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Index of reports
> Cases resulting in death (62)
Below is the selection of adverse event reports related to Lipitor (Atorvastatin) that includes cases resulting in death.
Reports 1 - 25 of 62 Next >>
Adverse event in 75 year old female receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from Canada on 2007-10-25
Patient: 75 year old female
Adverse reactions / side effects: Chest Discomfort
Adverse event resulted in: death
Suspect drug(s):
Losec
Administration route: Oral
Alendronate Sodium
Combivent
Flovent
Lasix
Lipitor
Metformin
Nitrazadon
Plaqueril
Prednisone
Serevent
Tylenol (Caplet)
Adverse event in 85 year old male receiving Lipitor (Atorvastatin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-23
Patient: 85 year old male, weighing 74.6 kg (164.1 pounds)
Adverse reactions / side effects: Oral Intake Reduced, Abdominal Pain, Vomiting, Nausea, Balance Disorder, Abasia, Chills, Dysuria, Pyrexia, Asthenia
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from Colombia on 2007-10-19
Patient: male
Adverse reactions / side effects: Sudden Death, Hypoaesthesia, Erythema, Fall
Adverse event resulted in: death
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2004-09-24
End date: 2007-10-04
Acuretic
Administration route: Oral
Indication: Hypertension
Start date: 2004-09-24
End date: 2007-10-04
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from United States on 2007-10-12
Patient: male
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from United States on 2007-10-09
Patient: male
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Norvasc
Lipitor
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from Ireland on 2007-07-31
Patient: female
Adverse reactions / side effects: Back Pain, Multi-Organ Failure, Pulmonary Haemorrhage, Rhabdomyolysis, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Cerebrovascular Disorder
Start date: 2005-12-16
End date: 2006-01-15
Lipitor
Indication: Blood Cholesterol Increased
Other drugs received by patient: Plavix; Pantoprazole Sodium; Centyl K; Mesulid; Atenogen; Istin; Orovite; Thiamine
Adverse event in 73 year old female receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification on 2007-07-19
Patient: 73 year old female
Adverse reactions / side effects: Jaundice, Respiratory Arrest, Acute Hepatic Failure, Hepatitis, Convulsion
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor (Atorvastatin)
Other drugs received by patient: Doxazosin Mesylate; Bendrofluazide; Amlodipine; Ramipril; Acetylsalicylic Acid SRT; CO-Proxamol; Lansoprazole; Gaviscon; Bactrim
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a individual with unspecified qualification from Ireland on 2007-07-12
Patient: female
Adverse reactions / side effects: Back Pain, Multi-Organ Failure, Pulmonary Haemorrhage, Rhabdomyolysis, Renal Failure Acute
Adverse event resulted in: death, hospitalization
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Cerebrovascular Disorder
Start date: 2005-12-16
End date: 2006-01-15
Lipitor
Indication: Blood Cholesterol Increased
Other drugs received by patient: Plavix; Pantoprazole Sodium; Centyl K; Mesulid; Atenogen; Istin; Orovite; Thiamine
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United Kingdom on 2007-07-10
Patient: male
Adverse reactions / side effects: Death, Overdose
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Netherlands on 2007-07-10
Patient: female
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-07-06
Patient: male
Adverse reactions / side effects: Death, Blood Triglycerides Increased, High Density Lipoprotein Decreased
Adverse event resulted in: death
Suspect drug(s):
Lipitor
Indication: High Density Lipoprotein Decreased
Lipitor
Indication: Blood Triglycerides Increased
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 male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United Kingdom on 2007-07-03
Patient: male
Adverse reactions / side effects: Death, Overdose
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
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):
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
Lipitor
Administration route: Oral
Start date: 2003-01-01
End date: 2004-09-27
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
Other drugs received by patient: Clopidogrel Bisulfate; Carvedilol; [composition Unspecified]
Adverse event in 80 year old female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Philippines on 2007-06-14
