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Index of reports
> Cases resulting in hospitalization (354)
> Cases with Liver Disorder (25)
Below is the selection of adverse event reports related to Lipitor (Atorvastatin) that includes cases resulting in hospitalization where reactions include liver disorder.
Reports 1 - 25 of 25 Next >>
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 male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-27
Patient: male, weighing 61.2 kg (134.6 pounds)
Adverse reactions / side effects: Jaundice, Malaise, Pancreatic Carcinoma, Anorexia, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Insulin; Amaryl; Novorapid; Novolin N
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-07-09
Patient: female, weighing 39.0 kg (85.8 pounds)
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Alfarol
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-08-27
End date: 2007-03-01
Alfarol
Administration route: Oral
Start date: 2007-05-01
Blopress
Administration route: Oral
Indication: Hypertension
Start date: 2001-08-27
End date: 2007-03-01
Blopress
Administration route: Oral
Start date: 2007-05-01
Lipitor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2001-08-27
End date: 2007-03-01
Lipitor
Administration route: Oral
Start date: 2007-05-01
Risedronate Sodium
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-08-27
End date: 2007-03-01
Risedronate Sodium
Administration route: Oral
Start date: 2007-05-01
Stogar
Administration route: Oral
Indication: Gastritis
Start date: 2001-08-27
End date: 2007-03-01
Stogar
Administration route: Oral
Start date: 2007-05-01
Adverse event in receiving Lipitor (Atorvastatin)
Reported by a pharmacist from United States on 2007-07-06
Patient:
Adverse reactions / side effects: Jaundice, Nausea, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-13
Patient: female
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Alfacalcidol
Dosage: daily dose:1mcg
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-08-27
End date: 2007-03-01
Alfacalcidol
Dosage: daily dose:1mcg
Administration route: Oral
Blopress
Dosage: daily dose:8mg
Administration route: Oral
Indication: Hypertension
Start date: 2001-08-27
End date: 2007-03-01
Blopress
Dosage: daily dose:8mg
Administration route: Oral
Lafutidine
Dosage: daily dose:10mg
Administration route: Oral
Indication: Gastritis
Start date: 2001-08-27
End date: 2007-03-01
Lafutidine
Dosage: daily dose:10mg
Administration route: Oral
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2001-08-27
End date: 2007-05-23
Risedronic Acid
Dosage: daily dose:10mg
Administration route: Oral
Indication: Osteoporosis
Start date: 2001-08-27
End date: 2007-03-01
Risedronic Acid
Dosage: daily dose:10mg
Administration route: Oral
Adverse event in 81 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-12
Patient: 81 year old female
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Blopress(candesartan Cilexetil)
Dosage: unk, unk, oral
Administration route: Oral
Indication: Hypertension
End date: 2007-05-01
Lipitor
Dosage: unk, unk, oral
Administration route: Oral
Indication: Hyperlipidaemia
Risedronate Sodium
Dosage: unk, unk, oral
Administration route: Oral
Indication: Osteoporosis
Stogar(lafutidine)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-08
Patient: female
Adverse reactions / side effects: Pancreatitis Acute, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Glyceol; Rinderon; Magnesium Oxide
Adverse event in 81 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-05
Patient: 81 year old female
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Benet Tablets 2.5mg
Administration route: Oral
Blopress Tablets 8
Administration route: Oral
Indication: Hypertension
End date: 2007-05-01
Lipitor
Administration route: Oral
Stogar
Administration route: Oral
Adverse event in 81 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-04
Patient: 81 year old female
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Alfacalcidol
Dosage: daily dose:1mcg
Administration route: Oral
Blopress
Dosage: daily dose:8mg
Administration route: Oral
Lafutidine
Dosage: daily dose:10mg
Administration route: Oral
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Risedronic Acid
Dosage: daily dose:10mg
Administration route: Oral
Adverse event in receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-05-25
Patient:
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Antibiotics
Lipitor
Dosage: daily dose:10mg-freq:daily
Administration route: Oral
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-05-22
Patient: female
