Calcium combined with Ergocalciferol

Reports:

Reaction Outcome Event Date Age Sex Weight Reported Reporter Country Treatment
Role Name
Urticaria Other Serious 9/7/2006 50 Female 9/8/2006 United States
Primary
Concomitant
Cardiac Murmur Hospitalization 4/24/2006 Female 160 lb 11/16/2006 Consumer Canada
Primary
Concomitant
Myocardial Infarction Death 9/21/2006 Female 130 lb 11/20/2006 Physician Canada
Primary
Concomitant
Toe Operation Other Serious 11/8/2006 Female 180 lb 12/1/2006 Consumer Canada
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2006 Female 12/5/2006 Physician United States
Primary
Secondary
Concomitant
Lymphadenectomy Other Serious 76 Female 174 lb 12/1/2006 United States
Primary
Concomitant
Cardiomegaly Other Serious 4/24/2006 Female 160 lb 12/14/2006 Consumer Canada
Primary
Concomitant
Underdose Other Serious 12/20/2006 Female 160 lb 12/30/2006 Other Health Professional Canada
Primary
Concomitant
Systemic Lupus Erythematosus Other Serious 12/12/2006 Female 135 lb 1/12/2007 Physician Canada
Primary
Concomitant
Drug Interaction Other Serious Male 317 lb 1/19/2007 Pharmacist United States
Primary
Interacting
Prescribed Overdose Other Serious 1/1/2006 Male 317 lb 2/2/2007 Pharmacist Denmark
Primary
Interacting
Prescribed Overdose Other Serious 1/1/2006 Male 317 lb 2/14/2007 Pharmacist Denmark
Primary
Interacting
Prescribed Overdose Other Serious 1/1/2006 Male 317 lb 2/14/2007 Pharmacist Denmark
Primary
Interacting
Rheumatoid Nodule Other Serious 60 Female 110 lb 2/23/2007 Physician Brazil
Primary
Concomitant
Sputum Discoloured Other Serious 12/6/2006 85 Male 2/14/2007 Belgium
Primary
Concomitant
Cyst Other Serious 6/12/2005 Male 185 lb 3/2/2007 Consumer United Kingdom
Primary
Concomitant
Renal Impairment Disability 2/1/2006 Female 3/7/2007 Physician Czech Republic
Primary
Concomitant
Upper Respiratory Tract Infection Hospitalization 1/21/2006 Female 110 lb 3/9/2007 Physician Canada
Primary
Concomitant
Sputum Discoloured Other Serious 12/6/2006 85 Male 3/6/2007 Belgium
Primary
Concomitant
Thymus Enlargement Hospitalization 1/1/2005 Female 118 lb 3/16/2007 Physician Canada
Primary
Concomitant
Urinary Tract Infection Hospitalization 12/1/2006 Female 194 lb 3/29/2007 Physician Germany
Primary
Concomitant
Neurological Infection Hospitalization 11/6/2004 Female 181 lb 4/2/2007 Czech Republic
Primary
Concomitant
Thymus Enlargement Hospitalization 1/1/2005 Female 118 lb 4/2/2007 Physician Canada
Primary
Concomitant
Malaise Other Serious 1/16/2007 43 Male 183 lb 4/19/2007 Physician United Kingdom
Primary
Concomitant
Injection Site Pain Disability 7/30/2007 Female 132 lb 8/27/2007 Other Health Professional United Kingdom
Primary
Concomitant
Chest Pain Hospitalization 7/7/2007 Female 155 lb 8/29/2007 Canada
Primary
Concomitant
Tendon Injury Hospitalization Female 251 lb 9/24/2007 Canada
Primary
Concomitant
Weight Bearing Difficulty Other Serious 1/1/2007 78 Female 9/20/2007 Consumer United States
Primary
Concomitant
Blood Calcium Decreased Other Serious 6/21/2007 Female 10/2/2007 Other Health Professional United Kingdom
Primary
Concomitant
Wound Drainage Hospitalization 5/1/2007 62 Male 170 lb 10/26/2007 Consumer United States
Primary
Concomitant
Psychomotor Hyperactivity Hospitalization 10/1/2007 Female 125 lb 11/2/2007 United States
Primary
Concomitant
Flatulence 10/1/2006 70 Female 11/19/2007 Consumer United States
Primary
Concomitant
Somnolence Life Threatening 9/25/2007 84 Female 11/26/2007 Other Health Professional United Kingdom
Primary
Secondary
Concomitant
