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Lipitor (Atorvastatin) - Adverse Event Reports - Disability

 



Index of reports > Cases resulting in disability (124)

     Myalgia (39)Abasia (26)Asthenia (25)Pain in Extremity (23)Muscular Weakness (23)Blood Creatine Phosphokinase Increased (18)Muscle Spasms (18)Fatigue (17)Gait Disturbance (17)Pain (12)

Below is the selection of adverse event reports related to Lipitor (Atorvastatin) that includes cases resulting in disability.

 Reports 1 - 25 of 124   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 physician from Australia on 2007-10-25

Patient: male, weighing 89.0 kg (195.8 pounds)

Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Drug Intolerance, Muscular Weakness, Musculoskeletal Discomfort, Gait Disturbance, Myocardial Infarction, Exercise Tolerance Decreased

Adverse event resulted in: disablity

Suspect drug(s):
Xanax
    Administration route: Oral
    Indication: Anxiety

Lipitor

Other drugs received by patient: Plavix; Cartia XT; Tritace; Multi-Vitamins; Nexium; Temaze; Panadol



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 female receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from Australia on 2007-10-19

Patient: female

Adverse reactions / side effects: Pain, Hypoaesthesia, Paraesthesia, Burning Sensation, Neuropathy Peripheral, Activities of Daily Living Impaired, Insomnia, Gait Disturbance, Unevaluable Event

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 male receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from Brazil on 2007-10-12

Patient: male

Adverse reactions / side effects: Burning Sensation, Coronary Artery Bypass, Hypertension

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: ALL Other Therapeutic Products; Selozok; Cardiac Therapy



Adverse event in male receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from United States on 2007-10-06

Patient: male

Adverse reactions / side effects: Renal Impairment, Abasia, Pain, Erectile Dysfunction, Liver Disorder, Disability

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor (Atorvastatin)



Adverse event in male receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from United States on 2007-10-06

Patient: male, weighing 86.4 kg (190.0 pounds)

Adverse reactions / side effects: Bedridden, Pain, Abasia, Liver Disorder, Impaired Driving Ability, Malaise, Unevaluable Event, Renal Failure Acute, Dyspnoea, Pain in Extremity, Diplegia, Cognitive Disorder, Cerebrovascular Accident, Hyperaesthesia, Lung Disorder, Insomnia, Swelling, Memory Impairment, Influenza Like Illness

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: Tylenol W / Codeine NO. 4; ALL Other Therapeutic Products; Advair Diskus 100 / 50; Acetylsalicylic Acid



Adverse event in male receiving Lipitor (Atorvastatin)

Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-07-27

Patient: male, weighing 100.0 kg (220.0 pounds)

Adverse reactions / side effects: Multi-Organ Failure, Pancreatitis Necrotising, Diabetes Mellitus, Asthenia

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: Ramipril



Adverse event in female receiving Lipitor (Atorvastatin)

Reported by a physician from France on 2007-07-26

Patient: female, weighing 93.0 kg (204.6 pounds)

Adverse reactions / side effects: Tendon Rupture, Pain

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor
    Administration route: Oral
    Indication: Hypercholesterolaemia

Lipitor
    Indication: Prophylaxis

Other drugs received by patient: Zanidip; Hyperium; Previscan; Gaviscon; Corvasal; Triatec; Esidrix; Omeprazole; Cordarone; Doliprane; Atarax; Pindolol



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 77 year old male receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from United Kingdom on 2007-07-13

Patient: 77 year old male

Adverse reactions / side effects: Pain in Extremity, Arthralgia, Arthritis, Mobility Decreased

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: Hypnotics and Sedatives; Ferrous Sulfate TAB; Amiloride Hydrochloride; Paracetamol; Warfarin Sodium; Aspirin; ALL Other Therapeutic Products; Frusemide; Beta Blocking Agents



Adverse event in female receiving Lipitor (Atorvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-12

