Halotestin 100 tabs (10 mg/1 tab)

Halotestin TN Pharma (Halotestin) improves strength and endurance. And in fact, this drug is the number one choice for weightlifters who are looking to increase their strength. When training before a competition, this drug can also be very useful in relieving the condition and burning fat. This is one of the strongest anabolic androgenic steroids, which is obtained from methyltestosterone with a modified structure in the chemical formula. This steroid has the highest anabolic and androgenic rating of 1900/850. Despite the fact that it has such high anabolic properties, its anabolic properties are considered almost zero! It acts more like an androgenic agent.

Long-term use of halotestin, like all 17-alkyd androgens, can cause very serious problems. There is a fairly large bouquet of possible side effects. Halotestin should not be taken concomitantly with antidiabetic drugs. In combination with nandrolone, primobolan depot, etc. leads to an increase in quality muscle mass.

Steroid Profile

• Anabolic activity - 1900% of testosterone
• Androgenic activity - 850% of testosterone (very high)
• Aromatization (conversion to estrogen) - absent
• Suppression of the hypothalamus-pituitary-testis axis - pronounced
• Liver toxicity - very high
• Method of administration - inside (tablets)
• Duration of action - 6-9 hours
• Detection time - 2 months

Pharmacological properties and effects of Halotestin

Fluoxymesterone was originally used as an agent with pronounced androgenic properties, used in the treatment of male hypogonadism and delayed puberty in men, for the treatment of breast cancer in women. Currently, medicine has abandoned its use. Halotestin is about five times more potent than methyltestosterone.

Halotestin (Fluoxymesterone) is similar in structure to methyltestosterone. It was developed by modifying testosterone at three positions: the 17 alpha methyl group, the 11-beta hydroxy group, and the 9 fluoro group.

The first chemical modification makes it possible to extend the half-life of the drug when taken orally and neutralize the destructive effect of the first passage through the liver, while maintaining the maximum concentration of the active substance in the blood.

The second modification is aimed at preventing the enzymatic transformation of the molecule by attaching aromatic rings to it, in other words, the drug does not turn into estrogens. The ability to block estrogen and prolactin receptors is supposed, which eliminates the risk of developing gynecomastia, edema and female-type fat deposition.

The last group determines the name of the drug (fluoxymesterone) and is aimed at increasing the androgenic activity of the drug (facilitates reduction in the 5a position, which leads to the formation of digitrotestosterone). This active form of the drug, which circulates in the blood, usually in small amounts, significantly exceeds the activity of testosterone and is able to bind strongly to androgen receptors in organ cells and muscle tissue.

It was also noted that the drug improves the aerobic performance of athletes in athletics. This is associated with the ability to stimulate erythropoiesis, the synthesis of hemoglobin. At the same time, a larger number of red blood cells is able to more efficiently transport oxygen to the cells.

Fluoxymesterone may be used for fat burning as it has been shown to enhance fatty acid oxidation in fast muscle fibers. Although for these purposes there are also safer and more effective anabolic agents, in particular winstrol, testosterone, oxandrolone.

Admission course

optimal dose of halotestin is 10 mg/day, it is not recommended to exceed a dose of 20 mg/day. In addition, long-term use of halotestin (more than 6 weeks) may not be safe for sexual function. Based on the ratio of benefits and harms, it is most advisable to conduct a course of Halotestin only before competitions in order to obtain two main effects of increasing physical strength and aggression.

Fluoxymesterone practically does not cause muscle tissue growth. Combinations of the drug with other anabolic agents also do not have special advantages.

Side effects

With an increased rate of formation of dihydrotestosterone from testosterone, hypertrophy and hyperplasia of the prostate, the development of prostate adenoma and, possibly, an increase in the likelihood of cancer are associated. The relatively easy ability of the drug to pass into dihydrotestosterone may further have adverse health effects in the context of its long-term use. Fluoxymesterone is estimated to be 19 times more anabolic than testosterone and 8.5 times more androgenic. Information about the activity of the drug was obtained experimentally.

Halotestin is toxic to the liver. Athletes who used the drug often report an increase and soreness of the organ. Studies show that the drug certainly leads to increased levels of liver enzymes, which indicates a steady process of increasing degradation of liver cells under the influence of fluoxymesterone. This fact is confirmed by literary sources.