Hypocalcaemia Other Serious 9/24/2007 Female 12/3/2007 Other Health Professional United States
Primary
Concomitant
Nausea Other Serious 1/1/2007 Female 11/21/2007 Physician United States
Primary
Concomitant
Reticulocyte Count Decreased Other Serious 1/1/2007 Male 198 lb 12/3/2007 Physician United States
Primary
Concomitant
Suicidal Ideation Other Serious 8/1/2007 42 Female 12/13/2007 Physician Argentina
Primary
Concomitant
Insomnia 6/1/2007 Male 236 lb 12/14/2007 Consumer United States
Primary
Concomitant
Contusion 7/26/2007 Female 130 lb 12/14/2007 United States
Primary
Concomitant
Joint Stiffness 6/1/2007 Male 169 lb 12/14/2007 Consumer United States
Primary
Concomitant
Injection Site Pain 4/1/2007 Female 145 lb 12/14/2007 Consumer United States
Primary
Concomitant
Arthralgia Female 201 lb 12/14/2007 Consumer United States
Primary
Concomitant
Injection Site Reaction 10/16/2007 Male 240 lb 12/14/2007 Consumer United States
Primary
Concomitant
Pyrexia 11/21/2007 Female 12/15/2007 United States
Primary
Concomitant
Haemolytic Anaemia Other Serious 1/16/2008 Male 2/20/2008 Other Health Professional United States
Primary
Concomitant
Tremor Other Serious 2/9/2008 Female 149 lb 2/20/2008 United States
Primary
Concomitant
Post Procedural Complication Other Serious 9/1/2007 Male 2/19/2008 Physician United States
Primary
Concomitant
Pain In Extremity Other Serious 11/1/2007 Female 160 lb 2/22/2008 Canada
Primary
Concomitant
Reticulocyte Count Decreased Other Serious 1/1/2007 Male 198 lb 2/27/2008 Physician United States
Primary
Concomitant
Sinusitis 2/1/2007 Female 175 lb 3/14/2008 United States
Primary
Concomitant
Injection Site Pain 12/1/2007 Female 79 lb 3/14/2008 Consumer United States
Primary
Concomitant
Headache 1/1/2008 Female 244 lb 3/15/2008 United States
Primary
Concomitant
Injection Site Urticaria 1/31/2008 Female 124 lb 3/15/2008 United States
Primary
Concomitant
Sinusitis 1/23/2008 Female 190 lb 3/15/2008 United States
Primary
Concomitant
Pruritus Other Serious 2/21/2008 72 Female 4/21/2008 United States
Primary
Secondary
Concomitant
Pain Hospitalization 10/22/2006 Female 139 lb 6/11/2008 United Kingdom
Primary
Concomitant
Sinusitis 1/23/2008 Female 190 lb 6/12/2008 United States
Primary
Concomitant
Alopecia 2/1/2008 Female 150 lb 6/12/2008 Consumer United States
Primary
Concomitant
Alopecia 2/11/2008 Female 150 lb 6/12/2008 United States
Primary
Concomitant
Injection Site Pain Female 135 lb 6/12/2008 Consumer United States
Primary
Concomitant
Stomatitis 12/1/2007 Female 192 lb 6/12/2008 Consumer United States
Primary
Concomitant
Headache 3/1/2008 Female 116 lb 6/12/2008 United States
Primary
Concomitant
Accidental Exposure 4/18/2008 Female 249 lb 6/12/2008 Consumer United States
Primary
Concomitant
Procedural Complication Female 6/12/2008 Physician United States
Primary
Concomitant
Skin Exfoliation 3/1/2008 Female 120 lb 6/12/2008 United States
Primary
Concomitant
Drug Ineffective 1/17/2008 Male 6/13/2008 Consumer United States
Primary
Concomitant
Viral Infection 1/1/2008 Female 113 lb 6/13/2008 Other Health Professional United States
Primary
Concomitant
Accidental Exposure 5/30/2008 Female 220 lb 6/13/2008 Consumer United States
Primary
Concomitant
Colonic Polyp Other Serious Male 170 lb 6/13/2008 Canada
Primary
Concomitant
Cardiac Failure Other Serious Male 6/19/2008 Other Health Professional United Kingdom
Primary
Concomitant
Thrombosis Hospitalization 8/1/2007 Female 156 lb 6/20/2008 United States
Primary
Concomitant
Pain In Extremity Other Serious 6/1/2008 Female 160 lb 6/27/2008 Canada
Primary
Concomitant
Cardiac Failure Other Serious Male 7/17/2008 Other Health Professional United Kingdom
