Aranesp combined with Venofer

Reports:

Reaction Outcome Event Date Age Sex Weight Reported Reporter Country Treatment
Role Name
Pancreatitis Other Serious 9/10/2003 Male 1/12/2006 Physician Portugal
Primary
Concomitant
Post Procedural Complication Hospitalization 9/1/2005 Male 2/9/2006 Other Health Professional Canada
Primary
Concomitant
Therapeutic Response Decreased Other Serious Female 3/6/2006 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Therapeutic Response Decreased Hospitalization 11/1/2005 Male 214 lb 3/20/2006 Physician United States
Primary
Secondary
Concomitant
Tachycardia Other Serious 4/5/2006 76 Male 4/14/2006 Physician Denmark
Primary
Secondary
Concomitant
Therapeutic Response Decreased Hospitalization 11/1/2005 Male 214 lb 4/14/2006 Physician United States
Primary
Secondary
Concomitant
Tongue Injury Hospitalization 6/19/2005 41 Male 4/18/2006 Physician Denmark
Primary
Concomitant
Rectal Polyp Other Serious 11/1/2004 58 Male 4/18/2006 Physician United Kingdom
Primary
Concomitant
Urinary Tract Infection Other Serious 11/1/2004 58 Male 5/3/2006 Physician United Kingdom
Primary
Concomitant
Reticulocyte Count Decreased Disability 3/1/2006 Female 118 lb 5/9/2006 Physician France
Primary
Secondary
Concomitant
Therapeutic Response Decreased Hospitalization 2/16/2006 Male 229 lb 5/12/2006 Physician United States
Primary
Concomitant
Therapeutic Response Decreased Other Serious 1/1/2005 Male 5/15/2006 Physician Canada
Primary
Secondary
Concomitant
Dyspepsia Other Serious 4/1/2005 Male 187 lb 5/17/2006 Physician Portugal
Primary
Concomitant
Rectal Haemorrhage Hospitalization 4/19/2006 Male 5/17/2006 Other Health Professional United States
Primary
Concomitant
Speech Disorder Hospitalization 10/14/2005 Female 136 lb 5/30/2006 Pharmacist United States
Primary
Concomitant
Urticaria Life Threatening 5/2/2006 Female 132 lb 6/7/2006 Other Health Professional United Kingdom
Primary
Concomitant
Wound Infection Staphylococcal Hospitalization 2/16/2006 Male 229 lb 6/13/2006 Physician United States
Primary
Concomitant
Reticulocyte Count Decreased Disability 3/1/2006 Female 118 lb 6/13/2006 Physician France
Primary
Secondary
Concomitant
Rectal Haemorrhage Hospitalization 1/1/2006 Male 6/16/2006 Other Health Professional United States
Primary
Concomitant
Sudden Death Death 50 Male 249 lb 6/29/2006 Other Health Professional United Kingdom
Primary
Concomitant
Platelet Count Decreased Female 6/22/2006 Pharmacist Canada
Primary
Concomitant
Thrombocytopenia Other Serious Female 6/28/2006 Pharmacist Canada
Primary
Concomitant
Therapeutic Response Decreased Other Serious 10/1/2005 45 Female 220 lb 7/21/2006 Physician United States
Primary
Secondary
Concomitant
Therapy Non-responder Other Serious 11/1/2004 58 Male 8/1/2006 United Kingdom
Primary
Concomitant
Therapeutic Response Decreased Other Serious 1/1/2006 Female 8/1/2006 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Haemoglobin Decreased 11/2/2005 Male 157 lb 8/4/2006 Physician United States
Primary
Concomitant
Haemoglobin Decreased 1/1/2005 89 Female 8/4/2006 Physician United States
Primary
Concomitant
Therapeutic Response Decreased 11/18/2005 Male 180 lb 8/4/2006 Physician United States
Primary
Secondary
Concomitant
Therapeutic Response Decreased 9/1/2005 Female 8/4/2006 Other Health Professional United States
Primary
Concomitant
Haemoglobin Decreased Other Serious 7/1/2006 Female 119 lb 8/18/2006 Physician
Primary
Concomitant
Nephrogenic Fibrosing Dermopathy Other Serious 9/1/2005 34 Female 95 lb 8/18/2006 Physician Netherlands
Primary
Concomitant
Therapeutic Response Decreased Other Serious 10/1/2005 45 Female 220 lb 9/15/2006 Physician United States
Primary
Secondary
Concomitant
Haemoglobin Decreased Other Serious 7/1/2006 Female 119 lb 9/25/2006 Physician
Primary
Concomitant
Systemic Lupus Erythematosus Other Serious 7/1/2006 Female 119 lb 11/6/2006 Physician
Primary
Concomitant
