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Index of reports
> Cases resulting in life threatening events (43)
> Cases with Drug Interaction (6)
Below is the selection of adverse event reports related to Zocor (Simvastatin) that includes cases resulting in life threatening events where reactions include drug interaction.
Adverse event in 74 year old male receiving Zocor (Simvastatin)
Reported by a physician from Denmark on 2007-07-30
Patient: 74 year old male, weighing 67.0 kg (147.4 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Dialysis, Drug Interaction, Urosepsis, Hypertension, Renal Failure Acute, Infarction
Adverse event resulted in: life threatening event
Suspect drug(s):
Zocor
Administration route: Oral
End date: 2007-06-12
Itraconazole
Administration route: Oral
Start date: 2007-06-05
End date: 2007-06-11
Adverse event in 64 year old receiving Zocor (Simvastatin)
Reported by a health professional (non-physician/pharmacist) from Denmark on 2007-05-08
Patient: 64 year old
Adverse reactions / side effects: Rhabdomyolysis, Drug Interaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-04-24
End date: 2006-11-01
Citalopram Hydrobromide
Administration route: Oral
Indication: Depression
Start date: 2006-04-24
End date: 2006-09-15
Citalopram Hydrobromide
Administration route: Oral
Start date: 2006-09-15
End date: 2006-11-01
Adverse event in 84 year old male receiving Zocor (Simvastatin)
Reported by a individual with unspecified qualification from United States on 2007-04-27
Patient: 84 year old male
Adverse reactions / side effects: Myoglobinuria, Hepatic Function Abnormal, Renal Impairment, Rhabdomyolysis, Drug Interaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Ketoconazole
Adverse event in 78 year old female receiving Zocor (Simvastatin)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-03-21
Patient: 78 year old female, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Paraparesis, Fatigue, Blood Creatine Phosphokinase Increased, Rhabdomyolysis, Sensation of Heaviness, Drug Interaction, Gait Disturbance, Asthenia, Myopathy
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2005-08-01
End date: 2007-01-30
Fusidic Acid
Administration route: Oral
Indication: Surgery
Start date: 2007-01-01
End date: 2007-01-30
Other drugs received by patient: Bendroflumethiazide; Dihydrocodeine; Ranitidine; Verapamil
Adverse event in 78 year old female receiving Zocor (Simvastatin)
Reported by a health professional (non-physician/pharmacist) from United Kingdom on 2007-02-22
Patient: 78 year old female, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased, Drug Interaction, Myopathy
Adverse event resulted in: life threatening event
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2005-08-01
End date: 2007-01-30
Fusidic Acid
Administration route: Oral
Indication: Surgery
Start date: 2007-01-01
End date: 2007-01-30
Other drugs received by patient: Bendroflumethiazide; Dihydrocodeine; Ranitidine; Verapamil
Adverse event in 64 year old receiving Zocor (Simvastatin)
Reported by a health professional (non-physician/pharmacist) from Denmark on 2007-01-22
Patient: 64 year old
Adverse reactions / side effects: Rhabdomyolysis, Drug Interaction
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Zocor
Administration route: Oral
Indication: Blood Cholesterol Increased
Start date: 2006-04-24
End date: 2006-11-01
Citalopram Hydrobromide
Administration route: Oral
Indication: Depression
Start date: 2006-04-24
End date: 2006-09-15
Citalopram Hydrobromide
Administration route: Oral
Start date: 2006-09-15
End date: 2006-11-01
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