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Index of reports
> Cases resulting in life threatening events (58)
Below is the selection of adverse event reports related to Crestor (Rosuvastatin) that includes cases resulting in life threatening events.
Reports 1 - 25 of 58 Next >>
Adverse event in female receiving Crestor (Rosuvastatin)
Reported by a physician from United States on 2007-10-31
Patient: female, weighing 71.7 kg (157.7 pounds)
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor
Dosage: crestor 10 mg 1 tablet daily oral
Administration route: Oral
Indication: Dementia
Start date: 2007-01-01
Crestor
Dosage: crestor 10 mg 1 tablet daily oral
Administration route: Oral
Indication: Dyslipidaemia
Start date: 2007-01-01
Crestor
Dosage: crestor 10 mg 1 tablet daily oral
Administration route: Oral
Indication: Hypertension
Start date: 2007-01-01
Adverse event in 68 year old female receiving Crestor (Rosuvastatin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-10-31
Patient: 68 year old female, weighing 59.5 kg (130.9 pounds)
Adverse reactions / side effects: Vomiting, Nausea, International Normalised Ratio Increased, Dehydration, Headache, Hepatitis, Haematemesis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Mirapex; Buspar; Aspirin; Fosamax; Gabapentin; Lortab; Nabumetone; Propranolol; Seroquel
Adverse event in 73 year old male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-10-24
Patient: 73 year old male, weighing 68.0 kg (149.6 pounds)
Adverse reactions / side effects: Blood Creatinine Increased, Anuria, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Crestor
Dosage: 2.5mg per day
Administration route: Oral
Start date: 2007-06-20
End date: 2007-09-25
Loxonin
Dosage: 60mg twice per day
Administration route: Oral
Start date: 2007-09-21
End date: 2007-09-23
Olmetec
Dosage: 2.5mg twice per day
Administration route: Oral
Indication: Cardiac Failure
End date: 2007-09-25
Valtrex
Dosage: 1000mg three times per day
Administration route: Oral
Indication: Herpes Zoster
Start date: 2007-09-21
End date: 2007-09-24
Other drugs received by patient: Artist; Neuquinon; Rabeprazole Sodium; Magnesium Oxide; Zolpidem
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-10-22
Patient: male, weighing 64.0 kg (140.8 pounds)
Adverse reactions / side effects: Cardiac Failure, Atrial Fibrillation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2006-06-17
End date: 2007-03-06
Crestor
Administration route: Oral
Start date: 2007-03-21
Other drugs received by patient: Aspirin; Ticlopidine HCL; Renivace; Amlodipine; Mucodyne; Astomin
Adverse event in female receiving Crestor (Rosuvastatin)
Reported by a physician from United States on 2007-10-09
Patient: female, weighing 92.5 kg (203.6 pounds)
Adverse reactions / side effects: Angioedema, Urticaria
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor
Dosage: 20 qd @ hs po
Administration route: Oral
Indication: Coronary Artery Disease
Start date: 2007-08-22
End date: 2007-08-23
Crestor
Dosage: 20 qd @ hs po
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-08-22
End date: 2007-08-23
Other drugs received by patient: Nadolol; Micardis; Aspirin; Metformin; Imdur
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-07-31
Patient: male
Adverse reactions / side effects: Hepatic Function Abnormal, Malaise, Anorexia, Disseminated Intravascular Coagulation, Pleural Effusion, Apallic Syndrome, Ascites
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Lipitor; Pravastatin
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-07-26
Patient: male
Adverse reactions / side effects: Hepatic Function Abnormal, Anorexia, Disseminated Intravascular Coagulation, Pleural Effusion, Apallic Syndrome, Respiration Abnormal, Ascites
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Lipitor; Pravastatin
Adverse event in 80 year old female receiving Crestor (Rosuvastatin)
Reported by a individual with unspecified qualification from United States on 2007-07-26
Patient: 80 year old female, weighing 53.1 kg (116.8 pounds)
Adverse reactions / side effects: Dyspnoea, Nausea, Chest Pain, Dizziness, Asthenia, Rash Pruritic
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-07-25
Patient: male
Adverse reactions / side effects: Hepatic Function Abnormal, Drug Ineffective, Disseminated Intravascular Coagulation, General Physical Health Deterioration, Apallic Syndrome, Ascites, Cholangitis, Anorexia, Pleural Effusion, Respiration Abnormal
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Lipitor; Pravastatin
Adverse event in female receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-06-27
Patient: female
