Gen-Fenofibrate Uses

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What is Gen-Fenofibrate?

Gen-Fenofibrate (Gen-Fenofibrate) helps reduce cholesterol and triglycerides (fatty acids) in the blood. High levels of these types of fat in the blood are associated with an increased risk of atherosclerosis (clogged arteries).

Gen-Fenofibrate is used to treat high cholesterol and high triglyceride levels.

Gen-Fenofibrate may also be used for purposes not listed in this medication guide.

Gen-Fenofibrate indications

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Primary Hypercholesterolemia or Mixed Dyslipidemia

Gen-Fenofibrate Capsules are indicated as adjunctive therapy to diet to reduce elevated low-density lipoprotein cholesterol (LDL-C), total cholesterol (total-c), Triglycerides (TG) and apolopoprotein B (Apo B), and to increase high-density lipoprotein cholesterol (HDL-C) in adult patients with primary hypercholesterolemia or mixed dyslipidemia.

Severe Hypertriglyceridemia

Gen-Fenofibrate Capsules are also indicated as adjunctive therapy to diet for treatment of adult patients with severe hypertriglyceridemia. Improving glycemic control in diabetic patients showing fasting chylomicronemia will usually obviate the need for pharmacologic intervention.

Markedly elevated levels of serum triglycerides (e.g. > 2,000 mg/dL) may increase the risk of developing pancreatitis. The effect of Gen-Fenofibrate therapy on reducing this risk has not been adequately studied.

Important Limitations of Use

Gen-Fenofibrate at a dose equivalent to 150 mg was not shown to reduce coronary heart disease morbidity and mortality in 2 large, randomized controlled trials of patients with type 2 diabetes mellitus.

How should I use Gen-Fenofibrate?

Use Gen-Fenofibrate capsules as directed by your doctor. Check the label on the medicine for exact dosing instructions.

Ask your health care provider any questions you may have about how to use Gen-Fenofibrate capsules.

Uses of Gen-Fenofibrate in details

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Use: Labeled Indications

Hypercholesterolemia or mixed dyslipidemia: Adjunctive therapy to diet for the reduction of low-density lipoprotein cholesterol (LDL-C), total cholesterol (total-C), triglycerides, and apolipoprotein B (apo B), and to increase high-density lipoprotein cholesterol (HDL-C) in adults with primary hypercholesterolemia or mixed dyslipidemia (Fredrickson types IIa and IIb). Use lipid-altering agents in addition to a diet restricted in saturated fat and cholesterol when response to diet and nonpharmacological interventions alone has been inadequate.

Note: While FDA-approved for hypercholesterolemia, Gen-Fenofibrate is not a first- or second-line choice; other agents may be more suitable (ACC/AHA [Stone 2013]). In addition, use is not recommended to lower LDL-C or raise HDL-C in the absence of hypertriglyceridemia.

Hypertriglyceridemia: Adjunctive therapy to diet for treatment of adult patients with severe hypertriglyceridemia (Fredrickson types IV and V hyperlipidemia).

Off Label Uses

Primary biliary cholangitis

Data from a single-center, retrospective cohort study support the use of Gen-Fenofibrate (in combination with ursodiol) in patients with primary biliary cholangitis (PBC) who have had an incomplete biochemical response to ursodiol monotherapy and showed significant improvement in alkaline phosphatase, a reduction in hepatic decompensation, and transplant-free survival improvement.

Gen-Fenofibrate description

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Each film-coated tablet contains Fenofibrate BP 160 mg. It also contains the following excipients: Pregelatinized starch maize, povidone, sodium lauryl sulphate, microcrystalline cellulose, crospovidone, anhydrous colloidal silica, sodium stearyl fumarate, purified water and opadry AMB OY-B-28920.

Gen-Fenofibrate is a lipid-regulating agent. The empirical formula is C20H21O4Cl and the molecular weight is 360.83. Gen-Fenofibrate is 2-[4-(4-chlorobenzoyl) phenoxy]-2-methyl-propanoic acid, 1-methylethyl ester.

Gen-Fenofibrate dosage

Gen-Fenofibrate Dosage

Generic name: Gen-Fenofibrate 160mg

Dosage form: tablet

The information at Drugs.com is not a substitute for medical advice. Always consult your doctor or pharmacist.

​The dose of Gen-Fenofibrate is 160 mg once daily.

​Patients should be placed on an appropriate lipid-lowering diet before receiving Gen-Fenofibrate and should continue this diet during treatment with Gen-Fenofibrate.

