Byetta combined with Coumadin

Reports:

Reaction Outcome Event Date Age Sex Weight Reported Reporter Country Treatment
Role Name
Weight Decreased Hospitalization 12/1/2005 47 Male 343 lb 1/6/2006 Physician United States
Primary
Secondary
Concomitant
Vomiting Hospitalization 12/12/2005 49 Male 257 lb 1/17/2006 Physician United States
Primary
Concomitant
Weight Decreased 1/1/2005 58 Male 302 lb 1/20/2006 Consumer United States
Primary
Concomitant
Chest Pain Hospitalization 2/26/2006 64 Female 195 lb 3/8/2006 Consumer United States
Primary
Concomitant
Injection Site Haemorrhage 12/11/2005 58 Male 1/20/2006 Consumer United States
Primary
Concomitant
Decreased Appetite 1/1/2005 Female 1/20/2006 Physician United States
Primary
Concomitant
International Normalised Ratio Increased 1/1/2005 Male 1/20/2006 Physician United States
Primary
Concomitant
Renal Failure Acute Required Intervention 2/18/2006 75 Female 3/10/2006 Other Health Professional United States
Primary
Secondary
Concomitant
Drug Ineffective Hospitalization 2/1/2006 62 Female 218 lb 3/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased 9/1/2005 64 Female 203 lb 1/20/2006 Consumer United States
Primary
Concomitant
Weight Decreased 10/20/2005 74 Female 142 lb 1/20/2006 Consumer United States
Primary
Secondary
Concomitant
Weight Decreased 10/1/2005 62 Male 326 lb 1/20/2006 United States
Primary
Concomitant
Nausea 11/8/2005 79 Male 250 lb 1/20/2006 Physician United States
Primary
Concomitant
Weight Decreased 11/17/2005 74 Male 230 lb 1/20/2006 Consumer United States
Primary
Concomitant
Injection Site Bruising 10/29/2005 82 Female 236 lb 1/20/2006 Consumer United States
Primary
Concomitant
Weight Decreased 9/1/2005 64 Male 217 lb 1/20/2006 Consumer United States
Primary
Concomitant
Dry Mouth 12/28/2005 55 Female 415 lb 1/20/2006 Consumer United States
Primary
Concomitant
Weight Decreased 11/17/2005 77 Male 265 lb 1/20/2006 Consumer United States
Primary
Concomitant
Weight Decreased 11/1/2005 81 Female 189 lb 1/20/2006 Consumer United States
Primary
Concomitant
Injection Site Pain 9/1/2005 Male 1/20/2006 Other Health Professional United States
Primary
Concomitant
Weight Decreased 10/10/2005 63 Male 302 lb 1/20/2006 Consumer United States
Primary
Concomitant
International Normalised Ratio Increased 1/1/2005 Male 1/20/2006 Other Health Professional United States
Primary
Secondary
Concomitant
International Normalised Ratio Increased 1/1/2005 Female 1/20/2006 Other Health Professional United States
Primary
Secondary
Concomitant
International Normalised Ratio Increased 12/15/2005 67 Male 1/20/2006 Other Health Professional United States
Primary
Concomitant
Weight Decreased 8/10/2005 51 Male 240 lb 1/20/2006 Physician United States
Primary
Concomitant
Stomach Discomfort 1/1/2005 76 Male 1/20/2006 Physician United States
Primary
Concomitant
Weight Decreased Hospitalization 2/1/2006 62 Female 218 lb 3/30/2006 Physician United States
Primary
Concomitant
Injection Site Haemorrhage 11/1/2005 78 Male 171 lb 1/20/2006 Consumer United States
Primary
Concomitant
Renal Failure Acute Hospitalization 2/26/2006 64 Female 195 lb 4/13/2006 Physician United States
Primary
Secondary
Concomitant
Pulmonary Embolism Hospitalization 4/1/2006 59 Male 4/27/2006 United States
Primary
Concomitant
Pulmonary Embolism Hospitalization 4/7/2006 59 Male 5/17/2006 United States
Primary
Concomitant
Wound Infection Life Threatening 3/23/2006 84 Male 223 lb 5/19/2006 Physician United States
Primary
Concomitant
Blood Glucose Increased 3/6/2006 80 Male 200 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 4/17/2006 69 Female 247 lb 5/31/2006 Physician United States
Primary
Concomitant
Weight Decreased 2/9/2006 Male 4/17/2006 Consumer United States
Primary
