|
Index of reports
> Cases resulting in disability (124)
> Cases with Myalgia (39)
Below is the selection of adverse event reports related to Lipitor (Atorvastatin) that includes cases resulting in disability where reactions include myalgia.
Reports 1 - 25 of 39 Next >>
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-30
Patient: female, weighing 56.7 kg (124.7 pounds)
Adverse reactions / side effects: Myalgia, Arthralgia, Diabetes Mellitus, Pain in Extremity, Musculoskeletal Stiffness, Renal Pain
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2007-03-12
End date: 2007-04-15
Lipitor
Indication: Hypercholesterolaemia
Other drugs received by patient: Nexium; Nexium; Nexium; Aspirin
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-10-29
Patient: male, weighing 62.6 kg (137.7 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Joint Stiffness, Arthropathy, Balance Disorder, C-Reactive Protein Increased, Muscle Injury, Myoglobin Blood Increased, Muscle Spasms, Myositis, Hypoaesthesia, Granuloma, Myopathy, Paraesthesia, Cerebral Infarction, Nervous System Disorder, Spinal Column Stenosis, Neuralgia, Abasia, Impaired Work Ability, Fall, Myalgia, Fatigue, Musculoskeletal Stiffness, Neuropathy, Amnesia, Cerebrovascular Accident, Enzyme Abnormality, Visual Disturbance, Joint Sprain, Arthritis, Asthenia, Face Injury, Spinal Cord Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Potassium Chloride; Antihypertensives; Procardia XL; Nifedipine
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a lawyer from United States on 2007-10-26
Patient: male, weighing 78.0 kg (171.6 pounds)
Adverse reactions / side effects: Nerve Injury, Neuropathy, Monoplegia, Pain in Extremity, Muscular Weakness, Ill-Defined Disorder, Amnesia, Myalgia, Fatigue, Insomnia, Muscle Injury, Gait Disturbance, Coordination Abnormal, Depression
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-10-19
Patient: male
Adverse reactions / side effects: Myalgia, Asthenia, Walking AID User
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
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 female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-07-18
Patient: female, weighing 81.8 kg (180.0 pounds)
Adverse reactions / side effects: Hypersensitivity, Pruritus, Abasia, Headache, Somnolence, Myalgia, Abnormal Dreams, Fatigue, DRY Mouth, Chest Pain, Heart Rate Irregular, Vomiting, Dyspnoea, Nausea, Dysgeusia, Arthralgia, Visual Disturbance, Diarrhoea, Insomnia, Heart Rate Increased, Angiopathy, Asthenia
Adverse event resulted in: disablity
Suspect drug(s):
Chantix
Indication: Smoking Cessation Therapy
Lipitor
Indication: Blood Cholesterol Increased
Codeine SUL TAB
Cholesterol
Indication: Blood Cholesterol Increased
Other drugs received by patient: Soma; Tylenol; Multivitamin
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-07-09
Patient: female, weighing 90.7 kg (199.5 pounds)
Adverse reactions / side effects: Diabetes Mellitus, Flatulence, Cardiomegaly, Muscle Enzyme Increased, Malaise, Muscle Injury, Oedema Peripheral, Aneurysm, Heart Rate Abnormal, Cardiac Failure Congestive, Blood Urine Present, Hypoaesthesia, Ill-Defined Disorder, Thyroid Disorder, Major Depression, Nervous System Disorder, Vascular Occlusion, Abasia, Benign Renal Neoplasm, Abdominal Pain Upper, Weight Increased, Myalgia, Fatigue, Dyspnoea Exertional, Abdominal Distension, Dizziness, Blood Creatine Phosphokinase MM Increased, Neuropathy, Gout, Muscular Weakness, Bladder Disorder, Arthritis, Asthenia
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Indication: Blood Cholesterol Increased
Start date: 1999-01-01
End date: 2002-03-01
Lipitor
Indication: Coronary Artery Disease
Lipitor
Indication: Hyperlipidaemia
Other drugs received by patient: Altace; Trazodone HCL; Paxil
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-07-09
Patient: female
Adverse reactions / side effects: Pain in Extremity, Pain of Skin, Abasia, Dementia, Muscular Weakness, Apathy, Myalgia, Fatigue, Arthralgia, Arthritis
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in 41 year old male receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from Norway on 2007-07-02
Patient: 41 year old male
Adverse reactions / side effects: Myalgia, Nervous System Disorder, Headache
Adverse event resulted in: disablity
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1993-09-01
End date: 1996-06-01
Zocor
Administration route: Oral
Start date: 1996-06-01
End date: 1998-01-01
Lipitor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1998-01-01
End date: 2003-09-01
Lescol
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-09-01
End date: 2003-10-01
Lescol
Administration route: Oral
Start date: 2003-10-21
End date: 2004-01-13
Mevacor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-10-01
End date: 2003-10-01
Other drugs received by patient: Albyl-E; Sorbangil; Kredex; Selo-ZOK
Adverse event in male receiving Lipitor (Atorvastatin)
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 Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Brazil on 2007-06-29
Patient: male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Myalgia, Vomiting, Hepatotoxicity, Chromaturia, Pyrexia
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Drug, Unspecified
Adverse event in male receiving Lipitor (Atorvastatin)
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 41 year old male receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-06-18
Patient: 41 year old male
Adverse reactions / side effects: Myalgia, Disturbance in Attention, Nervous System Disorder, Headache
