Previscan



Indications and Reactions:

Role Indications Reactions
Primary
Drug Use For Unknown Indication 20.0%
Pulmonary Hypertension 14.3%
Diarrhoea 8.6%
Hypothyroidism 8.6%
Myocardial Infarction 8.6%
Pancreatic Carcinoma Metastatic 8.6%
Angioplasty 5.7%
Atrial Fibrillation 5.7%
Helicobacter Infection 5.7%
Atherosclerosis Prophylaxis 2.9%
Hyperuricaemia 2.9%
Osteonecrosis 2.9%
Product Used For Unknown Indication 2.9%
Prophylaxis 2.9%
International Normalised Ratio Increased 17.6%
Septic Shock 17.6%
Bilirubin Conjugated Increased 5.9%
Blood Amylase Increased 5.9%
Blood Creatinine Increased 5.9%
Haematuria 5.9%
Hepatitis 5.9%
Melaena 5.9%
Muscle Haemorrhage 5.9%
Prothrombin Level Abnormal 5.9%
Rectal Haemorrhage 5.9%
Renal Failure 5.9%
Shock Haemorrhagic 5.9%
Secondary
Drug Use For Unknown Indication 31.4%
Product Used For Unknown Indication 15.0%
Atrial Fibrillation 12.0%
Hypertension 9.0%
Pulmonary Embolism 3.6%
Depression 2.8%
Deep Vein Thrombosis 2.8%
Type 2 Diabetes Mellitus 2.7%
Thrombosis Prophylaxis 2.6%
Cardiac Failure 2.5%
Arrhythmia 1.9%
Phlebitis 1.8%
Urinary Tract Infection 1.7%
Prophylaxis 1.6%
Bronchitis 1.5%
Essential Hypertension 1.4%
Pain 1.4%
Hypothyroidism 1.4%
Unevaluable Event 1.4%
Dyslipidaemia 1.3%
International Normalised Ratio Increased 20.3%
Vomiting 6.7%
Renal Failure Acute 6.6%
Rectal Haemorrhage 6.2%
Subdural Haematoma 5.9%
Toxic Skin Eruption 5.9%
Haematoma 5.5%
Muscle Haemorrhage 5.5%
Renal Failure 5.5%
Overdose 4.7%
Thrombocytopenia 4.5%
Neutropenia 3.8%
Shock Haemorrhagic 2.8%
Prothrombin Level Decreased 2.6%
Transaminases Increased 2.5%
Vascular Purpura 2.5%
Drug Rash With Eosinophilia And Systemic Symptoms 2.1%
Interstitial Lung Disease 2.1%
Peritoneal Haemorrhage 2.0%
Weight Decreased 2.0%
Concomitant
Drug Use For Unknown Indication 27.3%
Product Used For Unknown Indication 18.7%
Hypertension 11.1%
Atrial Fibrillation 8.9%
Cardiac Failure 3.8%
Multiple Myeloma 3.4%
Arrhythmia 2.7%
Type 2 Diabetes Mellitus 2.5%
Pain 2.4%
Thrombosis Prophylaxis 2.3%
Osteoporosis 2.0%
Unevaluable Event 1.9%
Prophylaxis 1.9%
Rheumatoid Arthritis 1.9%
Depression 1.8%
Diabetes Mellitus 1.8%
Insomnia 1.5%
Ill-defined Disorder 1.5%
Pulmonary Arterial Hypertension 1.4%
Hiv Infection 1.3%
Renal Failure Acute 19.3%
Renal Failure 10.7%
Thrombocytopenia 7.0%
Vomiting 6.7%
Malaise 4.7%
Somnolence 4.7%
Toxic Skin Eruption 4.7%
Weight Decreased 4.1%
Hyponatraemia 3.9%
Neutropenia 3.6%
Orthostatic Hypotension 3.6%
Pyrexia 3.5%
International Normalised Ratio Increased 3.3%
Lung Disorder 3.2%
Rhabdomyolysis 3.2%
Pancytopenia 2.9%
Sepsis 2.8%
Urinary Tract Infection 2.8%
Syncope 2.7%
Overdose 2.6%
Interacting
Drug Use For Unknown Indication 33.5%
Atrial Fibrillation 13.6%
Product Used For Unknown Indication 10.0%
Hypertension 5.1%
Unevaluable Event 4.9%
Bronchitis 3.3%
Back Pain 3.2%
Thrombosis Prophylaxis 3.2%
Arrhythmia 2.9%
Lung Disorder 2.8%
Urinary Tract Infection 2.3%
Depression 2.3%
Cardiac Failure 2.0%
Prophylaxis 2.0%
Type 2 Diabetes Mellitus 1.7%
Hypercholesterolaemia 1.6%
Pain 1.6%
Dyslipidaemia 1.4%
Phlebitis 1.4%
Sciatica 1.2%
International Normalised Ratio Increased 41.1%
Drug Interaction 7.3%
Overdose 5.5%
Rectal Haemorrhage 5.5%
Subdural Haematoma 5.5%
Melaena 5.2%
Muscle Haemorrhage 3.9%
International Normalised Ratio Decreased 2.9%
Shock Haemorrhagic 2.9%
Subcutaneous Haematoma 2.6%
Prothrombin Level Decreased 2.4%
Haematoma 2.1%
Haematuria 1.8%
Prothrombin Time Ratio Decreased 1.8%
Renal Failure 1.8%
Anaemia 1.6%
Pallor 1.6%
Respiratory Failure 1.6%
Wound Haemorrhage 1.6%
Gastrointestinal Haemorrhage 1.3%