https://hypermuscles.com/ Mon, 06 Jul 2026 01:34:28 +0000 MyBB https://hypermuscles.com/showthread.php?tid=1387 Mon, 07 Mar 2011 06:36:15 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1387
It has gained popularity in the bodybuilding community as a diuretic and muscle defining drug. Individuals interested in using the drostanolone propionate are those that are looking to add muscle hardness and density to their physiques, nearly always for the purpose of bodybuilding competitions.

Drostanolone propionate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.[citation needed] However, an already rather low body-fat level is needed for it to take full effect.[citation needed] Drostanolone propionate can promote increased strength while keeping body fat the same or even lowering it, something can help to prevent muscle loss while dieting.[citation needed] This can also allow strength athletes or those athletes in sports which have weight classes to increase performance without the risk of being raised into a higher weight class or add mass that may hinder performance.]]>
It has gained popularity in the bodybuilding community as a diuretic and muscle defining drug. Individuals interested in using the drostanolone propionate are those that are looking to add muscle hardness and density to their physiques, nearly always for the purpose of bodybuilding competitions.

Drostanolone propionate can increase muscle hardness and density, giving an individual a more complete appearance when competing on stage.[citation needed] However, an already rather low body-fat level is needed for it to take full effect.[citation needed] Drostanolone propionate can promote increased strength while keeping body fat the same or even lowering it, something can help to prevent muscle loss while dieting.[citation needed] This can also allow strength athletes or those athletes in sports which have weight classes to increase performance without the risk of being raised into a higher weight class or add mass that may hinder performance.]]> https://hypermuscles.com/showthread.php?tid=1386 Mon, 07 Mar 2011 06:35:49 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1386
Enanthat 500 by GenShi Labs is an injectable steroid which contains 250mg per 1ml of the Testosterone Enanthate.

Enanthat 500 (Testosterone Enanthate) testosterone is main androgen in body thus best mass and strength builder. Therefore athletes use this product very often to get above mentioned results.

Enanthat 500 (Testosterone Enanthate) is similar to Testosterone Cypionate even their half liveand active life periods are different, they are similar.

Enanthat 500 injections are normally less frequent for cypionate.

Testosterone is a product which is heavily used by beginners as well as veterans and both categories are very happy with results.]]>
Enanthat 500 by GenShi Labs is an injectable steroid which contains 250mg per 1ml of the Testosterone Enanthate.

Enanthat 500 (Testosterone Enanthate) testosterone is main androgen in body thus best mass and strength builder. Therefore athletes use this product very often to get above mentioned results.

Enanthat 500 (Testosterone Enanthate) is similar to Testosterone Cypionate even their half liveand active life periods are different, they are similar.

Enanthat 500 injections are normally less frequent for cypionate.

Testosterone is a product which is heavily used by beginners as well as veterans and both categories are very happy with results.]]> https://hypermuscles.com/showthread.php?tid=1385 Mon, 07 Mar 2011 06:35:22 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1385
Nandrolone Decanoate is used in the treatment of osteoporosis in postmenopausal women (though now not recommended) at a dose of 50 mg every three weeks. It is also used for some aplastic anaemias.

World wide "Deca" is one of the most widely used anabolic steroids. Its popularity is due to the simple fact that it exhibits many very favorable properties. Structurally nandrolone is very similar to testosterone, although it lacks a carbon atom at the 19th position (hence its other name 19-nortestosterone). The resulting structure is a steroid that exhibits much weaker androgenic properties than testosterone. Of primary interest is the fact that nandrolone will not break down to a more potent metabolite in androgen target tissues. You may remember this is a significant problem with testosterone. Although nandrolone does undergo reduction via the same (5-alpha reductase) enzyme that produces DHT from testosterone, the result in this case is dihydronandrolone. This metabolite is weaker than the parent nandroloness, and is far less likely to cause unwanted androgenic side effects. Strong occurrences of oily skin, acne, body/facial hair growth and hair loss occur very rarely. It is however possible for androgenic activity to become apparent with this as any steroid, but with nandrolone higher than normal doses are usually responsible.

