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Fugerel (Flutamide)
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Flutamide

Fugerel is used together with a luteinizing hormone-releasing hormone (LHRH) agonist to treat metastatic (cancer that has spread) prostate cancer in men. Fugerel belongs to the group of medicines called antiandrogens. It works by blocking the effects of androgen (a male hormone), to stop the growth and spread of cancer cells. This medicine is available only with your doctor's prescription. This product is available in the following dosage forms: Capsule.

Other names for this medication:
Flutamide, Andraxan, Drogenil, Etaconil, Flutamida, Flutan, Ftda, Fugerel, Odyne, Prostamide, Prostandril, Tafenil,

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Impact of a program for venous thromboembolism prophylaxis in hospitalized patients in four hospitals in Salvador Study of emotional intelligence and empathy in medical postgraduates. The second area occurred largely 2-3 mm lateral to the midline, in the area of the nucleus reticularis pontis caudalis rostrally, and the nuclei reticularis gigantocellularis and parvocellularis caudally. Neonatal screening for sickle cell disease in France: evaluation of the selective process.

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Many fish use pectoral fins exclusively for locomotion, and pectoral fins in most fish are integral to generating force during maneuvering. The expression of CD44 is regulated by IL-1beta, but binding of HMGA1 potentiates the transactivation of the CD44 promoter. Anthropogenic chemicals in the aquatic environment are known to cause reproductive disturbances in vertebrate and invertebrate organisms by interfering with the endocrine systems. Study of genetic stability of human bone marrow multipotent mesenchymal stromal cells.

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A growth medium for the production of a bacterin for immunization against infectious coryza. Studies meeting pre-defined inclusion criteria were assessed independently by two researchers for methodological quality and data extracted. Gender and the double burden of economic and social disadvantages on healthy eating: cross-sectional study of older adults in the EPIC-Norfolk cohort. The introduction of a negative charge at position 41 through the replacement of Cys-41 by either aspartate or glutamate reduced the enzymatic activities to very low but measurable levels, suggesting a charge-charge repulsive interaction between these residues and possibly one or both of the phosphates of NAD.

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The thioredoxin reductase (TrxR) isoenzymes, TrxR1 in cytosol or nucleus and TrxR2 in mitochondria, are essential mammalian selenocysteine (Sec)-containing flavoenzymes with a -Gly-Cys-Sec-Gly active site. Symptoms of acute posttraumatic stress disorder in prostate cancer patients following radical prostatectomy.

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