Patient: female

Adverse reactions / side effects: Gait Disturbance

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor (Atorvastatin)



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 male receiving Lipitor (Atorvastatin)

Reported by a lawyer from United States on 2007-07-06

Patient: male

Adverse reactions / side effects: Oral Intake Reduced, Rhabdomyolysis, Neurosis, Anhedonia, Respiratory Tract Infection Viral, Intervertebral Disc Degeneration, Carpal Tunnel Syndrome, Myositis, Back Pain, Renal Disorder, Cardiac Murmur, Cellulitis, Pain in Extremity, Angina Pectoris, Haemoptysis, Increased Viscosity of Bronchial Secretion, Musculoskeletal Pain, Muscular Weakness, Nasal Congestion, Hepatocellular Damage, Discomfort, Pulmonary Valve Incompetence, Diarrhoea, Dehydration, Mitral Valve Incompetence, Rash Maculo-Papular, Shock

Adverse event resulted in: hospitalization, disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: Altace; Lopressor; Aspirin; Plavix; Nitroglycerin; Vicodin; Mobic



Adverse event in female receiving Lipitor (Atorvastatin)

Reported by a physician from France on 2007-07-06

Patient: female, weighing 93.0 kg (204.6 pounds)

Adverse reactions / side effects: Tendon Rupture, Pain

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor
    Administration route: Oral
    Indication: Hypercholesterolaemia

Lipitor
    Indication: Prophylaxis

Other drugs received by patient: Zanidip; Hyperium; Previscan; Gaviscon; Corvasal; Triatec; Esidrix; Omeprazole; Cordarone; Doliprane; Atarax; Pindolol



Adverse event in female receiving Lipitor (Atorvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-06

Patient: female, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Cardiac Pacemaker Malfunction, Heart Rate Increased, Hepatic Failure, Paralysis, Cardiac Arrest

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor
    Indication: Blood Cholesterol Increased

Hypnotics and Sedatives
    Indication: Sedation

Other drugs received by patient: Synthroid



Adverse event in 53 year old female receiving Lipitor (Atorvastatin)

Reported by a consumer/non-health professional from United States on 2007-07-03

Patient: 53 year old female

Adverse reactions / side effects: Muscle Atrophy, Pain, Headache, Face Presentation, Weight Increased, Fatigue, Musculoskeletal Stiffness, Unevaluable Event, Muscle Spasms, Skin Disorder, Hypoaesthesia, Paraesthesia, Autoimmune Disorder, Activities of Daily Living Impaired, Insomnia, Swelling, DRY Eye

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor (Atorvastatin)

Other drugs received by patient: Zyrtec; Aleve



Adverse event in 44 year old male receiving Lipitor (Atorvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-03

Patient: 44 year old male, weighing 82.6 kg (181.6 pounds)

Adverse reactions / side effects: Dyspnoea, Nightmare, Palpitations, Atrioventricular Block Complete, Insomnia, Drug Interaction, Feeling Abnormal

Adverse event resulted in: life threatening event, hospitalization, disablity

Suspect drug(s):
Lipitor
    Dosage: 10 mg 1x a day
    Indication: Arterial Occlusive Disease
    Start date: 2007-01-01
    End date: 2007-02-01

Azithromycin
    Dosage: 1x a day 5 days
    Indication: Nasopharyngitis
    Start date: 2007-02-01



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 female receiving Lipitor (Atorvastatin)

Reported by a individual with unspecified qualification from United States on 2007-07-02

Patient: female, weighing 63.5 kg (139.7 pounds)

Adverse reactions / side effects: Cardiac Pacemaker Malfunction, Heart Rate Increased, Hepatic Failure, Paralysis, Cardiac Arrest

Adverse event resulted in: disablity

Suspect drug(s):
Lipitor
    Indication: Blood Cholesterol Increased

Hypnotics and Sedatives
    Indication: Sedation

Other drugs received by patient: Synthroid



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



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