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Index of reports
> Cases resulting in life threatening events (34)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in life threatening events.
Reports 1 - 25 of 34 Next >>
Adverse event in 65 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-25
Patient: 65 year old male
Adverse reactions / side effects: Mechanical Ileus, Gastroenteritis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Vasotec; Warfarin Potassium; Probucol
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 65 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-15
Patient: 65 year old male
Adverse reactions / side effects: Abdominal Pain, Mechanical Ileus, Diarrhoea, Anorexia, Gastrointestinal Sounds Abnormal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Vasotec; Warfarin Potassium; Probucol
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 65 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-05
Patient: 65 year old male
Adverse reactions / side effects: Mechanical Ileus, Diarrhoea, Eye Operation, Anorexia, Gastrointestinal Disorder
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 61 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Germany on 2007-07-30
Patient: 61 year old male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Hepatocellular Damage
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 52 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-24
Patient: 52 year old male
Adverse reactions / side effects: Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor; Nonsteroidal Anti-Inflammatory Drug (Unspecified)
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a individual with unspecified qualification from United States on 2007-07-10
Patient: male
Adverse reactions / side effects: Amyotrophic Lateral Sclerosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor
Dosage: 80 mg daily po
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2004-08-01
End date: 2006-12-21
Zetia
Dosage: 10 mg daily po
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2004-08-01
End date: 2006-12-21
Other drugs received by patient: Prilosec; Naproxen; Dutasteride -Avodart; Metoprolol -Toprol; Rilutek
Adverse event in 37 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-10
Patient: 37 year old female
Adverse reactions / side effects: Pruritus, Pain, Muscular Weakness, Hypoaesthesia, Tremor, Menstruation Irregular, Myalgia, Fatigue, Poor Peripheral Circulation, Musculoskeletal Stiffness, Feeling Abnormal, Asthenia
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 69 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Australia on 2007-07-06
Patient: 69 year old female, weighing 100.0 kg (220.0 pounds)
Adverse reactions / side effects: Adrenocortical Insufficiency Acute, Cough
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2007-03-01
End date: 2007-04-01
Zetia
Administration route: Oral
Start date: 2007-04-17
End date: 2007-04-18
Other drugs received by patient: Levothyroxine Sodium; [therapy Unspecified]; Zoton; [therapy Unspecified]; Vitamins (Unspecified)
Adverse event in 64 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-29
Patient: 64 year old male, weighing 105.0 kg (231.0 pounds)
Adverse reactions / side effects: Full Blood Count Abnormal, Thrombocytopenia, Epistaxis
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Arthrotec; Atorvastatin; Acetaminophen and Codeine Phosphate
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Australia on 2007-06-22
Patient: 50 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Ischaemia, Hepatitis Acute, Anaemia, Cardiac Output Decreased, Hepatic Enzyme Increased, Death, Renal Failure, Hepatomegaly, Chronic Hepatic Failure
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Coversyl (Perindopril Erbumine)
Administration route: Oral
Start date: 2004-08-19
Lasix
Indication: Ischaemia
Start date: 2003-01-01
Lasix
Indication: Left Ventricular Failure
Start date: 2003-01-01
Lipitor
Administration route: Oral
Start date: 2003-01-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2004-08-01
End date: 2004-09-27
Other drugs received by patient: Clopidogrel Bisulfate; Carvedilol; [composition Unspecified]
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Australia on 2007-06-13
Patient: 50 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Ischaemia, Hepatitis Acute, Anaemia, Cardiac Output Decreased, Cardiac Disorder, Hepatic Enzyme Increased, Death, Renal Failure, Hepatomegaly, Chronic Hepatic Failure
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Coversyl (Perindopril Erbumine)
Administration route: Oral
Start date: 2004-08-19
Lasix
Indication: Ischaemia
Start date: 2003-01-01
Lasix
Indication: Left Ventricular Failure
Start date: 2003-01-01
Lipitor
Administration route: Oral
Start date: 2003-01-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2004-08-01
End date: 2004-09-27
Other drugs received by patient: Clopidogrel Bisulfate; Carvedilol; [composition Unspecified]
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 male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-06-04
Patient: male
Adverse reactions / side effects: Haemoglobin Decreased, Renal Failure, Hepatic Failure, Blood Creatine Increased, Hepatic Enzyme Increased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor; Lopid
Adverse event in 52 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Netherlands on 2007-06-01
Patient: 52 year old female
Adverse reactions / side effects: Vanishing Bile Duct Syndrome, Biliary Fibrosis, Cholestasis, Hepatic Cirrhosis, Infection
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Atorvastatin Calcium
Adverse event in 56 year old female receiving Zetia (Ezetimibe)
Reported by a pharmacist from United Kingdom on 2007-05-31
Patient: 56 year old female
Adverse reactions / side effects: Fatigue, Suicidal Behaviour, Depression, Aggression
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Diclofenac; Lisinopril; Atorvastatin Calcium; Hormones (Unspecified)
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-30
Patient: 76 year old male
Adverse reactions / side effects: Fatigue, Blood Creatine Phosphokinase Abnormal, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
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: Gemfibrozil; Amiodarone; Lasix; [therapy Unspecified]
Adverse event in 76 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-29
Patient: 76 year old male
Adverse reactions / side effects: Fatigue, Blood Creatine Phosphokinase Normal, Blood Creatinine Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
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: Gemfibrozil; Amiodarone; Lasix; [therapy Unspecified]
Adverse event in 62 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-29
Patient: 62 year old male, weighing 90.0 kg (198.0 pounds)
Adverse reactions / side effects: Angioedema, Obstructive Airways Disorder
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Atorvastatin Calcium; Metoprolol; Perindopril
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-05-24
Patient: female, weighing 66.2 kg (145.7 pounds)
Adverse reactions / side effects: Poor Quality Sleep, Drug Hypersensitivity, Oedema Peripheral, Muscular Weakness, Nasal Congestion, Headache, Discomfort
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-18
Patient: female
Adverse reactions / side effects: Myalgia, Blood Creatine Phosphokinase Increased, Hepatic Enzyme Increased
Adverse event resulted in: life threatening event
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 64 year old male receiving Zetia (Ezetimibe)
Reported by a pharmacist from United States on 2007-05-17
Patient: 64 year old male
Adverse reactions / side effects: Inappropriate Schedule of Drug Administration, Dyspnoea, Chest Pain, Arteriogram Coronary Abnormal
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2006-01-01
End date: 2007-04-01
Zetia
Administration route: Oral
Start date: 2006-01-01
End date: 2006-01-01
Other drugs received by patient: Aspirin
Adverse event in 78 year old receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-15
Patient: 78 year old , weighing 51.0 kg (112.2 pounds)
Adverse reactions / side effects: Dementia, Amnesia
Adverse event resulted in: life threatening event
Suspect drug(s):
Rosuvastatin Calcium
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2004-12-01
Zetia
Administration route: Oral
Indication: Hypertension
Start date: 2005-02-01
Other drugs received by patient: Calcium Carbonate and Cholecalciferol; Bendroflumethiazide; Acetaminophen and Codeine Phosphate
Adverse event in 64 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-04
Patient: 64 year old male
Adverse reactions / side effects: Blood Creatinine Increased, Renal Failure Acute, Myopathy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Atorvastatin
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-03-01
End date: 2006-04-01
Atorvastatin
Administration route: Oral
Start date: 2006-04-01
End date: 2006-05-01
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-05-01
End date: 2006-06-15
Other drugs received by patient: Nifedipine
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