Systemic Lupus Erythematosus Other Serious 7/1/2006 Female 119 lb 11/27/2006 Physician
Primary
Concomitant
Nausea 11/17/2006 Male 12/18/2006 Pharmacist United States
Primary
Concomitant
Tumour Marker Increased Other Serious 7/1/2006 Female 134 lb 12/27/2006 Other Health Professional United States
Primary
Secondary
Concomitant
Therapeutic Response Decreased Other Serious 10/1/2005 45 Female 220 lb 1/3/2007 Physician United States
Primary
Secondary
Concomitant
Thrombosis Life Threatening 11/1/2006 77 Male 192 lb 1/22/2007 Other Health Professional France
Primary
Secondary
Concomitant
Vomiting Other Serious 7/25/2006 Male 132 lb 1/25/2007 Pharmacist United States
Primary
Concomitant
Pyrexia Life Threatening 11/29/2006 77 Male 192 lb 2/13/2007 Other Health Professional France
Primary
Secondary
Concomitant
Skin Ulcer Hospitalization 10/9/2006 63 Male 176 lb 2/9/2007 Physician France
Primary
Concomitant
Toxic Skin Eruption Hospitalization 10/9/2006 63 Male 176 lb 2/22/2007 Physician France
Primary
Concomitant
White Blood Cell Count Decreased Female 168 lb 2/28/2007 Consumer United States
Primary
Concomitant
Thrombosis Life Threatening 11/1/2006 Male 192 lb 3/2/2007 Other Health Professional France
Primary
Secondary
Concomitant
Drug Ineffective Hospitalization 6/13/2002 Male 3/8/2007 Physician Israel
Primary
Secondary
Concomitant
Skin Ulcer Haemorrhage Hospitalization 2/8/2006 Female 3/16/2007 Physician Spain
Primary
Concomitant
Tooth Loss Other Serious 1/1/2005 Female 127 lb 4/11/2007 United States
Primary
Concomitant
Thrombocytopenia Other Serious 5/1/2005 Female 4/17/2007 Other Health Professional United States
Primary
Concomitant
Loss Of Consciousness Hospitalization 3/23/2007 Female 5/4/2007 Physician Finland
Primary
Concomitant
Loss Of Consciousness Hospitalization 3/1/2007 Female 5/9/2007 Physician Finland
Primary
Concomitant
Vasculitis Other Serious 3/1/2007 Female 5/23/2007 Physician Finland
Primary
Concomitant
Vasculitis Other Serious 3/1/2007 Female 5/30/2007 Physician Finland
Primary
Concomitant
Therapeutic Response Decreased Other Serious Male 5/31/2007 Physician United Kingdom
Primary
Concomitant
Therapeutic Response Decreased Other Serious 3/1/2007 Male 198 lb 6/14/2007 Physician United Kingdom
Primary
Secondary
Concomitant
Loss Of Consciousness Hospitalization 1/27/2007 35 Female 6/18/2007 Physician France
Primary
Concomitant
Therapeutic Response Decreased Other Serious 3/1/2007 Male 198 lb 6/25/2007 Physician United Kingdom
Primary
Secondary
Concomitant
Therapeutic Response Decreased 8/1/2006 Female 6/26/2007 Other Health Professional United States
Primary
Concomitant
Vasculitis Other Serious 3/1/2007 Female 7/5/2007 Physician Finland
Primary
Concomitant
Red Blood Cell Sedimentation Rate Increased 7/9/2004 Female 200 lb 7/26/2007 Physician United States
Primary
Concomitant
Psoriasis Other Serious 10/1/2002 Male 8/2/2007 Physician Canada
Primary
Concomitant
Koebner Phenomenon Disability 8/1/2006 Male 149 lb 8/6/2007 Physician United Kingdom
Primary
Concomitant
Psoriasis Other Serious 10/1/2002 Male 8/15/2007 Physician Canada
Primary
Concomitant
Koebner Phenomenon Disability 8/1/2006 Male 149 lb 8/20/2007 Physician United Kingdom
Primary
Concomitant
Psoriasis Other Serious 10/1/2002 Male 9/5/2007 Physician Canada
Primary
Concomitant
Vision Blurred Hospitalization 7/30/2007 Female 9/6/2007 Physician Switzerland
Primary
Concomitant
Incorrect Dose Administered 1/1/2007 Male 9/7/2007 Physician France
Primary
Concomitant
Psoriasis Other Serious 10/1/2002 Male 9/13/2007 Physician Canada
Primary
Concomitant
Psoriasis Other Serious 10/1/2002 Male 9/28/2007 Physician Canada
Primary
Concomitant
Erythroplasia Other Serious 6/19/2007 Male 10/15/2007 Physician Finland
Primary
Concomitant
Chest Pain Life Threatening 8/31/2007 38 Male 10/16/2007 Consumer United States
Primary
Concomitant
Aplasia Pure Red Cell Other Serious 6/1/2007 Male 10/30/2007 Physician Finland
Primary
Concomitant