Concomitant
Nausea 2/6/2006 63 Female 343 lb 4/17/2006 Consumer United States
Primary
Concomitant
Rash Pruritic 2/1/2006 66 Male 228 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased 2/1/2006 61 Female 210 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased Life Threatening 3/1/2006 68 Male 265 lb 6/16/2006 Consumer United States
Primary
Secondary
Concomitant
Weight Decreased 1/6/2006 65 Male 230 lb 4/17/2006 Consumer United States
Primary
Secondary
Concomitant
International Normalised Ratio Increased 1/20/2006 53 Female 309 lb 4/17/2006 Consumer United States
Primary
Concomitant
Injection Site Irritation 11/22/2005 78 Female 4/17/2006 Consumer United States
Primary
Concomitant
Wound Haemorrhage 1/17/2006 55 Male 314 lb 4/17/2006 Consumer United States
Primary
Concomitant
Injection Site Bruising 11/29/2005 61 Male 200 lb 4/17/2006 Consumer United States
Primary
Concomitant
International Normalised Ratio Increased 1/1/2005 76 Male 4/17/2006 Physician United States
Primary
Concomitant
Blood Glucose Increased 3/6/2006 62 Male 218 lb 4/17/2006 Consumer United States
Primary
Concomitant
Injection Site Bruising 3/18/2006 70 Male 250 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased 12/1/2005 58 Male 220 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2006 74 Male 196 lb 4/17/2006 Consumer United States
Primary
Concomitant
Blood Glucose Increased 1/13/2006 61 Female 240 lb 4/17/2006 Consumer United States
Primary
Concomitant
International Normalised Ratio Abnormal 12/1/2005 54 Female 190 lb 4/17/2006 Consumer United States
Primary
Concomitant
Weight Decreased 2/2/2006 66 Female 215 lb 4/17/2006 Consumer United States
Primary
Concomitant
Blood Glucose Increased 3/11/2006 80 Male 200 lb 4/17/2006 Consumer United States
Primary
Concomitant
Glycosylated Haemoglobin Increased Hospitalization 1/1/2006 54 Male 6/28/2006 Consumer United States
Primary
Concomitant
International Normalised Ratio Increased 3/9/2006 61 Male 4/17/2006 Physician United States
Primary
Concomitant
Ventricular Hypertrophy Hospitalization 1/1/2006 54 Male 7/6/2006 Physician United States
Primary
Concomitant
Ecchymosis Female 8/1/2006 Consumer United States
Primary
Secondary
International Normalised Ratio Increased 1/1/2005 Female 8/1/2006 Other Health Professional United States
Primary
Secondary
Concomitant
International Normalised Ratio Increased 1/1/2005 Male 8/1/2006 Other Health Professional United States
Primary
Secondary
Weight Decreased 10/1/2005 74 Female 141 lb 8/1/2006 Consumer United States
Primary
Secondary
Concomitant
Unevaluable Event Other Serious Male 8/25/2006 Other Health Professional United States
Primary
Secondary
Concomitant
Vomiting 4/13/2006 74 Female 7/19/2006 Consumer United States
Primary
Concomitant
Polymenorrhoea 4/17/2006 45 Female 350 lb 7/19/2006 Consumer United States
Primary
Concomitant
Tooth Abscess 4/11/2006 70 Male 230 lb 7/19/2006 Consumer United States
Primary
Concomitant
Weight Decreased 4/1/2006 60 Female 240 lb 7/19/2006 Consumer United States
Primary
Concomitant
Contusion 4/11/2006 70 Male 245 lb 7/19/2006 Consumer United States
Primary
Concomitant
International Normalised Ratio Increased 4/19/2006 68 Female 7/19/2006 United States
Primary
Secondary
Concomitant
Throat Irritation 4/1/2006 69 Male 250 lb 7/19/2006 Consumer United States
Primary
Concomitant
Vaginal Haemorrhage 4/25/2006 72 Female 217 lb 7/19/2006 Consumer United States
Primary
Concomitant
Nausea 4/25/2006 71 Female 210 lb 7/19/2006 United States
Primary
Concomitant
International Normalised Ratio Increased 55 Male 7/19/2006 Other Health Professional United States
Primary
Secondary
Weight Decreased 6/21/2006 76 Female 17 lb 7/19/2006 Physician United States
Primary
Secondary
