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Index of reports
> Cases resulting in disability (1)
Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in disability.
Adverse event in 55 year old male receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-07-02
Patient: 55 year old male, weighing 127.0 kg (279.4 pounds)
Adverse reactions / side effects: Anxiety, Rhabdomyolysis, Insomnia, Mental Status Changes, Sleep Apnoea Syndrome
Adverse event resulted in: hospitalization, disablity
Suspect drug(s):
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-04-16
End date: 2007-04-13
Zetia
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-08-11
End date: 2007-04-13
Zetia
Administration route: Oral
Indication: LOW Density Lipoprotein Increased
Start date: 2006-08-11
End date: 2007-04-13
Other drugs received by patient: Toprol-XL; Toprol-XL; Nitrostat; Actos; Metformin; Aspirin; Clarinex
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