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Equi Test 525 is an injectable steroid made by Platinum Biotech, its active substance is:
Boldenone Undecyclenate 200mg
Testosterone Acetate 30mg
Testosterone Propionate 55mg
Testosterone Phenylpropionate 55mg
Testosterone Cypionate 85mg
Testosterone Decanoate 100mg
Deca Dura 300 is destinated for intramuscular injection and is made by Platinum Biotech, Europe. This steroid drug contains Nandrolone Decanoate.
Deca Dura 300 is a brand name of Platinum Biotech, the manufacturer of the drug containing the substance Nandrolone Decanoate. Although Nandrolone Decanoate is still contained in many generic compounds, almost every athlete connects this substance with Nandrolone Decanoate. Most common are the administrations of 50 mg/ml and 100 mg/ml. Deca Dura 300 is the most widespread and most commonly used injectable steroid. Its popularity is due to the simple fact that it exhibits many very favorable properties. Structurally Nandrolone is very similar to Testosterone.
Deca Dura 300 is a favorite to thousands of steroid users. In our recent survey, it was revealed that Nandrolone Decanoate is the most widely used anabolic steroid. It is easy on the liver and promotes good size and strength gains while reducing body fat.
Deca Dura 300 causes the muscle cell to store more nitrogen than it releases so that a positive nitrogen balance is achieved. A positive nitrogen balance is synonymous with muscle growth since the muscle cell, in this phase, assimilates (accumulates) a larger amount of protein than usual. The same manufacturer, however, points out on the package insert that a positive nitrogen balance and the protein building effect that accompany it will occur only if enough calories and proteins are supplied. One should know this since, otherwise, satisfying results with Deca Dura 300 cannot be obtained.
The highly anabolic effect of Deca Dura 300 is linked to a moderately androgenic component, so that a good gain in muscle mass and strength is obtained. At the same time, most athletes notice considerable water retention which, no doubt, is not as distinct as that with injectable testosterones but which in high doses can also cause a smooth and watery appearance.
Since Deca Dura 300 also stores more water in the connective tissues, it can temporarily ease or even cure existing pain in joints. This is especially good for those athletes who complain about pain in the shoulder, elbow, and knee, they can often enjoy pain-free workouts during treatment while using Deca Dura 300. Another reason for this is that it blocks the cortisone receptors thus allowing less cortisone to reach the muscle cells and the connective tissue cells. Athletes use this steroid, depending on their needs, for muscle buildup and in preparation for a competition.
It is suitable, even above average, to develop muscle mass since it promotes the protein synthesis and simultaneously leads to water retention. The optimal dose for this purpose lies between 200 and 600 mg per week. Scientific research has shown that best results can be obtained by the intake of 2 mg per pound of body weight. Those who take a dose of less than 200 mg per week will usually feel only a very light anabolic effect which, however, increases with a higher dosage.
The anabolic and consequent buildup effect of Deca Dura 300, up to a certain degree, depends on the dosage. In the range of approx. 200 to 600 mg per week, the anabolic effect increases almost proportionately to the dosage increase. If more than 600 mg per week are administered, the relationship of the positive to the negative effects shifts in favor of the latter.
In addition, at a dosage level above 600 mg per week, the anabolic effect no longer increases proportionately to the dosage increase, so that 1000 mg per week do not guarantee significantly better results than 600 mg per week.
Most male athletes experience good results by taking 400 mg per week. Steroid novices usually need only 200 mg per week.
Deca Dura 300 works very well for muscle buildup when combined with Dianabol (D-bol) and Testoviron Depot. The famous Dianabol (D-bol)/Deca Dura 300 stack results in a a fast and strong gain in muscle mass. Most athletes usually take 15 - 40 mg Dianabol (D-bol)/day and 200-400 mg Deca Dura 300 per week. Even faster results can be achieved with 400 mg Deca Dura 300 per week and 500 mg Sustanon per week. Athletes report an enormous gain in strength and muscle mass when taking 400 mg Deca Dura 300 per week, 500 mg Sustanon per week, and 30 mg Dianabol per day. Deca Dura 300 is a good basic steroid which, for muscle buildup, can be combined with many other steroids. Although it is not an optimal steroid when preparing for a competition, many athletes also achieve good results during this phase. Since Deca Dura 300 is a long-term anabolic, there is risk that with a higher dosage, the competing athlete will retain too much water. A conversion into estrogen, that means an aromatizing process, is possible with deca durabolin but usually occurs only at a dose of 400 mg per week.
During competitions with doping tests Deca Dura 300 must not be taken since the metabolites in the body can be proven in a urine analysis up to 18 months later. Those who do not fear testing can use Deca Dura 300 as a high-anabolic basic compound in a dosage of 400 mg per week. The androgens contained in 400 mg per week also help to accelerate the body's regeneration.
SIDE EFFECTS:
Side effects with this steroid are relatively low with dosages of 400 mg per week, androgenic caused side effects can occur. Most problems manifest themselves in high blood pressure and a prolonged time for blood clotting, which can cause frequent nasal bleeding and prolonged bleeding of cuts, as well as increased production of the sebaceous gland and occasional acne. Some athletes also report headaches and sexual overstimulation. When very high dosages are taken over a prolonged period, spermatogenesis can be inhibited in men, the testes produce less testosterone. The reason is that Deca Dura 300, like almost all steroids, inhibits the release of gonadotropins from the hypophysis.
Women with a dosage of up to 100 mg per week usually experience no major problems with Deca Dura 300. At higher dosages androgenic-caused virilization symptoms can occur, including deep voice (irreversible), increased growth of body hair, acne, increased libido, and possibly clitorishypertrophy. Since most female athletes get on well with Deca Dura 300 a dose of 50 mg per week is usually combined with Anavar 10 mg per day. Both compounds, when taken in a low dosage, are only slightly androgenic so that masculinizing side effects only rarely occur. Deca Dura 300, through its increased protein synthesis, also leads to a net muscle gain and Anavar, based on the increased phosphocreatine synthesis, leads to a measurable strength gain with very low water retention. Other variations of administration used by female athletes are Deca Dura 300 and Winstrol tablets, as well as Deca Dura 300 and Primobolan.
Testosterone Enanthate 300 is an injectable steroid made by Atlas Pharma, its active substance is Testosterone Enanthate.
Testosterone Enanthate is probably the most commonly used form of testosterone by both athletes and bodybuilders alike.
Testosterone Enanthate 300 is an oil based injectable steroid, which is designed to slowly release testosterone from the injection site. This slow release delivery leads to an elevation in testosterone levels lasting for approximately two weeks (it may even take as long as three weeks for the drug levels to fully diminish). Due to its relatively long activity level, Testosterone Enanthate is favored by the medical profession and is primarily used to treat cases of hypogonadism and similar disorders where low androgen levels are at fault. As with all testosterone products it has strong anabolic and androgenic activity. Gains in strength and muscle mass are notable, along with an increase in libido. It has also been noted that a relief in tendon pain and an increase in stamina are direct effects of Testosterone Enanthate 300 administration. This is probably due to increased water retention coupled with an increase in red blood cells – leading to a greater oxygen uptake in the blood.
Testosterone is a highly anabolic and androgenic hormone, it has an anabolic (muscle building) as well as anabolic rating of 100 each, respectively. Testosterone Enanthate 300 exerts the majority of its effects by promoting increased nitrogen retention in the muscle. Testosterone Enanthate 300 is also known to increases levels of the growth factor IGF-1 in both the muscle tissue as well as the liver. This steroid also increases the activity of satellite cells, which are cells that play an active role in repairing exercise-damaged muscle. Testosterone Enanthate 300 exerts these effects primarily by genomic mechanisms, meaning that it binds to the androgen receptor (AR) thus initiating gene transcription. This stimulation of the AR promotes various of the AR dependant mechanisms for both muscle gain and fat loss, as well as reducing catabolic glucocorticoid hormones, and increasing red blood cell production.