Aplasia Pure Red Cell Other Serious 6/1/2007 Male 11/27/2007 Physician Finland
Primary
Concomitant
Palmar-plantar Erythrodysaesthesia Syndrome Other Serious 1/1/2007 50 Male 1/4/2008 Other Health Professional Switzerland
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 1/7/2008 United States
Primary
Concomitant
Hypotension 12/26/2007 1/7/2008 United States
Primary
Concomitant
Syncope 1/2/2007 53 Female 201 lb 1/18/2008 United States
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 1/18/2008 United States
Primary
Concomitant
Swollen Tongue Hospitalization 12/26/2007 22 Female 139 lb 1/18/2008 United States
Primary
Concomitant
Loss Of Consciousness Other Serious 12/1/2007 77 Female 169 lb 1/22/2008 Other Health Professional United Kingdom
Primary
Concomitant
Haemolysis Other Serious 10/1/2007 Male 1/23/2008 Other Health Professional United States
Primary
Concomitant
Skin Induration Other Serious 9/1/2005 34 Female 95 lb 1/25/2008 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 1/30/2008 United States
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 1/30/2008 United States
Primary
Concomitant
Syncope 1/2/2007 53 Female 201 lb 1/30/2008 United States
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 1/30/2008 United States
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 2/1/2008 United States
Primary
Concomitant
Swollen Tongue Hospitalization 12/26/2007 22 Female 139 lb 2/1/2008 United States
Primary
Concomitant
Haemolysis Other Serious 10/1/2007 Male 2/6/2008 Other Health Professional United States
Primary
Concomitant
Restlessness 12/27/2007 75 Female 119 lb 2/16/2008 United States
Primary
Concomitant
Vomiting 12/26/2007 45 Female 163 lb 2/16/2008 United States
Primary
Concomitant
Nausea 12/27/2007 83 Female 93 lb 2/16/2008 United States
Primary
Concomitant
Vomiting 12/27/2007 55 Male 201 lb 2/16/2008 United States
Primary
Concomitant
Visual Disturbance 12/26/2007 66 Female 126 lb 2/16/2008 United States
Primary
Concomitant
Retching 1/2/2008 77 Female 157 lb 2/17/2008 United States
Primary
Concomitant
Hyperhidrosis 1/2/2008 62 Female 179 lb 2/17/2008 United States
Primary
Concomitant
Anaemia Other Serious 10/1/2007 Male 2/20/2008 Other Health Professional United States
Primary
Concomitant
Unresponsive To Stimuli 12/27/2007 65 187 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Syncope 1/2/2007 53 Female 201 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Vomiting 12/26/2007 45 Female 163 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Nausea 12/27/2007 83 Female 93 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Vomiting 12/27/2007 55 Male 201 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Swollen Tongue Hospitalization 12/26/2007 22 Female 139 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Retching 1/2/2008 77 Female 157 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Hyperhidrosis 1/2/2008 62 Female 179 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Visual Disturbance 12/26/2007 66 Female 126 lb 2/27/2008 Other Health Professional United States
Primary
Concomitant
Weight Decreased Hospitalization 12/1/2007 83 Male 170 lb 4/9/2008 Consumer United States
Primary
Concomitant
Therapeutic Response Decreased Other Serious 1/1/2007 Male 4/21/2008 Physician Sweden
Primary
Concomitant
Therapeutic Response Decreased Other Serious 1/1/2007 Male 5/1/2008 Physician Sweden
Primary
Concomitant
Therapeutic Response Decreased Other Serious 1/1/2007 Male 5/8/2008 Physician Sweden
Primary
Concomitant
Bone Marrow Failure Other Serious 1/1/2008 Female 5/27/2008 Physician Israel
Primary
Concomitant
Ventricular Fibrillation Other Serious 1/1/2007 Male 5/30/2008 Physician Sweden
Primary
Concomitant
Bone Marrow Failure Other Serious 4/1/2008 Female 150 lb 6/3/2008 Physician Israel
Primary
Concomitant
Urticaria Required Intervention 6/23/2008 64 Female 220 lb 6/30/2008 Other Health Professional United States
Primary
Concomitant
