Vitamin D



Combined with:

Asa
Yaz

Indications and Reactions:

Role Indications Reactions
Primary
Vitamin D Decreased 30.5%
Vitamin D Deficiency 20.3%
Temporal Arteritis 10.2%
Osteoporosis 6.8%
Bone Disorder 3.4%
Osteoporosis Prophylaxis 3.4%
Vitamin Supplementation 3.4%
Back Pain 1.7%
Bipolar Disorder 1.7%
Bone Density Abnormal 1.7%
Breast Feeding 1.7%
Heart Valve Replacement 1.7%
Hepatitis C 1.7%
Hypovitaminosis 1.7%
Osteopenia 1.7%
Osteoporotic Fracture 1.7%
Product Used For Unknown Indication 1.7%
Supplementation Therapy 1.7%
Vitamin D 1.7%
Vitamin D Abnormal 1.7%
Toxicity To Various Agents 13.3%
Medication Error 11.1%
Pain In Extremity 8.9%
Vomiting 8.9%
Rash 6.7%
Blood 25-Hydroxycholecalciferol Increased 4.4%
Diarrhoea 4.4%
Drug Dispensing Error 4.4%
Insomnia 4.4%
Overdose 4.4%
Pain 4.4%
Palpitations 4.4%
Visual Impairment 4.4%
Apnoea 2.2%
Blood Calcium Increased 2.2%
Carpal Tunnel Syndrome 2.2%
Cerebral Haemorrhage 2.2%
Cerebrovascular Accident 2.2%
Chest Pain 2.2%
Decreased Appetite 2.2%
Secondary
Product Used For Unknown Indication 39.1%
Drug Use For Unknown Indication 11.1%
Osteoporosis 5.7%
Hypertension 4.9%
Drug Exposure During Pregnancy 4.7%
Depression 3.6%
Pain 3.3%
Hypothyroidism 3.0%
Blood Cholesterol Increased 2.7%
Ill-defined Disorder 2.7%
Asthma 2.4%
Rheumatoid Arthritis 2.3%
Supplementation Therapy 2.1%
Fibromyalgia 2.0%
Prophylaxis 2.0%
Vitamin Supplementation 1.9%
Maternal Exposure During Pregnancy 1.7%
Diabetes Mellitus 1.6%
Osteoporosis Prophylaxis 1.6%
Vitamin D Deficiency 1.6%
Completed Suicide 11.4%
Vomiting 9.3%
Toxicity To Various Agents 7.9%
Drug Interaction 5.7%
Pain 5.7%
Tendonitis 5.7%
Drug Ineffective 5.0%
Pain In Extremity 5.0%
Nephrocalcinosis 4.3%
Rash 4.3%
Restless Legs Syndrome 4.3%
Visual Impairment 4.3%
Weight Increased 4.3%
White Blood Cell Count Decreased 4.3%
Constipation 3.6%
Tremor 3.6%
Dizziness 2.9%
Headache 2.9%
International Normalised Ratio Increased 2.9%
Pulmonary Hypertension 2.9%
Concomitant
Product Used For Unknown Indication 39.4%
Drug Use For Unknown Indication 8.8%
Osteoporosis 6.6%
Hypertension 5.6%
Rheumatoid Arthritis 5.5%
Pain 3.8%
Crohn's Disease 3.5%
Vitamin Supplementation 3.4%
Multiple Sclerosis 2.9%
Depression 2.4%
Supplementation Therapy 2.4%
Gastrooesophageal Reflux Disease 2.4%
Blood Cholesterol Increased 2.2%
Prophylaxis 2.2%
Asthma 1.8%
Diabetes Mellitus 1.7%
Anxiety 1.5%
Atrial Fibrillation 1.4%
Multiple Myeloma 1.3%
Hypothyroidism 1.2%
Vomiting 9.7%
Weight Decreased 9.3%
Nausea 6.3%
Pain 6.1%
Weight Increased 5.9%
Pain In Extremity 5.4%
Flushing 5.0%
Drug Ineffective 4.9%
Pruritus 4.9%
Death 4.6%
Urinary Tract Infection 4.5%
Pneumonia 4.2%
Fatigue 4.2%
Injection Site Pain 4.1%
Headache 3.9%
Pyrexia 3.6%
Dyspnoea 3.5%
Rash 3.5%
Diarrhoea 3.3%
Tremor 3.0%
Interacting
Product Used For Unknown Indication 27.8%
Vitamin D Deficiency 8.9%
Drug Use For Unknown Indication 7.8%
Blood Cholesterol Abnormal 5.6%
Vitamin Supplementation 5.6%
Depression 4.4%
Systemic Candida 4.4%
Back Disorder 3.3%
Back Pain 3.3%
Bladder Obstruction 3.3%
Fibromyalgia 3.3%
Hypertension 3.3%
Irritable Bowel Syndrome 3.3%
Blood Cholesterol Increased 2.2%
Blood Pressure High 2.2%
Gastrooesophageal Reflux Disease 2.2%
Hypersensitivity 2.2%
Major Depression 2.2%
Musculoskeletal Pain 2.2%
Neck Pain 2.2%
Drug Interaction 14.7%
Vitamin D Deficiency 14.7%
International Normalised Ratio Increased 8.8%
Somnolence 8.8%
Toxicity To Various Agents 8.8%
Dizziness 2.9%
Drug Administration Error 2.9%
Drug Effect Decreased 2.9%
Feeling Abnormal 2.9%
Heart Rate Increased 2.9%
Hepatic Enzyme Increased 2.9%
Low Density Lipoprotein Increased 2.9%
Musculoskeletal Discomfort 2.9%
Nephrocalcinosis 2.9%
Neutropenia 2.9%
Osteopenia 2.9%
Pancreatitis 2.9%
Thyroid Function Test Abnormal 2.9%
Treatment Noncompliance 2.9%
Type 1 Diabetes Mellitus 2.9%