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CAUTION SHOULD BE EXERCISED WHEN COUMARIN ANTICOAGULANTS ARE GIVEN IN CONJUNCTION WITH FENOFIBRATE TABLETS.
Low-density lipoprotein reduction: Is the risk worth the benefit?
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Phase I randomized, double-blind pilot study of micronized resveratrol (SRT501) in patients with hepatic metastases--safety, pharmacokinetics, and pharmacodynamics.
Aging, obesity, and the onset of renal disease also promote an increase in the prevalence of hypertension.
Life-years gained from modern cardiological treatments and population risk factor changes in England and Wales, 1981-2000.
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Risk factor specific sections follow, with the graded conclusions of the evidence review, normative tables and age-specific recommendations.
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In the presence of proliferative diabetic retinopathy (PDR) or severe non-PDR (NPDR), vigorous aerobic or resistance exercise may be contraindicated because of the risk of triggering vitreous hemorrhage or retinal detachment ().
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It may be gradually increased every 4-8 weeks up to maximal dose of Tricor 160 mg a day if triglycerides do not improve.
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The combined use of fenofibrate (fenofibrate (fenofibrate) ) and HMG-CoA reductase inhibitors should be avoided unless the benefit of further alterations in lipid levels is likely to outweigh the increased risk of this drug combination.
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DPP are cost-effective (), and actual cost data from the DPP and DPPOS confirm that lifestyle interventions are highly cost-effective ().
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In patients with hypertriglyceridemia and normal cholesterolemia with or without hyperchylomicronemia, treatment with fenofibrate at dosages equivalent to 150 mg fenofibrate per day decreased primarily very low density lipoprotein (VLDL), triglycerides and VLDL cholesterol.
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Cardiovascular Prevention in Clinical Practice (ESC and German Guidelines 2007).
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The A1C has several advantages to the FPG and OGTT, including greater convenience (since fasting is not required), evidence to suggest greater preanalytical stability, and less day-to-day perturbations during periods of stress and illness.
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Effects of K-877, a novel selective PPARα modulator (SPPARMα), in dyslipidaemic patients: A randomized, double blind, active- and placebo-controlled, phase 2 trial.
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The evidence for the first 4 bullets is reviewed in this section, while the evidence surrounding interventions for identified risk factors is addressed in the RF-specific sections of the guideline to follow.
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Results also point to a possible role for ongoing use of fenofibrate to treat diabetic retinopathy, if taken regularly.
Nuclear Hormone Receptor Modulators for the Treatment of Diabetes and Dyslipidemia.
Grimm, receiving consulting and lecture fees and grant support from Pfizer, Merck, and Novartis, consulting and lecture fees from Takeda, and lecture fees from AstraZeneca, Forest Laboratories, and Schering-Plough; Dr.
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The effects of fenofibrate on serum triglycerides were studied in two randomized, double-blind, placebo-controlled clinical trials of 147 hypertriglyceridemic patients.
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