https://hypermuscles.com/ Sun, 05 Jul 2026 21:38:10 +0000 MyBB https://hypermuscles.com/showthread.php?tid=43 Sun, 09 Aug 2009 14:34:35 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=43 (an oral blend of T3, Yohimbine and Clenbuterol)

Combines the synergistic fat burning power of beta adrenergic agonists) and alpha adrenergic antagonists (Yohimbine HCl), all to add the T3 characteristics of increase the metabolic rate by increasing Thyroid efficiency.

Clenbuterol - 37.5mcg

T3 - 25mcg

Yohimbine 5.4mg



Effects and Dosage
The blend is very potent combination of a beta and alpha antagonist.Clenbuterol and Yohimbine promote fat loss through the same adrenergic system, but the effects are achieved through different mechanisms. Clenbuterol is a known thermogenics shown to directly stimulate fat cells metabolism and accelerate the breakdown of triglycerides to form free fatty acids. The hormone glucagon released signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.Yohimbine, being an antagonist of alpha-2 receptors shifts the balance of sympathetic activity to ensure that lypolisis occurs. This increases synaptic Norepinephrine release, one of the body's own natural Lipolytic hormones. In effect, it acts as beta stimulating and alpha blocking properties, an ideal combination to stimulate fat loss.

Administration and Use:

Clenbuterol should be built up and tapered off gradually with dosage increases and decreases every 3-4 days and doses never exceeding 160 µg per day for safety measures. It is administered for periods of 2-3 weeks then discontinued for equal periods of time to prevent the body’s metabolic system the ability to adapt to the metabolic effects. For fat-burning goals Clenbuterol is often stacked with another fat-burning agent for quick effect, or alternated with another fat-burning agent by people who need to stay lean for a promote period. Usually T 3 is used for such purposes, with alternating cycles of 3 weeks each. If used together, cycles will not completely overlap!!! And a new adjustment is needed. A typical cycle for Clenbuterol might be 3 weeks, with the daily amounts being:

Day1-1 tablet

Day2-1 tablet

Day3-1 tablet

Day4-11/2 tablets

Day5-11/2 tablets

Day6-11/2 tablets

Day7-2 tablets

Day8-2 tablets

Day9-2 tablets

Day10-11/2 tablets

Day11-11/2 tablets

Day12-11/2 tablets

Day13-1 tablets

Day14-1 tablets

Day15-1 tablets

Day16-1/2tablet

Day17-1/2tablet

Day18-1/2tablet

Day19-1/2tablet

Day20-1/4tablet

Day21-1/4tablet

Then stopping for three weeks and recommencing.



Patients should be instructed that the expected benefits of CYX 3 may only be obtained when each tablet is swallowed with plain water the first thing upon arising for the day, at least 30 minutes before the first food, beverage, or medication of the day. Even ingestion with orange juice or coffee has been shown to markedly reduce the absorption of CYX 3



To facilitate delivery to the stomach and thus reduce the potential should be instructed to swallow CYX 3 with a full glass of tap water and not to lie down for at least 30 minutes and until after their first food of the day. Patients should not chew or suck on the tablet, or retain it in the mouth for a period longer than that required for swallowing, because a potential for side effects, not to take CYX 3 at bedtime or before arising for the day]]> (an oral blend of T3, Yohimbine and Clenbuterol)

Combines the synergistic fat burning power of beta adrenergic agonists) and alpha adrenergic antagonists (Yohimbine HCl), all to add the T3 characteristics of increase the metabolic rate by increasing Thyroid efficiency.

Clenbuterol - 37.5mcg

T3 - 25mcg

Yohimbine 5.4mg



Effects and Dosage
The blend is very potent combination of a beta and alpha antagonist.Clenbuterol and Yohimbine promote fat loss through the same adrenergic system, but the effects are achieved through different mechanisms. Clenbuterol is a known thermogenics shown to directly stimulate fat cells metabolism and accelerate the breakdown of triglycerides to form free fatty acids. The hormone glucagon released signals the breakdown of the triglycerides by hormone-sensitive lipase to release free fatty acids.Yohimbine, being an antagonist of alpha-2 receptors shifts the balance of sympathetic activity to ensure that lypolisis occurs. This increases synaptic Norepinephrine release, one of the body's own natural Lipolytic hormones. In effect, it acts as beta stimulating and alpha blocking properties, an ideal combination to stimulate fat loss.

