Ergocalciferol combined with Methotrexate

Reports:

Reaction Outcome Event Date Age Sex Weight Reported Reporter Country Treatment
Role Name
Somnolence Other Serious 50 Male 2/17/2006 Physician Portugal
Primary
Concomitant
Dyspnoea Other Serious 8/1/2005 52 Female 2/17/2006 Physician Spain
Primary
Concomitant
Vertigo Other Serious 10/1/2005 Male 234 lb 2/27/2006 Physician Portugal
Primary
Concomitant
Cerebrovascular Accident Other Serious 2/26/2006 Female 135 lb 3/9/2006 Consumer Canada
Primary
Concomitant
Cerebrovascular Accident Other Serious 2/26/2006 Female 135 lb 3/23/2006 Physician Canada
Primary
Concomitant
Mammogram Abnormal Other Serious 1/1/2006 46 Female 80 lb 3/28/2006 Other Health Professional United States
Primary
Concomitant
Lower Respiratory Tract Infection Death Female 88 lb 4/21/2006 Other Health Professional United Kingdom
Primary
Concomitant
Cerebrovascular Accident Other Serious 2/26/2006 Female 135 lb 4/21/2006 Physician Canada
Primary
Concomitant
Cerebrovascular Accident Other Serious 2/26/2006 Female 135 lb 5/11/2006 Physician Canada
Primary
Concomitant
Renal Disorder Other Serious 12/19/2003 Female 5/17/2006 Physician United Kingdom
Primary
Concomitant
Rectal Haemorrhage Hospitalization 5/17/2006 Female 180 lb 6/21/2006 Consumer Canada
Primary
Concomitant
Malaise Hospitalization 1/1/2005 12 Female 6/30/2006 Other Health Professional United Kingdom
Primary
Secondary
Concomitant
Lower Respiratory Tract Infection Death Female 88 lb 8/2/2006 Other Health Professional United Kingdom
Primary
Concomitant
Large Intestinal Haemorrhage Other Serious 6/28/2006 Female 8/4/2006 Consumer Canada
Primary
Concomitant
White Blood Cell Count Increased Death 10/28/2005 Female 88 lb 8/11/2006 Other Health Professional United Kingdom
Primary
Concomitant
Salivary Gland Mass Other Serious 1/1/2006 Female 240 lb 8/25/2006 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2006 Female 9/7/2006 Physician United States
Primary
Secondary
Concomitant
Pneumonia Hospitalization 7/22/2006 Female 130 lb 9/13/2006 Consumer Canada
Primary
Concomitant
Large Intestinal Haemorrhage Other Serious 7/12/2006 Female 9/22/2006 Physician Canada
Primary
Concomitant
Myocardial Infarction Death 9/21/2006 Female 130 lb 11/20/2006 Physician Canada
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2006 Female 12/5/2006 Physician United States
Primary
Secondary
Concomitant
Abortion Spontaneous Other Serious 12/2/2006 Female 145 lb 12/29/2006 Consumer Canada
Primary
Concomitant
Spinal Fracture Life Threatening 3/1/2005 Female 154 lb 1/25/2007 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
Sleep Apnoea Syndrome Hospitalization 8/17/2006 Female 3/9/2007 Physician United States
Primary
Concomitant
Thymus Enlargement Hospitalization 1/1/2005 Female 118 lb 3/16/2007 Physician Canada
Primary
Concomitant
Intermittent Claudication Hospitalization 3/1/2007 Male 43 lb 3/21/2007 France
Primary
Concomitant
Thymus Enlargement Hospitalization 1/1/2005 Female 118 lb 4/2/2007 Physician Canada
Primary
Concomitant
Drug Ineffective Hospitalization Female 140 lb 4/25/2007 Consumer Canada
Primary
Concomitant
Tongue Haemorrhage Hospitalization 4/8/2007 61 Female 4/27/2007 Physician Portugal
Primary
Concomitant
Carpal Tunnel Syndrome Other Serious Female 161 lb 4/30/2007 Consumer Canada
Primary
Concomitant
Yellow Skin Other Serious 10/1/2006 Male 154 lb 5/3/2007 Consumer Brazil
Primary
Concomitant