Weekly totals of 300-1000mg weekly are frequently used, and sometimes more for the highly advanced athlete. Due to the relatively long half life of Testosterone Enanthate 300 (4-5 days), injections are usually administered twice per week. This will allow stable blood levels to be maintained. When the level of steroid tapers down, a new injection is made, keeping everything fairly level. This is unlike Sustanon, which requires more frequent injections for the same effect. For a first cycle, 500 mg alone of Testosterone Enanthate 300, shot two times weekly (Monday and Thursday for example), for 10 weeks along with standard post cycle therapy would be very sufficient for good gains.
As the best mass builder available, Testosterone Enanthate 300 stacks well virtually everything and can also be used alone with high levels of success. Due to the longer half life of Testosterone Enanthate 300, a dose of 500 mg per week can be used for the first time user for a period of 10 weeks with very good results. Stacking oral steroids on a first cycle is generally considered uneccessary, because it is impossible to gauge your body's responsiveness to the individual steroids being used and determine which ones cause which side effects. For the more advanced athlete, doses of 500 - 1000 mg of Testosterone Enanthate 300 are also excellent for creating clear results within a 10 week period. More advanced athletes will often stack Testosterone Enanthate with Dianabol, Deca Durabolin, Primobolan or Equipose to create a powerful mass building stack.
All testosterones aromatize, and enanthate is no exception. The steroid user should be familiar with anti-estrogen compounds such as Nolvadex and Clomid and keep them on hand during cycle in case symptoms of gyno arise. Increases in water weight and fat weight should be expected, and the possibilities of gyno are always out there when using Testosterone Enanthate 300.
Standard post cycle therapy consisting of either Nolvadex or Clomid should take place after the cycle is over.
SIDE EFFECTS:
Side effects such as water retention usually occur when using Testosterone Enanthate. Gyno, increased rate of hair growth, back acne, increased blood pressure, and aggressiveness, both in the gym and out, are possible when using this steroid. The liver is accustomed to processing testosterone, so liver toxicity is normally not a concern except at extremely high doses.
300 - 1000mg per week.
Winsto 50 is an injectable steroid made by Euro-Med, its active substance is Stanozolol.
Winsto 50 is a popular brand name for the anabolic steroid Stanozolol. 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. Admittedly the anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a reliable builder. Its efficacy as an anabolic could even be comparable to Dianabol, however Winsto 50 does not carry with it the same tendency for water retention.
What is special about the injectable Winsto 50 is that its substance is not as is common in almost all steroids-dissolved in oil it is dissolved in water. Although almost every steroid-experienced bodybuilder knows this difference, the practical application of this knowledge rarely occurs: the injection-free intervals of the compound Winsto 50 must be distinctly shorter than with the other common steroids. Simplified, this means that Venaject 50-100 mg/ml must be injected much more frequently than the oil-dissolved steroids (e.g. Primobolan, Deca Durabolin, Sustanon 250, Parabolan, etc.). The reason for this is the relative low half-life time of steroids. Those dissolved in water must be injected at least every second day, and best results are observed at a daily injection of 50-100 mg. The substance Stanozolol is a precursor to the dihydrotestosterone and consequently, it prevents Winsto 50 from aromatizing into estrogens with water retention occurring only rarely. Based on these characteristics the main application of Winsto 50 is clearly defined in bodybuilding: preparation for a competition. Together with a calorie-reduced diet which is rich in protein Winsto 50 gives the muscles a continuously harder appearance. Winsto 50 is usually not used as the only steroid during dieting since, based on its low androgenic component, it does not reliably protect the athlete from losing muscle tissue. The missing, pronounced, androgenic effect is often balanced by a combined intake with Parabolan. The combination of Venaject 5O - 100 mg/day and Finaject 30 mg/day, until a few years ago, was THE competition stack. Since original Finaject has been phased out for years Parabolon has taken over its place. Depending on the athletes performance level, the athlete usually takes 50-100 mg Winsto 50 every l-2 days and Parabolan 76 mg/1.5 ml every 1-2 day. Although there is no scientific proof of a special combined action between Winsto 50 and Parabolan, based on several practical examples, a synergetic effect seems likely. Other steroids which athletes successfully combine with Winsto 50 during the preparation for a competition include Masteron, Equipose, Halotestin, Anavar, Testoviron Depot, Primobolan Depot, and HGH.
Winsto 50, however, is not only especially suited during preparation for a competition but also in a gaining phase. Since it does not cause water retention rapid weight gains with Winsto 50 are very rare. However a solid muscle gain and an over proportionally strong strength increase occur, usually remaining after use of the compound is discontinued. Bodybuilders who want to build up strength and mass often combine Winsto 50 with Dianabol (D-bol), Anadrol, Testoviron Depot, or Deca Durabolin. With a stack of 100 mg Anadrol/day, 50-100 mg Winsto 50/day, and 400 mg Deca Durabolin/week the user slowly gets into the dosage range of ambitious competing athletes. Older athletes and steroid novices can achieve good progress with either Winsto 50/Deca Durabolin or Winsto 50/Primobolan Depot. They use quite a harmless stack which normally does not lead to noticeable side effects. This leaves steroid novices with enough room for the "harder" stuff which they do not yet need in this phase Winsto 50 is mainly an anabolic steroid with a moderate, androgenic effect which, however can especially manifest itself in women dosing 50-100 mg/week and in men dosing higher quantities. Problems in female athletes usually occur when a quantity of 50-100 mg is injected twice weekly. The effect of Winsto 50 decreases considerably after a few days and thus an injection at least twice weekly is justified. However, an undesired accumulation of androgens in the female organism can occur, resulting in masculinization symptoms. Some deep female voices certainly originated with the intake of Winsto 50. However, a dose of 50-100 mg Winsto 50 every second day in ambitious female athletes is the rule rather than the exception. Other non-androgenic side effects can occur in men as well as in women, manifesting themselves in headaches, cramps, changes in the HDL and LDL values, and in rare cases, in high blood pressure. Possible liver damage can be estimated as very low when Winsto 50 is injected, however in large doses an elevation in the liver values is possible.
This steroid is often combined with other steroids depending on the desired result. For bulking purposes, a stronger androgen like testosterone, Dianabol or Anadrol 50 is usually added. Here it 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 contest and dieting phases we could alternately combine Winsto 50 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 otherwise addition compounds like Primobolan, Deca-Durabolin or Equipoise when wishing to stack this steroid. Here we should see good results and fewer side effects than is to be expected with standard androgen therapies.
SIDE EFFECTS:
Stanozolol tablets will also place a higher level of stress on the liver than the injectable Winstrol (which avoids the "first pass")During longer or higher dosed stanozolol cycles, liver values should therefore be watched closely through regular blood work. Although less common, the possibility of liver damage cannot be excluded with the Winsto 50 (Stanozolol) however. 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 amplified when adding other 17-AA oral compounds to a cycle of Winsto 50. When using such combinations, cautious users would make every effort to limit the length of the cycle (preferably 6 to 8 weeks).
50mg - 100mg per day
Oxandrolone is popular among bodybuilders because of its fabulous effects. It was a shame if Platinum Biotech with its reputation wouldn't make its own Oxandrolone. Oxandrolone by Platinum Biotech is called Anavar-50. Its strength is 50 mg per tablet and it is sold by 100 tablets.
This steroid is ideal for bulking purposes and it is commonly used during cutting phases of training. Who used this steroid probably know that it has two major advantages: it does not aromatize and it does not influence the body’s testosterone production. These two things are very, very important for body's health. No less importantly is that Anavar-50 does not retain liquid in the joints and the muscles.
This steroid is commonly used by bodybuilders, weightlifters and powerlifters. Weightlifters and powerlifters likes this steroid because it causes fabulous gains in strength without gaining body weight. This is very important for them because they don’t want to end up in higher weight class.
Anavar-50 itself does not cause noticeable muscle growth and strength. It can be combined with many steroids, like Deca Durabolin, Dianabol and various testosterone compounds. A combination that has been proven to be very effective is Oxandrolone and Halotestin 20 - 30 mg per day. The same effect will have Oxandrolone with 120 – 140 mcg of Clenbuterol daily. A good gain in muscle mass and strength is 200 mg of Deca Durabolin per week, 500 mg of Testosterone Enanthate per week and Anavar-50 25 mg daily.