Nandrolone Decanoate also show an extremely lower tendency for estrogen conversion. For comparison, the rate has been estimated to be only about 20% of that seen with testosterones. This is because while the liver can convert nandrolone to estradiol, in other more active sites of steroid aromatization such as adipose tissue nandrolone is far less open to this process". Consequently estrogen related side effects are a much lower concern with this drug. An anti-estrogen is likewise rarely needed with Deca, gynecomastia only a worry among sensitive individuals. At the same time water retention is not a usual concern. This effect can occur however, but is most often related to higher dosages. The addition of Proviron and/or Nolvadex should prove sufficient enough to significantly reduce any occurrence. Clearly Deca is a very safe choice among steroids. Actually, many consider it to be the best overall steroid for a man to use when weighing the side effects and results. It should also be noted that in HIV studies, Deca has been shown not only to be effective at safely bringing up the lean body weight of patient, but also to be beneficial to the immune system.]]>
Nandrolone Decanoate is used in the treatment of osteoporosis in postmenopausal women (though now not recommended) at a dose of 50 mg every three weeks. It is also used for some aplastic anaemias.

World wide "Deca" is one of the most widely used anabolic steroids. Its popularity is due to the simple fact that it exhibits many very favorable properties. Structurally nandrolone is very similar to testosterone, although it lacks a carbon atom at the 19th position (hence its other name 19-nortestosterone). The resulting structure is a steroid that exhibits much weaker androgenic properties than testosterone. Of primary interest is the fact that nandrolone will not break down to a more potent metabolite in androgen target tissues. You may remember this is a significant problem with testosterone. Although nandrolone does undergo reduction via the same (5-alpha reductase) enzyme that produces DHT from testosterone, the result in this case is dihydronandrolone. This metabolite is weaker than the parent nandroloness, and is far less likely to cause unwanted androgenic side effects. Strong occurrences of oily skin, acne, body/facial hair growth and hair loss occur very rarely. It is however possible for androgenic activity to become apparent with this as any steroid, but with nandrolone higher than normal doses are usually responsible.

Nandrolone Decanoate also show an extremely lower tendency for estrogen conversion. For comparison, the rate has been estimated to be only about 20% of that seen with testosterones. This is because while the liver can convert nandrolone to estradiol, in other more active sites of steroid aromatization such as adipose tissue nandrolone is far less open to this process". Consequently estrogen related side effects are a much lower concern with this drug. An anti-estrogen is likewise rarely needed with Deca, gynecomastia only a worry among sensitive individuals. At the same time water retention is not a usual concern. This effect can occur however, but is most often related to higher dosages. The addition of Proviron and/or Nolvadex should prove sufficient enough to significantly reduce any occurrence. Clearly Deca is a very safe choice among steroids. Actually, many consider it to be the best overall steroid for a man to use when weighing the side effects and results. It should also be noted that in HIV studies, Deca has been shown not only to be effective at safely bringing up the lean body weight of patient, but also to be beneficial to the immune system.]]> https://hypermuscles.com/showthread.php?tid=1384 Mon, 07 Mar 2011 06:34:44 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1384
Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys.

Boldenone was synthesized in an attempt to create a long-acting injectable Dianabol (Methandrostenolone), but in reality Equipoise acts nothing like Dianabol. The muscular gains made on a Boldenone cycle are usually slow and steady, resulting in quaility sustainable muscle, whereas Dianbol is a faster acting steroid designed for immediate weight gain. Another reason Boldenone is so popular for bulking is because it increases the appetite; this is also a reason many athletes will stay away from it pre-contest.

Boldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention.

It has a very long half-life, and can show up on a steroid test for up to 1.5 years, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use.