​Lipid levels should be monitored periodically. Therapy should be withdrawn in patients who do not have an adequate response after two months of treatment.

​Gen-Fenofibrate tablets can be given without regard to meals. Patients should be advised to swallow Gen-Fenofibrate tablets whole. Do not crush, break, dissolve, or chew tablets.

More about Gen-Fenofibrate (Gen-Fenofibrate)

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Gen-Fenofibrate interactions

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What other drugs will affect Gen-Fenofibrate?

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Coumarin Anticoagulants

Potentiation of coumarin-type anticoagulant effect has been observed with prolongation of the PT/INR.

Caution should be exercised when Gen-Fenofibrate is given in conjunction with coumarin anticoagulants. Gen-Fenofibrate may potentiate the anticoagulant effect of these agents resulting in prolongation of the PT/INR. To prevent bleeding complications, frequent monitoring of PT/INR and dose adjustment of the oral anticoagulant as recommended until the PT/INR has stabilized.

Immunosuppressants

Immunosuppressant agents such as cyclosporine and tacrolimus can impair renal function and because renal excretion is the primary elimination route of fibrate drugs including Gen-Fenofibrate capsules, there is a risk that an interaction will lead to deterioration of renal function. When immunosuppressants and other potentially nephrotoxic agents are co-administered with Gen-Fenofibrate capsules, the lowest effective dose of Gen-Fenofibrate capsules should be employed and renal function should be monitored.

Bile-Acid Binding Resins

Since bile-acid binding resins may bind other drugs given concurrently, patients should take Gen-Fenofibrate at least 1 hour before or 4 to 6 hours after a bile acid binding resin to avoid impeding its absorption.

Colchicine

Cases of myopathy, including rhabdomyolysis, have been reported with fenofibrates co-administered with colchicine, and caution should be exercised when prescribing Gen-Fenofibrate with colchicine.

Gen-Fenofibrate side effects

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What are the possible side effects of Gen-Fenofibrate?

Clinical Trials Experience

Because clinical studies are conducted under widely varying conditions, adverse reaction rates observed in the clinical studies of a drug cannot be directly compared to rates in the clinical studies of another drug and may not reflect the rates observed in practice.

Fenofibric acid is the active metabolite of Gen-Fenofibrate. Adverse events reported by 2% or more of patients treated with Gen-Fenofibrate and greater than placebo during double-blind, placebocontrolled trials are listed in Table 1. Adverse events led to discontinuation of treatment in 5.0% of patients treated with Gen-Fenofibrate and in 3.0% treated with placebo. Increases in liver tests were the most frequent events, causing discontinuation of Gen-Fenofibrate treatment in 1.6% of patients in double-blind trials.

Table 1: Adverse Events Reported by 2% or More of Patients Treated with Gen-Fenofibrate and Greater than Placebo During the Double-Blind, Placebo-Controlled Trials

BODY SYSTEM Adverse Event Gen-Fenofibrate*

(N = 439)

Placebo

(N = 365)

BODY AS A WHOLE
Abdominal Pain 4.6% 4.4%
Back Pain 3.4% 2.5%
Headache 3.2% 2.7%
DIGESTIVE
Nausea 2.3% 1.9%
Constipation 2.1% 1.4%
INVESTIGATIONS
Abnormal Liver Tests 7.5% 1.4%
Increased AST 3.4% 0.5%
Increased ALT 3.0% 1.6%
Increased Creatine Phosphokinase 3.0% 1.4%
RESPIRATORY
Respiratory Disorder 6.2% 5.5%
Rhinitis 2.3% 1.1%
* Dosage equivalent to 135 mg Gen-Fenofibrate

Clinical trials with Gen-Fenofibrate did not include a placebo-control arm. However, the adverse event profile of Gen-Fenofibrate was generally consistent with that of Gen-Fenofibrate. The following adverse events not listed above were reported in ≥ 3% of patients taking Gen-Fenofibrate alone:

Gastrointestinal Disorders: Diarrhea, dyspepsia

General Disorders and Administration Site Conditions: Pain

Infections and Infestations: Nasopharyngitis, sinusitis, upper respiratory tract infection

Musculoskeletal and Connective Tissue Disorders: Arthralgia, myalgia, pain in extremity

Nervous System Disorders: Dizzinesss

Postmarketing Experience

The following adverse events have been identified during postapproval use of Gen-Fenofibrate: rhabdomyolysis, pancreatitis, renal failure, muscle spasms, acute renal failure, hepatitis, cirrhosis, anemia, asthenia, and severely depressed HDL-cholesterol levels.