SIDE EFFECTS:
Anavar-50 is slightly toxic and shows only few side effects, but should not forget that as almost oral steroids it is 17-alpha-alkylated and the usage in high dosage and for a long period of time it can put stress on liver.
In medicine Oxymetholone was developed and used to help people with anemia and other diseases where weight loss was a concern. This compound is very effective for increasing appetite, gaining weight and strength, also it is increasing red blood cells count. Because of its effects, it is very popular nowadays in bodybuilding and other sports. EURO-MED has made its own Oxymetholone drug that is called Androlic 50. Its strength is 50 mg per tablet and it is sold by 100 tablets in EURO-MED original pack.
This steroid is very popular among bodybuilders and strength athletes, because it can be an alternative for D-bol. Androlic 50 offers the same results as D-bol, some times greater, but with fewer side effects. Usually, athletes report gains in mass up to 10 pounds in 2 weeks that are not uncommon for this steroid.
Why Oxymetholone is showing such good effects? This is the most asked question, but the answer is very simple. Because it increases the number of red bloods cells that allows the muscles to absorb more oxygen. To explain that, I will give you an example, the athlete can feel great power and strength even after several sets. The intake of Androlic 50 usually gives a fantastic and satisfying sensation, also it stimulates the body to regenerate faster. Only after few hours after a hard training, you can feel that you are ready now for more.
It is advised that the daily dosage of Androlic 50 should be in range of 0.5 – 0.8 mg per body weight. Also it is advised for those who like to take this steroid for the first time to limit the dosage to 50 mg per day and only after a week the dosage can be increased to 100 mg per day.
It is important to know that after discontinuing Oxymetholone, in a short period of time drastic reduction takes place and the user looks like before taking this steroid, that’s why it is need to continue the cycle with injectable steroids like testosterone or Sustanon for several weeks.
SIDE EFFECTS:
Unfortunately, Androlic 50 is at the same time the most harmful oral steroid, it is very toxic to liver because it is 17-alpha-alkylated. Also this steroid easily converts into estrogen, causes signs of feminization and water retention. That’s why it is required to take anti estrogens and diuretics.
Buy androlic 50 mg and get massive strength and maximum weight gain.
50 - 100mg per day
Dianabol is the branded name of Atlas Pharma. This lab is new on the market, but in a short period of time became well known by bodybuilders from all over the world because of its high quality products. The active substance in Dianabol is Methandienone, which is 10 mg per tab, also it is sold by 100 tabs per pack. This kind of drug is also known among bodybuilders as D-bol, Anabol, Dianabol, Methan, Methanabol, Dianabol etc.
Dianabol it is an oral steroid, which has a great effect on protein metabolism and its androgenic effect manifests itself in buildup of muscle mass and strength. Often it is called a "mass steroid", because in the first six weeks it is normal to gain 2 – 4 pounds of body weight per week. It is important to know that this steroid manifests itself in a noticeable retention of water and aromatizes easily. To avoid these effects it is recommended to take Nolvadex and Proviron.
The dosage should be coordinated with individual goals, for experienced bodybuilders the daily dose should be around 40 – 60 mg. Novices do not need to take more than 20 – 40 mg per day.
After eight weeks when the effect begins to slow down and you want to continue the cycle, the dosage of Dianabol should not be increased, it is enough to add such injectable steroids as Deca Durabolin or Primobolan. If you’ll choose Deca Durabolin, the dosage should be 200 mg per week, if Primobolan the same dosage of 200 mg per week should be enough. If you are either impatient or more advanced, you can start taking Dianabol 20 – 30 mgs daily and Deca Durabolin 200 – 400 mg per week.
If you are more interested in strength and less in body mass, than you can combine Dianabol with Oxandrolone or Stanozolol tablets.
SIDE EFFECTS:
As many other steroids, Dianabol has many potential side effects, but they are rare when the daily dosage is up to 20 mg. This steroid is I 7-alpha-alkylated, so it can be toxic to liver when it is taken in high dosage and for a long period of time. Dianabol strongly converts into estrogens and in some athletes causes gynecomastia. To avoid such effects it is recommended to take such drugs as Nolvadex and Proviron. Because of androgenic component the sebaceous gland is stimulated and it can cause acne vulgaris on the face, neck, chest, back and shoulders.
30 - 60 mg per day.
Stanozolol is one of the most popular and recognized anabolic steroid among bodybuilders, that’s why most of steroid manufacturers make use of this opportunity and has this drug in their production. An exception is not LA Pharma, which during years have proved that they can offer to users high quality steroids.
For stanozolol, LA Pharma uses the branded name Stanozolol 10. As you realized, the active component of Stanozolol 10 is Stanozolol and it is 10 mg per tablet. It is sold by 100 tablets in a sterile sachet.
The main reason why this steroid is so popular is maybe because it does not convert to estrogen and an anti estrogen drug is not needed while using stanozolol. Also it does not give water retention and not giving gynecomastia.
The daily dosage of Stanozolol 10 is usually 35 – 75 mg. Most often it is not taken alone, usually it is taken in combination with other steroids depending on desired goals. Testosterone, D-bol or Oxymetholone is added for bulking purposes. In this case stanozolol will balance out the cycle a bit, giving good anabolic effect with lower estrogenic activity. The result of this combination should be a gain in muscle mass with a low level of water and fat retention.
Stanozolol 10 can be used in combination with Trenbolone or Halotestin. Such combination is usually for contests and dieting phases. The result should be a strongly defined and hard look of muscularity.
SIDE EFFECTS:
Stanozolol is a 17-alpha-alkylated, that’s why for those who take this steroid for a long period of time and in high doses, liver toxicity should be a concern. Due to the liver toxicity it is recommended to those who take this steroid to limit their cycles to six weeks or less. If you decided to run Stanozolol 10 for a longer period of time, you should monitor your liver values via blood test to ensure that no damage occurs.
Other side effects are: acne, prostate enlargement and aggravation of male pattern baldness. As i said earlier, to avoid dramatic side effects the dosage and the time of using should be strictly monitored.
35 - 75mg per day
T3-50 is an weight loss drug, it is also known as Cytomel. This drug is manufactured by Platinum Biotech.
T3-50 is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodide-thyronine. The thyroid of a healthy person usually produces two hormones, the better known L-thyroxine and the aforementioned L-triiodine-thyronine. Since T3-50 is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-T3-50 is clearly the stronger and more effective of these two hormones. This makes T3-50 more effective than the commercially available L-T4 compounds such as L-thyroxine or Synthroid.
Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking T3-50, which causes a faster conversion of carbohydrates, proteins and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means increased fat burning. Competing bodybuilders, in particular, use T3-50 during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of T3-50 report that by the simultaneous intake of steroids, the steroids become more effective, most likely as the result of the faster conversion of protein.
It is important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, one tablet every 3-4 days. Taking T3-50 for too long and/or at too high a dosage can result in a permanent thyroid deficiency. After doing such, one might need to be treated with a drug like T3-50 for life. It is also a good idea to first consult your physician and have your thyroid function tested. An undiagnosed hyperfunction would not mix well with the added hormone. An athlete should also be sure never to purchase an injectable form of the drug. It is generally an emergency room product, much too powerful for athletic use. Since T3-50 is the most powerful thyroid hormone athletes are using, this is generally not the starting point for a beginner. Before using such a powerful item, it is a good idea to become familiar with a weaker substance. The highly popular Triacana is very mild, allowing the user much more latitude (from severe side effects) than T3-50. An in-between point is Synthroid (synthetic T-4), still weaker in action than T3-50. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.
Until recently, T3-50 was used by bodybuilders and female bodybuilders, in particular on a daily basis over several months to remain "hard" and in good shape all year round. Believe us when we tell you that to a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and defined look in photos, eat fast food and iron this out by taking T3-50. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of T3-50, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat.
T3-50 is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given todays standards. A drastic reduction of food and calories below the 1000 calorie/day mark can often be avoided by taking T3-50. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of T3-50 in a reasonable dosage is certainly "healthier" than an extreme hunger diet.