Although commonly compared to nandrolone, boldenone lacks progesterone receptor interaction and all the associated progestinic side effects. Boldenone can, however, produce mild androgenic side effects. Oily skin, acne, increased aggression and hair loss are all possible with this compound but rare. Boldenone does reduce to a more potent androgen dihydroboldenone via the 5-alpha-reductase enzyme (analogous to the conversion of testosterone to dihydrotestosterone (DHT), however its affinity for this interaction in the human body is low to nonexistent. Suppression of the HPTA, water retention, possible increase in acne and possible conversion to estrogen, high blood pressure are all side effects associated with Boldenone.

Boldenone is often used by bodybuilders in both off-season and pre-contest. Boldenone is well known for increasing vascularity while preparing for a bodybuilding contest. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the 'base' of the stack.

Common bodybuilding doses range between 200 mg to 400 mg/week but could be as high as 800 mg/week. The medical advised dosage is 1mg per kilogram of bodyweight every 2-3 weeks.

Many bodybuilders will find that it is a good replacement drug for Nandrolone.]]>
Boldenone will increase nitrogen retention, protein synthesis, increases appetite and stimulates the release of erythropoietin in the kidneys.

Boldenone was synthesized in an attempt to create a long-acting injectable Dianabol (Methandrostenolone), but in reality Equipoise acts nothing like Dianabol. The muscular gains made on a Boldenone cycle are usually slow and steady, resulting in quaility sustainable muscle, whereas Dianbol is a faster acting steroid designed for immediate weight gain. Another reason Boldenone is so popular for bulking is because it increases the appetite; this is also a reason many athletes will stay away from it pre-contest.

Boldenone has a low rate of aromatization (about 50% of Testosterone), which means it does not convert to estrogen easily and does not cause very much water retention.

It has a very long half-life, and can show up on a steroid test for up to 1.5 years, due to the long undecylenate ester attached to the parent steroid. Trace amounts of the drug can easily be detected for months after discontinued use.

Although commonly compared to nandrolone, boldenone lacks progesterone receptor interaction and all the associated progestinic side effects. Boldenone can, however, produce mild androgenic side effects. Oily skin, acne, increased aggression and hair loss are all possible with this compound but rare. Boldenone does reduce to a more potent androgen dihydroboldenone via the 5-alpha-reductase enzyme (analogous to the conversion of testosterone to dihydrotestosterone (DHT), however its affinity for this interaction in the human body is low to nonexistent. Suppression of the HPTA, water retention, possible increase in acne and possible conversion to estrogen, high blood pressure are all side effects associated with Boldenone.

Boldenone is often used by bodybuilders in both off-season and pre-contest. Boldenone is well known for increasing vascularity while preparing for a bodybuilding contest. If intended to assist in bodybuilding, the drug is taken as part of a steroid stack of other anabolic steroids, usually with a potent androgen like testosterone as the 'base' of the stack.

Common bodybuilding doses range between 200 mg to 400 mg/week but could be as high as 800 mg/week. The medical advised dosage is 1mg per kilogram of bodyweight every 2-3 weeks.

Many bodybuilders will find that it is a good replacement drug for Nandrolone.]]> https://hypermuscles.com/showthread.php?tid=1383 Mon, 07 Mar 2011 06:34:13 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1383 https://hypermuscles.com/showthread.php?tid=1382 Mon, 07 Mar 2011 06:33:43 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1382
Stanozolol, commonly sold under the name Winstrol (oral) and Winstrol Depot (intra-muscular), was developed by Winthrop Laboratories in 1962. It is a synthetic anabolic steroid derived from testosterone, and has been approved by the FDA for human use.

Unlike most injectable anabolic steroids, Stanozolol is not esterified and is sold as an aqueous suspension, or in oral tablet form. The drug has a large oral bioavailability, due to a C17 ?-alkylation which allows the hormone to survive first pass liver metabolism when ingested. It is because of this that Stanozolol is also sold in tablet form.

Stanozolol is also one of the few compounds that women can take safely, as its anabolic:androgenic ratio is quite skewed towards anabolism.

Stanozolol has been used on both animal and human patients for a number of conditions. In humans, it has been demonstrated to be successful in treating anaemia and hereditary angioedema. Veterinarians may prescribe the drug to improve muscle growth, red blood cell production, increase bone density and stimulate the appetite of debilitated or weakened animals.

