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Index of reports
> Cases resulting in life threatening events (66)
Below is the selection of adverse event reports related to Lipitor (Atorvastatin) that includes cases resulting in life threatening events.
Reports 1 - 25 of 66 Next >>
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Norway on 2007-10-31
Patient: male
Adverse reactions / side effects: Myalgia, Rhabdomyolysis, Compartment Syndrome, Drug Interaction, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient possibly interacting with the suspect drug:
Rinexin
Administration route: Oral
Indication: Upper Respiratory Tract Infection
Start date: 2007-07-01
End date: 2007-07-08
Other drugs received by patient: Cosylan; Penicillin V Potassium; Acetaminophen; Rhinocort
Adverse event in 60 year old male receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-10-15
Patient: 60 year old male
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Coagulopathy, Drug Interaction, Pyrexia, Myalgia, Nephrolithiasis, Pyelectasia, Oedema Peripheral, Muscle Spasms, Cough, Back Pain, Haemorrhage Urinary Tract, Haematuria, Anaemia, Benign Prostatic Hyperplasia, Renal Cyst, Flank Pain, Dehydration
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Coumadin
Administration route: Oral
End date: 2007-07-25
Lipitor
Administration route: Oral
Indication: Hyperlipidaemia
End date: 2007-07-25
Targretin
Administration route: Oral
End date: 2007-07-25
Zolinza
Administration route: Oral
Indication: Mycosis Fungoides
Start date: 2007-07-13
End date: 2007-07-25
Other drugs received by patient: Paxil; Ritalin; Megace; Synthroid; Toprol-XL; Omega-3 Marine Triglycerides; Prinivil; Zantac; Hydroxyzine Hydrochloride
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-10-12
Patient: female, weighing 63.6 kg (140.0 pounds)
Adverse reactions / side effects: Cerebrovascular Accident
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-10-11
Patient: male, weighing 59.9 kg (131.7 pounds)
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event
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 female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-10-01
Patient: female, weighing 84.8 kg (186.6 pounds)
Adverse reactions / side effects: Peripheral Coldness, Muscle Atrophy, Flatulence, Fall, Liver Disorder, Walking AID User, OFF Label USE, Hypokinesia, Neuropathy Peripheral, Balance Disorder, Unevaluable Event, Muscle Spasms, Loss of Control of Legs, Pain in Extremity, Ill-Defined Disorder, Staphylococcal Infection, Insomnia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2001-01-01
End date: 2004-01-01
Lipitor
Indication: Pain
Other drugs received by patient: Diovan
Adverse event in 44 year old female receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-31
Patient: 44 year old female, weighing 99.8 kg (219.5 pounds)
Adverse reactions / side effects: Activities of Daily Living Impaired, Muscular Weakness
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-30
Patient: female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Aspirin
Dosage: daily dose:100mg
Administration route: Oral
Indication: Angina Pectoris
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-04-10
End date: 2007-05-13
Other drugs received by patient: Diltiazem HCL; Nitorol R; Epadel; Candesartan Cilexetil
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 47 year old female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-07-24
Patient: 47 year old female, weighing 73.9 kg (162.7 pounds)
Adverse reactions / side effects: Weight Decreased, Abdominal Pain, Pain, Constipation, Weight Abnormal, Fatigue, Gastrointestinal Pain, Gastrointestinal Disorder, Abdominal Distension, Decreased Appetite
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor
Dosage: 20 mg qd po
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2003-01-01
End date: 2007-05-09
Lipitor
Dosage: 20 mg qd po
Administration route: Oral
Indication: Cardiac Disorder
Start date: 2003-01-01
End date: 2007-05-09
Lipitor
Dosage: 20 mg qd po
Administration route: Oral
Indication: Prophylaxis
Start date: 2003-01-01
End date: 2007-05-09
Other drugs received by patient: Buspar; Valtrex; Ditropan XL; Imipramine; Premarin; Multi-Vitamin; Glucosamine-Chondroitin; Fish OIL
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-23
Patient: female, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Ventricular Tachycardia, Cardiogenic Shock, Hypokalaemia
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Losartan Potassium; Aldactone; Piretanide; Thyradin S; Constan; Nitorol R; Allopurinol
Adverse event in 34 year old male receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-17
Patient: 34 year old male, weighing 102.1 kg (224.5 pounds)
Adverse reactions / side effects: Adverse Drug Reaction, Nervous System Disorder, Lactic Acidosis, Apoptosis, Melas Syndrome, Cerebrovascular Accident
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-13
Patient: female
Adverse reactions / side effects: Interstitial Lung Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Aspirin
Dosage: daily dose:100mg
