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Index of reports
> Cases resulting in disability (39)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in disability.
Reports 1 - 25 of 39 Next >>
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 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, 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 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 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 70 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-26
Patient: 70 year old male
Adverse reactions / side effects: Myositis, Myopathy
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Zocor
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 67 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-03
Patient: 67 year old female, weighing 66.0 kg (145.2 pounds)
Adverse reactions / side effects: Diarrhoea, Abdominal Distension
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 72 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-03
Patient: 72 year old male, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Abdominal Discomfort, Abdominal Pain Lower, Diarrhoea, Abdominal Distension, Abdominal Pain Upper, Eructation
Adverse event resulted in: disablity
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Triglycerides Increased
Start date: 2007-06-01
End date: 2007-06-22
Zetia
Administration route: Oral
Indication: Aortic Arteriosclerosis
Start date: 2007-06-01
End date: 2007-06-22
Other drugs received by patient: Coumadin; Ubidecarenone; Vitamins (Unspecified); Allegra
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 male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-06-29
Patient: male, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Weight Decreased, Muscle Atrophy, Blood Creatine Phosphokinase Increased, 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 Succinate
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-06-25
Patient: male, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Weight Decreased, Muscle Atrophy, Blood Creatine Phosphokinase Increased, Dyspnoea, Pain in Extremity, Fear, Myalgia, Anxiety, Facial Paresis, Hyperphagia, Joint Range of Motion Decreased, Amyotrophic Lateral Sclerosis, 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 Succinate
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 male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-22
Patient: male, weighing 79.8 kg (175.6 pounds)
Adverse reactions / side effects: Weight Decreased, Muscle Atrophy, Blood Creatine Phosphokinase Increased, Dyspnoea, Pain in Extremity, Fear, Myalgia, Facial Paresis, Hyperphagia, Joint Range of Motion Decreased, Amyotrophic Lateral Sclerosis, 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 Succinate
Adverse event in 47 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-05-14
Patient: 47 year old male
Adverse reactions / side effects: Sleep Disorder, Headache
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Aspirin; Metoprolol; Pravastatin Sodium; Ramipril
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-05-11
Patient: female
Adverse reactions / side effects: Muscular Weakness
Adverse event resulted in: disablity
Suspect drug(s):
Rosuvastatin Calcium
Administration route: Oral
Zetia
Administration route: Oral
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-05-07
Patient: male
Adverse reactions / side effects: Myalgia, Weight Decreased, Blood Creatine Phosphokinase Increased, Muscle Atrophy, Asthenia, Disability, RED Blood Cell Sedimentation Rate Increased
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Indication: Hypercholesterolaemia
Zetia
Adverse event in 77 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-02
Patient: 77 year old female
Adverse reactions / side effects: Gout
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Allopurinol; Coreg; Aspirin; Furosemide; Glimepiride; Prinivil; Prevacid; Omega-3 Marine Triglycerides; Calcium (Unspecified)
Adverse event in 77 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-04-26
Patient: 77 year old female
Adverse reactions / side effects: Back Pain, Vomiting, Paranasal Sinus Hypersecretion, Syncope, Malaise, Feeling Hot, Cholecystitis, Gallbladder Disorder, Gait Disturbance, Asthenia, Joint Lock
Adverse event resulted in: disablity
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
End date: 2006-11-01
Zetia
Administration route: Oral
Start date: 2006-01-01
End date: 2006-01-01
Other drugs received by patient: Prozac
Adverse event in 63 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-24
Patient: 63 year old female
Adverse reactions / side effects: Eyelid Oedema, Erythema of Eyelid, Urticaria, Pain, Eyelids Pruritus, Eyelid Exfoliation
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor; Metoprolol; Aspirin
Adverse event in 63 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-04-19
Patient: 63 year old female
Adverse reactions / side effects: Eyelid Oedema, Erythema of Eyelid, Urticaria, Pain, Eyelids Pruritus, Eyelid Exfoliation
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor; Metoprolol; Aspirin
Adverse event in 42 year old male receiving Zetia (Ezetimibe)
Reported by a physician from United Arab Emirates on 2007-04-18
Patient: 42 year old male, weighing 162.0 kg (356.4 pounds)
Adverse reactions / side effects: Myalgia, Blood Creatine Phosphokinase Increased, Hepatic Enzyme Increased
Adverse event resulted in: disablity
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in 73 year old female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-04-13
Patient: 73 year old female
Adverse reactions / side effects: Antinuclear Antibody Positive, Pruritus, Systemic Lupus Erythematosus Rash, Complement Factor C3 Increased
Adverse event resulted in: disablity
Suspect drug(s):
Diovan
End date: 2007-02-01
Hydrochlorothiazide
End date: 2007-02-01
Zetia
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2007-01-01
Other drugs received by patient: Simvastatin; Prevacid; Toprol-XL; Aspirin
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