Stanozolol is one of the Anabolic steroids commonly used as an ergogenic aid and is banned from use in sports competition under the auspices of the International Association of Athletics Federations (IAAF).
Use in bodybuilding

Like other anabolic steroids, stanozolol is classified as a Schedule III controlled substance under federal regulation. In New York, the state legislature classifies analbolic steroids under DEA Schedule II.

Used illegally in bodybuilding, typically "stacked" with other testosterone-based anabolic steroids, Stanozolol is liked by many due to the fact it causes strength increases without excess weight-gain, promotes increases in vascularity, and will not convert to estrogen. It also does not cause excess water retention, and even sometimes is thought to have a diuretic effect on the body.

Stanozolol is commonly used by athletes and bodybuilders alike to lose fat while retaining lean body mass. It is usually used in a cutting cycle, to help preserve lean body mass while metabolizing adipose, although it has not been proven conclusively that it has any special fat-burning properties.

It is presented most commonly as a 50 mg/mL injection or a 50 mg tablet. However, recently 100 mg/mL versions have become available. A common dosage can be 25-100 mg/day, with optimal results usually seen at 50 mg/day. It is reduced to micrometer particles in aqueous suspension and does not have a typical elimination half-life. Authentic Stanozol can easily be seen, because it will separate in its container if left undisturbed for a number of hours (the micronized crystal will fall to the bottom, and the water suspension will rise to the top). It has a white, milky colour.

It should be taken no more than 48 hours apart, with some users preferring to inject every day, or even twice a day, to maintain serum levels.

An alternative to Stanozolol is Furazabol. Furazabol's effects are virtually identical to Stanzolol except that instead of having an extremely adverse effect on cholesterol values, Furazabol actually improves a person's blood lipid profile (at therapeutic doses, not performance enhancing ones).Sold under the trade name Mitolan, Furazabol is a standard treatment in Japan for hyperlipemia.]]>
Stanozolol, commonly sold under the name Winstrol (oral) and Winstrol Depot (intra-muscular), was developed by Winthrop Laboratories in 1962. It is a synthetic anabolic steroid derived from testosterone, and has been approved by the FDA for human use.

Unlike most injectable anabolic steroids, Stanozolol is not esterified and is sold as an aqueous suspension, or in oral tablet form. The drug has a large oral bioavailability, due to a C17 ?-alkylation which allows the hormone to survive first pass liver metabolism when ingested. It is because of this that Stanozolol is also sold in tablet form.

Stanozolol is also one of the few compounds that women can take safely, as its anabolic:androgenic ratio is quite skewed towards anabolism.

Stanozolol has been used on both animal and human patients for a number of conditions. In humans, it has been demonstrated to be successful in treating anaemia and hereditary angioedema. Veterinarians may prescribe the drug to improve muscle growth, red blood cell production, increase bone density and stimulate the appetite of debilitated or weakened animals.

Stanozolol is one of the Anabolic steroids commonly used as an ergogenic aid and is banned from use in sports competition under the auspices of the International Association of Athletics Federations (IAAF).
Use in bodybuilding

Like other anabolic steroids, stanozolol is classified as a Schedule III controlled substance under federal regulation. In New York, the state legislature classifies analbolic steroids under DEA Schedule II.

Used illegally in bodybuilding, typically "stacked" with other testosterone-based anabolic steroids, Stanozolol is liked by many due to the fact it causes strength increases without excess weight-gain, promotes increases in vascularity, and will not convert to estrogen. It also does not cause excess water retention, and even sometimes is thought to have a diuretic effect on the body.

Stanozolol is commonly used by athletes and bodybuilders alike to lose fat while retaining lean body mass. It is usually used in a cutting cycle, to help preserve lean body mass while metabolizing adipose, although it has not been proven conclusively that it has any special fat-burning properties.

