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Tricor

Tricor is used with a low-fat diet, exercise, and sometimes with other medications to reduce the amounts of fatty substances such as cholesterol and triglycerides in the blood and to increase the amount of HDL (high-density lipoprotein; a type of fatty substance that decreases the risk of heart disease) in the blood.

Other names for this medication:
Antilip, Apteor, Catalip, Controlip, Craveril, Docfenofi, Einecs, Elipsia, Fegenor, Fenobeta, Fenobrat, Fenobrate, Fenofibrate, Fenofibrato, Fenofibratum, Fenoglide, Fenohexal, Fenosup, Fibrafen, Fulcro, Grofibrat, Katalip, Lexemin, Lifen, Liperial, Lipidcare, Lipidil, Lipilfen, Lipired, Lipirex, Lipivim, Lipofen, Lipohexal, Lipolin, Lofibra, Lowlip, Minuslip, Nolipax, Normalip, Normolip, Nuozhituo, Procetofen, Stanlip, Supralip, Trigent, Triglide, Trilipix, Trolip, Xafenor, Zumafib

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Also known as: Fenofibrate

Description

Tricor is the medication of high quality, which is taken in treatment of high triglyceride levels and high cholesterol with diet changes. The target of this perfect remedy is the treatment of high triglyceride levels and high cholesterol with diet changes. Tricor is also known as Fenofibrate, Fenofibric acid, Lipicard, Lofibra, Lipanthyl, Fenocor-67. Tricor is acting by increasing enzyme which breaks down fats in the blood. It is fibrate (lipid-lowering agent). Generic name of Tricor is Fenofibrate. Brand names of Tricor are Tricor, Tricor, Antara, Triglide, Lofibra, Lipofen.

Dosage

Usual Adult Dose of Tricor 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 Tricor 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 Tricor dosage information

Overdose

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

Storage

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 Tricor 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.

Contraindications

You should not take Tricor if you are allergic to fenofibrate, or if you have:

severe kidney disease (or if you are on dialysis); liver disease; or gallbladder disease.

Do not breast-feed while using this medicine, and for at least 5 days after your last dose.

To make sure Tricor is safe for you, tell your doctor if you have ever had:

kidney disease; liver disease; or gallbladder problems.

Fenofibrate can cause the breakdown of muscle tissue, which can lead to kidney failure. This happens more often in women, in older adults, or people who have kidney disease, diabetes, or poorly controlled hypothyroidism (underactive thyroid).

It is not known whether this medicine will harm an unborn baby. Tell your doctor if you are pregnant or plan to become pregnant.

Tricor is not approved for use by anyone younger than 18 years old.

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To our knowledge, this is the first study to show that endoscopic biopsy granulomas in patients with uncomplicated (non-stricturing, non-penetrating) CD predict the subsequent development of SCD. A TMJ OA synthetic database will be created next, and evaluated by expert radiologists, and this will serve to evaluate how sensitive the current radiological diagnosis tools are. With nuclei, significantly less propenal is formed, although the yield of free base is equivalent to that from purified DNA. Rationale and indications for biological treatment of psychiatric disorders. In vivo pharmacokinetic/pharmacodynamic profiles of valnemulin in an experimental intratracheal Mycoplasma gallisepticum infection model. The primary mechanisms of DDIs are based on pharmacokinetics (PK) and pharmacodynamics (PD). Audiological medicine encompasses the diagnosis and management of disorders of hearing and balance. Adsorption experiments in simulated gastrointestinal fluid and real gastric juice were carried out.

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This variability was partly explained by climatic conditions during late gestation. However, little is known about how genes interact with positive traits to affect well-being. We ultimately conclude that improved professional self-regulation is a reasonable starting place for oocyte donation. Detailed chromosome analysis clobetasol lotion cost failed to reveal any evidence for spontaneous chromosome instability in lymphocytes from patients with multiple endocrine neoplasia, type 2 (MEN-2), whereas, with one exception, lymphocytes from MEN-2 patients were significantly more sensitive to chromosome damage by bleomycin and, to a lesser extent, MNNG than those from controls. The two highly competitive, monoclonal antibodies (MAs), UM 5.1 and UM 8.1, recognize on the E2 glycoprotein of Semliki Forest virus different determinants as indicated by the absence of cross-reactive anti-idiotypic antibodies in rabbit immune sera induced against these highly neutralizing MAs. Similar numbers of hilar Prox1-expressing cells were observed in PND30 and 60 Swiss Webster mice. These findings highlight the critical role of miR-137-c-Met nexus in CRC development and reveal Mecp2-regulated epigenetic silence causes the downregulation of miR-137 in colorectal adenoma and carcinoma. Study on the consistency of doctor-report outcomes and patient-report outcomes in symptoms of traditional Chinese Medicine: a small sample size trial in diabetics. Prevalence, virulence factor genes and antibiotic resistance of Bacillus cereus sensu lato isolated from dairy farms and traditional dairy products.

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Focus should be on high risk patients with (1) large polyps, severe dysplasia and advanced villous change, (2) synchronous polyps and invasive cancer, and (3) familial and other multiple polyposis disorders. Protective role of coffee in non-alcoholic fatty liver disease (NAFLD). Species differences in release of arachidonate metabolites in response to inhaled diluted diesel exhaust. Ethanol exposure for 4 h decreased biotinylated surface expression of GABA(A) receptor alpha1 subunits and reduced zolpidem (100 nM) enhancement of GABA-evoked currents. We calculated standardised mean differences (SMDs), with odds ratios (ORs) for dichotomous data. Anti-tumor effect of matrine combined with cisplatin on rat models of cervical cancer. Antibodies that compete with Notch1 ligand binding or that bind to the negative regulatory region can act as potent inhibitors of Notch1 signaling. There is a direct linear relationship between olanzapine dose and plasma concentration. NIHSS, MMSE, BBS, FMA, and stroke side predicted most HRQOL domains.

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In contrast to total phospholipid, a specific phospholipid class, ethanolamine plasmalogen, decreased from ectoderm to endoderm. An experimental study of the life-cycle of the fresh-water spongeEphydatia fluvitilis in its natural surroundings. The avidin-biotin immunoperoxidase and the immunogold-silver staining (IGSS) techniques were used. GC patients with positive cMet or FGFR2 gene amplification may potentially benefit from cMet or FGFR2 targeted therapies or combined targeted therapy. Data on two days 24-h dietary recall or record, anthropometry, physical activity and screen time were recorded. We probed the molecular mechanism of transcriptional regulation by MrpJ using transcriptional reporters and chromatin immunoprecipitation (ChIP). The behaviour of MMPs may be significantly different in men and women and may also differ in cases of cirrhosis of various aetiologies.

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