Adverse reactions / side effects: Pancreatitis Acute, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Glyceol; Rinderon; Magnesium Oxide
Adverse event in 58 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-05-07
Patient: 58 year old female
Adverse reactions / side effects: Pancreatitis, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Glyceol; Rinderon; Magnesium Oxide
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-04-27
Patient: male
Adverse reactions / side effects: Liver Disorder, Hepatic Cirrhosis
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-04-04
Patient: female
Adverse reactions / side effects: Rash, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Blopress
Dosage: daily dose:8mg
Administration route: Oral
Indication: Hypertension
Farom
Dosage: daily dose:600mg
Administration route: Oral
Indication: Upper Respiratory Tract Infection
Start date: 2006-11-18
End date: 2006-11-24
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-09-06
End date: 2006-12-04
Niflan
Dosage: daily dose:225mg
Administration route: Oral
Indication: Upper Respiratory Tract Infection
Start date: 2006-10-20
End date: 2006-12-04
Adverse event in 65 year old male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-03-30
Patient: 65 year old male
Adverse reactions / side effects: Jaundice, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Ticlopidine Hydrochloride; Acetylsalicylic Acid SRT
Adverse event in 75 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-03-27
Patient: 75 year old female
Adverse reactions / side effects: Liver Operation, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in 65 year old male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-03-19
Patient: 65 year old male
Adverse reactions / side effects: Jaundice, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Ticlopidine Hydrochloride; Acetylsalicylic Acid SRT
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-03-15
Patient: male
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Warfarin Potassium; Warfarin Potassium; Iohexol
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-03-13
Patient: male
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Warfarin Potassium; Warfarin Potassium; Iohexol
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-03-09
Patient: female, weighing 50.8 kg (111.8 pounds)
Adverse reactions / side effects: Hypersensitivity, Nausea, Drug Ineffective, Headache, Convulsion, Liver Disorder, Suicidal Ideation, Weight Increased, Dysstasia, Malaise, Pharyngeal Oedema, Hepatic Cyst, Insomnia, Abdominal Distension, Dizziness, Depression, Oedema Mouth, Feeling Abnormal, Drug Interaction Inhibition
Adverse event resulted in: hospitalization
Suspect drug(s):
Benadryl
Lipitor
Indication: Blood Cholesterol Increased
Xanax
Indication: Depression
Zyrtec
Indication: Multiple Allergies
Other drugs received by patient possibly interacting with the suspect drug:
Chantix
Indication: Smoking Cessation Therapy
Start date: 2007-02-01
End date: 2007-02-01
Contrast Media
Indication: Computerised Tomogram
Start date: 2007-02-01
End date: 2007-02-01
Other drugs received by patient: Crestor; Zocor; ALL Other Therapeutic Products; Dyazide; Oxygen; Zelnorm; Prevacid
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-03-05
Patient: female
Adverse reactions / side effects: Nasopharyngitis, Gamma-Glutamyltransferase Increased, Alanine Aminotransferase Increased, Aspartate Aminotransferase Increased, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Laennec
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-02-15
Patient: female
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Magnesium Oxide; Aspirin
Adverse event in 71 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-02-09
Patient: 71 year old female
Adverse reactions / side effects: Cholangitis, Rash, Upper Respiratory Tract Inflammation, Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Blopress
Dosage: daily dose:8mg
Administration route: Oral
Indication: Hypertension
Farom
Dosage: daily dose:600mg
Administration route: Oral
Indication: Upper Respiratory Tract Infection
Start date: 2006-11-18
End date: 2006-11-24
Lipitor
Dosage: daily dose:10mg
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-09-06
End date: 2006-12-04
Niflan
Dosage: daily dose:225mg
Administration route: Oral
Indication: Upper Respiratory Tract Infection
Start date: 2006-10-20
End date: 2006-12-04
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-02-07
Patient: male
Adverse reactions / side effects: Liver Disorder
Adverse event resulted in: hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Warfarin Potassium; Warfarin Potassium; Iohexol
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