Administration and Use:

Clenbuterol should be built up and tapered off gradually with dosage increases and decreases every 3-4 days and doses never exceeding 160 µg per day for safety measures. It is administered for periods of 2-3 weeks then discontinued for equal periods of time to prevent the body’s metabolic system the ability to adapt to the metabolic effects. For fat-burning goals Clenbuterol is often stacked with another fat-burning agent for quick effect, or alternated with another fat-burning agent by people who need to stay lean for a promote period. Usually T 3 is used for such purposes, with alternating cycles of 3 weeks each. If used together, cycles will not completely overlap!!! And a new adjustment is needed. A typical cycle for Clenbuterol might be 3 weeks, with the daily amounts being:

Day1-1 tablet

Day2-1 tablet

Day3-1 tablet

Day4-11/2 tablets

Day5-11/2 tablets

Day6-11/2 tablets

Day7-2 tablets

Day8-2 tablets

Day9-2 tablets

Day10-11/2 tablets

Day11-11/2 tablets

Day12-11/2 tablets

Day13-1 tablets

Day14-1 tablets

Day15-1 tablets

Day16-1/2tablet

Day17-1/2tablet

Day18-1/2tablet

Day19-1/2tablet

Day20-1/4tablet

Day21-1/4tablet

Then stopping for three weeks and recommencing.



Patients should be instructed that the expected benefits of CYX 3 may only be obtained when each tablet is swallowed with plain water the first thing upon arising for the day, at least 30 minutes before the first food, beverage, or medication of the day. Even ingestion with orange juice or coffee has been shown to markedly reduce the absorption of CYX 3



To facilitate delivery to the stomach and thus reduce the potential should be instructed to swallow CYX 3 with a full glass of tap water and not to lie down for at least 30 minutes and until after their first food of the day. Patients should not chew or suck on the tablet, or retain it in the mouth for a period longer than that required for swallowing, because a potential for side effects, not to take CYX 3 at bedtime or before arising for the day]]> https://hypermuscles.com/showthread.php?tid=42 Sun, 09 Aug 2009 14:31:59 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=42
Thyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT). Both hormones are stored in the thyroid colloid as thyroglobulin.

Thyroid hormone preparations belong to two categories (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid) and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity.]]>
Thyroid hormone drugs are natural or synthetic preparations containing tetraiodothyronine (T4, levothyroxine) sodium or triiodothyronine (T3, liothyronine) sodium or both. T4 and T3 are produced in the human thyroid gland by the iodination and coupling of the amino acid tyrosine T4 contains four iodine atoms and is formed by the coupling of two molecules of diiodotyrosine (DIT). T3 contains three atoms of iodine and is formed by the coupling of one molecule of DIT with one molecule of monoiodotyrosine (MIT). Both hormones are stored in the thyroid colloid as thyroglobulin.

Thyroid hormone preparations belong to two categories (1) natural hormonal preparations derived from animal thyroid, and (2) synthetic preparations. Natural preparations include desiccated thyroid and thyroglobulin. Desiccated thyroid is derived from domesticated animals that are used for food by man (either beef or hog thyroid) and thyroglobulin is derived from thyroid glands of the hog. The United States Pharmacopeia (USP) has standardized the total iodine content of natural preparations. Thyroid USP contains not less than (NLT) 0.17 percent and not more than (NMT) 0.23 percent iodine, and thyroglobulin contains not less than (NLT) 0.7 percent of organically bound iodine. Iodine content is only an indirect indicator of true hormonal biologic activity.]]> https://hypermuscles.com/showthread.php?tid=41 Sun, 09 Aug 2009 14:30:56 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=41

Clenbutaplex is a β2 adrenergic agonist with some similarities to ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenic drug. It causes an increase in aerobic capacity, CNS stimulation, and an increase in blood pressure and oxygen transportation. It increases the rate at which fat and protein is used up in the body at the same time as slowing down the storage of glycogen. It is commonly used for smooth muscle relaxant properties. These mean that it is a bronchodilator, and tocolytic.]]>

Clenbutaplex is a β2 adrenergic agonist with some similarities to ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenic drug. It causes an increase in aerobic capacity, CNS stimulation, and an increase in blood pressure and oxygen transportation. It increases the rate at which fat and protein is used up in the body at the same time as slowing down the storage of glycogen. It is commonly used for smooth muscle relaxant properties. These mean that it is a bronchodilator, and tocolytic.]]> https://hypermuscles.com/showthread.php?tid=40 Sun, 09 Aug 2009 14:29:36 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=40

Turanaplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.


