralogy of Fallot Thrombocytopenia Due to Platelet Alloimmunization Thrombocytopenic Purpura, Autoimmune Transposition of the Great Arteries Trichohepatoenteric Syndrome 2 Univentricular Heart Urinary System Disease Vascular Disease Ventricular Fibrillation, Paroxysmal Familial, 1 Viral Infectious Disease Visceral Steatosis