Primary
Concomitant
Acute Coronary Syndrome Other Serious 4/8/2008 Male 176 lb 7/24/2008 Canada
Primary
Concomitant
Hypoaesthesia Other Serious 4/8/2008 Male 176 lb 8/12/2008 Canada
Primary
Concomitant
Sleep Apnoea Syndrome Other Serious 1/1/2008 Female 8/12/2008 Physician United States
Primary
Concomitant
Myalgia Hospitalization 4/30/2008 Female 8/20/2008 Other Health Professional United States
Primary
Concomitant
Pruritus Other Serious 2/21/2008 72 Female 135 lb 7/24/2008 United States
Primary
Secondary
Concomitant
Weight Decreased 10/1/2006 Female 132 lb 8/22/2008 Consumer United States
Primary
Concomitant
Drug Ineffective 3/1/2008 Female 128 lb 8/19/2008 Physician United States
Primary
Concomitant
Prothrombin Time Prolonged Male 8/27/2008 Consumer United States
Primary
Secondary
Concomitant
Rash Generalised 10/1/2007 Female 180 lb 8/27/2008 Consumer United States
Primary
Concomitant
Dysphonia 1/1/2008 Male 168 lb 8/27/2008 Other Health Professional United States
Primary
Concomitant
Rash 4/15/2008 Female 143 lb 8/27/2008 Consumer United States
Primary
Concomitant
Stomach Discomfort 6/3/2008 Male 228 lb 8/27/2008 United States
Primary
Concomitant
Hospitalisation Hospitalization Female 144 lb 8/28/2008 Canada
Primary
Concomitant
Swelling Face 5/13/2008 Female 8/29/2008 Physician United States
Primary
Concomitant
Feeling Hot 8/29/2008 United States
Primary
Concomitant
Dizziness 6/21/2008 Female 106 lb 8/29/2008 United States
Primary
Concomitant
Skin Burning Sensation 6/19/2008 Female 8/29/2008 United States
Primary
Concomitant
Unevaluable Event 5/23/2008 Female 8/29/2008 United States
Primary
Concomitant
Flushing Female 8/29/2008 United States
Primary
Concomitant
Pruritus 7/1/2008 Female 8/29/2008 United States
Primary
Concomitant
Resuscitation Life Threatening 4/30/2008 Female 195 lb 9/10/2008 Other Health Professional United States
Primary
Concomitant
Fall 5/1/2008 Female 178 lb 9/12/2008 United States
Primary
Concomitant
Throat Irritation 5/30/2008 Female 130 lb 9/12/2008 United States
Primary
Concomitant
Paraesthesia Male 195 lb 9/12/2008 Pharmacist United States
Primary
Concomitant
Accidental Exposure 6/4/2008 Female 150 lb 9/12/2008 Consumer United States
Primary
Concomitant
Skin Tightness 7/1/2008 Female 256 lb 9/12/2008 Consumer United States
Primary
Concomitant
Stomach Discomfort 8/20/2008 Female 220 lb 9/13/2008 Consumer United States
Primary
Concomitant
Accidental Exposure 8/20/2008 Female 135 lb 9/13/2008 United States
Primary
Concomitant
Wound Infection Other Serious 1/1/2006 Female 9/30/2008 United States
Primary
Concomitant
Sensory Disturbance Other Serious 10/7/2008 Male 205 lb 10/28/2008 Other Health Professional United States
Primary
Concomitant
Pain In Extremity Other Serious 6/1/2008 Female 160 lb 11/20/2008 Canada
Primary
Concomitant
Palpitations 8/28/2008 Female 11/26/2008 United States
Primary
Concomitant
Nausea 8/1/2008 Female 169 lb 11/26/2008 United States
Primary
Concomitant
Flushing 9/1/2008 Female 11/26/2008 United States
Primary
Concomitant
Paraesthesia 9/1/2008 Female 11/26/2008 United States
Primary
Concomitant
Muscle Spasms 9/23/2008 Female 130 lb 11/26/2008
Primary
Concomitant
Paraesthesia 10/26/2008 Female 11/26/2008 United States
Primary
Concomitant
Pruritus 10/29/2008 Female 11/26/2008 United States
Primary
Secondary
Concomitant
Nervousness Female 11/26/2008 United States
Primary
Concomitant
Hypotension Hospitalization 9/22/2008 Male 165 lb 12/10/2008 Canada
Primary
Concomitant
Vision Blurred 8/1/2007 Male 250 lb 12/12/2008 Consumer United States
