Halotestin steroid information
Halotestin is an oral steroid. Its fluoxymesterone substance is a precursor of methyltestosterone which, through changes in the chemical structure, was made much more androgenic than test-osterone. The anabolic component of Halotestin is only slightly pronounced. Based on its characteristics Halotestin is used mainly when the athlete is more interested in a strength buildup rather than in a muscle gain. Powerlifters and weightlifters who must stay within a certain weight class often use Halotestin because they are primarily interested in a strength gain without adding body weight. In bodybuilding this drug is almost exclusively taken during preparation for a competition. With a lower body fat content Halotestin gives the bodybuilder a distinctive muscle hardness and sharpness. Although the muscle diameter does not increase, it appears more massive since the muscle den-sity is improved. The fact that a daily dose of up to 20 mg does not cause water and salt retention makes it even more desirable. During a diet, Halotestin helps the athlete get through difficult, intense training while increasing the aggressiveness of many us-ers. This is another reason why it is so popular among powerlifters, weightlifters, football players, and, in particular, boxers. The generally observed dose is normally 20-40 mg/day. Bodybuilders are usually satisfied with 20-30 mg/day while powerlifters often take 40 mg/day or more. The daily dosage is usually split into two equal amounts and taken mornings and evenings with plenty of fluids. Since the tablets are 1 7-alpha alky-lated, they can be taken during meals without any loss in effect.

The 11 beta-hydroxyl group also inhibits aromatization, making estrogen production impossible with this steroid. Estrogenic side effects such as water retention, fat fain and gynecomastia are similarly not a concern when taking this substance. Strong androgenic side effects are to be expected though, and in many cases are unavoidable. Oily skin and acne a very common for instance, at times requiring sensitive individuals to seek some form of topical or even prescription drug treatment to keep it under control. Clearly Halotestin is a strong androgen, and definitely one female athletes should stay away from. Masculinizing side effects can be intense, and may occur very rapidly with this substance. Hair loss is an additional worry, making Halotestin® a poor choice for those with an existing condition. Aggression may also become very pronounced with this drug. This effect is often desired by users looking to "harness" this in order to increase the intensity of workouts or a competition. Even women daring enough to take Dianabol should think twice about this compound, as virilization symptoms are most often permanent.

The "hardening" effect of Halotestin would therefore be somewhat similar to that seen with trenbolone, although it will be without the same level of mass gain. Clearly non-aromatizing androgens such as Halotestin and trenbolone can play an important role during contest preparations. Although Halotestin appears to be more androgenic than testosterone, the anabolic effect of it is not very strong. This makes it a great strength drug, but not the best for gaining serious muscle mass. The predominant effect seen when taking Halotestin is a harder, more dense look to the muscles without a notable size increase. It is therefore very useful for athletes in weight-restricted sports like wrestling, powerlifting and boxing. When the competitor has an acceptably low body fat percentage, the strong androgen level (in absence of excess estrogen) can elicit an extremely hard and defined ("ripped") look to the muscles. The shift in androgen/estrogen ratio additionally seems to bring about a state in which the body may be more inclined to burn off excess fat and prevent new fat storage. The strength gained from each cycle will not be accompanied by a great weight increase, allowing most competitors to stay within a specified weight range. Halotestin also makes an excellent drug for bodybuilding contest preparation.

The main concern with this steroid is that it can be a very toxic drug. This is due to the fact that fluoxymesterone is a 17 alpha alkylated compound, its structure altered to survive oral administration. As we discuss throughout this book, l7alpha alkylation can be very harsh to the liver. One should also resist the temptation to stack this drug with other alkylated orals if possible, and instead opt for orals without this alteration or esterified injectable compounds (which will not add to the strain on the liver). The possibility of damage is therefore a legitimate concern with Halotestin, especially when used at higher doses or for prolonged periods of time. The total daily dosage is likewise best kept in the range of 20-40mg, used for no longer than 8 weeks. After which an equally long break (at a minimum) should be taken from all c17-AA orals.

In cutting phases a mild anabolic such as Deca-Durabolin or Equipoise might be a good addition, as both provide good anabolic effect without excessive estrogen buildup. Here Halotestin will provide a well needed androgenic component, helping to promote a more solid and defined gain in muscle mass than obtained with an anabolic alone. A mix of 400-800mg Testosterone enanthate and 20-30mg Halotestin for example, should prove to be an exceptional stack for strength and muscle gain. This however would be accompanied by a more significant level of side effects, both compounds exhibiting strong androgenic activity in the body. Perhaps Primobolan Depot would even be a better choice, as with such a combination there is no buildup of estrogen (and likewise even less worry of water and fat retention). For mass we could alternately use an injectable testosterone.

Fluoxymesterone also seem to depress endogenous testosterone levels rather quickly with use, despite its complete lack of estrogen conversion. One therefore should consider ancillary drug use at the conclusion of each cycle in order to help restore the normal release of androgens in the body. Using a combination of HCG and Clomid/Nolvadex is of course the best option, the two drugs working well together to restore normal hormonal functioning. Although estrogen is not a problem with Halotestin, the use of an antiestrogen such as Nolvadex or Clomid is still indicated when discontinuing a cycle. Since HCG stimulates aromatase activity in the Leydig's cells, here Nolvadex/Clomid help by blocking the activity of any excess estrogen that may be produced. Afterward they will also block the inhibitory effect of endogenous estrogens on the hypothalamus, stimulating the enhanced release of gonadotropins and supporting the normal biosynthesis of testosterone.

So far, so good," you will say, but unfortunately, this is not so since Halotestin is a very toxic steroid. Besides Anadrol 50 and Methyltestosterone it is the oral steroid with the most side effects. Those who would like to try Halotestin should limit the intake to 4-6 weeks and take no more than 20-30 mg daily Fluoxymesterone puts extremely high stress on the liver and is thus potentially liver damaging. Other frequently- observed side effects are increased pro-duction of the sebaceous gland (which goes hand in hand with acne), nasal bleeding, headaches, gastrointestinal pain, and reduced pro-duction of the body's own hormones. Men become easily irritable and aggressive. Gynecomastia and high blood pressure caused by edemas do not occur with Halotestin. Do not be surprised, however, when on Halotestin's package insert you read the words "gynecomastia" and "edemas." This standard warning, due to legal provisions, is included in all strong androgenic steroids. Women should avoid Halotestin since it can cause substantol and in part irreversible virilization symptoms.