Swelling 6/19/2006 76 Female 200 lb 7/19/2006 Consumer United States
Primary
Concomitant
Nausea 1/1/2006 60 Female 315 lb 7/19/2006 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 7/17/2006 73 Male 192 lb 9/12/2006 United States
Primary
Concomitant
Weight Decreased 4/1/2006 59 Female 207 lb 7/19/2006 Consumer United States
Primary
Concomitant
Weight Decreased 5/1/2006 69 Male 300 lb 7/19/2006 Consumer United States
Primary
Concomitant
Weight Decreased Female 7/19/2006 Consumer United States
Primary
Concomitant
Nausea 5/2/2006 76 Female 7/19/2006 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 7/18/2006 73 Male 192 lb 10/6/2006 Physician United States
Primary
Concomitant
Vision Blurred Hospitalization 8/1/2006 68 Female 10/20/2006 Consumer United States
Primary
Secondary
Concomitant
Injection Site Irritation Other Serious 10/1/2006 67 Female 300 lb 10/26/2006 Consumer United States
Primary
Concomitant
Peripheral Arterial Occlusive Disease Hospitalization 5/18/2006 81 Male 237 lb 10/30/2006 Physician United States
Primary
Concomitant
Infective Thrombosis Hospitalization 10/13/2006 76 Female 170 lb 11/2/2006 Consumer United States
Primary
Concomitant
Surgery Hospitalization 12/1/2005 Female 11/17/2006 Physician United States
Primary
Concomitant
Vision Blurred Hospitalization 8/1/2006 68 Female 11/17/2006 Physician United States
Primary
Secondary
Concomitant
Injection Site Irritation Other Serious 10/1/2006 67 Female 300 lb 11/16/2006 Physician United States
Primary
Concomitant
Retinal Vascular Thrombosis Hospitalization 62 Female 158 lb 12/12/2006 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 6/15/2006 50 Female 12/21/2006 Physician United States
Primary
Concomitant
Atrial Fibrillation 7/1/2006 50 Male 10/16/2006 Other Health Professional United States
Primary
Concomitant
Weight Decreased 6/28/2006 70 Male 220 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 6/1/2006 68 Female 203 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 7/12/2006 77 Male 160 lb 10/16/2006 Consumer United States
Primary
Secondary
Concomitant
Vertigo 9/3/2006 66 Female 176 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2006 72 Male 265 lb 10/16/2006 Consumer United States
Primary
Concomitant
Tremor 9/3/2006 67 Male 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2006 Female 10/16/2006 Other Health Professional United States
Primary
Concomitant
Vision Blurred 9/11/2006 61 Female 231 lb 10/16/2006 Other Health Professional United States
Primary
Concomitant
Pain In Extremity 7/1/2006 59 Female 205 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Increased Other Serious 9/15/2006 56 Male 280 lb 2/8/2007 Physician United States
Primary
Concomitant
Weight Increased Other Serious 9/15/2006 56 Male 280 lb 2/12/2007 Physician United States
Primary
Concomitant
Weight Decreased 8/1/2006 71 Female 190 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Increased 9/8/2006 70 Male 216 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 6/1/2006 75 Female 10/16/2006 Consumer United States
Primary
Concomitant
Injection Site Haemorrhage 7/24/2006 72 Male 10/16/2006 Consumer United States
Primary
Concomitant
Injection Site Bruising 7/1/2006 65 Female 10/16/2006 Consumer United States
Primary
Concomitant
Prothrombin Time Prolonged 5/1/2006 69 Male 250 lb 10/16/2006 Consumer United States
Primary
Concomitant
Somnolence 8/1/2006 63 Female 189 lb 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 4/1/2006 31 Female 228 lb 10/16/2006 Consumer United States
Primary
Concomitant
Injection Site Pain 7/1/2006 55 Female 10/16/2006 Consumer United States
Primary
Concomitant
Weight Decreased 7/1/2006 76 Male 206 lb 10/16/2006 Consumer United States
Primary
Concomitant
