Trenbolone – a powerful anabolic steroid used previously in veterinary medicine to increase muscle mass and appetite in livestock.

To increase the duration of action Trenbolone is not used in its original form, as a rule esterified derivatives are used: trenbolone acetate (with the shortest duration of action) and trenbolone enanthate. After introduction into the muscle, trenbolone esters are gradually decomposed by plasma lipase, providing a prolonged supply of the active substance to the blood. It has a powerful anabolic effect, but has many side effects, so it is not the best choice.

Each ml of Trenbolone Mix contains 150 mg of Trenbolone Acetate 50mg, Trenbolone Hexahydrobenzylcarbonate 50mg, Trenbolone Enanthate 50mg.

Boldenone (Equipoise) – can be used instead of primobolan, however, it should be noted that it significantly increases appetite.

Boldenone was created as a long-acting version of methandrostenolone, however, a steroid was obtained that has completely different properties, despite the chemical similarity of the molecules. Boldenone is a Dianabol molecule that lacks the 17-alpha-methyl group (this part of the molecule allows Dianabol to pass through the liver without breaking down).

Boldenone Equipoise is chemically a testosterone molecule that has a double bond between 1 and 2 carbon atoms. This modification made boldenone as powerful as testosterone in its anabolic properties, while the androgenic properties of the drug are half as pronounced. However, practice shows that Equipoise allows you to get lower results than the equivalent amount of testosterone.

Also, this connection inhibits the process of aromatization (conversion to estrogen) of the drug. Athletes almost never notice side effects of boldenone associated with estrogen (gynecomastia, edema, increased pressure), even if the dose reaches 1 g per week. This means that during the course of Equipoise there is no need to take antiestrogens.

Low androgenic activity allows women to use equipoise. Virilization phenomena occur quite rarely, compared with other drugs. Boldenone is one of the few injectable drugs that can be used in female bodybuilding with the least risk of side effects.

Strombafort (active ingredient – stanozolol, also known as Stanoger, Winstrol, Stanover, Nabolik, Stanazolik, Strombajekt, Stromba, Menabol, Stanol, Terabon, Cetabone) is an anabolic steroid available in tablets and solution for injection (Strombaject Aqua). This is a synthetic 17α-methylated steroid, a derivative of dihydrotestosterone, which differs greatly from natural steroids by the addition of + 3,2-pyrazole. Unlike most injectable forms, stanozolol is an aqueous suspension of a free substance.

Strombafort in tablets has high bioavailability and stability (it does not break down in the liver when passed) due to the alkyl group in alpha-17 position, however, this makes stanozolol in tablets toxic to the liver. However, the injection form is also not without this drawback, the difference in toxicity and bioavailability of both forms of the steroid is minimal.

Strombafort differs in greater availability and much lower cost from Oxandrolone. The course is structured in a similar way. To reduce liver toxicity, an injection form (50 mg / day) can be used, since when taken orally, the entire drug passes through it, while the suspension is only partially (from the systemic circulation). Although, on the other hand, the indicated oral dosage is not hazardous to health, while injections are very painful and abscesses develop relatively often.

Strombafort tablet can be consumed in 2-3 doses (most in the first half of the day) on an empty stomach. Optionally, after a cycle, you can drink hepatoprotectors to restore the liver.

Chorionic gonadotropin – it is a hormone that is produced by the placenta during pregnancy, and then is excreted unchanged in the urine, from where it is extracted and purified to obtain drugs. Chorionic gonadotropin has the same biological effects as luteinizing hormone, which is formed in the pituitary gland.

In bodybuilding, the use of chorionic gonadotropin is justified and even necessary during a course of anabolic steroids for the prevention of testicular atrophy. In this case, its use is safe, since the dose of the drug is much lower, in addition, chorionic gonadotropin eliminates some side effects of anabolic steroids, as well as preserve the gained muscle mass.

This drug has many controversial administration protocols. However, recent studies have shown a clear need for the use of gonadotropin in long courses (more than 6 weeks). This allows you to recover much faster after the course. The recommendations in the courses are based on the experience of Western andrologists. If gonadotropin was not administered on the course, blast-therapy is necessary.

Cabergoline (Dostinex) – inhibits the secretion of prolactin, which allows you to completely eliminate the negative progestin effect of Nandrolone on sexual function, reduce the risk of gynecomastia.

Cabergoline (active ingredient) – suppresses the secretion of prolactin, in addition to enhances libido and erection, significantly reduces the recovery time between sexual intercourse, and also lowers blood pressure. Cabergoline belongs to the ergot alkaloids derivative, according to the mechanism of action – a dopamine (D2) receptor agonist. It is a more modern and safe analogue of bromocriptine.

The drug allows you to almost completely eliminate the main side effects of such steroids as Nandrolone Decanoate (Deca) and Trenbolone. One of the effects caused by a decrease in prolactin concentration is a decrease in fluid retention in the tissues, which gives an increase in dry muscle mass.

Aromatase inhibitors (Anastrozol, Exedrol, Letrozol)- are required even at low dosages of testosterone, since the level of aromatization of testosterone is high, so there is a need to prevent estrogenic side effects (fluid accumulation, gynecomastia, suppression of the axis of the hypothalamus-pituitary-testes). Low dosages of anastrozole are used, which allow maintaining the level of estrogen necessary for the body, while increasing relief and accelerating recovery. Confirmation are numerous reviews of Western athletes and qualified specialists. Ideally, the intake of IA is carried out under the control of the tests (they are prescribed if the level of estradiol is elevated), but it should be remembered that gynecomastia is often irreversible. An indirect sign of excessive estrogen suppression is a decrease in libido and erectile dysfunction, in which case the dosage of IA should be reduced.

Clomed – is the basis of post-cycle therapy, which begins 3-5 days after the final injection. Clomed is needed to restore the axis of the hypothalamus-pituitary-testes, which is suppressed by anabolic drugs. The drug activates the secretion of endogenous testosterone.

Tamoxifen should not be used. Tamoxifen is not recommended in this case, since studies have shown the ability to increase the number and sensitivity of progesterone receptors.