Winstrol Tablets 500 10mg (Stanozolol)

Product Details:

What is Supplied:

Winstrol (Stanozolol) 500 x 10mg tablets.

Description:

Winstrol is the most widely recognized trade name for the drug stanozolol. Stanozolol is a derivative of dihydrotestosterone, chemically altered so that the hormone's anabolic (tissue-building) properties are greatly amplified and its androgenic activity minimized. Stanozolol is classified as an "anabolic" steroid, and exhibits one of the strongest dissocations of anabolic to androgenic effect among commercially available agents. It also cannot be aromatized into estrogens. Stanozolol is the second most widely used oral steroid, succeeded in popularity only by Dianabol (methandrostenolone). It is favored for its ability to promote muscle growth without water-retention, making it highly valued by dieting bodybuilders and competitive athletes.

Side Effects (Estrogenic):

Stanozolol is not aromatized by the body, and is not measurably estrogenic. An anti-estrogen is not necessary when using this steroid, as gynecomastia should not be a concern even among sensitive individuals. Since estrogen is the usual culprit with water retention, stanozolol instead produces a lean, quality look to the physique with no fear or excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are major concerns. Stanozolol is also very popular among athletes in combination strength/speed sports such as Track and Field. In such disciplines one usually does not want to carry around excess water weight, and may find the raw muscle-growth brought about by stanozolol to be quite favorable over the lower quality mass gains of aromatizable agents.

Side Effects (Androgenic):

Although Winstrol Stanozolol is classified as an anabolic steroid, androgenic side effects are still common with this substance. This may include bouts of oily skin, acne, and body/facial hair growth. Anabolic/androgenic steroids may also aggravate male pattern hair loss. Women are also warned of the potential virilizing effects of anabolic/androgenic steroids. These may include a deepening of the voice, menstrual irregularities, changes in skin texture, facial hair growth, and clitoral enlargement. Additionally, the 5-alpha reductase enzyme does not metabolize stanozolol, so its relative androgenicity is not affected by finastride. Stanozolol is a steroid with relatively low androgenic activity in relation to its tissue-building actions, making the threshold for strong androgenic side effects comparably higher than more androgenic agents such as testosterone, methandrostenolone, or fluoxymesterone.

Side Effects (Hepatotoxicity):

Stanozolol is a c17-alpha alkylated compound. This alteration protects the drug from deactivation by the liver, allowing a very high percentage of the drug entry into the bloodstream following oral adminstration. C17-alpha alkylated anabolic/androgenic steroids can be hepatotoxic. Prolonged or high exposure may result in liver damage. In rare instances life threatening dysfunction may develop. It is advisable to visit a physician periodically during each cycle to monitor liver function and overall health. Intake of c17-alpha alkylated steroids is commonly limited to 6 - 8 weeks, in an effort to avoid escalating liver strain.

When administering Oral Steroids we recommend you use our LIV-52 8 Week Steroid Liver Protector Kit which can be found under the category Liver Detoxification Kits.

Side Effects (Cardiovascular):

Anabolic/androgenic steroids can have deleterious effects on serum cholesterol. This includes a tendancy to reduce HDL (good) cholesterol values and increase LDL (bad) cholesterol values, which may shift the HDL to LDL balance in a direction that favors greater risk of arteriosclerosis. The relative impact of an anabolic/androgenic steroid on serum lipids is dependent on the dose, route of administration (oral vs. injectable) type of steroid (aromatizable or non-aromatizable), and level of resistance to hepatic metabolism. Stanozolol has a strong effect on the hepatic management of cholesterol due to its structural resistance to liver breakdown, non-aromatizable nature, and route of administration. Studies using an oral dose of 6mg per day for six weeks demonstrated a mean serum HDL reduction of 33% in healthy male weight-training subjects, which was combined with a 29% increase in serum LDL. Anabolic/androgenic steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and support left ventricular hypertrophy, all potentially increasing the risk of cardiovascular disease and myocardial infarction.

Side Effects (Testosterone Suppression):

All anabolic/androgenic steroids when taken in doses sufficient to promote muscle gain are expected to suppress endogenous testosterone production. Stanozolol is no exception, and is noted for its strong influence on the hypothalamic-pituitary-testicular axis. Clinical studies giving 10mg per day to healthy male subjects for 14 days caused the mean plasma testosterone level to fall by 55%. Without the intervention of testosterone-stimulating substances testosterone levels should return to normal within 1 - 4 months of drug secession. Note that prolonged hypogonadotrophic hypogonadism can develop secondary to steroid abuse, necessitating medical intervention.

We provide On Cycle and Post Cycle Therapy Kits in the category Cycle Therapy. If you are cycling Winstrol alone we recommend you to use either a Nolvadex alone or Clomid alone Post Cycle Therapy Kit. However, if you are stacking Winstrol with other anabolic/androgenic steroids such as Testosterone or Deca-Durabolin, we recommend you run the hCG On Cycle Therapy Kit and run a Clomid + Nolvadex 6 Week Post Cycle Therapy. This will help you to maintain/restore your endogenous testosterone production maximizing gains and minimizing gains lost when you conclude your cycle.

Administration (Men):

The usual dosage for physique- or performance-enhancing purposes is between 15mg and 25mg per day, or three to five 5mg tablets, taken for no longer than 6 - 8 weeks. Injectable Winstrol is generally recommended at a clinical dosage of one 50mg injection every 2 - 3 weeks. When used for physique- or performance-enhancing purposes, a dosage of 50mg every other day is most commonly applied. Veterinary stanozolol preparations with a larger particle size will be more slowly dispersed by the body, and are commonly given at 75mg every third day. Doses of 50mg per day with injectable stanozolol are not uncommon, although probably not advised. Note that injectable forms of the drugs are expected to have, milligram for milligram, a greater anabolic effect than oral.

Stanozolol is often combined with other steroids for a more dramatic result. For example, while bulking one might opt to add in 200 - 400mg of testosterone ester (cypionate, enanthate, or propionate) per week. The result should be a considerable gain in new muscle mass, with a more comfortable level of water and fat retention than if taking a higher dose of testosterone alone. For dieting phases, one might alternately combine stanozolol with a non-aromatizing steroid such as 150mg per week of a trenbolone ester or 200 - 300mg of Primobolan (methenolone enantahte). Such stacks are highly favored for increasing definition and muscularity. An in-between (lean mass gain) might be to add in 200 - 400mg of a low estrogenic compound like Deca-Durabolin (nandrolone decanoate) or Equipose (boldenone undecylenate).

Administration (Woman):

When Winstrol used for physique- or performance enhancing purposes, a dosage of 5mg to 10mg daily is most common, taken for no longer than 4 - 6 weeks. Injectable Winstrol is generally recommended at a clinical dose of 50mg every 2 - 3 weeks. The injectable is usually not advised for women for physique- or performance-enhancing purposes, as it allows for less control over blood hormone levels. Those women who absolutely must use the injectable commonly administer 25mg every 3 or 4 days. Although this compound is weakly androgenic, the risk of virilization symptoms cannot be completely excluded, even at therapeutic doses.