Archive | August, 2010

Sustanon 250 (Injectable)

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Sustanon 250 (Injectable)

Posted on 31 August 2010 by admin

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Alternative names:

Sostenon 250
Sustenon 250

Veterinary products:

Deposterone

Therapeutic dose:

1 mL every 3 weeks

Description

Sustanon contains four different testosterones:
Testosterone propionate 30 mg
Testosterone phenylpropionate 60 mg
Testosterone isocaproate 60 mg
Testosterone decanoate 100 mg

Sustanon 250 has considerable anabolic and androgenic properties. It was designed to maximize the synergistic effect of using four testosterones. The variation in half-life times of the testosterones means that the product is fast-acting and remains effective for several weeks. Total plasma testosterone levels peak approximately 24–48 hours after administration. Plasma testosterone levels return to the lower limit of the normal range in males in approximately 21 days. Sustanon is predominantly used as testosterone  replacement therapy in the treatment of male hypogonadal disorders such as eunuchoidism (following castration), hypopituitarism, endocrine impotence, decreased libido and disorders of spermatogenesis. Testosterone therapy may also be indicated for the prevention and treatment of osteoporosis in hypogonadal males.

Street information

Sustanon 250 has a reputation for being very effective at increasing both size and strength. The adverse effects of water retention and aromatization leading to  gynaecomastia are considered to be less pronounced than in long-acting testosterone injections.



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Stanozolol (Injectable)

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Stanozolol (Injectable)

Posted on 31 August 2010 by admin

Anabolex Dianabol Dbol D bol Methandrostenolone Steroid

Alternative names:

Androstanazole
Methylstanazole

Proprietary names:

Stromba (50 mg/mL)
Stromaject (50 mg/mL)
Winstrol Depot (50 mg/mL)

Veterinary product:

Winstrol V (50 mg/mL)

Therapeutic dose:

Men: 25-50mg per day

Description

Stanozolol is considered by many steroid users to have relatively low androgenic properties. As it is a water-based, injectable steroid, it has a relatively short half-life.

This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth. The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a good, reliable builder of muscle. Its anabolic properties could even be comparable to Dianabol, but Stanozolol does not have the same tendency for water retention. There are many injectable versions of this steroid produced.

Since stanozolol is not capable of converting into estrogen, an anti-estrogen is not necessary when using this steroid, gynecomastia is not a concern even among the most sensitive individuals. Since estrogen is also the cause of water retention, instead of bulk look, Stanozolol produces a lean, quality look with no fear of excess subcutaneous fluid retention. This makes it a great steroid to use during cutting cycles, when water and fat retention are a major concern. It is also very popular among athletes in combination strength/speed sports such as Track and Field.

The usual dosage for men is 25-50mg per day. It is often combined with other steroids depending on the desired result. For bulking purposes, a stronger androgen like testosterone, Dianabol or Anadrol is usually added. Here Stanozolol will balance out the cycle a bit, giving us good anabolic effect with lower overall estrogenic activity than if taking such steroids alone. The result should be a considerable gain in new muscle mass, with a more comfortable level of water and fat retention. For cutting phases Stanozolol can be combined with a non-aromatizing androgen such as trenbolone or Halotestin. Such combinations should help bring about the strongly defined, hard look of muscularity so sought after among bodybuilders. Older, more sensitive individuals can add compounds like Primobolan, Deca-Durabolin or Equipoise when wishing to stack this steroid. Here they should see good results and fewer side effects than with standard androgen therapies.

Women usually take around 5-10mg daily. Although female athletes usually find stanozolol very tolerable, the injectable version is usually off limits.

With the structural (c17-AA) alteration, the tablets will also place a higher level of stress on the liver than the injectable (which avoids the “first pass”). During longer or higher dosed cycles, liver values should therefore be watched closely through regular blood work. Although less common, there is still a possibility of liver damage occuring with the injectable form. While it does not enter the body through the liver, it is still broken down by it, providing a lower (but more continuous) level of stress. Such stress would of course be increased with the addition of other c17-AA oral compounds to a cycle of Winstrol. When using such combinations, cautious users would make every effort to limit the length of the cycle (preferably 6 to 8 weeks) and take some form of liver protectants. It should also be noted that both versions of Winstrol have been linked to strong adverse changes in HDL/LDL cholesterol levels. This side effect is common with anabolic steroid therapy, and obviously can become a health concern as the dose/duration of intake increase above normal. The oral version should have a greater impact on cholesterol values than the injectable due to the method of administration, and may therefore be the worse choice of the two for those concerned and this side effect.

The oral use of stanozolol can also have a profound impact on levels of SHBG (sex hormone-binding globulin). This is a characteristic of all anabolic/androgenic steroids, however its potency and form of administration make Stanozolol particularly noteworthy in this regard. Since plasma binding proteins such as SHBG act to temporarily constrain steroid hormones from exerting activity, this effect would provide a greater percentage of free (unbound) steroid hormone in the body. This may amount to an effective mechanism in which stanozolol could increase the potency of a concurrently used steroid. To further this purpose one could also addition Proviron, which has an extremely high affinity for SHBG. This affinity may cause Proviron to displace other weaker substrates for SHBG (such as testosterone), another mechanism in which the free hormone level may be increased. Adding Stanozolol and Proviron to your next testosterone cycle may therefore prove very useful,, markedly enhancing the free state of this potent muscle building androgen.