It is presented most commonly as a 50 mg/mL injection or a 50 mg tablet. However, recently 100 mg/mL versions have become available. A common dosage can be 25-100 mg/day, with optimal results usually seen at 50 mg/day. It is reduced to micrometer particles in aqueous suspension and does not have a typical elimination half-life. Authentic Stanozol can easily be seen, because it will separate in its container if left undisturbed for a number of hours (the micronized crystal will fall to the bottom, and the water suspension will rise to the top). It has a white, milky colour.

It should be taken no more than 48 hours apart, with some users preferring to inject every day, or even twice a day, to maintain serum levels.

An alternative to Stanozolol is Furazabol. Furazabol's effects are virtually identical to Stanzolol except that instead of having an extremely adverse effect on cholesterol values, Furazabol actually improves a person's blood lipid profile (at therapeutic doses, not performance enhancing ones).Sold under the trade name Mitolan, Furazabol is a standard treatment in Japan for hyperlipemia.]]> https://hypermuscles.com/showthread.php?tid=1381 Mon, 07 Mar 2011 06:33:07 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1381
Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively long metabolic half-life of trenbolone enanthate dosages should be once a week. Trenbolone acetate injections are commonly split into at least once every two days.

The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.]]>
Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively long metabolic half-life of trenbolone enanthate dosages should be once a week. Trenbolone acetate injections are commonly split into at least once every two days.

The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.]]> https://hypermuscles.com/showthread.php?tid=1380 Mon, 07 Mar 2011 06:32:39 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1380
Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.

The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.]]>
Bodybuilders have been known to use the drug in order to increase body mass more effectively than by weight training alone. A normal bodybuilding dosage can range from 200 mg/week up to 1400 mg/week. Due to the relatively short metabolic half-life of trenbolone acetate, dosages should commonly be split into injections at least once every two days. Trenbolone enanthate can be injected once a week.

The 2006 book Game of Shadows alleges that baseball superstar Barry Bonds used this drug in 2001, when he set the current single-season home run record.

Trenbolone compounds have a binding affinity for the androgen receptor three times as high as that of testosterone. Once metabolised, the drugs have the effect of increasing nitrogen uptake by muscles, leading to an increase in the rate of protein synthesis. It also has the secondary effects of stimulating appetite, reducing the amount of fat being deposited in the body, and decreasing the rate of catabolism. Trenbolone has proven popular with anabolic steroid users as it is not metabolised by aromatase or 5?-reductase into estrogenic compounds such as estradiol, or into DHT. This means that it also does not cause any water retention normally associated with highly androgenic steroidal compounds like testosterone or methandrostenolone. It is also loved by many for the dramatic strength increases commonly experienced with it. Some short-term side effects include insomnia, high blood pressure, increased aggression and libido. However, since women will suffer virilization effects even at small doses, this drug should not be taken by a female. Urban wisdom/myth in bodybuilding culture, states that the use of the drug over extended periods of time can lead to kidney damage. The kidney toxicity has not yet been proven, and scientific evidence supporting the idea is suspiciously absent from the bodybuilding community that perpetuates this idea. The origin of this myth most likely has to do with the rust colored oxidized metabolites of trenbolone which are excreted in urine and often mistaken for blood. After Schänzer (Clin Chem 1996; 42(7): 1001-1020, Metabolism of anabolic androgenic steroids) trenbolone and 17epi-trenbolone are both excreted (in urine) as conjugates that can be hydrolyzed with beta-glucuronidase. This implies that trenbolone leaves the body as beta-glucuronides or sulfates, that means mostly non metabolized.]]> https://hypermuscles.com/showthread.php?tid=1379 Mon, 07 Mar 2011 06:32:11 +0000 Cornish_Celt]]> https://hypermuscles.com/showthread.php?tid=1379 Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: 250-1000 mg/week (males only)
Acne: Yes
Water Retention: Yes
High Blood Pressure: Yes
Liver Toxic: Low
Aromatization: Yes
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Testosterone blend typically contains four different testosterone esters: Testosterone propionate (30 mg); testosterone phenylpropionate (60 mg); testosterone isocaproate (60mg); and testosterone decanoate (100 mg), although a lower dosed version is also produced. An intelligently "engineered" testosterone, Sustanon is designed to provide a fast yet extended release of testosterone. The propionate and phenylpropionate esters in this product are quickly utilized, releasing into circulation within the first four days. The remaining esters are much slower to release, staying active in the body for about two and three weeks (respectively).

