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Calutol (Bicalutamide)

Calutol belongs to a group of medicines known as anti-androgens. This means that it blocks the actions of male sex hormones called androgens and it also reduces the amount of male hormones (such as testosterone) that your body produces. In prostate cancer, the cancer cells need the male hormone testosterone to grow and multiply well. Hormone treatments like Calutol block the effect of testosterone on prostate cancer cells. This slows down the growth of the cancer. Calutol also helps to reduce symptom 'flares' and side-effects from other treatments which may be used for the cancer, or following surgery.

Other names for this medication:
Bicalutamide, Casodex, Bicalox, Bicalutamida, Bicusan, Bidrostat, Caluran, Calutide, Calutol, Capro, Cosudex, Imda, Lutamidal, Probic, Zolacos,

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Calutol is used with another medication (gonadotropin-releasing hormone (GnRH) agonists; such as leuprolide or goserelin) to treat metastatic prostate cancer (cancer that started in the prostate and has spread to other parts of the body). Calutol is in a class of medications called nonsteroidal antiandrogens. It works by blocking the effect of androgen (a male hormone), to stop the growth and spread of cancer cells.

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Compositional effects on the hydrogen storage properties of Mg(NH2)2-2LiH-xKH and the activity of KH during dehydrogenation reactions. Potentialities of preventing progressive and complicated myopia in the light of present-day knowledge Proteomic analyses of normal and glaucomatous human optic nerve were pursued for insights into the molecular pathology of primary open-angle glaucoma (POAG). Nutrient transfer across the equine placenta: correlation of structure and function.

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Taken together, HCQ increases the apoptosis of rheumatoid synoviocytes by activating caspase-3, and also sensitizes rheumatoid synoviocytes to Fas-mediated apoptosis. Olfactory bulbs were examined using freeze substitution, silver trapping of chloride and intensification techniques at light and electron microscopic level. We conclude that one of the mechanisms of tamoxifen in normal breast tissue include tipping of the angiogenic balance into an anti-angiogenic state and that flaxseed has limited effects on the pro-angiogenic factors whereas the anti-angiogenic endostatin may be modified by diet. Part of the IgE binding to mould and yeast allergen extracts is due to cross-reacting glycoproteins.

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Data collection included face-to-face interviews using a structured questionnaire. Med19 promotes bone metastasis and invasiveness of bladder urothelial carcinoma via bone morphogenetic protein 2. Immunized nematode-infected mice produced significantly lower levels of malaria-specific antibody than nematode-free mice produced. The tamsulosin side effects syncope and collapse normal serum-calcium and magnesium of the rat: their relation to sex and age.

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Although the link between CMV and IBD is not clear, the immunomodulator properties of the virus may play a role in the evolution of IBD. The frequency of X-ray-induced hprt mutations citalopram too high dose levothyroxine is slightly enhanced in the hamster mutant cells treated with the same dose. Inhibition of cholesterol synthesis ex vivo and in vivo by fluvastatin, a new inhibitor of 3-hydroxy-3-methylglutaryl coenzyme A reductase. Purification and characterization of a thermostable xylanase from Saccharopolyspora pathumthaniensis S582 isolated from the gut of a termite.

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Developmental changes in the cochlear hair cell mechanotransducer channel and their regulation by transmembrane channel-like proteins. It is well known that high frequency of tobacco consumption is associated with psychological dependence. IL-22 increased the phosphorylation of diclofenac epolamine vs lidocaine toxicity signal transducer and activator of transcription3, the expression of matrix metalloproteinase 9, and the invasion in PANC1 and BxPC3 cells in vitro while silencing of IL-22R RNA caused opposite effects.

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