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Index of reports
> Cases resulting in other serious reactions (152)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in other serious reactions.
Reports 1 - 25 of 152 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 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 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 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 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 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 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 40 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-18
Patient: 40 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Aldolase Increased
Suspect drug(s):
Crestor
Administration route: Oral
Zetia
Other drugs received by patient: Unspecified Beta Blocker
Adverse event in 58 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-18
Patient: 58 year old female
Adverse reactions / side effects: Myalgia, Ageusia, Alopecia
Suspect drug(s):
Zetia (Ezetimibe)
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
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-17
Patient: male, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Weight Decreased, Blood Creatine Phosphokinase Increased, Muscle Atrophy, Muscle Contractions Involuntary, Fear, Myalgia, Facial Paresis, Joint Range of Motion Decreased, Amyotrophic Lateral Sclerosis, Blood Cholesterol Increased, Dyspnoea, Pain in Extremity, Chromaturia, Anxiety, Hyperphagia, Asthenia, Disability, RED Blood Cell Sedimentation Rate Increased
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hypercholesterolaemia
Lipitor
Indication: Blood Cholesterol Increased
Zetia
Other drugs received by patient: Norvasc; Metoprolol
Adverse event in 62 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-10-17
Patient: 62 year old female, weighing 120.0 kg (264.0 pounds)
Adverse reactions / side effects: Myalgia, Influenza Like Illness
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Atenolol; Furosemide; Glimepiride; Isosorbide
Adverse event in 66 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-16
Patient: 66 year old male, weighing 73.5 kg (161.7 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Sensory Disturbance
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 71 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-15
Patient: 71 year old male
Adverse reactions / side effects: Muscle Disorder
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Candesartan Cilexetil
Adverse event in 77 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-15
Patient: 77 year old female
Adverse reactions / side effects: Photosensitivity Reaction
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Omeprazole
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 72 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-12
Patient: 72 year old male, weighing 74.8 kg (164.7 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Musculoskeletal Pain, Cognitive Disorder, Myalgia, Fatigue, Gait Disturbance, Muscle Spasms, Pain in JAW
Suspect drug(s):
Crestor
Dosage: 5mgm daily po
Administration route: Oral
Start date: 2007-10-02
End date: 2007-10-09
Zetia
Dosage: 10 mgm daily po
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-04-10
End date: 2006-09-02
Adverse event in 70 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-11
Patient: 70 year old male
Adverse reactions / side effects: Bone Marrow Failure, Aplastic Anaemia
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: [therapy Unspecified]
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-11
Patient: male
Adverse reactions / side effects: Hypersensitivity, Stevens-Johnson Syndrome
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 62 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-10
Patient: 62 year old male
Adverse reactions / side effects: Hepatic Function Abnormal
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor
Adverse event in 58 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-08
Patient: 58 year old female, weighing 75.0 kg (165.0 pounds)
Adverse reactions / side effects: Herpes Zoster
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Levoxyl; Topamax; Ranitidine; Allergenic Extract
Adverse event in 60 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-10-08
Patient: 60 year old female, weighing 53.0 kg (116.6 pounds)
Adverse reactions / side effects: Myalgia, Amyotrophic Lateral Sclerosis, Drug Administration Error, Underdose
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2004-03-01
End date: 2004-03-01
Zetia
Administration route: Oral
Start date: 2004-03-01
End date: 2005-03-01
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 male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-10-05
Patient: male
Adverse reactions / side effects: Renal Impairment, Rhabdomyolysis
Suspect drug(s):
Crestor
Administration route: Oral
Zetia
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