|
This is an index of reports of adverse events (side effects, adverse reactions, etc.) related to Tricor (Fenofibrate). Click on the relevant link below to view a selection of reports according to the event's seriousness level and/or the nature of the side effect / adverse reaction. Or scroll down to view a sample of recent reports further on this page.
Our database includes reports from Jan 2007 to Dec 2007. The information is not vetted and should not be cosidered as verified clinical evidence.
All cases (53)
Cases resulting in a serious event (47)
Cases resulting in death (9)
Cases resulting in life threatening events (2)
Cases resulting in hospitalization (14)
Cases resulting in disability (1)
Cases resulting in other serious reactions (30)
Below is a sample of reports where side effects / adverse reactions may be related to Tricor (Fenofibrate). For a complete list and/or a specific selection of reports, please use the links in the index above.
Adverse event in 84 year old male receiving Tricor (Fenofibrate)
Reported by a individual with unspecified qualification from United States on 2007-10-29
Patient: 84 year old male, weighing 95.3 kg (209.6 pounds)
Adverse reactions / side effects: Abdominal Pain, Pruritus, Abasia, Muscular Weakness, Fall, Constipation, Myalgia, Balance Disorder, Sexual Dysfunction, Bladder Disorder
Suspect drug(s):
Tricor (Fenofibrate)
Adverse event in 78 year old female receiving Tricor (Fenofibrate)
Reported by a physician from Japan on 2007-10-24
Patient: 78 year old female
Adverse reactions / side effects: Nephritis Interstitial, Blood Cholesterol Increased
Suspect drug(s):
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-07-24
End date: 2007-08-21
Zetia
Administration route: Oral
Indication: Hypercholesterolaemia
Start date: 2007-07-24
End date: 2007-08-21
Adverse event in 49 year old female receiving Tricor (Fenofibrate)
Reported by a consumer/non-health professional from United States on 2007-10-22
Patient: 49 year old female, weighing 66.7 kg (146.7 pounds)
Adverse reactions / side effects: Confusional State, Abdominal Pain, Nausea, Muscular Weakness, Myalgia, Fatigue, Dyspepsia, Insomnia, Dizziness, Renal Pain, Coordination Abnormal, Feeling Abnormal
Suspect drug(s):
Tricor (Fenofibrate)
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 male receiving Tricor (Fenofibrate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-07-27
Patient: male, weighing 95.5 kg (210.1 pounds)
Adverse reactions / side effects: Renal Failure, Rhabdomyolysis, Drug Interaction
Suspect drug(s):
ACE Inhibitor NOS
Indication: Drug USE FOR Unknown Indication
Ephedra MIX
Indication: Weight Loss Diet
Start date: 2007-06-01
Ibuprofen
Indication: Migraine
Tricor
Indication: Drug USE FOR Unknown Indication
Start date: 2005-01-01
Other drugs received by patient possibly interacting with the suspect drug:
Lovastatin
Dosage: low dose
Indication: Drug USE FOR Unknown Indication
Start date: 2007-01-18
End date: 2007-05-01
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a consumer/non-health professional from United States on 2007-07-25
Patient: female, weighing 73.2 kg (161.0 pounds)
Adverse reactions / side effects: Weight Increased, Vomiting, Nausea, Blood Cholesterol Increased, Bronchitis
Suspect drug(s):
Chantix
Tricor
Indication: Blood Cholesterol Increased
Other drugs received by patient: Atenolol; Clonazepam
Adverse event in 59 year old male receiving Tricor (Fenofibrate)
Reported by a individual with unspecified qualification from United States on 2007-07-23
Patient: 59 year old male, weighing 137.9 kg (303.4 pounds)
Adverse reactions / side effects: Dysstasia, Pain in Extremity, Activities of Daily Living Impaired, Gait Disturbance
Suspect drug(s):
Tricor (Fenofibrate)
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 50 year old male receiving Tricor (Fenofibrate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-29
Patient: 50 year old male
Adverse reactions / side effects: Rhabdomyolysis, Renal Failure, Drug Interaction
Suspect drug(s):
Tricor (Fenofibrate)
Other drugs received by patient possibly interacting with the suspect drug:
