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Halotestex Tablets

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Alternative names:

Halotestex, Fluoxymesterone, Halotestin, Android-F, Ultandren, Hysterone Tabs, Stenox, Ora-Testryl, Halobolic 10

Supplier

British Dragon

Packaging

10 mg 100 tabs

Description:

Halotestex is the British Dragon brand name for the steroid fluoxymesterone. Structurally fluoxymesterone is a derivative of testosterone, differing from our base androgen by three structural alterations (specifically 17alpha-methyl, 11 beta-hydroxy and 9-fluoro group additions). The result is a potent oral steroid that exhibits extremely strong androgenic properties. This has a lot to due with the fact that it is derived from testosterone, and as such shares important similarities to this hormone. Most importantly, like testosterone Halotestex appears to be a good substrate for the 5-alpha reductase enzyme. This is evidenced by the fact that a large number of its metabolites are found to be 5-alpha reduced androgens, which coupled with its outward androgenic nature, suggests it is converting to a much more active steroid in androgen responsive target tissues such as the skin, scalp and prostate.

The 11beta-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. Hair loss is an additional worry, making Halotestex 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. Clearly Halotestex 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. Even women daring enough to take Dianabol should think twice about this compound, as virilization symptoms are most often permanent.

Although Halotestex 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 Halotestex is a harder, more dense look to the muscles without a notable size increase. It is therefore very useful for athletes in eight-restricted sports like wrestling, power lifting and boxing. 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. Halotestex also makes an excellent drug for bodybuilding contest preparation. 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 androgenestrogen 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 "hardening" effect of Halotestex 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 Halotestex and trenbolone can play an important role during contest preparations.

The main concern with Halotestex 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 page, alpha alkylation can be very harsh to the liver. The possibility of damage is therefore a legitimate concern with Halotestex, especially when used at higher doses or for prolonged periods of time. The total daily dosage is likewise se best kept in the range of 20-40 mg, used for no longer than 8 weeks. After which an equally long break (at a minimum) should be taken from all c17-AA orals. 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).

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 Halotestex 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. 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. A mix of 400-800 mg testosterone enanthate and 20-30 mg Halotestex 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.

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 ClomidNolvadex is of course the best option, the two drugs working well together to restore normal hormonal functioning. Although estrogen is not a problem with Halotestex, 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 NolvadexClomid 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.

Since Halotestex is only used for a few specific purposes, it is not in high demand among athletes. Likewise it is not a very popular item on the black market. Investing in the manufacture of a counterfeit version would probably not pay off well, no doubt the reason we haven't seen any yet. All of the various forms of Halotestex could therefore be assumed legitimate when found in circulation. Currently the most popular item found on the black market is the Stenox brand from Mexico, sold in boxes of 20 tablets. Although the dosage of these tablets is only 2.5 mg, the low price usually asked for this preparation more than compensates. Overall, Halotestex is an effective steroid for a narrow range of uses, and is probably not the most ideal product for the recreational user.

Side effects:

llmedicines may cause side effects, but many people have no, or minor,side effects. Check with your doctor if any of these most COMMON sideeffects persist or become bothersome:

Changes insexual desire; absence of menstrual flow; acne; breast swelling ortenderness; deepening of voice; growth of facial hair; headache;irregular menstrual flow; mood changes; painful, prolonged erection;swelling of the clitoris.

Seek medical attention right away if any of these SEVERE side effects occur:

Severeallergic reactions (rash; hives; difficulty breathing; tightness in thechest; swelling of the mouth, face, lips, or tongue); ankle swelling;change in skin color; nausea; vomiting; weight gain.

Thisis not a complete list of all side effects that may occur. If you havequestions or need medical advice about side effects, contact yourdoctor or health care provider.
Effects with other drugs

Androgensmay increase sensitivity to oral anticoagulants. Dosage of theanticoagulant may require reduction in order to maintain satisfactorytherapeutic hypoprothrombinemia.

Concurrent administration of oxyphenbutazone and androgens may result in elevated serum levels of oxyphenbutazone.

In diabetic patients, the metabolic effects of androgens may decrease blood glucose and, therefore, insulin requirements.