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Index of reports
> Cases resulting in life threatening events (2)
Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in life threatening events.
Adverse event in 43 year old male receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-10-22
Patient: 43 year old male, weighing 87.4 kg (192.3 pounds)
Adverse reactions / side effects: Hyperlipidaemia, Acute Hepatic Failure
Adverse event resulted in: life threatening event, hospitalization
Suspect drug(s):
Tricor (Fenofibrate)
Adverse event in male receiving Tricor (Fenofibrate)
Reported by a physician from Japan on 2007-04-30
Patient: male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Dermatitis, Neuroleptic Malignant Syndrome
Adverse event resulted in: life threatening event
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-01-22
End date: 2007-01-29
Tricor
Administration route: Oral
Start date: 2007-01-22
End date: 2007-01-29
Other drugs received by patient: Zestril; Norvasc; Amaryl; Lipitor; Bezatol SR
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