As for the dosage, one should be very careful since T3-50 is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25 mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100 mcg/day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also important that T3-50 not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and not be ended abruptly.
SIDE EFFECTS:
One should take caution if considering using this drug. T3-50 comes with an extensive list of warnings and precautions which are not to be ignored. Side effects include, but are not limited to, heart palpitations, agitation, shortness of breath, irregular heartbeat, sweating, nausea, headaches, and psychic/metabolic disorders. It is a powerful hormone, and one that could potentially alter the normal functioning of the body if misused. When administering T3-50, one must remember to increase the dosage slowly. Generally one 25 mcg tablet is taken on the first day, and the dosage is thereafter increased by one tablet every three of four days for a maximum dosage of 100 mcg. This will help the body adjust to the increased thyroid hormone, hopefully avoiding any sudden "shock" to the system. The daily dose is also to be split evenly throughout the day, in an effort to keep blood levels steadier. Women are more sensitive to the side effects of T3-50 than men, and usually opt to take no more than 50 mcg daily.
Astralean is an weight loss drug, its active substance is Clenbuterol. This drug is manufactured by Alpha Pharma.
Clenbuterol belongs to the class of drugs classified as sympathomimetics. Sympathomimetic drugs are compounds that mimic or imitate the effects of the hormone epinephrine (adrenaline) and the hormone/neurotransmitter norepinephrine (noradrenaline).
Clenbuterol is a popular drug prescribed as a decongestant and bronchodilator and commonly used by sufferers of asthma. However, it is now becoming popular as a dietary supplement endorsed as an effective slimming pill.
Astralean is on of the most popular and potent cutting agents available. Astralean is known to burn fat with thermogenic properties and also build lean muscle mass. Clenbuterol is a potent, long-lasting bronchodilator that is used in some European countries to treat asthma and related lung disorders. However, the drug is also a potent thermogenic agent and can selectively decrease fat and increase lean muscle mass. This property of Astralean has made it a widely abused drug among many individuals. Because of this selective partitioning effect, the drug is widely abused by both amateur and professional athletes around the world.
Many bodybuilders, as well as other athletes, find Astralean beneficial because of its thermogenic abilities. As a thermogenic it increases blood pressure, stimulating the heart muscles. This stimulation, in turn, leads to an increase in body temperature. In addition, Astralean boosts glycogenolysis, or the breakdown of glycogen. This process results to release of glycogen into the bloodstream (in the form of glucose) and renders the body incapable of storing or using more glycogen. This hikes the rate at which fat and protein are used up in the body for these three essential purposes – energy production, for recycling of their molecular components, or for their excretion. This is how Astralean users lose adipose (fat) tissues.
Astralean is also particularly appealing to bodybuilders and other athletes because it heightens aerobic capacity. Aerobic means "with oxygen", and refers to the use of oxygen in the body's metabolic or energy-generating process. In simple terms, Astralean improves oxygen transportation via increased blood pressure. This makes Clenbuterol a staple of many endurance athletes’ drug protocol.
This drug is also used as an anabolic agent although its anabolism effect remains a contentious issue. In several animal studies, it has exhibited anabolism resulting to muscle gains. However, this has not been observed on human subjects.
The recommended regimen with this drug is to gradually ramp up its dosage. Slowly build up the intake each day until an effective and comfortable range is established. This way, most of the drug’s effects can be avoided, specifically its negative effect on blood pressure. Males typically take 2-8 tablets a day while females take 2 - 4 tablets a day.
The length of time this drug is to be cycled is dependent on the goal of the user. If your objective is to lose fat, Astralean highest efficacy is observed when taken in a period of 4 - 6 weeks. During this phase, it is important to monitor temperature increase or decrease.
Remember that as a thermogenic this drug works by elevating the temperature, and thus a decrease or a drop in temperature means its losing its potency. This also signals that you need to break for at least several weeks. Increasing the dosage or prolonging the intake will prove to be ineffective and a total waste of money since the decreased efficacy may mean that the body is growing immune or resistant to its effects.
To heighten its fat-burning ability, many stack Astralean with other drugs such as the thyroid hormone Cytomel. This stack is great during contest preparation or cutting cycle when bodybuilders need to get rid of undesirable fat without sacrificing caloric intake.
Astralean is also typically stacked with non-aromatizing anabolic steroids, those that do not cause water retention. This stack regimen induces the so-called synergistic effect of drugs.
Astralean dosage is dependent on body weight and can be optimized by measuring the body temperature. Athletes usually take 5 - 7 tablets, 100 - 140 mcg per day. For women 80 - 100 mcg/day is usually sufficient. It is advisable to begin Astralean by taking only one tablet on the first day and then increasing the dosage by one tablet each of the following days until the desired maximum dosage is reached. The compound is usually taken over a period of 8 - 10 weeks.
SIDE EFFECTS:
Possible side effects of Astralean include restlessness, palpitations, tremor (involuntary trembling of fingers), headache, increased perspiration, insomnia, muscle spasms, increased blood pressure, and nausea. Individuals who have been diagnosed of cardio-vascular problems should not take Astralean.
Use a pyramid starting from 20mcg to 120-150 mcg and finishing 20mcg.
Clenbuterol-40 is an weight loss drug, its active substance is Clenbuterol. This drug is manufactured by Platinum Biotech.
Clenbuterol belongs to the class of drugs classified as sympathomimetics. Sympathomimetic drugs are compounds that mimic or imitate the effects of the hormone epinephrine (adrenaline) and the hormone/neurotransmitter norepinephrine (noradrenaline).
Clenbuterol is a popular drug prescribed as a decongestant and bronchodilator and commonly used by sufferers of asthma. However, it is now becoming popular as a dietary supplement endorsed as an effective slimming pill.
Clenbuterol-40 is on of the most popular and potent cutting agents available. Clenbuterol-40 is known to burn fat with thermogenic properties and also build lean muscle mass. Clenbuterol is a potent, long-lasting bronchodilator that is used in some European countries to treat asthma and related lung disorders. However, the drug is also a potent thermogenic agent and can selectively decrease fat and increase lean muscle mass. This property of Clenbuterol-40 has made it a widely abused drug among many individuals. Because of this selective partitioning effect, the drug is widely abused by both amateur and professional athletes around the world.
Many bodybuilders, as well as other athletes, find Clenbuterol-40 beneficial because of its thermogenic abilities. As a thermogenic it increases blood pressure, stimulating the heart muscles. This stimulation, in turn, leads to an increase in body temperature. In addition, Clenbuterol-40 boosts glycogenolysis, or the breakdown of glycogen. This process results to release of glycogen into the bloodstream (in the form of glucose) and renders the body incapable of storing or using more glycogen. This hikes the rate at which fat and protein are used up in the body for these three essential purposes – energy production, for recycling of their molecular components, or for their excretion. This is how Clenbuterol-40 users lose adipose (fat) tissues.
Clenbuterol-40 is also particularly appealing to bodybuilders and other athletes because it heightens aerobic capacity. Aerobic means "with oxygen", and refers to the use of oxygen in the body's metabolic or energy-generating process. In simple terms, Clenbuterol-40 improves oxygen transportation via increased blood pressure. This makes Clenbuterol a staple of many endurance athletes’ drug protocol.
This drug is also used as an anabolic agent although its anabolism effect remains a contentious issue. In several animal studies, it has exhibited anabolism resulting to muscle gains. However, this has not been observed on human subjects.
The recommended regimen with this drug is to gradually ramp up its dosage. Slowly build up the intake each day until an effective and comfortable range is established. This way, most of the drug’s effects can be avoided, specifically its negative effect on blood pressure. Males typically take 2-8 tablets a day while females take 2 - 4 tablets a day.
The length of time this drug is to be cycled is dependent on the goal of the user. If your objective is to lose fat, Clenbuterol-40 highest efficacy is observed when taken in a period of 4 - 6 weeks. During this phase, it is important to monitor temperature increase or decrease.