Primary
Secondary
Concomitant
Visual Impairment 4/1/2008 Female 250 lb 12/12/2008 United States
Primary
Concomitant
Red Blood Cell Sedimentation Rate Increased 3/1/2008 Male 172 lb 12/12/2008 United States
Primary
Concomitant
Injection Site Pain 4/1/2008 Male 180 lb 12/12/2008 Consumer United States
Primary
Concomitant
Injection Site Urticaria 9/18/2008 Female 175 lb 12/12/2008 Consumer United States
Primary
Concomitant
Vitamin D Decreased 9/1/2008 Female 130 lb 12/12/2008 United States
Primary
Concomitant
Injection Site Rash 9/26/2008 Female 12/12/2008 United States
Primary
Concomitant
Rheumatoid Arthritis 10/18/2008 Female 12/12/2008 Physician United States
Primary
Concomitant
Urinary Retention Hospitalization 11/23/2008 72 Male 203 lb 12/30/2008 Other Health Professional United Kingdom
Primary
Secondary
Concomitant
White Blood Cell Count Increased Hospitalization 9/8/2008 Female 194 lb 1/8/2009 Physician United States
Primary
Concomitant
Transaminases Increased 6/1/2008 Female 143 lb 1/12/2009 Physician United States
Primary
Concomitant
Urinary Retention Hospitalization 11/23/2008 72 Male 203 lb 1/16/2009 Other Health Professional United Kingdom
Primary
Secondary
Concomitant
White Blood Cell Count Increased Hospitalization 9/8/2008 Female 194 lb 1/23/2009 Physician United States
Primary
Concomitant
Urinary Retention Hospitalization 11/23/2008 72 Male 203 lb 2/3/2009 Other Health Professional United Kingdom
Primary
Secondary
Concomitant
Fatigue 11/1/2007 Male 155 lb 2/5/2009 Physician United States
Primary
Concomitant
Focal Segmental Glomerulosclerosis Other Serious 55 Female 2/5/2009 United States
Primary
Concomitant
Nervousness Female 2/24/2009 United States
Primary
Concomitant
Hyperhidrosis 11/14/2008 Female 2/24/2009 United States
Primary
Concomitant
Skin Burning Sensation 11/24/2008 Female 2/24/2009 United States
Primary
Concomitant
Hypertension Other Serious 55 Female 2/25/2009 Other Health Professional United States
Primary
Concomitant
Osteopenia 48 Female 3/12/2009 Other Health Professional United States
Primary
Concomitant
Rash Life Threatening 3/17/2009 64 Female 4/23/2009 Pharmacist United Kingdom
Primary
Concomitant
White Blood Cell Count Increased Hospitalization 9/8/2008 Female 194 lb 4/30/2009 Physician United States
Primary
Concomitant
Vertigo 5/1/2006 64 Female 149 lb 4/30/2009 Consumer United States
Primary
Concomitant
Interacting
Humerus Fracture Disability 6/7/2009 Female 153 lb 6/18/2009 Other Health Professional United States
Primary
Concomitant
Weight Decreased Hospitalization 4/26/2008 85 Female 7/17/2009 Lawyer United States
Primary
Concomitant
Humerus Fracture Disability 6/7/2009 Female 153 lb 7/31/2009 Other Health Professional United States
Primary
Concomitant
Weight Decreased Hospitalization 4/26/2008 85 Female 8/3/2009 Lawyer United States
Primary
Concomitant
Weight Decreased Hospitalization 4/26/2008 85 Female 8/10/2009 Lawyer United States
Primary
Concomitant
Pain 7/1/2008 Female 8/21/2009 United States
Primary
Concomitant
Flushing 8/1/2008 Female 8/21/2009 United States
Primary
Concomitant
Trichorrhexis 7/1/2008 Female 8/21/2009 United States
Primary
Concomitant
Pruritus 9/1/2008 Female 8/21/2009 United States
Primary
Concomitant
Hot Flush 10/27/2008 Female 140 lb 8/22/2009 Consumer United States
Primary
Concomitant
Diarrhoea 1/1/1979 Female 140 lb 8/25/2009 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 4/26/2008 85 Female 8/26/2009 United States
Primary
Concomitant
Injection Site Pain 1/1/2007 Female 120 lb 9/11/2009 Consumer United States
Primary
Concomitant

Drug Data