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Apteor (Fenofibrate)

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Apteor is a fibric acid derivative like clofibrate and gemfibrozil. Apteor is used to treat primary hypercholesterolemia, mixed dyslipidemia, severe hypertriglyceridemia. Apteor was granted FDA approval on 31 December 1993.

Other names for this medication:
Controlip, Craveril, Docfenofi, Einecs, Febira, Fenobrat, Fenobrate, Fenocap, Fenofib, Fenofibrat, Fenoglide, Fenoratio, Fenosup, Fibrafen, Fibral, Grofibrat, Hafenthyl, Katalip, Lexemin, Lifibrat, Lipanthyl, Lipcor, Liperial, Lipicard, Lipidcare, Lipidof, Lipilfen, Lipivim, Lipofen, Lipohexal, Lipsin, Lofat, Lofibra, Lowlip, Minuslip, Naftilan, Nofiate, Nolipax, Normolip, Nubrex, Nuozhituo, Procetofen, Supralip, Tilene, Triglide, Trilipix, Trolip, Versamid, Xafenor, Zumafib

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Also known as: Fenofibrate


{name} (fenofibrate) belongs to a group of drugs known as "fibrates." It 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).

{name} is used along with a proper diet to help to treat high cholesterol and high triglyceride levels.

In addition to eating a proper diet (such as a low-cholesterol/low-fat diet), other lifestyle changes that may help {name} work better include exercising, losing weight if overweight, and stopping smoking.


Usual Adult Dose of Apteor for Hyperlipoproteinemia Type IIa (Elevated LDL): 145 mg orally once a day.

Usual Adult Dose for Hyperlipoproteinemia Type IIb (Elevated LDL + VLDL): 145 mg orally once a day.

Usual Adult Dose for Hyperlipoproteinemia Type IV (Elevated VLDL): 48 to 145 mg orally once a day. Usual Adult Dose for Hyperlipoproteinemia Type V (Elevated Chylomicrons + VLDL): 48 to 145 mg orally once a day. Usual Geriatric Dose of Apteor for Hyperlipoproteinemia: 48 mg orally once a day. Increases in dosage should occur only after evaluating the effects on renal function and lipid levels at this dose, with a maximum recommended dose of 145 mg/24 hours.

Detailed Apteor dosage information


Seek emergency medical attention or call the Poison Help line at 1-800-222-1222.


Store at room temperature between 15 and 30 degrees C (59 and 86 degrees F) away from moisture and heat. Keep container tightly closed. Throw away any unused medicine after the expiration date. Keep out of the reach of children.

Side effects

The most common side effects associated with Apteor are:

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Side effect occurrence does not only depend on medication you are taking, but also on your overall health and other factors.


Do not take Apteor if you are allergic to its components. Do not take Apteor if you're pregnant or you plan to have a baby, or you are a nursing mother. Apteor can ham your baby. Be careful with Apteor if you suffer from liver cirrhosis, hepatitis, severe kidney disease, gallbladder disease, diabetes, kidney, liver, heart disease, hypothyroidism. Be careful with Apteor if you are taking such medicines as blood thinner (warfarin (such as Coumadin)); fluvastatin (such as Lescol), cholesterol-lowering medicines (lovastatin (such as Mevacor), simvastatin (such as Zocor), cerivastatin (such as Baycol), pravastatin (such as Pravachol), atorvastatin (such as Lipitor), cyclosporine (such as Gengraf, Neoral, Sandimmune). If you experience drowsiness and dizziness while taking Apteor you should avoid any activities such as driving or operating machinery. Avoid alcohol. Elderly people should be very careful with Apteor. Keep low-cholesterol and low-fat diet. Do not stop taking Apteor suddenly.

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Effects of Floral Scent, Color and Pollen on Foraging Decisions and Oocyte Development of Common Green Bottle Flies. We also developed a computational tool for the automated design of gene regulation programs using recombinase-based state machines. To our knowledge, this is the first report of secondary metabolites from the marine hydrothermal vent mussel B. Twenty- four postpartum rabbits were randomly assigned into sham shock group (group P), shock group without interventions (group P0), conventional fluid resuscitation group (group PNL), and limited fluid resuscitation group (group PLH), and the model of severe uncontrolled hemorrhagic shock was established in the latter 3 groups. To examine the threshold in disease activity associated with switching biologic treatment regimens in rheumatoid arthritis (RA) patients in real-world clinical practice.

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