Adverse reactions / side effects: Pneumonia Aspiration, Myopathy
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Selbex; Cercine
Adverse event in 39 year old male receiving Crestor (Rosuvastatin)
Reported by a physician from United States on 2007-06-25
Patient: 39 year old male
Adverse reactions / side effects: Rhabdomyolysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-25
Patient: male
Adverse reactions / side effects: Blood Bilirubin Increased
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor
Administration route: Oral
Start date: 2006-08-01
End date: 2007-02-01
Norvir
Indication: HIV Infection
Start date: 2006-12-01
End date: 2007-02-01
Reyataz
Indication: HIV Infection
Start date: 2006-12-01
End date: 2007-02-01
Truvada
Dosage: 1 tablet daily
Indication: HIV Infection
Start date: 2006-12-01
End date: 2007-02-01
Other drugs received by patient: Altace; Atenolol; Ambien; Aspirin; Vitamin CAP; Vitamin E; Fish OIL; Lorazepam
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-06-18
Patient: male, weighing 60.2 kg (132.4 pounds)
Adverse reactions / side effects: Blood Alkaline Phosphatase Increased, Blood Bilirubin Increased, Dyspnoea, Cellulitis, Hepatic Function Abnormal, Visual Field Defect, Alanine Aminotransferase Increased, Hemiparesis, Dysarthria, Cardiac Failure, Cerebral Infarction, Gamma-Glutamyltransferase Increased, C-Reactive Protein Increased, Coronary Artery Restenosis, Aspartate Aminotransferase Increased
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2005-12-21
End date: 2006-03-02
Crestor
Administration route: Oral
Start date: 2006-03-28
End date: 2006-07-03
Crestor
Administration route: Oral
Start date: 2006-07-04
End date: 2006-12-03
Other drugs received by patient: NU-Lotan; Allopurinol; Omepral; Euglucon; Cardenalin; Amlodin; Ticlopidine HCL; Prorenal; Sigmart; Aspirin; Pursennid; Mevalotin; Nitorol; Nitroderm; Albuminar; Predopa; Liple; Alprostadil; Metilon; Lasix; Mucodyne; Bisolvon; Hanp; Perdipine; Cefamezin Alpha
Adverse event in receiving Crestor (Rosuvastatin)
Reported by a consumer/non-health professional from France on 2007-06-14
Patient:
Adverse reactions / side effects: Alveolitis, Overdose, Interstitial Lung Disease, Haemoptysis, C-Reactive Protein Increased, Body Temperature Increased, Pleurisy, General Physical Health Deterioration, Inflammation
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Altace
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2006-10-01
End date: 2007-03-27
Cordarone / 00133102 /
Dosage: 100 mg, qd
Administration route: Oral
Start date: 2004-07-01
End date: 2007-03-27
Cosopt / 01419801 /
Indication: Glaucoma
End date: 2007-03-27
Crestor
Dosage: 5 mg, qd
Administration route: Oral
Start date: 2006-10-01
End date: 2007-03-27
Detensiel / 00802601 /
Dosage: 10 mg, qd
Administration route: Oral
Start date: 2006-08-03
End date: 2007-03-27
Other drugs received by patient: Mopral / 00661201 /; Previscan / 00789001 /
Adverse event in 73 year old female receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-06-14
Patient: 73 year old female
Adverse reactions / side effects: Renal Failure, Rhabdomyolysis
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Blopress
Administration route: Oral
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-05-08
End date: 2007-05-09
Other drugs received by patient: Mobic; Amlodin
Adverse event in 66 year old female receiving Crestor (Rosuvastatin)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-06-12
Patient: 66 year old female
Adverse reactions / side effects: Haemorrhage, Drug Interaction, Shock
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient possibly interacting with the suspect drug:
Warfarin Sodium
Administration route: Oral
Indication: Deep Vein Thrombosis
Start date: 2006-08-01
End date: 2006-09-01
Other drugs received by patient: Atenolol; Bendrofluazide; Ramipril; Levothyroxine Sodium
Adverse event in 83 year old male receiving Crestor (Rosuvastatin)
Reported by a individual with unspecified qualification from France on 2007-06-12
Patient: 83 year old male
Adverse reactions / side effects: Alveolitis, Overdose, Interstitial Lung Disease, Haemoptysis, Pleurisy, General Physical Health Deterioration
Adverse event resulted in: life threatening event
Suspect drug(s):
Bisoprolol Fumarate
Dosage: 10 mg (10 mg, 1 d)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-08-03
End date: 2007-03-27
Cordarone
Dosage: 100 mg (100 mg, 1 d)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2004-07-01
End date: 2007-03-27
Cosopt
Indication: Glaucoma
End date: 2007-03-27
Crestor
Dosage: 5 mg (5 mg, 1 d)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-03-27