Adverse event resulted in: disablity
Suspect drug(s):
Lescol
Dosage: 40 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-09-01
End date: 2003-10-01
Lescol
Dosage: 40 mg/d
Administration route: Oral
Start date: 2003-10-21
End date: 2004-01-13
Lipitor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1998-01-01
End date: 2003-09-01
Mevacor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-10-01
End date: 2003-10-01
Zocor
Dosage: 10 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1993-09-01
End date: 1996-06-01
Zocor
Dosage: 40 mg, qd
Administration route: Oral
Start date: 1996-06-01
End date: 1998-01-01
Other drugs received by patient: Ezetrol; Selo-ZOK; Albyt-E; Sorbangil; Kredex; Seroxat
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-11
Patient: male
Adverse reactions / side effects: Myalgia, Drug Ineffective, Abasia, Intervertebral Disc Degeneration, Muscular Weakness, Muscle Spasms
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Crestor
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Australia on 2007-06-08
Patient: male, weighing 82.0 kg (180.4 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Pain in Extremity, Liver Disorder, Exercise Tolerance Decreased, Myalgia, Aspartate Aminotransferase Increased, Muscle Injury, Blood Disorder, Muscle Disorder
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Acetylsalicylic Acid SRT
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-01
Patient: female, weighing 90.7 kg (199.5 pounds)
Adverse reactions / side effects: Diabetes Mellitus, Flatulence, Cardiac Disorder, Cardiomegaly, Malaise, Oedema Peripheral, Muscle Injury, Aneurysm, Heart Rate Abnormal, Cardiac Failure Congestive, Blood Urine Present, Hypoaesthesia, Renal Cyst, Thyroid Disorder, Major Depression, Nervous System Disorder, Vascular Occlusion, Abasia, Benign Renal Neoplasm, Abdominal Pain Upper, Weight Increased, Myalgia, Neuropathy Peripheral, Fatigue, Dyspnoea Exertional, Abdominal Distension, Dizziness, Neuropathy, Gout, Muscular Weakness, Bladder Disorder, Arthritis, Asthenia
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Altace
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-01
Patient: female
Adverse reactions / side effects: Myalgia, Gait Disturbance, Muscle Spasms
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-05-26
Patient: female
Adverse reactions / side effects: Myalgia, Bedridden
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
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 male receiving Lipitor (Atorvastatin)
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 female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-05-04
Patient: female, weighing 81.8 kg (180.0 pounds)
Adverse reactions / side effects: Dyspnoea, Hypersensitivity, Abasia, Headache, Myalgia, Arthralgia, Heart Rate Increased, Chest Pain, Insomnia, Angiopathy
Adverse event resulted in: disablity
Suspect drug(s):
Chantix
Indication: Smoking Cessation Therapy
Lipitor
Indication: Blood Cholesterol Increased
Codeine SUL TAB
Cholesterol
Indication: Blood Cholesterol Increased
Other drugs received by patient: Soma; Tylenol; Vitamins
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-04-28
Patient: male
Adverse reactions / side effects: Myalgia, Drug Ineffective, Abasia, Intervertebral Disc Degeneration
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Crestor
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Netherlands on 2007-04-13
Patient: male, weighing 71.0 kg (156.2 pounds)
Adverse reactions / side effects: Weight Increased, Myalgia, Fatigue, Pruritus, Arthralgia, Chest Pain, Erectile Dysfunction, Muscle Spasms
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Stent Placement
Bisoprolol Fumarate
Administration route: Oral
Indication: Stent Placement
Start date: 2003-08-01
End date: 2006-09-01
Other drugs received by patient: Ascal Cardio; Seretide
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-03-23
Patient: male, weighing 62.6 kg (137.7 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Impaired Work Ability, Abasia, Joint Stiffness, Myalgia, Arthropathy, Fatigue, Balance Disorder, Muscle Injury, Musculoskeletal Stiffness, Muscle Spasms, Scoliosis, Myositis, Hypoaesthesia, Amnesia, Myopathy, Paraesthesia, Enzyme Abnormality, Loss of Employment, Cerebral Infarction, Gait Disturbance, Arthritis, Asthenia, Spinal Column Stenosis, Neuralgia
Adverse event resulted in: disablity
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Potassium Acetate; Antihypertensives; Procardia XL; Nifedipine
Adverse event in 41 year old male receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from Norway on 2007-03-20
Patient: 41 year old male
Adverse reactions / side effects: Myalgia, Disturbance in Attention, Nervous System Disorder, Headache
Adverse event resulted in: disablity
Suspect drug(s):
Lescol
Dosage: 40 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-09-01
End date: 2003-10-01
Lescol
Dosage: unk, unk
Start date: 2003-10-21
End date: 2004-01-13
Lipitor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1998-01-01
End date: 2003-09-01
Mevacor
Dosage: 20 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2003-10-01
End date: 2003-10-01
Zocor
Dosage: 10 mg, qd
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 1993-09-01
End date: 1996-06-01
Zocor
Dosage: 40 mg, qd
Administration route: Oral
Start date: 1996-06-01
End date: 1998-01-01
Other drugs received by patient: Ezetrol; Selo-ZOK; Albyt-E; Sorbangil; Kredex
Page 1 Next >>
|