Knee Arthroplasty Hospitalization 5/14/2007 Female 126 lb 5/25/2007 Consumer Canada
Primary
Concomitant
Cardiomyopathy Hospitalization 4/17/2007 8 Male 57 lb 6/11/2007 Other Health Professional France
Primary
Secondary
Concomitant
Hypertrophic Cardiomyopathy Hospitalization 4/17/2007 8 Male 5/31/2007 France
Primary
Secondary
Concomitant
Purulent Discharge Hospitalization 5/14/2007 Female 126 lb 6/29/2007 Consumer Canada
Primary
Concomitant
Spinal Fracture Life Threatening 3/1/2005 Female 154 lb 7/13/2007 Belgium
Primary
Concomitant
Incision Site Infection Hospitalization Female 130 lb 7/23/2007 Canada
Primary
Concomitant
Tongue Haemorrhage Hospitalization 4/8/2007 61 Female 7/25/2007 Physician Portugal
Primary
Concomitant
Knee Arthroplasty Hospitalization 9/26/2006 Female 8/3/2007 Belgium
Primary
Concomitant
Injection Site Pain Disability 7/30/2007 Female 132 lb 8/27/2007 Other Health Professional United Kingdom
Primary
Concomitant
Nephrolithiasis Other Serious 3/14/2007 61 Female 9/11/2007 United States
Primary
Concomitant
Tendon Injury Hospitalization Female 251 lb 9/24/2007 Canada
Primary
Concomitant
Gait Disturbance Hospitalization 3/1/2007 Male 43 lb 10/9/2007 France
Primary
Concomitant
Synovitis Hospitalization 3/1/2007 Male 43 lb 10/16/2007 France
Primary
Concomitant
Psychomotor Hyperactivity Hospitalization 10/1/2007 Female 125 lb 11/2/2007 United States
Primary
Concomitant
Renal Cyst Hospitalization 1/1/2007 Female 11/9/2007 Czech Republic
Primary
Concomitant
Insomnia 6/1/2007 Male 236 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
Tearfulness 10/10/2007 Female 162 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
Injection Site Bruising 9/13/2007 Female 150 lb 12/14/2007 Physician
Primary
Concomitant
Thoracic Vertebral Fracture Hospitalization 1/3/2008 83 Female 1/25/2008 Belgium
Primary
Concomitant
Thoracic Vertebral Fracture Hospitalization 1/3/2008 83 Female 2/6/2008 Belgium
Primary
Concomitant
Migraine Other Serious Female 138 lb 2/27/2008 Canada
Primary
Concomitant
Ischaemia Hospitalization 2/8/2008 Female 3/12/2008 Brazil
Primary
Concomitant
Carpal Tunnel Syndrome Other Serious 2/1/2007 Female 125 lb 3/13/2008 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2007 Female 3/14/2008 Czech Republic
Primary
Concomitant
Pain In Extremity Other Serious 3/6/2008 Male 3/14/2008 United States
Primary
Concomitant
Injection Site Pain 12/1/2007 Female 79 lb 3/14/2008 Consumer United States
Primary
Concomitant
Accidental Exposure 1/4/2008 Female 175 lb 3/15/2008 Other Health Professional United States
Primary
Concomitant
Speech Disorder Hospitalization 2/8/2008 Female 198 lb 3/18/2008 Brazil
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2007 Female 3/21/2008 Czech Republic
Primary
Concomitant
Lymphoma Other Serious 3/1/2008 Female 222 lb 3/28/2008 Physician United States
Primary
Concomitant
Speech Disorder Hospitalization 2/8/2008 Female 198 lb 4/7/2008 Brazil
Primary
Concomitant
Upper Limb Fracture Other Serious 3/6/2008 Male 4/11/2008 United States
Primary
Concomitant
Thoracic Vertebral Fracture Hospitalization 1/3/2008 83 Female 4/8/2008 Physician Belgium
Primary
Concomitant
Salpingectomy Other Serious 6/14/2007 Female 132 lb 5/2/2008 United States
Primary
Concomitant
Speech Disorder Hospitalization 2/8/2008 Female 198 lb 5/12/2008 Brazil
Primary
Concomitant
Thoracic Vertebral Fracture Hospitalization 1/3/2008 83 Female 5/29/2008 Belgium