Remember that as a thermogenic this drug works by elevating the temperature, and thus a decrease or a drop in temperature means its losing its potency. This also signals that you need to break for at least several weeks. Increasing the dosage or prolonging the intake will prove to be ineffective and a total waste of money since the decreased efficacy may mean that the body is growing immune or resistant to its effects.
To heighten its fat-burning ability, many stack Clenbuterol-40 with other drugs such as the thyroid hormone Cytomel. This stack is great during contest preparation or cutting cycle when bodybuilders need to get rid of undesirable fat without sacrificing caloric intake.
Clenbuterol-40 is also typically stacked with non-aromatizing anabolic steroids, those that do not cause water retention. This stack regimen induces the so-called synergistic effect of drugs.
Clenbuterol-40 dosage is dependent on body weight and can be optimized by measuring the body temperature. Athletes usually take 5 - 7 tablets, 100 - 140 mcg per day. For women 80 - 100 mcg/day is usually sufficient. It is advisable to begin Clenbuterol-40 by taking only one tablet on the first day and then increasing the dosage by one tablet each of the following days until the desired maximum dosage is reached. The compound is usually taken over a period of 8 - 10 weeks.
SIDE EFFECTS:
Possible side effects of Clenbuterol-40 include restlessness, palpitations, tremor (involuntary trembling of fingers), headache, increased perspiration, insomnia, muscle spasms, increased blood pressure, and nausea. Individuals who have been diagnosed of cardio-vascular problems should not take Clenbuterol-40.
T3-Cytomel is an weight loss drug, it is also known as Cytomel. This drug is manufactured by LA Pharma.
T3-Cytomel is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodide-thyronine. The thyroid of a healthy person usually produces two hormones, the better known L-thyroxine and the aforementioned L-triiodine-thyronine. Since T3-Cytomel is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-T3-Cytomel is clearly the stronger and more effective of these two hormones. This makes T3-Cytomel more effective than the commercially available L-T4 compounds such as L-thyroxine or Synthroid.
Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking T3-Cytomel, which causes a faster conversion of carbohydrates, proteins and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means increased fat burning. Competing bodybuilders, in particular, use T3-Cytomel during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of T3-Cytomel report that by the simultaneous intake of steroids, the steroids become more effective, most likely as the result of the faster conversion of protein.
It is important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, one tablet every 3-4 days. Taking T3-Cytomel for too long and/or at too high a dosage can result in a permanent thyroid deficiency. After doing such, one might need to be treated with a drug like T3-Cytomel for life. It is also a good idea to first consult your physician and have your thyroid function tested. An undiagnosed hyperfunction would not mix well with the added hormone. An athlete should also be sure never to purchase an injectable form of the drug. It is generally an emergency room product, much too powerful for athletic use. Since T3-Cytomel is the most powerful thyroid hormone athletes are using, this is generally not the starting point for a beginner. Before using such a powerful item, it is a good idea to become familiar with a weaker substance. The highly popular Triacana is very mild, allowing the user much more latitude (from severe side effects) than T3-Cytomel. An in-between point is Synthroid (synthetic T-4), still weaker in action than T3-Cytomel. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.
Until recently, T3-Cytomel was used by bodybuilders and female bodybuilders, in particular on a daily basis over several months to remain "hard" and in good shape all year round. Believe us when we tell you that to a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and defined look in photos, eat fast food and iron this out by taking T3-Cytomel. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of T3-Cytomel, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat.
T3-Cytomel is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given todays standards. A drastic reduction of food and calories below the 1000 calorie/day mark can often be avoided by taking T3-Cytomel. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of T3-Cytomel in a reasonable dosage is certainly "healthier" than an extreme hunger diet.
As for the dosage, one should be very careful since T3-Cytomel is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25 mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100 mcg/day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also important that T3-Cytomel not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and not be ended abruptly.
SIDE EFFECTS:
One should take caution if considering using this drug. T3-Cytomel comes with an extensive list of warnings and precautions which are not to be ignored. Side effects include, but are not limited to, heart palpitations, agitation, shortness of breath, irregular heartbeat, sweating, nausea, headaches, and psychic/metabolic disorders. It is a powerful hormone, and one that could potentially alter the normal functioning of the body if misused. When administering T3-Cytomel, one must remember to increase the dosage slowly. Generally one 25 mcg tablet is taken on the first day, and the dosage is thereafter increased by one tablet every three of four days for a maximum dosage of 100 mcg. This will help the body adjust to the increased thyroid hormone, hopefully avoiding any sudden "shock" to the system. The daily dose is also to be split evenly throughout the day, in an effort to keep blood levels steadier. Women are more sensitive to the side effects of T3-Cytomel than men, and usually opt to take no more than 50 mcg daily.
25 - 100 mcg per day
Aroma-25 is an post cycle steroid, it is also known as Aromasin and is made by Platinum Biotech.
Aroma-25 is a steroidal suicide aromatase inhibitor, which means that it lowers estrogen production in the body by blocking the aromatase enzyme, the enzyme responsible for estrogen synthesization.
Exemestane was developed to fight breast cancer in post-menopausal women, who need a particularly aggressive therapy, and for whom first line defenses such as SERMS (Tamoxifen) have not worked. This should be our first clue in inferring that this stuff is pretty strong, or at least stronger than some of the other compounds which are used to fight breast cancer.
Aroma-25 averages an 85% rate of estrogen suppression, so it´s clearly a very effective agent for bodybuilders and other athletes wanting to avoid estrogen related side effects such as gyno, acne, or water-retention brought on by aromatizing steroids. Specifically, Aroma-25 dose this by selectively inhibiting aromatase activity in a time-dependent and irreversible manner.
As with most of the compounds in this class, it also causes a reasonable rise in testosterone levels, and as you may have guessed, this rise in testosterone means that Aroma-25 can also cause androgenic sides. As you can see from the chart below, exemestane is very effective at both lowering estrogen (estradiol) and raising testosterone: Estrogen and androgen plasma levels after 10 d of daily exemestane (25 or 50 mg) in healthy young males. To convert to Systeme International units: estradiol, picomoles per liter; estrone, picomoles per liter; androstenedione, nanomoles per liter; and testosterone, nanomoles per liter.
So we can see that 25 mgs is a very effective dose from that chart, right? As an added benefit, exemestane not only increases testosterone and lowers estrogen, but it also increases IGF levels. Additionally Worth noting is that Aroma-25 may possibly be less harsh on blood lipids than some of the other (similar) compounds we use in the world of bodybuilding or athletics. It also has, at best no effect on IGF, and at worst could lower it. AI´s are very tricky with regards to inconsistencies in IGF levels.
Unfortunately, you need to take Exemestane for a week to reach steady blood plasma levels of it, and exemestane has a half life of 27 hours.
The ability of exemestane to lower estrogen levels by the aforementioned 85% makes it a very nice choice for use in any cycle where aromatizing steroids are used. In addition, since it´s not too harsh at all on blood lipid profiles, it´s a very good choice for longer cycles. It´s ability to raise both testosterone levels also seem to suggest that it would be a very nice addition to a Post-Cycle-Therapy (PCT).
SIDE EFFECTS:
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Exemestane: anxiety; back, joint, muscle, or limb pain; constipation; coughing; diarrhea; dizziness; fatigue; flu-like symptoms; hair loss; headache; hot flashes; increased or decreased appetite; increased sweating; joint pain; nausea; stomach pain or upset; tiredness; trouble sleeping; weight gain; vomiting.
Letrozole-2.5 is an post cycle steroid, it is also known as Femara and is made by Platinum Biotech.
Letrozole-2.5 is a third generation aromatase inhibitor. Like most aromatase inhibitors it was developed to fight breast cancer by inhibiting aromatization via the aromatase enzyme. It is similar to Arimidex, however Letrozole-2.5 is much more potent in it's ability and is used primarily when other treatments such as selective estrogen receptor modulators have failed to produce results. This is why the majority of the research about Letrozole has been conducted on post-menopausal women, but of course some of the findings can be translated over for the benefit of athletes.
