Fenofibrate Disease Interactions
There are 5 disease interactions with fenofibrate:
Fenofibrate (Includes Fenofibrate) ↔ Liver Disease
Severe Potential Hazard, High plausibility
Applies to: Liver Disease
The use of fenofibrate is contraindicated in patients with active liver disease or unexplained, persistent elevations of serum transaminases. Fenofibrate therapy is associated with dose-related hepatotoxicity, including biochemical abnormalities of liver function, hepatitis (hepatocellular, chronic active, as well as cholestatic) and, rarely, cirrhosis. Therapy with fenofibrate should be administered cautiously in patients with a history of liver disease and/or heavy alcohol use. Liver function tests, including serum transaminase levels, should be performed at baseline and periodically throughout the duration of therapy. Patients who develop elevated ALT or AST levels during therapy should be monitored until abnormalities resolve. Therapy should be withdrawn if elevations persist above 3 times the upper limit of normal.
Fenofibrate (Includes Fenofibrate) ↔ Renal Dysfunction
Severe Potential Hazard, High plausibility
Applies to: Renal Dysfunction
The use of fenofibrate is contraindicated in patients with significantly impaired renal function. The rate of clearance of fenofibric acid has been shown to decrease substantially when CrCl is below 50 mL/min, with drug accumulation during chronic dosing. Increased adverse effects, including rhabdomyolysis (with or without secondary renal failure) and severe hyperkalemia, have been associated with the use of fibric acid derivatives in patients with renal insufficiency. Therapy with fenofibrate should be administered cautiously in patients with mild or moderate renal impairment. Close clinical monitoring is recommended during therapy.
Fibric Acid Derivatives (Includes Fenofibrate) ↔ Biliary Cirrhosis
Severe Potential Hazard, High plausibility
Applies to: Biliary Cirrhosis
The use of fibric acid derivatives is contraindicated in patients with primary biliary cirrhosis. These agents may further raise the already elevated cholesterol in these patients.
Fibric Acid Derivatives (Includes Fenofibrate) ↔ Cholelithiasis
Severe Potential Hazard, High plausibility
Applies to: Gallbladder Disease
The use of fibric acid derivatives is contraindicated in patients with gallbladder disease. A significantly increased incidence of cholelithiasis has been observed in patients treated with the fibric acid derivative, clofibrate, presumably because of increased cholesterol excretion into the bile. Based on two separate studies (the WHO study and the Coronary Drug Project study), clofibrate use was associated with twice the risk of developing cholelithiasis and cholecystitis requiring surgery. Due to their structural and pharmacologic similarities, use of other fibric acid derivatives may be expected to carry the same risk.
Fibric Acid Derivatives (Includes Fenofibrate) ↔ Rhabdomyolysis
Severe Potential Hazard, Moderate plausibility
Applies to: Myoneural Disorder, Myopathy
Severe myopathy, including rhabdomyolysis with acute renal failure secondary to myoglobinuria, has been reported rarely with the use of fibric acid derivatives. The myopathy may be dose-related and is characterized by muscle aches and/or weakness in conjunction with increases in creatine phosphokinase (CPK) values exceeding 10 times the upper limit of normal. Therapy with fibric acid derivatives should be administered cautiously in patients with preexisting myopathy or a myoneural disorder, since it may delay the recognition or confound the diagnosis of a drug-induced musculoskeletal effect. Patients should be advised to report promptly any unusual muscle pain, tenderness or weakness, particularly if accompanied by malaise or fever. Periodic CPK determinations may be considered in some patients, although the value of such monitoring is uncertain. Therapy should be withdrawn if markedly elevated CPK levels occur or if drug-related myopathy is diagnosed or suspected.
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fenofibrate drug Interactions
There are 74 drug interactions with fenofibrate
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Drug Interaction Classification
The classifications below are a general guideline only. It is difficult to determine the relevance of a particular drug interaction to any individual given the large number of variables.
| Major | Highly clinically significant. Avoid combinations; the risk of the interaction outweighs the benefit. |
| Moderate | Moderately clinically significant. Usually avoid combinations; use it only under special circumstances. |
| Minor | Minimally clinically significant. Minimize risk; assess risk and consider an alternative drug, take steps to circumvent the interaction risk and/or institute a monitoring plan. |
Do not stop taking any medications without consulting your healthcare provider.
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