Halotestin (Fluoxymesterone-10mgs)

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Description

Halotestin (Fluoxymesterone-10mgs) is the popular commercial name of an oral steroid with the active ingredient Fluoxymesterone. This steroid is very similar to testosterone and is used to treat low testosterone levels in males, breast cancer in females, Delayed Puberty and Hypogonadism
Which represent steroid fluoxymesterone is characterized with high anabolic Halotestin and androgenic proprieties that are similar to testosterone.Being Widely used by athletes this drug is not strong mass building steroid. Its main purpose is to increase strength and aggression. Often Bodybuilders take fluoxymesterone in time they are preparing for Halotestin contests.Being both anabolic and androgenic Often this drug is used to treat breast cancer, hypogonadism. It is also known because of its propriety of blocking the estrogen production, that’s mean to help bodybuilders to Halotestin Avoid Such side effects as gyno or water retention. Making part of 7alpha-methylated compound, fluoxymesterone is toxic on liver. Halotestin Bodybuilders usually take 10-20 mgs per workout. Because of its powerful Halotestin androgenic proprieties women are not advised to take fluoxymesterone.After taking fluoxymesterone sportsmen report following side effects: liver damaging, increase production of the sebaceous gland, headaches, gastrointestinal pain.Fluoxymesterone is produced by many pharmaceutical companies such as: fluoxymesterone (Genesis), Halotestin (Hubei).

 

Halotestin Tablets contain fluoxymesterone, an androgenic hormone.

Fluoxymesterone is a white or nearly white, odorless, crystalline powder, melting at or about 240° C, with some decomposition. It is practically insoluble in water, sparingly soluble in alcohol, and slightly soluble in chloroform.

The chemical name for fluoxymesterone is androst-4-en-3-one, 9-fluoro-11,17-dihydroxy-17-methyl-, (11β,17β)-. The molecular formula is C20H29FO3 and the molecular weight 336.45.

Endogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorus, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein.

Androgens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor.

During exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH).

Inactivation of testosterone occurs primarily in the liver.

The half-life of fluoxymesterone after oral administration is approximately 9.2 hours.

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