In terms of how these effects can be used to the benefit of bodybuilders and strength athletes, Letrozole-2.5 is primarily used to ward any estrogenic side effects caused by the administration of anabolic steroids. This steroid has been show to have the capability of reducing the level of estrogen in users' bodies by up to 96-98%. This would seemingly be enough in itself to make the compound a desirable one with which steroid users would be interested in. However Letrozole-2.5 also has been shown to increase the amount of lutenizing hormone, follicle stimulating hormone, and sex hormone binding globulin in users. When you combine these attributes with the fact that it will help protect against gynocomastia, water retention and other estrogenic side effects letrozole obviously can fulfill many users' needs.
There are some animal studies that have suggested that Letrozole can help to reduce or even eliminate pre-existing gynocomastia as well. Of course there are some limits to this research as it has never been conducted using human subjects but it does demonstrate that there may be a mechanism by which this could occur. Anecdotally some users have reported that they have experienced a reduction in their own pre-existing gynocomastia, but of course these reports have their limits as they were not conducted with the scientific controls in place.
Interestingly, it takes approximately 60 days to get a steady blood plasma level of letrozole once administration of the drug begins. This may necessitate that a user begin using the compound prior to beginning their cycle if they wish for the effects to be at full strength once their cycle begins. This may also hinder the ability of the compound to respond quickly if a user begins administration of the drug to counteract some side effects that have appeared quickly.
Anecdotally users have reported seeing good results using doses ranging from about 25 mgs per day to 5 mgs per day. However these doses do vary quite widely from user to user, including dosing schedules. Some have reported using the compound every other day or every third day with good results. Also, doses reported have ranged from 25 mgs to as much as 2.5 mgs per day.
Despite this anecdotal evidence it should be noted that doses as low as 100 micrograms can cause the maximum inhibition of the aromatase enzyme. It is therefore advisable that users experiment with their dosages to find what levels can be maintained for the compound to be fully effective, while minimizing side effects. Of course if a user is trying to treat side effects that have already appeared one may want to err on the side of using too much Letrozole-2.5 and face those side effects rather than dealing with something like gynocomastia. However, the severity of the condition will likely determine this in most cases.
The maximum dosage that a user would want to use would be 2.5 mgs per day. It has been shown in numerous studies that this dosage will eliminate nearly all of the estrogen in the body in nearly all individuals. Any dose that is higher than this would simply be unneeded.
Despite the ability to increase the amount of lutenizing hormone, follicle stimulating hormone, and sex hormone binding globulin in users Letrozole-2.5 can be counterproductive if used during post-cycle therapy. This is due to the ability of the compound to drive estrogen levels too low during use. Once the compound is discontinued this can result in a "rebound effect" in estrogen levels with these becoming quite high, something that should be avoided during or after post-cycle therapy. Anastrozole could be seen as an alternative to Letrozole-2.5 in this capacity as it seemingly does not have such a potent effect. The detrimental effect that letrozole has on blood lipid levels is another reason why many will avoid it's use during post-cycle therapy, and this is discussed below.
SIDE EFFECTS:
It should be noted that in theory if one was to consistently suppress your natural estrogen levels for a long period of time, this would negatively impact your health, including your cholesterol. Due to the ability of Letrozole-2.5 to inhibit estrogen so much, this should definitely be a concern to most users. However the research that has focused on the relationship between use of letrozole and cholesterol levels is rather inconsistent in it's findings. Many studies have concluded that the compound is detrimental to both a user's HDL and LDL cholesterol levels, while other research has found no link. Obviously individuals are best served to monitor their cholesterol while using any compound via blood tests however barring that, letrozole should simply not be run for extended periods of time if at all possible. Doing so could cause serious medical complications.
Along with the issues related to blood lipids is the fact that many users complain that their libido is dramatically reduced when using the compound. This is related to the fact that estrogen is partly responsible for the regulation of an individual's sex drive. Since Letrozole-2.5 is so potent it can often drive estrogen levels too low and this inhibits a user's libido. To avoid this users can lower dosages, but some anecdotally report that even extremely low doses of the drug can cause problems. If this is the case a less potent compound such as exemestane or anastrozole may be a more appropriate option.
Nolvo-20 is an post cycle steroid and is made by Platinum Biotech. The active substance is Nolvo-20 Citrate.
Nolvo-20 is probably the most popular ancillary drug for male steroid users who wish to avoid the estrogen like effects caused by the use of anabolic steroids. Nolvo-20 Citrate binds to estrogen receptors thus blocking the hormones action on target tissues and achieving an anti-estrogenic effect.
Also worth noting is the fact that Nolvo-20 is an estrogen agonist in the liver and is capable of mimicking estrogen in this organ. At first glance you may wonder why this could be considered a good thing, however, when you realize that estrogen positively effects HDL (good) cholesterol values in the liver its value in this instance becomes obvious. As you know, steroid use tends to suppress HDL levels and raise LDL levels significantly leading to increased cholesterol levels and cardiac risk. Adding Nolvo-20 may therefore form a protective function in this case, although it certainly does not save the liver from all the other hazards involved with the use of c-17 alpha alkylated orals.
Nolvo-20 Citrate is a selective estrogen receptor modulator. Selective estrogen receptor modulators can act as estrogen receptor agonists or antagonists. This activity of Nolvo-20 Citrate is tissue selective, effecting those estrogen receptors located in the liver, breast, and bone. When the Nolvo-20 molecule binds to this receptor, the estrogen is blocked and can not have any influence, thereby remaining inactive in that tissue. By doing so, an "anti-estrogenic" effect is achieved. The drug was developed and still used to treat breast cancer. It is often used as a first option due to its mild nature in comparison to aromatase inhibitors. Of course one would want to use the mildest compound possible when dealing with estrogen levels in women, but one could afford to be more aggressive in dealing with male strength athletes or bodybuilders.
In terms of its use in steroid users, Nolvo-20 can help in two ways. Firstly due to the binding affinity of the compound it is able to help in the prevention of gynocomastia. Nolvo-20 will compete with estrogen for the estrogen receptors in certain tissues, including the breast, and if it can bind to the receptor estrogen will not have an opportunity to interact with receptor and therefore gynocomastia should not be able to develop. When using anabolic steroids that can convert to estradiol (estrogen) this protection against gynocomastia can be invaluable. However it should be noted that Nolvo-20 Citrate will not eliminate the estrogen or disallow the conversion to occur. Instead it attempts to counteract the effects of circulating estrogen in the body in those tissues that the drug effects. Therefore there is no evidence that Nolvo-20 has any effects counteracting etrogenic side effects that are unrelated to the tissues that are not in the breast, liver or bone. Namely there is no real causal connection to any reduction in water retention and acne in users that begin taking Nolvo-20 citrate as it relates to estrogen.
The second, and possibly more beneficial, aspect of Nolvo-20 for steroid users is its ability to increase the production of luteinizing hormone and follicle stimulating hormone, and therefore increasing testosterone. This ability is why it is often used by steroid users during their post-cycle therapy. There are numerous studies that indicate that Nolvo-20 Citrate can increase the levels of these hormones quite dramatically. Nolvo-20 does this by blocking the negative feedback inhibition caused by estrogen at the hypothalamus and pituitary, and this in turn will help to increase the production of these hormones. Unlike clomiphine citrate, Nolvo-20 citrate has also been shown to increase luteinizing hormone responsiveness to gonadotropin releasing hormone. Clomiphine Citrate can lower this responsiveness over time.
In terms of dosing for combating gynocomastia that has begun to form, there is very little research. The limited research that does exist does point to the fact that doses of 20-40 mgs per day are effective in treating the existing condition. However, anecdotally users have reported sometimes using doses of 60-80 mgs per day. These doses may have more to do with users impatience rather than the need for higher doses, as no research indicates that such doses are needed. It should be noted as well however that Nolvo-20 may have no effect on existing gynocomastia in some individuals. Many users have indicated that the compound will only help alleviate symptoms if the gynocomstia has not been apparent for a long period of time. Of course, this is all subjective and the effectiveness of the drug can only be determined on a trial and error basis.
