Solostar



Indications and Reactions:

Role Indications Reactions
Primary
Type 2 Diabetes Mellitus 61.7%
Diabetes Mellitus 10.9%
Type 1 Diabetes Mellitus 10.9%
Device Therapy 4.8%
Product Used For Unknown Indication 2.0%
Type Ii Diabetes Mellitus 1.8%
Hypertension 1.7%
Blood Pressure 1.3%
Cardiac Disorder 0.7%
Pain 0.7%
Rash 0.7%
Cardiac Failure Congestive 0.6%
Depression 0.6%
Blood Cholesterol 0.4%
Seasonal Allergy 0.4%
Affective Disorder 0.2%
Atrial Fibrillation 0.2%
Blood Cholesterol Abnormal 0.2%
Blood Cholesterol Increased 0.2%
Blood Glucose Decreased 0.2%
Device Malfunction 32.4%
Injury Associated With Device 17.8%
Product Quality Issue 14.2%
Malaise 3.6%
Visual Impairment 3.6%
Wrong Drug Administered 3.2%
Hypoglycaemia 2.8%
Visual Acuity Reduced 2.8%
Feeling Abnormal 2.4%
Injection Site Pain 2.0%
Nausea 2.0%
Pain 2.0%
Unevaluable Event 2.0%
Injection Site Haemorrhage 1.6%
Vomiting 1.6%
Weight Decreased 1.6%
Blood Glucose Increased 1.2%
Hyperglycaemia 1.2%
Overdose 1.2%
Tremor 1.2%
Secondary
Type 2 Diabetes Mellitus 54.6%
Product Used For Unknown Indication 12.8%
Diabetes Mellitus 10.5%
Type 1 Diabetes Mellitus 6.4%
Device Therapy 5.5%
Type Ii Diabetes Mellitus 2.2%
Hypertension 1.9%
Blood Pressure 1.7%
Diabetes 0.7%
Prophylaxis 0.5%
Insulin-requiring Type 2 Diabetes Mellitus 0.5%
Depression 0.3%
Pain 0.3%
Diabetic Neuropathy 0.3%
Type I Diabetes Mellitus 0.3%
Asthma 0.3%
Blood Glucose 0.3%
Thyroid Disorder 0.3%
Blood Glucose Increased 0.3%
Hyperlipidaemia 0.2%
Device Malfunction 52.2%
Product Quality Issue 16.0%
Blood Glucose Increased 4.4%
Visual Impairment 4.0%
Visual Acuity Reduced 2.7%
Wrong Drug Administered 2.4%
Weight Decreased 2.1%
Hypoglycaemia 2.1%
Malaise 1.4%
Weight Increased 1.3%
Hyperglycaemia 1.2%
Hospitalisation 1.2%
Injection Site Pain 1.2%
Tremor 1.2%
Death 1.2%
Vision Blurred 1.2%
Cerebrovascular Accident 1.1%
Myocardial Infarction 1.1%
Pneumonia 1.0%
Injection Site Haemorrhage 1.0%
Concomitant
Type 2 Diabetes Mellitus 59.7%
Diabetes Mellitus 17.3%
Device Therapy 6.7%
Type 1 Diabetes Mellitus 4.5%
Product Used For Unknown Indication 3.2%
Hypertension 2.4%
Cardiac Disorder 1.2%
Anticoagulant Therapy 0.8%
Blood Cholesterol 0.8%
Blood Pressure 0.5%
Gastrooesophageal Reflux Disease 0.4%
Pain 0.4%
Renal Disorder 0.4%
Sleep Disorder 0.4%
Atrial Fibrillation 0.3%
Diabetes 0.3%
Osteoporosis 0.3%
Thyroid Disorder 0.3%
Affective Disorder 0.2%
Arrhythmia 0.2%
Visual Acuity Reduced 17.2%
Visual Impairment 12.0%
Weight Decreased 6.8%
Death 6.4%
Myocardial Infarction 6.4%
Weight Increased 6.4%
Cerebrovascular Accident 5.2%
Malaise 4.4%
Cardiac Disorder 4.0%
Neoplasm Malignant 3.6%
Blood Glucose Increased 3.2%
Adverse Event 2.8%
Pancreatic Carcinoma 2.8%
Pneumonia 2.8%
Renal Disorder 2.8%
Renal Failure 2.8%
Tremor 2.8%
Vision Blurred 2.8%
Arthropathy 2.4%
Incorrect Product Storage 2.4%
Interacting
Type 2 Diabetes Mellitus 80.0%
Hypertension 20.0%
Drug Interaction 100.0%