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Index of reports
> Cases resulting in hospitalization (14)
> Cases with Haemoglobin Decreased (3)
Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in hospitalization where reactions include haemoglobin decreased.
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-07-20
Patient: female, weighing 101.0 kg (222.2 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Anaemia, Bone Marrow Failure, Renal Failure Acute, Hepatic Enzyme Increased
Adverse event resulted in: hospitalization
Suspect drug(s):
Tricor
Indication: Blood Triglycerides Increased
Start date: 2006-10-01
End date: 2007-04-01
Tricor
Indication: LOW Density Lipoprotein Increased
Tricor
Indication: High Density Lipoprotein Decreased
Other drugs received by patient: Metoprolol Succinate; Olmesartan Medoxomil; Hydrochlorothiazide
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-06-11
Patient: female, weighing 101.0 kg (222.2 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Bone Marrow Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Tricor
Indication: Blood Triglycerides Increased
Start date: 2006-10-01
End date: 2007-04-01
Tricor
Indication: LOW Density Lipoprotein Increased
Tricor
Indication: High Density Lipoprotein Decreased
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-05-04
Patient: female, weighing 101.0 kg (222.2 pounds)
Adverse reactions / side effects: Haemoglobin Decreased, Bone Marrow Failure
Adverse event resulted in: hospitalization
Suspect drug(s):
Tricor
Indication: Blood Triglycerides Increased
Start date: 2006-10-01
End date: 2007-04-01
Tricor
Indication: LOW Density Lipoprotein Increased
Tricor
Indication: High Density Lipoprotein Decreased
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