As with all testosterone products, Sustanon is a strong anabolic with pronounced androgenic activity. It is mainly used as a bulking drug, providing good gains in strength and muscle mass. Although it does convert to estrogen, as is the nature of testosterone, this injectable is noted as being slightly more tolerable than cypionate or enanthate. Such observations are only issues of timing however. With Sustanon, blood levels of testosterone are building more slowly, so side effects do not set in as fast. For equal blood hormone levels however, testosterone will break down equally without regard to ester. Also correlating with estrogen, water retention would be noticeable with Sustanon, unless steps were taken to minimize estrogen.
Many individuals like to use a combination of Nolvadex & Proviron, while others use an anti-aromatase like Arimidex, Femara, or Aromasin, to help control estrogen related side effects.

Being a strong androgen, we can expect the typical side effects. This includes oily skin, acne body/facial hair growth and premature balding. The addition of Proscar/Propecia should be able to minimize such side effects, as it will limit the conversion of testosterone to DHT (dihydrotestosterone) . Sustanon will also suppress natural testosterone production rather quickly. The use of HCG and/or Clomid/Nolvadex are necessary at the conclusion of a cycle in order to avoid a hormonal crash. Remember though, Sustanon will remain active in the body for up to a month after your last injection was given. Beginning you post cycle drug therapy immediately after the steroid has been discontinued will not be very effective. Instead, HCG or Clomid/Nolvadex should be delayed three weeks, until you are near the point where blood androgen levels have dropped significantly.]]> Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: 250-1000 mg/week (males only)
Acne: Yes
Water Retention: Yes
High Blood Pressure: Yes
Liver Toxic: Low
Aromatization: Yes
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Testosterone blend typically contains four different testosterone esters: Testosterone propionate (30 mg); testosterone phenylpropionate (60 mg); testosterone isocaproate (60mg); and testosterone decanoate (100 mg), although a lower dosed version is also produced. An intelligently "engineered" testosterone, Sustanon is designed to provide a fast yet extended release of testosterone. The propionate and phenylpropionate esters in this product are quickly utilized, releasing into circulation within the first four days. The remaining esters are much slower to release, staying active in the body for about two and three weeks (respectively).

As with all testosterone products, Sustanon is a strong anabolic with pronounced androgenic activity. It is mainly used as a bulking drug, providing good gains in strength and muscle mass. Although it does convert to estrogen, as is the nature of testosterone, this injectable is noted as being slightly more tolerable than cypionate or enanthate. Such observations are only issues of timing however. With Sustanon, blood levels of testosterone are building more slowly, so side effects do not set in as fast. For equal blood hormone levels however, testosterone will break down equally without regard to ester. Also correlating with estrogen, water retention would be noticeable with Sustanon, unless steps were taken to minimize estrogen.
Many individuals like to use a combination of Nolvadex & Proviron, while others use an anti-aromatase like Arimidex, Femara, or Aromasin, to help control estrogen related side effects.

Being a strong androgen, we can expect the typical side effects. This includes oily skin, acne body/facial hair growth and premature balding. The addition of Proscar/Propecia should be able to minimize such side effects, as it will limit the conversion of testosterone to DHT (dihydrotestosterone) . Sustanon will also suppress natural testosterone production rather quickly. The use of HCG and/or Clomid/Nolvadex are necessary at the conclusion of a cycle in order to avoid a hormonal crash. Remember though, Sustanon will remain active in the body for up to a month after your last injection was given. Beginning you post cycle drug therapy immediately after the steroid has been discontinued will not be very effective. Instead, HCG or Clomid/Nolvadex should be delayed three weeks, until you are near the point where blood androgen levels have dropped significantly.]]>