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Index of reports
> Cases resulting in hospitalization (14)
> Cases with Rhabdomyolysis (3)
Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in hospitalization where reactions include rhabdomyolysis.
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
Adverse event in 56 year old female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-06-29
Patient: 56 year old female
Adverse reactions / side effects: Renal Failure, Rhabdomyolysis, Hepatic Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Crestor
Administration route: Oral
Tricor
Other drugs received by patient: Diabetic Medication; Blood Pressure Medication
Adverse event in 49 year old male receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-05-31
Patient: 49 year old male, weighing 117.3 kg (258.1 pounds)
Adverse reactions / side effects: Rhabdomyolysis, Haematuria, Blood Creatinine Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Tricor (Fenofibrate)
Other drugs received by patient: Benicar / Hydrochlorothiazide
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