For use during post-cycle therapy users have anecdotally indicated that doses ranging between 20 and 40 mgs per day are average. These doses have been shown to significantly raise levels of testosterone, luteinizing hormone and follicle stimulating hormone. Most users have reported when using Nolvo-20 for their post-cycle therapy they will administer the drug for a minimum of three weeks. A maximum length has not necessarily been established due to the few side effects associated with the compound. In this case, this compound can be run for as long as wanted with little to no concern being needed to be paid to potential side effects. See the below section for more details.
Some users have used Nolvo-20 for the purpose of helping raise their HDL (good) cholesterol values. In theory it is thought that since the compound is an estrogen agonist in the liver and therefore is capable of activating the estrogen receptor and mimicking the actions of the hormone in the organ that it may help improve cholesterol levels as estrogen does. However this effect is rather slight and won’t significantly improve a user’s HDL levels very noticeably at all. This is especially true when one factors in the dramatic effect that most anabolic steroids have on these levels. For this reason, Nolvo-20 should not be relied upon for this purpose.
SIDE EFFECTS:
One of the possible side effects associated with use of Nolvo-20 is the possible reduction of insulin-like growth factor levels. If these levels are reduced this could suppress the gains an individual can make slightly. However this reduction, if it actually exists, would not be overly significant with gains in muscle mass only being marginally reduced for the most part.
Another effect of use of Nolvo-20 may be vision problems. Recently, there has been some information from researchers that indicates corneal, retinal and optic nerve abnormalities seen in patients using the drug could be related to its use. Anecdotally a small number of steroid users have reported that they have suffered from visual problems while using this drug as well. After discontinuation of the drug these symptoms seemingly dissipate. However there is simply not enough research on the subject to know whether permanent damage could occur. More research needs to be conducted.
Other than these concerns, there is little in the way that long-term use of Nolvo-20 could cause damage to in the human body. It is seemingly safe in terms of possible effects to the body’s hormonal production, other than the one relating to insulin-like growth factor, and endocrine system. For the vast majority of users the compound is relatively side effect free and well tolerated.
Provinon-25 is an post cycle steroid, this drug contains Mesterolone and is made by Platinum Biotech.
Provinon-25 is a synthetic, orally effective androgen which does not have any anabolic characteristics. Provinon-25 is used in school medicine to ease or cure disturbances caused by a deficiency of male sex hormones. Many athletes, for this reason, often use Provinon-25 at the end of a steroid treatment in order to increase the reduced testosterone production. This, however is not a good idea since Mesterolone has no effect on the body own testosterone production but as mentioned in the beginning only reduces or completely eliminates the dysfunctions caused by the testosterone deficiency. These are in particular impotence which is mostly caused by an androgen deficiency that can occur after the discontinuance of steroids, and infertility which manifests itself in a reduced sperm count and a reduced sperm quality. Provinon-25 is therefore taken during a steroid administration or after discontinuing the use of the steroids, to eliminate a possible impotency or a reduced sexual interest. This, however does not contribute to the maintenance of strength and muscle mass after the treatment.
Some competitive bodybuilders will also add Mesterolone to their pre-contest preparation as many believe that it will improve muscle density and hardness. This could be attributed to the ability of the compound to decrease water retention and reduce the amount of circulating estrogen in the body, similar to many other androgenic compounds. However, as discussed earlier, there are several other drugs that could be substituted for mesterolone that are much more effective for this prupose.
Many steroid users who have had adverse reactions to testosterone, or otherwise do not wish to use testosterone in their cycle, will often add Mesterolone to their cycles for it's ability to increase the libido of a user. Often times when a user does not include testosterone, or simply not enough testosterone in relation to the other compounds that he is using, libido will be reduced and including Mesterolone may help alleviate this. Obviously, the dihydrotestosterone effect of the compound plays a key role in this process.
This drug is also favored by many during contest preparations, when a lower estrogen/high androgen level is particularly sought after. This is especially beneficial when anabolics like Winstrol, Oxandrolone and Primobolan are being used alone, as the androgenic content of these drugs is relatively low. Provinon-25 can supplement a wellneeded androgen, and bring about an increase in the hardness and density of the muscles. Women in particular find a single 25 mg tablet will efficiently shift the androgen/estrogen ratio, and can have a great impact on the physique. Since this is such a strong androgen however, extreme caution should be taken with administration. Higher dosages clearly have the potential to cause virilization symptoms quite readily. For this reason females will rarely take more than one tablet per day, and limit the length of intake to no longer than four or five weeks. One tablet used in conjunction with 10 or 20 mg of Nolvadex can be even more efficient for muscle hardening, creating an environment where the body is much more inclined to burn off extra body fat (especially in female trouble areas like the hips and thighs).
Provinon-25 is therefore taken during a steroid administration or after discontinuing the use of the steroids, to eliminate a possible impotency or a reduced sexual interest. This, however does not contribute to the maintainance of strength and muscle mass after the treatment.
There are other better suited compounds for this like HCG and Clomid. For this reason Provinon-25 is unfortunately cunsidered by many to be a useless and unnecessary compound.
The majority of male users will find that dosing in the range of 25 to 100 milligrams per day of mesterolone will be enough to acheive their desired results. Females most often remain at about 25 milligrams per day, but many have experimented with levels far higher. Due to the active life of the compound, splitting the dosage of the drug so that it can be taken twice per day is beneficial, but the effects of the compound should remain for a full twenty four hours so it is not completely necessary.
Due to the fact that many other compounds are available that are much more potent and effective than Mesterolone for the same purposes, it is seemingly unnecessary to increase a user's dosage far higher than 100 mgs per day. Instead one would most likely be better served to switch compounds are try a much more potent drug if the desired results are not acheived.
SIDE EFFECTS:
The side effects of Provinon-25 in men are low at a dosage of 2-3 tablets/day so that Provinon-25, taken for example in combination with a steroid cycle, can be used comparatively without risk over several weeks. Since it is well-tolerated by the liver liver dysfunctions do not occur in the given dosages. For athletes who are used to acting under the motto "more is better" the intake of Provinon-25 could have a paradoxical effect. The most common side effect of Provinon-25 or in this case, secondary symptom is in part a distinct sexual over-stimulation and in some cases continuous penis erection. Since this condition can be painful and lead to possible damages, a lower dosage or discontinuing the compound are the only sensible solutions. Female athletes should use it with caution since possible androgenic side effects cannot be excluded. Women who want to give Provinon-25 a try should not take more than one 25 mg tablet per day. Higher dosages and periods of intake of more than four weeks considerably increase the risk of virilization symptoms. Female athletes who have no difficulties with this drug obtain good results with 25 mg Provinon-25/day and 20 mg Nolvadex/day and, in combination with a diet, report an accelerated fat breakdown and continuously harder muscles.
Like any drug, Provinon-25 also is associated with some rare side effects. While the side effects do not occur in all individuals, they are quite disturbing. The side effects include: painful erections, loss of libido, general fatigue, deepening of voice, hair growth, acne, oily skin.
Clomifin-50 is an post cycle steroid, this drug is also known as Clomid and is made by Platinum Biotech.
Clomiphene Citrate is not an anabolic/androgenic steroid. Since it is a synthetic estrogen it belongs, however, to the group of sex hormones. In school medicine Clomiphene Citrate is normally used to trigger ovulation. Clomiphene Citrate also has a strong influence on the hypothalamohypophysial testicular axis. It stimulates the hypophysis to release more gonadotropin so that a faster and higher release of FSH (follicle stimulating hormone) and LH (luteinizing hormone) occurs. This results in an elevated endogenous (body's own) testosterone level. Clomiphene Citrate is especially effective when the body's own testosterone production, due to the intake of anabolic/androgenic steroids, is suppressed. In most cases Clomiphene Citrate can normalize the testosterone level and the spermatogenesis (sperm development) within 10- 14 days. For this reason Clomiphene Citrate is primarily taken after steroids are discontinued. At this time it is extremely important to bring the testosterone production to a normal level as quickly as possible so that the loss of strength and muscle mass is minimized. Even better results can be achieved if Clomiphene Citrate is combined with HCG or when Clomiphene citrate is used after the intake of HCG.
