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Index of reports
> Cases resulting in hospitalization (124)
> Cases with Rhabdomyolysis (14)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in hospitalization where reactions include rhabdomyolysis.
Adverse event in 42 year old male receiving Zetia (Ezetimibe)
Reported by a pharmacist from United States on 2007-10-30
Patient: 42 year old male, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Coumadin; Coreg; Spironolactone
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Sweden on 2007-10-24
Patient: 50 year old male
Adverse reactions / side effects: Rhabdomyolysis, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Candesartan Cilexetil
Administration route: Oral
Start date: 2007-04-01
Candesartan Cilexetil
Administration route: Oral
End date: 2007-08-06
Rosuvastatin Calcium
Administration route: Oral
Start date: 2006-01-01
Rosuvastatin Calcium
Administration route: Oral
Zetia
Administration route: Oral
Start date: 2006-01-01
Zetia
Administration route: Oral
Other drugs received by patient: Bisoprolol; Bisoprolol; Insulin; Enalapril Maleate; Enalapril Maleate; Isosorbide Mononitrate; Aspirin; Insulin Lispro
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Sweden on 2007-10-22
Patient: 50 year old male
Adverse reactions / side effects: Rhabdomyolysis, Dizziness, Hypoaesthesia, Myoglobin Blood Increased, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Candesartan Cilexetil
Administration route: Oral
Start date: 2007-04-01
Candesartan Cilexetil
Administration route: Oral
End date: 2007-08-06
Rosuvastatin Calcium
Administration route: Oral
Start date: 2006-01-01
Rosuvastatin Calcium
Administration route: Oral
Zetia
Administration route: Oral
Start date: 2006-01-01
Zetia
Administration route: Oral
Other drugs received by patient: Bisoprolol Fumarate; Bisoprolol Fumarate; Insulin Human, Isophane; Enalapril Maleate; Enalapril Maleate; Isosorbide Mononitrate; Aspirin; Insulin Lispro
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Sweden on 2007-10-18
Patient: 50 year old male
Adverse reactions / side effects: Rhabdomyolysis, Dizziness, Hypoaesthesia, Myoglobin Blood Increased, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Candesartan Cilexetil
Administration route: Oral
Start date: 2007-04-01
Candesartan Cilexetil
Administration route: Oral
End date: 2007-08-06
Rosuvastatin Calcium
Administration route: Oral
Start date: 2006-01-01
Rosuvastatin Calcium
Administration route: Oral
Zetia
Administration route: Oral
Start date: 2006-01-01
Zetia
Administration route: Oral
Other drugs received by patient: Bisoprolol Fumarate; Bisoprolol Fumarate; Insulin Human, Isophane; Enalapril Maleate; Enalapril Maleate; Isosorbide Mononitrate; Aspirin; Insulin Lispro
Adverse event in 42 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-15
Patient: 42 year old male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Coronary Artery Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2006-01-01
End date: 2007-08-16
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2006-01-01
End date: 2007-08-16
Other drugs received by patient: Coumadin; Coreg
Adverse event in 42 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-05
Patient: 42 year old male, weighing 86.0 kg (189.2 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Coronary Artery Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
End date: 2007-08-16
Zetia
Administration route: Oral
Indication: Blood Cholesterol
End date: 2007-08-16
Other drugs received by patient: Coumadin; Coreg
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-06
Patient: female, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Blood Creatine Phosphokinase Increased, Diabetes Mellitus, Hypocalcaemia, Muscle Spasms
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Hypercholesterolaemia
Prednisone TAB
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Adverse event in 55 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-02
Patient: 55 year old male, weighing 127.0 kg (279.4 pounds)
Adverse reactions / side effects: Anxiety, Rhabdomyolysis, Insomnia, Mental Status Changes, Sleep Apnoea Syndrome
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-04-16
End date: 2007-04-13
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-08-11
End date: 2007-04-13
Zetia
Administration route: Oral
Indication: LOW Density Lipoprotein Increased
Start date: 2006-08-11
End date: 2007-04-13
Other drugs received by patient: Toprol-XL; Toprol-XL; Nitrostat; Actos; Metformin; Aspirin; Clarinex
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-07
Patient: 76 year old male
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lopid
End date: 2007-04-01
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-04-01
End date: 2007-04-01
Zocor
End date: 2007-04-01
Other drugs received by patient: Amiodarone; Lasix; [therapy Unspecified]; Zestril
Adverse event in 54 year old female receiving Zetia (Ezetimibe)
Reported by a pharmacist from United States on 2007-05-22
Patient: 54 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Myositis, Rhabdomyolysis, Chest Pain, Cardiac Enzymes Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 49 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from France on 2007-04-30
Patient: 49 year old male, weighing 130.0 kg (286.0 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Renal Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Albuterol; Furosemide; Diltiazem Hydrochloride; Fluticasone Propionate and Salmeterol Xinafoate; Zolpidem Tartrate; Aspirin Lysine; Nitroglycerin; Acetaminophen
Adverse event in 70 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-01-24
Patient: 70 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Dyspnoea, Rhabdomyolysis, Hyperkalaemia, Hyperphosphataemia, Urinary Tract Infection, General Physical Health Deterioration, Haemoglobin Decreased, Malaise, Renal Tubular Necrosis, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-07-01
End date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-03-20
End date: 2005-07-01
Zetia
Administration route: Oral
Start date: 2006-02-01
End date: 2006-04-01
Zetia
Administration route: Oral
Start date: 2006-04-01
Other drugs received by patient: Valsartan; Aspirin; Hydrochlorothiazide; Atenolol; Atenolol; Dimenhydrinate; Aspirin and Caffeine, Citrated and Codeine Phosphate; Aspirin and Caffeine, Citrated and Codeine Phosphate
Adverse event in 70 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-01-19
Patient: 70 year old female, weighing 63.0 kg (138.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Dyspnoea, Rhabdomyolysis, Hyperkalaemia, Hyperphosphataemia, Urinary Tract Infection, General Physical Health Deterioration, Haemoglobin Decreased, Malaise, Renal Tubular Necrosis, Muscle Spasms, Renal Failure Acute
Adverse event resulted in: hospitalization
Suspect drug(s):
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-07-01
End date: 2006-04-01
Rosuvastatin Calcium
Administration route: Oral
Start date: 2005-03-20
End date: 2005-07-01
Zetia
Administration route: Oral
Start date: 2006-02-01
End date: 2006-04-01
Zetia
Administration route: Oral
Start date: 2006-04-01
Other drugs received by patient: Valsartan; Aspirin; Hydrochlorothiazide; Atenolol; Atenolol; Dimenhydrinate; Aspirin and Caffeine, Citrated and Codeine Phosphate; Aspirin and Caffeine, Citrated and Codeine Phosphate
Adverse event in 49 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from France on 2007-01-18
Patient: 49 year old male, weighing 130.0 kg (286.0 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Renal Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Albuterol; Furosemide; Diltiazem Hydrochloride; Fluticasone Propionate and Salmeterol Xinafoate; Zolpidem Tartrate; Aspirin Lysine; Nitroglycerin; Acetaminophen
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