Turanaplex formula is white tablet coated in a peach protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]>

Turanaplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.


Turanaplex formula is white tablet coated in a peach protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]> https://hypermuscles.com/showthread.php?tid=39 Sun, 09 Aug 2009 14:28:40 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=39

Oxyplex(Oxymetholone) is a synthetic anabolic-androgenic steroid hormone that is structurally related to the male hormone testosterone. Synthetic androgens are used to treat a variety of conditions including hypogonadism and delayed puberty. Androgens are also used to correct hereditary angioneurotic edema, manage carcinoma of the breast, promote a positive nitrogen balance following injury or surgery, and stimulate erythropoiesis.

Considerable amounts of androgens are consumed by athletes in attempts to improve athletic performance. Oxyplex is used to promote weight gain and counteract weakness and emaciation resulting from debilitating diseases, such as advanced HIV infection, and after serious infections, burns, trauma, or surgery. It is marketed as a human prescription drug for the treatment of bone marrow failure anemias and deficient red cell production anemias.]]>

Oxyplex(Oxymetholone) is a synthetic anabolic-androgenic steroid hormone that is structurally related to the male hormone testosterone. Synthetic androgens are used to treat a variety of conditions including hypogonadism and delayed puberty. Androgens are also used to correct hereditary angioneurotic edema, manage carcinoma of the breast, promote a positive nitrogen balance following injury or surgery, and stimulate erythropoiesis.

Considerable amounts of androgens are consumed by athletes in attempts to improve athletic performance. Oxyplex is used to promote weight gain and counteract weakness and emaciation resulting from debilitating diseases, such as advanced HIV infection, and after serious infections, burns, trauma, or surgery. It is marketed as a human prescription drug for the treatment of bone marrow failure anemias and deficient red cell production anemias.]]> https://hypermuscles.com/showthread.php?tid=38 Sun, 09 Aug 2009 14:27:17 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=38

Primoplex is indicated in the treatment of refractory deficient red cell production anemias. These may include aplastic anemia, myelofibrosis, myelosclerosis, agnogenic myeloid metaplasia, and hypoplastic anemias caused by malignancy or myelotoxic drugs.

Primoplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.

Primoplex (Methenolone Acetate) has been used in certain countries to counteract catabolic states, for example after major trauma.


Primoplex 25 is white tablet coated in a green protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]>

Primoplex is indicated in the treatment of refractory deficient red cell production anemias. These may include aplastic anemia, myelofibrosis, myelosclerosis, agnogenic myeloid metaplasia, and hypoplastic anemias caused by malignancy or myelotoxic drugs.

Primoplex is indicated in conditions such as chronic infections, extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein sparing effects. These agents are adjuncts to, and not replacements for, conventional treatment of these disorders.

Primoplex (Methenolone Acetate) has been used in certain countries to counteract catabolic states, for example after major trauma.


Primoplex 25 is white tablet coated in a green protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]> https://hypermuscles.com/showthread.php?tid=37 Sun, 09 Aug 2009 14:25:12 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=37

Fluoxymesterone (Haloplex) is an androgenic steroid that is only useful to a small select group of athletes who seeks very specific goals. Athletes tend to use it to increase strength and aggression in the gym or in competitions such as strongman contests, fighting (like boxing) or MMA. The lack of estrogenic activity makes Halotestin perfect for pre-fight usage – as weigh-ins would not be effected by water retention. Even in such an events, Fluoxymesterone usage is usually limited to mere few weeks rather then cycled like real steroids for months.

Fluoxymesterone (Haloplex) has poor binding to the AR. Studies have shown the effects to be mostly non-AR mediated. However, it is considered a very toxic oral drug, and a poor choice in most bodybuilding/steroid use applications.

The half life of Fluoxymesterone (Haloplex) is commonly misunderstood. The rumored belief is that 30-90 minutes is the half-life but this rumor is false, the half life of Fluoxymesterone is about 9.5 hours.]]>

Fluoxymesterone (Haloplex) is an androgenic steroid that is only useful to a small select group of athletes who seeks very specific goals. Athletes tend to use it to increase strength and aggression in the gym or in competitions such as strongman contests, fighting (like boxing) or MMA. The lack of estrogenic activity makes Halotestin perfect for pre-fight usage – as weigh-ins would not be effected by water retention. Even in such an events, Fluoxymesterone usage is usually limited to mere few weeks rather then cycled like real steroids for months.