Statin Therapy (Statin Therapy)
Dosage: low dose
Indication: Drug USE FOR Unknown Indication
Start date: 2005-12-01
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 2007-06-25
Patient: female
Adverse reactions / side effects: Blood Triglycerides Increased
Suspect drug(s):
Crestor
Administration route: Oral
Tricor
Adverse event in 42 year old female receiving Tricor (Fenofibrate)
Reported by a individual with unspecified qualification from United States on 2007-06-25
Patient: 42 year old female
Adverse reactions / side effects: Blood Creatine Phosphokinase Increased
Suspect drug(s):
Crestor
Administration route: Oral
Tricor
Zetia
Other drugs received by patient: Darvocet; Neurontin
Adverse event in 50 year old male receiving Tricor (Fenofibrate)
Reported by a health professional (non-physician/pharmacist) from United States on 2007-06-20
Patient: 50 year old male
Adverse reactions / side effects: Rhabdomyolysis, Renal Failure
Suspect drug(s):
Tricor (Fenofibrate)
Adverse event in 30 year old male receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-06-19
Patient: 30 year old male
Adverse reactions / side effects: Renal Failure Acute
Suspect drug(s):
Tricor
Administration route: Oral
Indication: Drug USE FOR Unknown Indication
Tricor
Start date: 2006-12-01
Other drugs received by patient: Lisinopril; Valsartan
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-06-14
Patient: female, weighing 83.9 kg (184.6 pounds)
Adverse reactions / side effects: Weight Increased, Myalgia, Colonic Polyp, Fatigue, Colon Cancer, Pain in Extremity, Alopecia, Asthenia, Myopathy
Suspect drug(s):
Lipitor
Dosage: daily dose:10mg
Indication: Blood Cholesterol Increased
Tricor
Zoloft
Indication: Depression
Zoloft
Indication: Anxiety
Other drugs received by patient: Clonazepam
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 male receiving Tricor (Fenofibrate)
Reported by a physician from Japan on 2007-05-31
Patient: male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Drug Eruption
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-01-22
End date: 2007-01-29
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-01-22
End date: 2007-01-29
Other drugs received by patient: Zestril; Norvasc; Amaryl; Lipitor; Bezatol SR
Adverse event in female receiving Tricor (Fenofibrate)
Reported by a physician from United States on 2007-05-31
Patient: female, weighing 103.9 kg (228.5 pounds)
Adverse reactions / side effects: Abdominal Pain, Blood Creatine Phosphokinase Increased, Alanine Aminotransferase Increased, Myopathy, Muscle Spasms
Suspect drug(s):
Tricor
Dosage: 145 mg daily po
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-10-04
End date: 2007-05-25
Zetia
Dosage: 10 mg daily po
Administration route: Oral
Indication: Drug Ineffective
Start date: 2006-11-15
End date: 2007-05-25
Zetia
Dosage: 10 mg daily po
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2006-11-15
End date: 2007-05-25
Other drugs received by patient: Hydrochlorothiazide; Metformin HCL; Prilosec
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 male receiving Tricor (Fenofibrate)
Reported by a physician from Japan on 2007-05-30
Patient: male, weighing 70.0 kg (154.0 pounds)
Adverse reactions / side effects: Drug Eruption
Suspect drug(s):
Crestor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-01-22
End date: 2007-01-29
Tricor
Administration route: Oral
Indication: Hyperlipidaemia
Start date: 2007-01-22
End date: 2007-01-29
Other drugs received by patient: Zestril; Norvasc; Amaryl; Lipitor; Bezatol SR
Adverse event in 59 year old male receiving Tricor (Fenofibrate)
Reported by a consumer/non-health professional from United States on 2007-05-30
Patient: 59 year old male
Adverse reactions / side effects: Photosensitivity Reaction
Suspect drug(s):
Byetta
Dosage: 10 mcg; bid; sc; 5 mcg; bid; sc
Indication: Diabetes Mellitus non-Insulin-Dependent
Start date: 2007-02-01
End date: 2007-03-01
Byetta
Dosage: 10 mcg; bid; sc; 5 mcg; bid; sc
Indication: Diabetes Mellitus non-Insulin-Dependent
Start date: 2007-03-01
Tricor
Indication: Blood Cholesterol
Start date: 2006-12-01
|
