1. What is Halotestin?
Fluoromethandrostenolone is a powerful anabolic steroid, a steroid derived from testosterone, more precisely, the end product of structural changes of methandrostenolone; Halotestin is a 17AA steroid with hepatotoxicity, half-life 6-8 hours, initially introduced in the late 50s under the trade name “Halotestin,” and was originally advertised as having various medical effects. It was initially introduced in the late 1950s under the trade name “Halotestin.” It was initially advertised as having various medical effects, initially used to treat muscle atrophy, male androgen deficiency disorders, muscle tissue repair, malnutrition, and fracture healing. It was also used to treat problems caused by long-term cortisone use, paraplegia (hemiplegia), and breast cancer. It has been effective in treating burns, a rare approved medical treatment for post-menopausal osteoporosis in women, as well as for female breast cancer and male sex hormone deficiency. However, it is not commonly used in treatment.
In the field of competitive sports Halo is known in the sports world as one of the most powerful and fastest-acting steroids. Its anabolic rate is extremely high at 1900, and the androgenic rate at 850. The structural addition of hydroxyl groups to carbon 11 inhibits aromatization and greatly enhances androgenic properties; the aforementioned anabolic rate of 1900 is actually substantial at 0 in the human body and works mainly through androgenic activity. So fluoxymesterone does not allow the user to increase muscle mass; Halotestin is known for the strength to gain it brings to the user; often in the fat loss cycle, the last phase of the athlete a few weeks before the competition, halotestin can improve the athlete’s condition, and excessive diet harsh period, when it comes to side effects compared to other steroids, it is indeed more “prominent” But the harder, the more effective than the other, the more toxic, that’s the constant truth.
Here is to emphasize: use of fluoxymesterone avoid other 17aa toxic oral use together
2. Fluoxymesterone action?
It has a powerful effect in raising red blood cells; it can increase the number of red blood cells in the blood, and red blood cell pressure, which is the key to improving muscle endurance and strength. It also has a fat loss effect; it helps control fatty acid oxidation in the liver and increases the number of mitochondria in fast muscle fibers; plus, it works with red blood cells to give people with low body fat percentage a better visual shock.
Fluorometholone is suitable for powerlifters fighters love to use in the weeks before the competition for strength growth “strongest” without one; for weeks before the competition, bodybuilders in power to improve and aggression to improve the characteristics, and it’s helpful in the late diet brutal description of not enough to eat at the same time the last stage also energy drained existence of powerlessness, Halotestin helps you through the final phase, making you drier and tighter, needing low sebum to have a change in status. Otherwise, it is meaningless.
The effect of testosterone is very powerful, he has a special purpose, the main effect is to increase the strength and “aggression” “aggressive” impact, more of this “aggression” used in training will make You are more focused on training passion for making you more powerful, which will not change human nature, will not let you use the ability to lose judgment of right and wrong, if the attack on others, which has long been eliminated, no one wants to use to become a mad dog. Still, for people who are already jerks irritable, use may change the bad jerk, so weigh their suitability? For the sensible person, this “beast aggression” will make him more focused, efficient, and passionate before the game.
Side effects (estrogen):
Fluorometholone is not aromatized by the body and does not measure estrogenicity. Anti-estrogen is unnecessary when using this steroid, as gynecomastia does not occur much in sensitive individuals. Since estrogen is a common cause of water maintenance, this steroid can produce a lean body appearance without the fear of excess subcutaneous fluid retention. This makes it a very beneficial steroid for the cutting cycle when water and fat storage are the main concerns.
Side effects (androgens):
Fluoxymesterone is classified as an androgen. Androgenic side effects are common for this substance, and side effects may include oily skin, acne, and body/facial hair growth flare-ups. Anabolic/androgenic steroids may also aggravate male pattern baldness. Men who are genetically prone to male pattern baldness may need to choose a gentler, less androgenic anabolic steroid. As potent as androgens are, such steroids may also increase aggressiveness. Women are also warned about the potential worsening effects of anabolic/androgenic steroids. These may include deepening of the voice, irregular menstruation, changes in skin texture, facial hair growth, and clitoral enlargement.
Fluoxymesterone appears to be a good substrate for 5-alpha reductase. Many of its metabolites are derived from 5-alpha-reduced androgens, so this point can be demonstrated, as can its exo-androgenic nature, which suggests that this steroid is being converted into a more active steroid in androgen-responsive target tissues. Concurrent use of finasteride or dutasteride reduces the relative androgenicity of fluoxymesterone.
It is also noteworthy that fluoxymesterone has been shown to have general androgenic properties. In human studies published in 1961, steroids showed a stronger tendency to promote penile enlargement than other androgenic effects such as hair growth, libido, and voice changes. Fluoxymesterone provides a slightly different androgenic state than testosterone, thus proving that it is somewhat possible to actually formulate the drug’s effects within a broad range of androgenic actions. Fluoxymesterone is still considered an androgen, but studies like the one described above suggest that it may not provide androgenic biological activity equivalent to testosterone.
Side effects (hepatotoxicity):
Fluoromethandrostenolone is a c17-alpha alkylated compound. This alteration protects the drug from hepatic inactivation, allowing a very high percentage of the drug to enter the bloodstream after oral administration. c17-alpha alkylated anabolic/androgenic steroids may be hepatotoxic. Prolonged or high levels of use may lead to liver damage. In extreme cases, life-threatening dysfunction may occur. Regular visits to the physician during each cycle are recommended to monitor liver function and overall health. c17-alpha alkylated steroid ingestion is typically limited to 6-8 weeks to avoid elevated liver strain. A study of nine male subjects taking 20 mg of fluoxymesterone for two weeks showed it resulted in the majority of patients (6/9) noting abnormal sulfoximine metabolism (BSP) retention, which is a marker of hepatic stress.
The use of liver detoxification supplements such as Liver Stabilizer, Liv-52, or Essentiale Forte is recommended when taking any hepatotoxic anabolic/androgenic steroids.
Side effects (cardiovascular):
Anabolic/androgenic steroids can have harmful effects on serum cholesterol. This includes a tendency to lower HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may convert HDL to LDL in balance, leading to a greater risk of atherosclerosis. The relative effects of anabolic/androgenic steroids on serum lipids depend on the dose, route of administration (oral vs. injectable), type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Fluoxymesterone is structurally resistant to hepatic cholesterol, and the route of administration is highly productive on the liver. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and cause left ventricular hypertrophy, which may increase cardiovascular disease and myocardial infarction risk.
To help reduce cardiovascular stress, it is recommended to maintain an active cardiovascular exercise program and minimize the intake of saturated fat, cholesterol, and simple carbohydrates during AAS use. Supplementation with fish oil (4 grams per day) and natural cholesterol/antioxidant formulas such as Lipid Stabil or products with similar ingredients are also recommended.
Side effects (testosterone suppression):
All anabolic/androgenic steroids are expected to inhibit endogenous testosterone production when taken at doses sufficient to promote muscle gain. Without the intervention of testosterone-stimulating substances, testosterone levels should return to normal within 1-4 months of the drug split. Long-term muscular dystrophy hypogonadism may occur secondary to steroid abuse and require medical intervention.
Studies in which nine healthy male subjects were given up to 12 weeks of 10 mg, 20 mg, or 30 mg of fluoxymesterone have demonstrated strong suppression of endogenous testosterone levels but inconsistent effects on gonadotropin levels. Although not fully understood, fluoxymesterone is thought to have a direct inhibitory effect on inhibitory gonadotropin-mediated testicular steroidogenesis.
