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Tricor (Fenofibrate) - Adverse Event Reports - Hospitalization - Hepatic Enzyme Increased

 



Index of reports > Cases resulting in hospitalization (14) > Cases with Hepatic Enzyme Increased (3)

Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in hospitalization where reactions include hepatic enzyme increased.

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 68 year old female receiving Tricor (Fenofibrate)

Reported by a consumer/non-health professional from United States on 2007-05-17

Patient: 68 year old female

Adverse reactions / side effects: Drug Toxicity, Overdose, Wrong Drug Administered, Hepatic Enzyme Increased, Influenza Like Illness

Adverse event resulted in: hospitalization

Suspect drug(s):
Avandia
    Dosage: po
    Administration route: Oral
    End date: 2007-04-01

Glucophage
    Dosage: po
    Administration route: Oral
    End date: 2007-04-01

Humulin 70 / 30
    Dosage: sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    End date: 2007-04-01

Lipitor
    Dosage: po
    Administration route: Oral
    End date: 2007-04-01

Symlin
    Dosage: 15 mcg; bid; sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    End date: 2007-04-01

Symlin
    Dosage: 15 mcg; bid; sc
    Indication: Diabetes Mellitus non-Insulin-Dependent
    Start date: 2006-10-01

Tricor
    Dosage: po
    Administration route: Oral
    End date: 2007-04-01

Vasotec
    End date: 2007-04-01



Adverse event in 63 year old female receiving Tricor (Fenofibrate)

Reported by a physician from Puerto Rico on 2007-03-16

Patient: 63 year old female

Adverse reactions / side effects: Jaundice, Myalgia, Rash, Hepatitis Toxic, Hepatic Enzyme Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)

Other drugs received by patient: Levothyroxine Sodium

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