Street information

The injectable versions of Stanozolol (both human and veterinary) are far more popular than the tablet forms. Although gains are considered to be achieved slowly with this product, its low incidence of water retention makes it popular as a pre-contest drug.

Stromba has a reputation for being fast-acting and quickly excreted from the body, as it is water based rather than oil based. Therefore, it is common to find it being injected several times a week.



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Stanozolol (Oral)

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Stanozolol (Oral)

Posted on 31 August 2010 by admin

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Alternative names:

Androstanazole
Methylstanazole

Proprietary names:

Stromba (5 mg)
Winstrol (2 mg)

Therapeutic dose:

2.5–10 mg daily

Stanozolol has anabolic and androgenic properties and has been used in the treatment of vascular manifestations of Behçet’s syndrome and in the management of hereditary angio-oedema. Stanozolol, when given for prolonged periods, has been associated with elevated liver function results as it is a 17-alpha-alkylated compound.

This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth. The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a ggod, reliable builder of muscle. Its anabolic properties could even be comparable to Dianabol, but Stanozolol does not have the same tendency for water retention. Stanozolol also contains the same c17 methylation we see with Dianabol, an alteration used so that oral administration is possible. To spite this design however, there are many injectable versions of this steroid produced.

Since stanozolol is not capable of converting into estrogen, an anti-estrogen is not necessary when using this steroid, gynecomastia is not a concern even among the most sensitive individuals. Since estrogen is also the cause of water retention, instead of bulk look, Stanozolol produces a lean, quality look with no fear of excess subcutaneous fluid retention. This makes it a great steroid to use during cutting cycles, when water and fat retention are a major concern. It is also very popular among athletes in combination strength/speed sports such as Track and Field.

It is often combined with other steroids depending on the desired result. For bulking purposes, a stronger androgen like testosterone, Dianabol or Anadrol is usually added. Here Stanozolol will balance out the cycle a bit, giving us good anabolic effect with lower overall estrogenic activity than if taking such steroids alone. The result should be a considerable gain in new muscle mass, with a more comfortable level of water and fat retention. For cutting phases Stanozolol can be combined with a non-aromatizing androgen such as trenbolone or Halotestin. Such combinations should help bring about the strongly defined, hard look of muscularity so sought after among bodybuilders. Older, more sensitive individuals can add compounds like Primobolan, Deca-Durabolin or Equipoise when wishing to stack this steroid. Here they should see good results and fewer side effects than with standard androgen therapies.

With the structural (c17-AA) alteration, the tablets will also place a higher level of stress on the liver than the injectable (which avoids the “first pass”). During longer or higher dosed cycles, liver values should therefore be watched closely through regular blood work. Although less common, there is still a possibility of liver damage occuring with the injectable form. While it does not enter the body through the liver, it is still broken down by it, providing a lower (but more continuous) level of stress. Such stress would of course be increased with the addition of other c17-AA oral compounds to a cycle of Stanozolol. When using such combinations, cautious users would make every effort to limit the length of the cycle (preferably 6 to 8 weeks) and take some form of liver protectants. It should also be noted that both versions of Stanozolol have been linked to strong adverse changes in HDL/LDL cholesterol levels. This side effect is common with anabolic steroid therapy, and obviously can become a health concern as the dose/duration of intake increase above normal. The oral version should have a greater impact on cholesterol values than the injectable due to the method of administration, and may therefore be the worse choice of the two for those concerned and this side effect.

The oral use of stanozolol can also have a profound impact on levels of SHBG (sex hormone-binding globulin). This is a characteristic of all anabolic/androgenic steroids, however its potency and form of administration make Stanozolol particularly noteworthy in this regard. Since plasma binding proteins such as SHBG act to temporarily constrain steroid hormones from exerting activity, this effect would provide a greater percentage of free (unbound) steroid hormone in the body. This may amount to an effective mechanism in which stanozolol could increase the potency of a concurrently used steroid. To further this purpose one could also addition Proviron, which has an extremely high affinity for SHBG. This affinity may cause Proviron to displace other weaker substrates for SHBG (such as testosterone), another mechanism in which the free hormone level may be increased. Adding Stanozolol and Proviron to your next testosterone cycle may therefore prove very useful,, markedly enhancing the free state of this potent muscle building androgen.

Street information

Stanozolol tablets have a reputation for causing gastrointestinal discomfort after  prolonged use. Both the tablets and the injection form are not considered to aromatize. Tablets are often taken in divided doses to reduce the gastric irritation. This practice is popular with female users, as it reduces the risks of virilization that is associated with large amounts of androgens in the female system.



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Methenolone Enanthate (Injectable)

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Methenolone Enanthate (Injectable)

Posted on 31 August 2010 by admin

Anabolex Dianabol Dbol D bol Methandrostenolone Steroid

Alternative names:

Metenolone enantate
Metenolone enanthate
Methenolone oenanthate

Proprietary names:

Primobolan Depot (50 mg/mL, 100 mg/mL)

Description

Methenolone enanthate is the long-acting injectable version of Primobolan tablets (methenolone acetate).

Street information

Primobolan Depot has a reputation for having low androgenic properties causing little aromatization, water retention or liver damage. It is generally considered to be a much milder Anabolic Steroid than nandrolone decanoate.



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