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
Overdose 3/7/2008 Female 142 lb 6/12/2008 United States
Primary
Concomitant
Rheumatoid Arthritis 9/1/2006 Male 6/12/2008 Consumer United States
Primary
Concomitant
Eye Infection 4/1/2008 Female 152 lb 6/12/2008 Consumer United States
Primary
Concomitant
Headache 3/1/2008 Female 116 lb 6/12/2008 United States
Primary
Concomitant
Throat Irritation 4/12/2008 Female 204 lb 6/12/2008 United States
Primary
Concomitant
Accidental Exposure 4/18/2008 Female 249 lb 6/12/2008 Consumer United States
Primary
Concomitant
Skin Exfoliation 3/1/2008 Female 120 lb 6/12/2008 United States
Primary
Concomitant
Viral Infection 1/1/2008 Female 113 lb 6/13/2008 Other Health Professional United States
Primary
Concomitant
Injection Site Irritation 1/15/2008 Female 158 lb 6/13/2008 United States
Primary
Concomitant
Injection Site Haemorrhage Hospitalization 5/9/2008 Male 195 lb 6/13/2008 Consumer United States
Primary
Concomitant
Accidental Exposure 5/30/2008 Female 220 lb 6/13/2008 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 1/1/2007 Female 6/27/2008 Czech Republic
Primary
Concomitant
Thoracic Vertebral Fracture Hospitalization 1/3/2008 83 Female 6/24/2008 Belgium
Primary
Concomitant
Hernia Other Serious 3/12/2008 Female 165 lb 7/3/2008 United States
Primary
Concomitant
Carpal Tunnel Decompression Other Serious 8/15/2008 Female 143 lb 8/29/2008 Consumer United States
Primary
Concomitant
Constipation Hospitalization 3/10/2008 Female 9/5/2008 United States
Primary
Concomitant
Constipation Hospitalization 3/10/2008 Female 9/12/2008 United States
Primary
Concomitant
Injection Site Swelling 1/1/2000 Female 132 lb 9/12/2008 Consumer United States
Primary
Concomitant
Respiratory Tract Congestion 1/1/2005 Female 9/12/2008 Consumer United States
Primary
Concomitant
Rash 5/29/2008 Female 142 lb 9/12/2008 United States
Primary
Concomitant
Oropharyngeal Pain Male 180 lb 9/12/2008 Consumer United States
Primary
Concomitant
Pain 6/1/2008 Female 215 lb 9/12/2008
Primary
Concomitant
Contusion 7/3/2008 Female 158 lb 9/12/2008 United States
Primary
Concomitant
Rheumatoid Arthritis 1/1/2008 Male 170 lb 9/12/2008 Consumer United States
Primary
Concomitant
Rheumatoid Arthritis 6/1/2008 Female 145 lb 9/12/2008 Consumer United States
Primary
Concomitant
Visual Acuity Reduced Female 185 lb 9/12/2008 Consumer United States
Primary
Concomitant
Urticaria 3/1/2008 Female 200 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
Emphysema 5/1/2008 Female 200 lb 9/13/2008 United States
Primary
Secondary
Concomitant
Pancreatitis Hospitalization 3/1/2006 Male 200 lb 10/27/2008 Consumer United States
Primary
Concomitant
Renal Failure Other Serious 4/1/2003 Female 10/31/2008 Other Health Professional United States
Primary
Secondary
Concomitant
Emphysema 5/1/2008 Female 200 lb 12/12/2008
Primary
Secondary
Concomitant
Arthralgia 8/27/2008 Female 195 lb 12/12/2008 Consumer United States
Primary
Concomitant
Urticaria 8/28/2008 Female 12/12/2008 United States
Primary
Concomitant
Injection Site Pain 5/1/2008 Female 115 lb 12/12/2008 Consumer United States
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
Rheumatoid Arthritis 8/1/2008 Female 330 lb 12/12/2008 Other Health Professional United States
Primary
Concomitant
Gingival Bleeding 1/1/2008 Female 12/12/2008 Consumer United States
Primary
Concomitant
Injection Site Pain 6/1/2007 Female 220 lb 12/12/2008 Other Health Professional United States
