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Tricor (Fenofibrate) - Adverse Event Reports - Hospitalization

 



Index of reports > Cases resulting in hospitalization (14)

     Rhabdomyolysis (3)Hepatic Enzyme Increased (3)Haemoglobin Decreased (3)Bone Marrow Failure (3)Renal Failure (2)Rash (1)Drug Toxicity (1)Acute Hepatic Failure (1)Hepatitis Toxic (1)Renal Failure Acute (1)

Below is the selection of adverse event reports related to Tricor (Fenofibrate) that includes cases resulting in hospitalization.

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 40 year old male receiving Tricor (Fenofibrate)

Reported by a consumer/non-health professional from United States on 2007-10-09

Patient: 40 year old male, weighing 100.0 kg (220.0 pounds)

Adverse reactions / side effects: Psychotic Disorder

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)

Other drugs received by patient: Clozapine; Quetiapine Fumarate; Esomeprazole Magnesium



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 male receiving Tricor (Fenofibrate)

Reported by a physician from United States on 2007-07-06

Patient: male

Adverse reactions / side effects: Renal Failure

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)

Other drugs received by patient: Warfarin Sodium; Clopidogrel; Unspecified Medication



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 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 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



Adverse event in 33 year old male receiving Tricor (Fenofibrate)

Reported by a pharmacist from United States on 2007-05-31

Patient: 33 year old male, weighing 98.0 kg (215.6 pounds)

Adverse reactions / side effects: Pancreatitis Acute, Blood Triglycerides Increased

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)

Other drugs received by patient: Quetiapine; Crestor; Depakote ER



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 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



Adverse event in male receiving Tricor (Fenofibrate)

Reported by a physician from United States on 2007-04-12

Patient: male

Adverse reactions / side effects: Neuropathy

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)



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



Adverse event in 67 year old male receiving Tricor (Fenofibrate)

Reported by a consumer/non-health professional from United States on 2007-02-23

Patient: 67 year old male, weighing 109.0 kg (239.8 pounds)

Adverse reactions / side effects: Cholelithiasis

Adverse event resulted in: hospitalization

Suspect drug(s):
Tricor (Fenofibrate)

Other drugs received by patient: Clopidogrel Bisulfate; Amlodipine Besylate; Atorvastatin Calcium; Trazodone HCL

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