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Index of reports
> Cases resulting in death (16)
> Cases with Cardiac Disorder (3)
Below is the selection of adverse event reports related to Zetia (Ezetimibe) that includes cases resulting in death where reactions include cardiac disorder.
Adverse event in 50 year old male receiving Zetia (Ezetimibe)
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 male receiving Zetia (Ezetimibe)
Reported by a physician from Australia on 2007-06-07
Patient: male
Adverse reactions / side effects: Death, Chronic Hepatic Failure, Cardiac Disorder
Adverse event resulted in: death
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Simvastatin
Adverse event in male receiving Zetia (Ezetimibe)
Reported by a physician from Australia on 2007-04-02
Patient: male
Adverse reactions / side effects: Death, Chronic Hepatic Failure, Cardiac Disorder
Adverse event resulted in: death
Suspect drug(s):
Zetia (Ezetimibe)
Other drugs received by patient: Zocor
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