Primary
Concomitant
Injection Site Rash 9/26/2008 Female 12/12/2008 United States
Primary
Concomitant
Swelling 10/1/2008 Male 180 lb 12/12/2008 United States
Primary
Concomitant
Urinary Tract Infection Hospitalization 9/1/2008 Female 12/12/2008 Other Health Professional United States
Primary
Concomitant
White Blood Cells Urine Positive 1/1/2008 Female 12/12/2008 United States
Primary
Concomitant
Injection Site Pain 7/1/2008 Female 12/12/2008 Physician United States
Primary
Concomitant
Injection Site Pain 1/1/2006 Male 12/12/2008 Physician United States
Primary
Concomitant
Rheumatoid Arthritis 10/18/2008 Female 12/12/2008 Physician United States
Primary
Concomitant
Rash 1/1/2008 Female 12/12/2008 Consumer United States
Primary
Concomitant
Injection Site Irritation 11/14/2008 Female 140 lb 12/12/2008 Consumer United States
Primary
Concomitant
Incorrect Dose Administered 11/11/2008 Female 230 lb 12/12/2008 Consumer United States
Primary
Concomitant
Injection Site Pain Female 12/12/2008 Consumer United States
Primary
Concomitant
Incorrect Dose Administered 11/24/2008 Female 149 lb 12/12/2008 United States
Primary
Concomitant
Constipation Hospitalization 3/10/2008 Female 12/19/2008 United States
Primary
Concomitant
White Blood Cell Count Decreased Hospitalization 11/6/2008 2 Male 29 lb 12/29/2008 Other Health Professional United States
Primary
Concomitant
White Blood Cell Count Increased Hospitalization 9/8/2008 Female 194 lb 1/8/2009 Physician United States
Primary
Concomitant
White Blood Cell Count Increased Hospitalization 9/8/2008 Female 194 lb 1/23/2009 Physician United States
Primary
Concomitant
Urinary Tract Infection 10/25/2008 Female 3/14/2009 United States
Primary
Concomitant
Arthralgia 11/29/2008 Female 98 lb 3/14/2009 United States
Primary
Concomitant
Product Quality Issue Hospitalization 6/1/2008 63 Male 3/12/2009 Consumer 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
Dizziness Other Serious 4/2/2009 Female 130 lb 5/6/2009 Physician United States
Primary
Concomitant
Vomiting Other Serious 4/14/2009 12 Female 6/1/2009 France
Primary
Secondary
Concomitant
Injection Site Pain 3/6/2009 Female 156 lb 6/11/2009 Consumer United States
Primary
Concomitant
Incorrect Dose Administered 6/16/2007 Female 210 lb 9/11/2009 Consumer United States
Primary
Concomitant
Incorrect Dose Administered 7/8/2007 Female 182 lb 9/11/2009 Consumer United States
Primary
Concomitant
Injection Site Pain 4/1/2007 Female 145 lb 9/12/2009 Consumer United States
Primary
Concomitant
Wrong Technique In Drug Usage Process 9/13/2007 Female 150 lb 9/12/2009 Physician
Primary
Concomitant
Incorrect Dose Administered 1/4/2008 Female 175 lb 9/12/2009 Other Health Professional United States
Primary
Concomitant
Wrong Technique In Drug Usage Process 4/18/2008 Female 249 lb 9/12/2009 Consumer United States
Primary
Concomitant
Injection Site Haemorrhage Hospitalization 5/9/2008 Male 195 lb 9/12/2009 Consumer United States
Primary
Concomitant
Injection Site Extravasation 5/30/2008 Female 220 lb 9/12/2009 Consumer United States
Primary
Concomitant
Rheumatoid Arthritis 8/1/2008 Female 330 lb 9/12/2009 Other Health Professional United States
Primary
Concomitant
Wrong Technique In Drug Usage Process 5/1/2008 Female 115 lb 9/12/2009 Consumer United States
Primary
Concomitant
Incorrect Dose Administered 7/3/2008 Female 158 lb 9/12/2009 United States
Primary
Concomitant

Drug Data