Serum Ferritin Decreased Hospitalization 4/1/2008 71 Male 7/21/2008 Other Health Professional Switzerland
Primary
Secondary
Concomitant
Therapeutic Response Decreased Other Serious 3/1/2007 60 Male 8/6/2008 Consumer United States
Primary
Secondary
Concomitant
Bone Marrow Failure Other Serious 4/1/2008 Female 150 lb 8/11/2008 Physician Israel
Primary
Concomitant
Ventricular Fibrillation Other Serious 1/1/2007 Male 8/21/2008 Physician Sweden
Primary
Concomitant
Skin Induration Other Serious 9/1/2005 34 Female 95 lb 8/21/2008 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Skin Induration Other Serious 9/1/2005 34 Female 95 lb 8/22/2008 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Malaise Other Serious 12/1/2007 Female 169 lb 8/27/2008 Other Health Professional United Kingdom
Primary
Concomitant
Therapeutic Response Decreased Other Serious 3/1/2007 Male 198 lb 8/28/2008 Physician United Kingdom
Primary
Secondary
Concomitant
Skin Induration Other Serious 9/1/2005 34 Female 95 lb 9/2/2008 Other Health Professional Netherlands
Primary
Secondary
Concomitant
Sepsis Hospitalization 1/1/2008 36 Female 146 lb 9/10/2008 Physician Germany
Primary
Secondary
Concomitant
Aplasia Pure Red Cell Other Serious 5/1/2006 81 Female 104 lb 10/14/2008 Physician United Kingdom
Primary
Secondary
Concomitant
Myelodysplastic Syndrome Other Serious 9/6/2008 Male 10/17/2008 Other Health Professional United States
Primary
Concomitant
Sepsis Other Serious 2/25/2008 Male 321 lb 10/23/2008 Physician Greece
Primary
Secondary
Concomitant
Hiccups Hospitalization 9/3/2008 54 Male 10/31/2008 Physician Sweden
Primary
Concomitant
Convulsion Hospitalization 4/29/2008 Female 121 lb 11/5/2008 Physician Switzerland
Primary
Concomitant
Myelodysplastic Syndrome Other Serious 9/6/2008 Male 11/6/2008 Other Health Professional United States
Primary
Concomitant
Sepsis Other Serious 2/25/2008 Male 321 lb 11/24/2008 Physician Greece
Primary
Secondary
Concomitant
Pulmonary Embolism Other Serious 4/29/2008 Female 121 lb 12/1/2008 Physician Switzerland
Primary
Concomitant
Pancreatitis Acute Other Serious 11/4/2008 64 Male 11/19/2008 Other Health Professional Switzerland
Primary
Concomitant
Pancreatitis Acute Hospitalization 10/27/2008 44 Female 11/19/2008 Other Health Professional Switzerland
Primary
Concomitant
Atrial Fibrillation Other Serious 4/5/2006 76 Male 12/2/2008 Physician Denmark
Primary
Secondary
Concomitant
Myelodysplastic Syndrome Other Serious 9/6/2008 Male 12/4/2008 Other Health Professional United States
Primary
Concomitant
Aplasia Pure Red Cell Other Serious Female 117 lb 12/9/2008 Physician Sweden
Primary
Secondary
Concomitant
Aplasia Pure Red Cell Other Serious Female 117 lb 12/22/2008 Physician Sweden
Primary
Secondary
Concomitant
Orthopnoea Hospitalization 12/16/2008 Male 175 lb 12/26/2008 Greece
Primary
Concomitant
Pyrexia Hospitalization 11/22/2008 Female 216 lb 12/29/2008 Greece
Primary
Concomitant
Peritonitis Other Serious 11/2/2007 59 Female 11/25/2008 Other Health Professional United States
Primary
Concomitant
Cardio-respiratory Arrest Death 6/30/2008 78 Female 128 lb 1/8/2009 Greece
Primary
Concomitant
Orthopnoea Hospitalization 12/16/2008 73 Male 172 lb 1/21/2009 Greece
Primary
Concomitant
Coronary Artery Disease Hospitalization 1/13/2009 73 Male 172 lb 1/21/2009 Greece
Primary
Concomitant
Aplasia Pure Red Cell Other Serious Female 117 lb 1/22/2009 Physician Sweden
Primary
Secondary
Concomitant
Pyrexia Hospitalization 11/22/2008 51 Female 216 lb 1/30/2009 Greece
Primary
Concomitant
Type 2 Diabetes Mellitus Other Serious 11/15/2004 Male 218 lb 2/3/2009 Physician United States
Primary
Secondary
Concomitant
Pancreatitis Acute Hospitalization 10/27/2008 44 Female 1/27/2009 Ireland
Primary
Concomitant
Pancreatitis Acute Other Serious 11/4/2008 64 Male 1/27/2009 Physician Ireland
Primary
Concomitant
Tubulointerstitial Nephritis Other Serious 1/24/2009 71 Male 143 lb 2/23/2009 Physician Netherlands
Primary
Concomitant

Drug Data