Vena Cava Thrombosis Other Serious 4/1/2006 Female 240 lb 3/16/2007 Consumer United States
Primary
Concomitant
Oesophagitis Hospitalization 12/13/2006 63 Female 280 lb 3/15/2007 Physician United States
Primary
Concomitant
Vena Cava Thrombosis Other Serious 4/1/2006 Female 240 lb 4/6/2007 Consumer United States
Primary
Concomitant
International Normalised Ratio Increased Other Serious 7/13/2006 Male 3/30/2007 Physician United States
Primary
Secondary
Concomitant
Prothrombin Time Prolonged 60 Female 1/12/2007 Physician United States
Primary
Concomitant
Weight Decreased 64 Male 246 lb 1/12/2007 Physician United States
Primary
Concomitant
Oxygen Saturation Decreased 34 Female 1/12/2007 Other Health Professional United States
Primary
Concomitant
International Normalised Ratio Decreased 1/1/2006 63 Male 309 lb 1/12/2007 Other Health Professional United States
Primary
Concomitant
Weight Decreased 8/1/2006 63 Female 1/12/2007 Consumer United States
Primary
Concomitant
Weight Decreased 7/1/2006 76 Male 275 lb 1/12/2007 Consumer United States
Primary
Concomitant
Faeces Discoloured 10/23/2006 62 Male 1/12/2007 Consumer United States
Primary
Concomitant
Weight Decreased 8/1/2006 66 Male 275 lb 1/12/2007 Consumer United States
Primary
Concomitant
Weight Increased 10/1/2006 40 Female 590 lb 1/12/2007 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2006 65 Male 285 lb 1/12/2007 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2006 72 Female 216 lb 1/12/2007 Consumer United States
Primary
Concomitant
Hepatic Enzyme Increased 10/15/2006 69 Female 1/12/2007 Consumer United States
Primary
Concomitant
Vomiting 11/21/2006 61 Female 400 lb 1/12/2007 Consumer United States
Primary
Concomitant
Renal Impairment 12/7/2006 57 Female 1/12/2007 Consumer United States
Primary
Concomitant
Vomiting Hospitalization 10/17/2006 57 Female 196 lb 1/12/2007 Consumer United States
Primary
Concomitant
Cardiac Disorder Hospitalization 4/14/2007 73 Male 5/3/2007 Consumer United States
Primary
Concomitant
Dyspnoea Hospitalization 1/1/2007 73 Male 6/14/2007 Consumer United States
Primary
Concomitant
Stomach Discomfort Female 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2007 53 Male 4/10/2007 Consumer United States
Primary
Concomitant
Injection Site Bruising 3/22/2007 70 Male 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 1/1/2007 69 Female 203 lb 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 12/1/2006 77 Male 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased Hospitalization 6/1/2006 77 Male 192 lb 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 3/7/2007 69 Female 210 lb 4/10/2007 Consumer United States
Primary
Secondary
Concomitant
International Normalised Ratio Increased 3/7/2007 59 Male 4/10/2007 Consumer United States
Primary
Secondary
Concomitant
Nausea 2/1/2007 70 Female 210 lb 4/10/2007 Consumer United States
Primary
Concomitant
Vomiting Hospitalization 10/17/2006 57 Female 196 lb 4/10/2007 Physician United States
Primary
Concomitant
Weight Decreased 7/10/2006 66 Male 275 lb 4/10/2007 Physician United States
Primary
Concomitant
Painful Respiration 11/1/2006 33 Female 211 lb 4/10/2007 Other Health Professional United States
Primary
Concomitant
Weight Decreased 12/22/2006 63 220 lb 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 1/10/2007 73 Female 128 lb 4/10/2007 Consumer United States
Primary
Concomitant
Drug Dispensing Error 1/10/2007 41 Female 185 lb 4/10/2007 Consumer United States
Primary
Concomitant
Weight Decreased 7/1/2006 76 Male 206 lb 4/10/2007 Consumer United States
Primary
Concomitant
Weight Fluctuation 8/1/2006 63 Female 185 lb 4/10/2007 Consumer United States
Primary
Concomitant
Rectal Haemorrhage 3/2/2007 59 Female 220 lb 4/10/2007 Consumer United States
Primary
Concomitant

Drug Data