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Index of reports
> Cases resulting in other serious reactions (152)
> Cases with Myalgia (34)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in other serious reactions where reactions include myalgia.
Reports 1 - 25 of 34 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 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 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 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 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 68 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-10-04
Patient: 68 year old female
Adverse reactions / side effects: Myalgia, Gait Disturbance
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-06-15
End date: 2007-06-17
Zetia
Administration route: Oral
Start date: 2007-06-18
End date: 2007-06-18
Adverse event in 68 year old female receiving Zetia (Ezetimibe)
Reported by a physician from Japan on 2007-07-27
Patient: 68 year old female
Adverse reactions / side effects: Myalgia, Gait Disturbance
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-06-15
End date: 2007-06-17
Zetia
Administration route: Oral
Start date: 2007-06-18
End date: 2007-06-18
Adverse event in 79 year old female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-24
Patient: 79 year old female, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Myalgia, Nausea, Asthenia, Mobility Decreased
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Bendroflumethiazide; Valsartan
Adverse event in 45 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Canada on 2007-07-20
Patient: 45 year old male, weighing 117.0 kg (257.4 pounds)
Adverse reactions / side effects: Myositis, Myalgia, Hypoaesthesia
Suspect drug(s):
Zetia (Ezetimibe)
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-07-17
Patient: male
Adverse reactions / side effects: Myalgia, Back Pain, Muscle Injury
Suspect drug(s):
Lipitor
Lovastatin
Zetia
Adverse event in female receiving Zetia (Ezetimibe)
Reported by a physician from United States on 2007-07-11
Patient: female, weighing 53.5 kg (117.7 pounds)
Adverse reactions / side effects: Blood Thyroid Stimulating Hormone, Pain in Extremity, Muscular Weakness, Exercise Tolerance Decreased, Discomfort, Myalgia, Fatigue, Limb Discomfort, Muscle Fatigue, Emotional Disorder, Gait Disturbance, Spinal Operation
Suspect drug(s):
Drug, Unspecified
Indication: Blood Cholesterol Increased
Start date: 2006-11-01
End date: 2006-12-01
Lipitor
Indication: Blood Cholesterol Increased
Start date: 2004-01-01
End date: 2006-07-01
Vytorin
Indication: Blood Cholesterol Increased
Zetia
Indication: Blood Cholesterol Increased
Start date: 2007-02-01
End date: 2007-03-01
Zocor
Indication: Blood Cholesterol Increased
Other drugs received by patient: Synthroid; Acyclovir; Premarin; Zoloft; Diovan; Hydrochlorothiazide
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 male receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-06-22
Patient: male
Adverse reactions / side effects: Myalgia, Back Pain, Muscle Injury
Suspect drug(s):
Lipitor
Lovastatin
Zetia
Adverse event in 52 year old male receiving Zetia (Ezetimibe)
Reported by a physician from Ireland on 2007-06-13
Patient: 52 year old male
Adverse reactions / side effects: Myalgia, Chromaturia, Deafness, Ocular Icterus, Psoriatic Arthropathy
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Lipitor
Adverse event in 60 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-06-07
Patient: 60 year old female
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 female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-06-04
Patient: female
Adverse reactions / side effects: Myalgia, Oesophageal Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Actonel
Lipitor
Zetia
Dosage: daily dose:10mg
Indication: Blood Cholesterol Increased
Other drugs received by patient: Synthroid
Adverse event in 56 year old male receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-25
Patient: 56 year old male, weighing 98.9 kg (217.5 pounds)
Adverse reactions / side effects: Myalgia, Abdominal Pain, Blood Amylase Increased, Lipase Increased
Suspect drug(s):
Vytorin
Dosage: see image
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2005-02-01
End date: 2006-02-01
Vytorin
Dosage: see image
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2005-02-01
End date: 2006-02-01
Vytorin
Dosage: see image
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-02-01
End date: 2007-03-15
Vytorin
Dosage: see image
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-02-01
End date: 2007-03-15
Zetia
Dosage: 10 mg/qod/po
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-02-01
End date: 2007-03-15
Other drugs received by patient: Norvasc; Prevacid; Aspirin; Glucosamine; Niacin; Omega-3 Marine Triglycerides; Multi-Vitamins
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 female receiving Zetia (Ezetimibe)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-05-21
Patient: female, weighing 90.7 kg (199.5 pounds)
Adverse reactions / side effects: Blood Pressure Increased, Rhabdomyolysis, Tendon Rupture, Body Temperature Increased, Nausea, Hypotension, Stomach Discomfort, Fall, Weight Increased, Myalgia, Compression Fracture, Vitamin D Decreased
Suspect drug(s):
Calcium Chloride
Indication: Osteoporosis
Calcium Chloride
Lipitor
Indication: Blood Cholesterol Increased
Start date: 2005-01-01
End date: 2005-01-01
Zetia
Indication: Blood Cholesterol Increased
Start date: 2005-01-01
End date: 2005-01-01
Zometa
Indication: Osteoporosis
Other drugs received by patient: Zestril; Vitamin D; Vitamin D; Hydrochlorothiazide; Prozac; Ranitidine Hydrochloride; Other Combinations OF Nutrients; Diltiazem; Klonopin; Oxycontin
Adverse event in 60 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-05-17
Patient: 60 year old female
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 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 60 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-05-01
Patient: 60 year old female
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 77 year old female receiving Zetia (Ezetimibe)
Reported by a consumer/non-health professional from United States on 2007-04-30
Patient: 77 year old female
Adverse reactions / side effects: Abdominal Pain, Lymphadenopathy, Haemorrhage, Chills, Pain, Wheezing, Headache, Pyrexia, Abdominal Pain Upper, Hand Deformity, Myalgia, Fatigue, Lymph Node Pain, DRY Throat, Chest Pain, Oedema Peripheral, Abdominal Distension, Adverse Event, Pharyngolaryngeal Pain, Aneurysm, Muscle Spasms, Back Pain, Gingival Bleeding, Dyspnoea, Dysphagia, Blood Urine Present, Coronary Artery Disease, Muscular Weakness, Rash, Arthralgia, Asthenia
Suspect drug(s):
Zetia
Administration route: Oral
Indication: Blood Cholesterol
Start date: 2003-12-01
End date: 2006-06-28
Zetia
Administration route: Oral
Other drugs received by patient: Singulair; Tricor; Nystatin; Quinine; Prilosec; Asmanex Twisthaler; Albuterol; Levothyroxine Sodium; Plavix; Spiriva; Xalatan
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