Administration route: Oral
Indication: Angina Pectoris
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hyperlipidaemia
Other drugs received by patient: Diltiazem HCL; Nitorol R; Epadel; Blopress
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from United States on 2007-07-10
Patient: male
Adverse reactions / side effects: Amyotrophic Lateral Sclerosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor
Dosage: 80 mg daily po
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2004-08-01
End date: 2006-12-21
Zetia
Dosage: 10 mg daily po
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2004-08-01
End date: 2006-12-21
Other drugs received by patient: Prilosec; Naproxen; Dutasteride -Avodart; Metoprolol -Toprol; Rilutek
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Netherlands on 2007-07-10
Patient: male, weighing 79.0 kg (173.8 pounds)
Adverse reactions / side effects: Pulmonary Fibrosis
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Metformin HCL
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-09
Patient: female, weighing 72.0 kg (158.4 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Ventricular Tachycardia, Cardiogenic Shock
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Losartan Potassium; Aldactone; Piretanide; Thyradin S; Constan; Nitorol R; Allopurinol
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-09
Patient: female, weighing 77.0 kg (169.4 pounds)
Adverse reactions / side effects: Chest Discomfort, Dizziness Postural, Oedema Peripheral, Pulmonary Embolism, Deep Vein Thrombosis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Actos
Administration route: Oral
Indication: Diabetes Mellitus
Start date: 2006-05-08
End date: 2007-04-14
Lipitor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-08-21
End date: 2007-04-14
Lipitor
Indication: Hyperlipidaemia
Soleton
Administration route: Oral
Indication: Analgesia
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a pharmacist from Japan on 2007-07-06
Patient: male
Adverse reactions / side effects: Death, Rhabdomyolysis
Adverse event resulted in: death, life threatening event
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Tenormin; Cough and Cold Preparations; Cough and Cold Preparations
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):
Azithromycin
Dosage: 1x a day 5 days
Indication: Nasopharyngitis
Start date: 2007-02-01
Lipitor
Dosage: 10 mg 1x a day
Indication: Arterial Occlusive Disease
Start date: 2007-01-01
End date: 2007-02-01
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-29
Patient: male, weighing 81.6 kg (179.5 pounds)
Adverse reactions / side effects: Arthropathy, Dysstasia, Coronary Artery Occlusion, Abasia, Gallbladder Disorder, Muscle Rigidity, Exercise Tolerance Decreased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Lisinopril; Lopressor
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-27
Patient: female, weighing 64.4 kg (141.7 pounds)
Adverse reactions / side effects: Weight Decreased, Nightmare, Pruritus, Nausea, Ovarian Cyst Ruptured, Irritability, Anxiety, Malaise, Dyspepsia
Adverse event resulted in: life threatening event
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-22
Patient: male, weighing 95.5 kg (210.0 pounds)
Adverse reactions / side effects: Myalgia, Coronary Artery Occlusion, Muscle Spasms
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Plavix; ALL Other Therapeutic Products
Adverse event in 50 year old male receiving Lipitor (Atorvastatin)
Reported by a physician from Australia on 2007-06-22
Patient: 50 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Ischaemia, Hepatitis Acute, Anaemia, Cardiac Output Decreased, Hepatic Enzyme Increased, Death, Renal Failure, Hepatomegaly, Chronic Hepatic Failure
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
Coversyl (Perindopril Erbumine)
Administration route: Oral
Start date: 2004-08-19
Lasix
Indication: Ischaemia
Start date: 2003-01-01
Lasix
Indication: Left Ventricular Failure
Start date: 2003-01-01
Lipitor
Administration route: Oral
Start date: 2003-01-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Hypertension
Start date: 2004-08-01
End date: 2004-09-27
Zetia
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2004-08-01
End date: 2004-09-27
Other drugs received by patient: Clopidogrel Bisulfate; Carvedilol; [composition Unspecified]
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-22
Patient: female, weighing 77.0 kg (169.4 pounds)
Adverse reactions / side effects: Chest Discomfort, Dizziness Postural, Oedema Peripheral, Pulmonary Embolism, Deep Vein Thrombosis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Actos
Administration route: Oral
Indication: Diabetes Mellitus
Start date: 2006-05-08
End date: 2007-04-10
Lipitor
Administration route: Oral
Indication: Hypercholesterolaemia
Lipitor
Indication: Hyperlipidaemia
Soleton
Dosage: freq:every day
Administration route: Oral
Indication: Analgesic Effect
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from United Kingdom on 2007-06-14
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
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