Patient: 80 year old female
Adverse reactions / side effects: Cardio-Respiratory Arrest, Acute Myocardial Infarction
Adverse event resulted in: death
Suspect drug(s):
Lipitor
Administration route: Oral
Norvasc
Administration route: Oral
Adverse event in 60 year old male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United Kingdom on 2007-06-14
Patient: 60 year old male
Adverse reactions / side effects: Pancreatitis Acute
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in 50 year old male receiving Lipitor (Atorvastatin)
Reported by a physician from Australia on 2007-06-13
Patient: 50 year old male, weighing 80.0 kg (176.0 pounds)
Adverse reactions / side effects: Ischaemia, Hepatitis Acute, Anaemia, Cardiac Output Decreased, Cardiac Disorder, Hepatic Enzyme Increased, Death, Renal Failure, Hepatomegaly, Chronic Hepatic Failure
Adverse event resulted in: death, life threatening event, hospitalization
Suspect drug(s):
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
Lipitor
Administration route: Oral
Start date: 2003-01-01
End date: 2004-09-27
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
Other drugs received by patient: Clopidogrel Bisulfate; Carvedilol; [composition Unspecified]
Adverse event in 51 year old male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Canada on 2007-06-07
Patient: 51 year old male
Adverse reactions / side effects: Malaise, Pancreatic Carcinoma, Myocardial Infarction, Hepatocellular Damage
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-04
Patient: male
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Japan on 2007-06-04
Patient: male
Adverse reactions / side effects: Agranulocytosis, Hepatic Function Abnormal, Histiocytosis Haematophagic, Pneumonia, Disseminated Intravascular Coagulation, Sepsis
Adverse event resulted in: death, disablity
Suspect drug(s):
Lipitor
Dosage: daily dose:20mg
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-12-20
End date: 2007-01-21
Mucosta
Dosage: daily dose:300mg
Administration route: Oral
Indication: Gastric Ulcer
Other drugs received by patient: Caltan; Takepron; Warfarin Sodium; Adalat; Astomin; Mucodyne; Frandol; Pursennid
Adverse event in 80 year old female receiving Lipitor (Atorvastatin)
Reported by a consumer/non-health professional from Philippines on 2007-06-01
Patient: 80 year old female
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Lipitor
Administration route: Oral
Norvasc
Administration route: Oral
Adverse event in female receiving Lipitor (Atorvastatin)
Reported by a physician from Ireland on 2007-05-21
Patient: female
Adverse reactions / side effects: Renal Failure
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in receiving Lipitor (Atorvastatin)
Reported by a physician from Canada on 2007-05-17
Patient:
Adverse reactions / side effects: Rhabdomyolysis, Dialysis
Adverse event resulted in: death
Suspect drug(s):
Lipitor (Atorvastatin)
Adverse event in 63 year old female receiving Lipitor (Atorvastatin)
Reported by a physician from United States on 2007-05-11
Patient: 63 year old female
Adverse reactions / side effects: Drug Toxicity, Completed Suicide
Adverse event resulted in: death
Suspect drug(s):
Diphenhydramine HCL
Administration route: Oral
Indication: Suicide Attempt
Phenobarbital TAB
Administration route: Oral
Indication: Suicide Attempt
Carbon Monoxide
Indication: Suicide Attempt
Diazepam
Indication: Suicide Attempt
Carbamazepine
Indication: Suicide Attempt
Lipitor
Indication: Suicide Attempt
Nitroglycerin
Indication: Suicide Attempt
Albuterol
Indication: Suicide Attempt
Nasonex
Indication: Suicide Attempt
Levoxyl
Indication: Suicide Attempt
Enalapril
Indication: Suicide Attempt
Prevacid
Indication: Suicide Attempt
Unspecified Vitamins
Indication: Suicide Attempt
Adverse event in male receiving Lipitor (Atorvastatin)
Reported by a physician from Australia on 2007-05-11
Patient: male, weighing 128.6 kg (282.9 pounds)
Adverse reactions / side effects: Death
Adverse event resulted in: death
Suspect drug(s):
Lipitor
Administration route: Oral
Indication: Hypercholesterolaemia
Clozapine
Dosage: daily dose:350mg
Administration route: Oral
Indication: Schizophrenia
Start date: 2005-10-14
End date: 2007-01-17
Clozapine
Metformin HCL
Dosage: text:500
Administration route: Oral
Indication: Diabetes Mellitus
Diamicron
Dosage: daily dose:30mg
Administration route: Oral
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