Triamtec(5 MG, Capsule) (Ramipril)
Dosage: 10 mg (10 mg, 1 d)
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Start date: 2006-10-01
End date: 2007-03-27
Other drugs received by patient: Mopral(capsule) (Omeprazole); Previscan(tablet) (Fluindione)
Adverse event in 59 year old male receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-06-11
Patient: 59 year old male
Adverse reactions / side effects: Convulsion
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor (Rosuvastatin)
Adverse event in 57 year old female receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-06-11
Patient: 57 year old female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Cardiopulmonary Failure, Pulmonary Oedema
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Amaryl; Mexitil; Calblock; Lendormin; Mevalotin
Adverse event in 58 year old male receiving Crestor (Rosuvastatin)
Reported by a consumer/non-health professional from United States on 2007-06-07
Patient: 58 year old male, weighing 77.1 kg (169.6 pounds)
Adverse reactions / side effects: Activities of Daily Living Impaired, Chest Pain, Gait Disturbance
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor
Dosage: 500 mg -i think- 1 daily po
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2005-11-01
End date: 2006-11-15
Crestor
Dosage: 500 mg -i think- 1 daily po
Administration route: Oral
Indication: Blood Triglycerides Increased
Start date: 2005-11-01
End date: 2006-11-15
Adverse event in 83 year old male receiving Crestor (Rosuvastatin)
Reported by a health professional (non-physician/pharmacist) from France on 2007-06-06
Patient: 83 year old male
Adverse reactions / side effects: Alveolitis, Interstitial Lung Disease
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Cordarone
Administration route: Oral
Start date: 2004-07-01
End date: 2007-03-27
Cosopt
Indication: Glaucoma
End date: 2007-03-27
Crestor
Administration route: Oral
Start date: 2006-08-01
End date: 2007-03-27
Detensiel
Administration route: Oral
Start date: 2004-07-01
End date: 2007-03-27
Triatec
Administration route: Oral
Start date: 2006-10-01
End date: 2007-03-27
Other drugs received by patient: Omeprazole; Previscan
Adverse event in 33 year old male receiving Crestor (Rosuvastatin)
Reported by a individual with unspecified qualification from United States on 2007-05-31
Patient: 33 year old male, weighing 102.1 kg (224.5 pounds)
Adverse reactions / side effects: Myalgia, Muscle Swelling, Contusion, Oedema Peripheral, Muscular Weakness, Testicular Swelling, Excessive Exercise, Muscle Enzyme Increased
Adverse event resulted in: life threatening event, hospitalization, disablity
Suspect drug(s):
Crestor (Rosuvastatin)
Adverse event in 64 year old male receiving Crestor (Rosuvastatin)
Reported by a pharmacist from United States on 2007-05-30
Patient: 64 year old male, weighing 71.2 kg (156.6 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Metabolic Acidosis, Hyperkalaemia, Haemodialysis, Renal Failure Acute
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Aceon
Dosage: 8 mg orally daily
Administration route: Oral
Indication: Hypertension
Crestor
Indication: Hyperlipidaemia
Glucophage
Dosage: 500 mg orally daily
Administration route: Oral
Indication: Diabetes Mellitus
Adverse event in male receiving Crestor (Rosuvastatin)
Reported by a physician from Czech Republic on 2007-05-18
Patient: male
Adverse reactions / side effects: Torsade DE Pointes, Sick Sinus Syndrome, Drug Interaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient possibly interacting with the suspect drug:
Sedacoron
Dosage: during dialysis
Indication: Atrial Fibrillation
Start date: 2007-04-24
End date: 2007-04-24
Sedacoron
Dosage: during dialysis
Start date: 2007-04-26
End date: 2007-04-26
Sedacoron
Administration route: Oral
Start date: 2007-04-26
End date: 2007-04-28
Other drugs received by patient: Calcium Carbonicum; Eprex; Ferrlecit; Furorese; Hypnogen; Milurit; Tagren; Tagren; Tagren; Rocaltrol; Ranisan; Betahirex; Prolekofen; Fosrenol; Enelbin Retard; Enelbin Retard; Enelbin Retard
Adverse event in female receiving Crestor (Rosuvastatin)
Reported by a physician from Japan on 2007-05-15
Patient: female, weighing 58.0 kg (127.6 pounds)
Adverse reactions / side effects: Renal Tubular Disorder, Vomiting, Convulsions Local, Blood Creatine Phosphokinase Increased, Anorexia, Hyponatraemia, Muscle Spasms
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Crestor (Rosuvastatin)
Other drugs received by patient: Mevalotin; Dogmatyl; Tasuomin; PL; Transamin; Dasen; Amaryl; Norvasc; Preran; Alosenn
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