Because these events are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

Gen-Fenofibrate contraindications

See also:
What is the most important information I should know about Gen-Fenofibrate?

Hypersensitivity to Gen-Fenofibrate or fenofibric acid or to any of the excipients of Gen-Fenofibrate.

Severe renal impairment/insufficiency, including those receiving dialysis.

Active liver disease/dysfunction/insufficiency, including those with primary biliary cirrhosis and unexplained persistent liver function abnormalities eg, persistent elevations in serum transaminases. Pre-existing gallbladder disease.

Photoallergy or phototoxic reaction during treatment with fibrates or ketoprofen.

Chronic or acute pancreatitis with the exception of acute pancreatitis due to severe hypertriglyceridemia.

Gen-Fenofibrate contains lecithin soya as an excipient and therefore, Gen-Fenofibrate should not be taken with allergic to peanut or arachis oil or soya lecithin, or related products due to the risk of hypersensitivity reactions.

Use in lactation: Gen-Fenofibrate should not be used in nursing mothers. Because of the potential for tumorigenicity seen in animal studies, a decision should be made whether to discontinue nursing or to discontinue Gen-Fenofibrate, taking into account the importance of Gen-Fenofibrate to the mother. There are no data on the excretion of Gen-Fenofibrate and/or its metabolites into breast milk.

Use in children: Safety and effectiveness in pediatric patients aged <18 years have not been established.



Active ingredient matches for Gen-Fenofibrate:

Fenofibrate in Canada.


Unit description / dosage (Manufacturer)Price, USD
Gen-Fenofibrate 200 mg x 100's

List of Gen-Fenofibrate substitutes (brand and generic names):

Capsule; Oral; Fenofibrate 200 mg
Gen-Fenofibrate Micro 200 mg x 100's
Hafenthyl Supra 160 mg x 3 Blister x 10 Tablet
Hafenthyl 100 mg x 3 Blister x 10 Tablet
Hafenthyl 200 mg x 3 Blister x 10 Tablet
Hafenthyl 300 mg x 3 Blister x 10 Tablet
Hyperchol 100 mg x 4 x 12's (Ikapharmindo)$ 16.74
Hyperchol 300 mg x 3 x 10's (Ikapharmindo)$ 27.90
Hyperchol 200 M 200 mg x 5 x 6's (Ikapharmindo)$ 31.00
Lexemin 300 mg x 10 x 10's (Unison)
Lexemin 100 mg x 10 x 10's (Unison)
Lexemin / micronized 200 mg x 10 x 10's (Unison)
Lexemin 300 mg x 10 x 10's (Unison)
Lexemin / micronized 160 mg x 10 x 10's (Unison)
Lexemin 160 mg x 10 x 10's (Unison)
Lexemin cap 100 mg 10 x 10's (Unison)
Lexemin cap 300 mg 10 x 10's (Unison)
Lexemin tab 160 mg / micronized 10 x 10's (Unison)
Lexemin FC tab 160 mg 10 x 10's (Unison)
Lifemore 200 mg x 10 Blister x 10 Tablet
Lifemore 200 mg x 1 Bottle 100 Tablet
Lifen 500 mg
Lifen 200M 200 mg x 3 x 10's$ 33.48
Lifenoz-U 160 mg
Lifibrat 100 mg x 4 Blister x 10 Tablet, 10 Blister x 10 Tablet
Lifibrat 200 mg x 3 Blister x 10 Tablet, 10 Blister x 10 Tablet
Lifibrat 300 mg x 3 Blister x 10 Tablet, 10 Blister x 10 Tablet
Lifibrat 100 mg x 4 Blister x 10 Tablet
Lifibrat 100 mg x 10 Blister x 10 Tablet
Lifibrat 200 mg x 3 Blister x 10 Tablet

References

  1. DailyMed. "FENOFIBRATE: DailyMed provides trustworthy information about marketed drugs in the United States. DailyMed is the official provider of FDA label information (package inserts).". https://dailymed.nlm.nih.gov/dailyme... (accessed September 17, 2018).
  2. PubChem. "fenofibrate". https://pubchem.ncbi.nlm.nih.gov/com... (accessed September 17, 2018).
  3. DrugBank. "fenofibrate". http://www.drugbank.ca/drugs/DB01039 (accessed September 17, 2018).

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Information checked by Dr. Sachin Kumar, MD Pharmacology

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