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Index of reports
> Cases resulting in a serious event (294)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in a serious event.
Reports 1 - 25 of 294 Next >>
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-10-31
Patient: female, weighing 69.9 kg (153.7 pounds)
Adverse reactions / side effects: Weight Decreased, Malabsorption, Myalgia, Depression, Feeling Abnormal, Exercise Tolerance Decreased
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 65 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-31
Patient: 65 year old female
Adverse reactions / side effects: Hepatic Function Abnormal
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Crestor
Adverse event in 60 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Israel on 2007-10-30
Patient: 60 year old female
Adverse reactions / side effects: Anaphylactic Shock
Suspect drug(s):
Zetia (Ezetimibe)
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 60 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Australia on 2007-10-29
Patient: 60 year old female
Adverse reactions / side effects: Limb Discomfort, Paraesthesia
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 71 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-29
Patient: 71 year old female, weighing 93.0 kg (204.6 pounds)
Adverse reactions / side effects: Myalgia, Pain in Extremity, Pain, Muscular Weakness, Gait Disturbance
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Protonix; Dicyclomine Hydrochloride; Nitroglycerin; Effexor XR; Xanax; Lortab; Vitamins (Unspecified); Metronidazole; Dimethyl Sulfone; Flaxseed; Zonalon; Advair Diskus 100 / 50; Minocycline; Premarin; Atenolol; Diltiazem Hydrochloride; Furosemide; Cyanocobalamin; Nizoral; Nizoral 2% Shampoo; Betamethasone; Plaquenil; Humira; Isoniazid; Nitroglycerin; Valtrex; Requip
Adverse event in 60 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-26
Patient: 60 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Hepatic Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Ursodiol; Phospholipids (Unspecified); Allopurinol; Pioglitazone Hydrochloride; Amlodipine Besylate
Adverse event in 58 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Australia on 2007-10-26
Patient: 58 year old female, weighing 99.0 kg (217.8 pounds)
Adverse reactions / side effects: Hypoaesthesia, Skin Tightness, Paraesthesia
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 71 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-25
Patient: 71 year old male, weighing 105.0 kg (231.0 pounds)
Adverse reactions / side effects: Abdominal Pain, Diarrhoea, Pelvic Pain, Constipation, Deep Vein Thrombosis
Adverse event resulted in: disablity
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-06-01
End date: 2006-01-01
Zetia
Administration route: Oral
Start date: 2007-01-01
End date: 2007-02-01
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2006-06-01
End date: 2006-01-01
Zetia
Administration route: Oral
Start date: 2007-01-01
End date: 2007-02-01
Other drugs received by patient: Cozaar; Cozaar; Toprol-XL; Toprol-XL; Synthroid; Spiriva; Albuterol
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-25
Patient: female
Adverse reactions / side effects: Thrombocytopenic Purpura
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-25
Patient: female, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Myalgia, Muscle Spasms
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lasix; Levothyroxine Sodium; Fosamax; Enalapril Maleate; Amaryl; Elavil; Sular
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 80 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-24
Patient: 80 year old male
Adverse reactions / side effects: Hepatic Function Abnormal
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Amlodipine Besylate; Benzbromarone; Valsartan; AST-120; Magnesium Oxide
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-24
Patient: male
Adverse reactions / side effects: Anxiety, Abdominal Pain, Back Pain, Tendon Disorder, Pyrexia, Erectile Dysfunction
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lexapro; Xanax; Lipitor; Levitra
Adverse event in 71 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from Spain on 2007-10-24
Patient: 71 year old male
Adverse reactions / side effects: Hyperkalaemia, Oedema
Adverse event resulted in: hospitalization
Suspect drug(s):
Chlorthalidone and Spironolactone
Administration route: Oral
Start date: 2006-01-01
End date: 2006-07-12
Rosiglitazone Maleate
Administration route: Oral
Start date: 2006-01-01
End date: 2006-07-12
Zetia
Administration route: Oral
Start date: 2006-01-01
End date: 2006-07-12
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 78 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-24
Patient: 78 year old female
Adverse reactions / side effects: Nephritis Interstitial, Blood Cholesterol Increased
Suspect drug(s):
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-07-24
End date: 2007-08-21
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-07-24
End date: 2007-08-21
Adverse event in 56 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-23
Patient: 56 year old female
Adverse reactions / side effects: Pneumonia, Hepatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Amlodipine Besylate; Amlodipine Besylate
Adverse event in 61 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Netherlands on 2007-10-23
Patient: 61 year old male
Adverse reactions / side effects: Fibrosis, Hepatitis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor
Start date: 2001-01-01
End date: 2005-03-24
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2004-11-04
End date: 2005-03-24
Other drugs received by patient: Isosorbide Dinitrate; Phenprocoumon; Metoprolol Tartrate; Dipyridamole; Colestid
Adverse event in 34 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Belgium on 2007-10-23
Patient: 34 year old male, weighing 104.0 kg (228.8 pounds)
Adverse reactions / side effects: Gamma-Glutamyltransferase Increased, Aspartate Aminotransferase Increased, Alanine Aminotransferase Increased, Intentional Drug Misuse
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Type IIA Hyperlipidaemia
Start date: 2006-11-22
Zetia
Administration route: Oral
Indication: Type IIA Hyperlipidaemia
Start date: 2006-11-22
End date: 2007-02-27
Zetia
Administration route: Oral
Start date: 2007-02-28
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 male receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: male, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Alopecia, Gait Disturbance
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 60 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United Kingdom on 2007-10-19
Patient: 60 year old female
Adverse reactions / side effects: Systemic Lupus Erythematosus
Suspect drug(s):
Prednisolone
Zetia
Administration route: Oral
Adverse event in 49 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United Kingdom on 2007-10-19
Patient: 49 year old male
Adverse reactions / side effects: Retinal Tear, Laboratory Test Abnormal, Fungal Skin Infection, Vitreous Detachment, Uveitis, Immunosuppression
Adverse event resulted in: hospitalization
Suspect drug(s):
Atorvastatin Calcium
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2004-01-01
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2004-06-01
Other drugs received by patient: Viagra
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from Belgium on 2007-10-18
Patient: male
Adverse reactions / side effects: Hepatic Neoplasm Malignant
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Atorvastatin Calcium
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