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% |
|
|