Products

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

 

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Fluoxymestherone

 

Fluoxymesterone is an oral derivative of the male hormone testosterone. Unlike testosterone, Halotestex does not convert to estrogen. Therefore, estrogen-related side effects such as fat deposition, water retention, and gynecomastia do not occur. Fluoxymesterone has powerful androgenic properties. It is particularly noted for increased strength without significant additional weight gain. Side effects include aggression, oily skin, and virilization. Fluoxymesterone is considered to be very toxic to the liver, and thus must be used with caution and for short durations only.

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gallery/Fluo
gallery/Fluoxymesterone
gallery/Methandienone
gallery/Methelonone
gallery/Oxandrolona
gallery/Oxymetholona
gallery/BTS-PRO
gallery/Stanozolol

Methandienone

 

Methandienone does not react strongly with the androgen receptor, instead relying on activity not mediated by the receptor for its effects these include dramatic increases in protein synthesis, glycogenolysis and muscle strength over a short space of time. In high doses (30 mg or more per day), side effects such as gyndecomastia, high blood pressure, acne and male pattern baldness may begin to occur. The drug causes severe masculinising effect in women even at low doses. Without the administration of aromatase inhibitors, estrogenic effect will appear over time in men. Many users will combat the estrogenic side effects with Tamoxifen or clomid

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Methenolone

 

Methenolone Act is a mild oral anabolic with extremely low androgenic activity, meaning that there is only a minimal chance of typical steroid side-effects. It does not convert to estrogen and, therefore, estrogen-caused water retention and fat deposition will not occur from using it. Methenolone increases the conversion of protein to lean muscle tissue through its anabolic activity. Because Methenolone Act has virtually no androgen (i.e., masculinizing) effects, it can generally be used safely by women.

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Oxandrolone

 

Although Oxandrolone is an ooral steroid, and has been alpha/alkylated to survive oral ingestion and the first pass through the liver. It´s still relatively mild in that respect too..., the unique chemical configuration of oxandrolone both confers a resistance to liver metabolism as well as noticable anabolic activity. It would also appear that Oxandrolone appears not to exhibit the serious hepatotoxic effects (jaundice attributed to the c17alpha-alkylated AASs. Oxandrolone has even been used successfully in some stuidies to heal cutaneous wounds ot to improve respiratory function. Both of these novel propieties could make it a good choice for in--season use for boxers, Mixed MArtial Arts competitors, and other such athletes.

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Oxymetholone

 

Oxymetholone is a strong and efficient oral steroid with an androgenic effect that is quite effective in increasing muscle mass and strength. For this reason, dramatic increases in strength and muscle mass can be achieved in a short period of time, with a fairly significant increase in body weight. This anabolic steroid is widely used among bodybuilders and athletes..

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BTS-PRO

 

BTS-PRO - Sibutramine usually as sibutramide hydrochloride monohydrate, is an orally administred agent for the treatment of obesity it is a centrally-acting serotonin-norepinephrine reuplake inhibitor structurally related to amphetamines, althrough its mechanism of action is disctinct.

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Stanozolol

 

Stanozolol is prescribed for chronic infections, for conditions such as extensive surgery, (corticosteroid-induced Myopathy, decubitus ulcers, burns), or severe trauma wich require reversal of catabolic processes or protein-sparing effects. Th is used in addition to, and not as replacements for, conventional treatment for these disorders.

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