Fluoxymesterone (Haloplex) has poor binding to the AR. Studies have shown the effects to be mostly non-AR mediated. However, it is considered a very toxic oral drug, and a poor choice in most bodybuilding/steroid use applications.

The half life of Fluoxymesterone (Haloplex) is commonly misunderstood. The rumored belief is that 30-90 minutes is the half-life but this rumor is false, the half life of Fluoxymesterone is about 9.5 hours.]]> https://hypermuscles.com/showthread.php?tid=36 Sun, 09 Aug 2009 14:24:20 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=36

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.

Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).


Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.


Stanoplex is used in the treatment of hereditary angioedema.


Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.

Stanoplex 50 is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]>

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.

Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).


Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.


Stanoplex is used in the treatment of hereditary angioedema.


Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.

Stanoplex 50 is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]> https://hypermuscles.com/showthread.php?tid=35 Sun, 09 Aug 2009 14:23:11 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=35

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.

Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).

Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.

Stanoplex is used in the treatment of hereditary angioedema.

Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.


The new Stanoplex 10 formula is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]>

Stanoplex is prescribed for chronic infections, for conditions such as extensive surgery, [corticosteroid-induced myopathy, decubitus ulcers, burns] , or severe trauma, which require reversal of catabolic processes or protein-sparing effects. This is used in addition to, and not as replacements for, conventional treatment of these disorders.

Stanoplex is effective in raising hemoglobin concentrations in some cases of aplastic anemia (congenital or idiopathic).

Stanoplex is indicated in the prophylaxis of hereditary angioedema to decrease the frequency and severity of attacks.

Stanoplex is used in the treatment of hereditary angioedema.

Stanoplex is indicated in the treatment of conditions associated with decreased fibrinolytic activity due to antithrombin III deficiency or excess fibrinogen. These conditions may include cutaneous vasculitis, scleroderma of Raynaud's disease, vasculitis of Behcet's disease, and complications of deep vein thrombosis such as venous lipodermatosclerosis. Stanozolol is indicated in the prevention of recurrent venous thrombosis associated with antithrombin III deficiency. Stanozolol may be of benefit in patients susceptible to or with a history of thromboembolism for the treatment of vascular disorders associated with these forms of reduced fibrinolytic activity.


The new Stanoplex 10 formula is white tablet coated in a yellow protective cover that will prevent absorption in the stomach, thus allowing for correct absorption in the lower intestine.]]> https://hypermuscles.com/showthread.php?tid=34 Sun, 09 Aug 2009 14:22:27 +0000 Robbie]]> https://hypermuscles.com/showthread.php?tid=34

Methanoplex 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 gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimiplex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid .

The 17α-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid's affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, Methanoplex is significantly more active than an equivalent quantity of testosterone , resulting in rapid growth of muscle tissue. However, the concomitant elevation in estrogen levels - a result of the aromatization of Methanoplex - results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a "steroid cycle", to facilitate rapid strength increases and the appearance of great size, while compounds such as Testaplex or Decaplex with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own.]]>

Methanoplex 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 gynaecomastia , high blood pressure , acne and male pattern baldness may begin to occur. The drug causes severe masculinising effects in women even at low doses. Without the administration of aromatase inhibitors such as Arimiplex , estrogenic effects will appear over time in men. Many users will combat the estrogenic side effects with Tamoxiplex or Clomid .

The 17α-methylation of the steroid does allow it to pass through the liver without being broken down allowing it to be taken orally. It also has the effect of decreasing the steroid's affinity for sex hormone binding globulin , a protein that de-activates steroid molecules and prevents them from further reactions with the body. As a result, Methanoplex is significantly more active than an equivalent quantity of testosterone , resulting in rapid growth of muscle tissue. However, the concomitant elevation in estrogen levels - a result of the aromatization of Methanoplex - results in significant water retention. This gives the appearance of great gains in mass and strength, which prove to be temporary once the steroid is discontinued and water weight drops. Because of this, it is often used by bodybuilders only at the start of a "steroid cycle", to facilitate rapid strength increases and the appearance of great size, while compounds such as Testaplex or Decaplex with long acting esters build up in the body to an appreciable amount capable of supporting anabolic function on their own.]]>