Paradoxically, although Clomiphene Citrate is a synthetic estrogen it also works as an anti-estrogen. The reason is that Clomiphene Citrate has only a very low estrogenic effect and thus the stronger estrogens which, for example, form during the aromatization of steroids, are blocked at the receptors. These would include those that develop during the aromatizing of steroids. This does not prevent the steroids from aromatizing but the increased estrogen is mostly deactivated since it cannot at-tach to the receptors. The increased water retention and the possible signs of feminization can thus be reduced or even completely avoided. Since the antiestrogenic effect of Clomiphene Citrate is lower than those found in Proviron, Nolvadex, and Teslac it is mainly taken as a testosterone stimulant. Clomifin-50 is a medication that promotes the production of the body's own stimulating hormone, gonadotropin, which in turn increases the testosterone level. It is, for example, administered to women as a so-called anti-estrogen to trigger ovulation ("ovulation stimulator").
Originally developed as a female fertility aid, Clomifin-50 has been popular among steroid users for quite some time now as a post-cycle therapy compound used to help recover natural testosterone production. The compound works by partially or completely blocking the effects of estrogen in the body. This is due to the fact that it is a synthetic estrogen with both agonist and antagonist properties. With a similar structure to that of tamoxifen citrate, Clomifin-50 blocks the ability of estrogen to bind with receptors in certain tissues, these being located in the hypothalamus and being suprapituitary, although this is a somewhat contentious claim. Tamoxifen Citrate is selective to those receptors in the liver, breast, and bone. So in terms of use as a fertility drug in women, Clomifin-50 helps to eliminate the negative feedback of estrogens on the hypothalamic-pituitary-ovarian axis and increases the production of luteinizing hormone and follicle stimulating hormone. This induces ovulation.
Therefore if these results can be translated to strength athletes and bodybuilders, this ability to raise the levels of luteinizing hormone and follicle stimulating hormone should be quite impressive. An increase in these hormones will result in an increase in testosterone production in users. This of course is something that is desperately desired when coming off of anabolic steroids. If testosterone levels can be raised quickly after a cycle a user is much more likely to maintain more of his gains than if he suffered through a crash in testosterone levels and his natural production came back slowly, all the while having to combat the increased levels of estrogen and cortisol.
While it is true that Clomifin-50 has many "anti-estrogen" properties, there are a multitude of better options. It's is relatively weak in comparison to tamoxifen citrate and the anti-aromatase compounds that are available are much more potent in terms of controlling and/or eliminating estrogenic side effects that are likely to develop. The primary duty of clomiphine citrate should be left to post-cycle therapy.
Of course due to the fact that there is little research to do with the use of Clomifin-50 as it relates to steroid users, much of what we know about the dosing of it has been from anecdotal reports. For the most part users will maintain doses of the drug between 25 mgs to 150 mgs per day on a consistent basis. Often times users will "frontload" the compound using doses of between 200-300 mgs on the first day of their post-cycle therapy and then reduce the subsequent doses. However the side effects associated with large doses of the compound may hinder some individuals' abilities to do this.
Some users also advocate tapering the dose of Clomifin-50 during the last few weeks of administration. However this is more a practice that is based upon theory rather than solid medical evidence of it's productivity.
In terms of dosing length it seems that at least 3 weeks of Clomifin-50 therapy is recommended by users. Of course each has their own preferences along with individual recovery schedules. Also the types of compounds used and the duration of a cycle will of course influence the time it takes for a user to recover and the need for a lengthy post-cycle therapy. Due to the lack of serious side effects associated with the drug, as well as the fact that there is no risk of toxicity with the Clomifin-50, users are able to use the compound for months on end with seemingly no significant negative consequences.
Male users generally find that a daily intake of 50-100 mg over a four to six weeks period will bring testosterone production back to an acceptable level. This raise in testosterone should occur slowly but evenly throughout the period of intake. Since an immediate boost in testosterone is often desirable, many prefer to combine Clomid with HCG for the first week or two after the steroids have been removed. The kick-start from HCG also helps to restore the normal ability for the testes to respond to endogenous LH, which may be hindered for some time after the cycle is ended due to a prolonged state of inactivity. Once the HCG is stopped, the user continues treatment with Clomid alone. HCG should not be used for longer than two or three weeks though, as the resulting increased testosterone and estrogen levels may again initiate negative feedback inhibition at the hypothalamus. When planning your ancillary drug program, it is also important to remember that injectable steroids can stay active for a long duration. Using ancillary drugs the first week after a long acting injectable like Sustanon has been stopped may prove to be wholly ineffective. Instead, the athlete should wait for two to three weeks, to a point where androgen levels will be diminishing. Here the body will be primed and ready to restore testosterone production.
Clomid and HCG are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time. There is also no exact method for using the two drugs in this manner. Some have experimented by periodically administering small doses of HCG along with one or two tablets of Clomid, perhaps for a few days at a stretch followed by a longer break. An on/off schedule would be implemented; for fear that this combination may lose some effectiveness if used continuously for this purpose. This method of intake may prove to be effective, although it is really much more feasible to stimulate testosterone production after the cycle than to try and maintain it for the long duration during.
SIDE EFFECTS:
Despite these rather inconvenient side effects, for the most part Clomifin-50 can be run for extended periods of time with no worries of serious negative consequences. Potentially things such as hot flashes, nausea, dizziness, and headaches may occur but anecdotally users report that these symptoms are quite rare. However emotional side effects along with vision problems are frequently reported with use of this drug. Visual tracers or blurry vision are often reported by users, even some who use extremely low doses of the compound. These are often reported to become more pronounced at night. However if this symptom becomes unbearable, it quickly dissipates after administration of the compound is ceased.
In terms of the emotional side effects associated with Clomifin-50, some users complain that they become depressed, irritable or more emotional in general when using the drug. This can primarily be explained by way of Clomifin-50 being a synthetic estrogen. By introducing a type of estrogen into a user's system some effects should be expected. Coupled with the fact that the natural testosterone production of the user is already suppressed this obviously could lead to some difficulties. Of course some users find these effects much more pronounced than others, with many finding Clomifin-50 intolerable while others have little to no side effects.
Another possible effect of use of the compound is increased acne. This is a direct result in the shifting hormonal balance that a user would be experiencing while coming off of anabolic steroids and the introduction of Clomifin-50 to their system. An increase in production of seminal fluid may also be experienced by some users and therefore the volume of ejaculate may well noticeably increase as well.
Modafinil from Platinum Biotech allows you to stay awake for a very long time without feeling tired. The dosage varies from once 100 mg per day to twice 200 mg per day.
The central stimulatory effect of Modafin dependents on the dose and time of use. The Modafin blocks the reuptake of norepinephrine from noradrenergic terminals on neurons sleep inducer.
Modafin is a stimulant used in the treatment of narcolepsy and hypersomnia Idiopathic composed of the modafinil molecule.
It allows people with unusual fatigue staying awake without influencing the work efficiency. Often used by students during their blockade.
The central stimulatory effect of Modafin dependents on the dose and time of use. The Modafin blocks the reuptake of norepinephrine from noradrenergic terminals on neurons sleep inducer.
A vital organ of the human body, the liver performs many critical functions and plays a leading role in metabolism and digestion, along with assimilating and processing carbohydrates, proteins, and lipids, and detoxifying the body of bilious secretions and unhealthy elements.
Silymarin, a vegetable agent extracted from milk thistle (Silybum marianum) which is a component of Samarin, protects the liver against all harmful influences and promotes the recovery of healthy cells in the liver.
Begin treatment with a reasonable daily dose of silymarin, 3 times daily take 1 capsule of Samarin 140.
Taking Samarin has no side effects; however, in isolated cases, mild laxative effects were observed.
3 times daily take 1 capsule
Anazole is an post cycle steroid, its active substance is Anastrozole and is made by Alpha Pharma.
Anazole is a potent and selective non-steroidal aromatase inhibitor indicated for the treatment of advanced breast cancer in post-menopausal women with disease progression following tamoxifen therapy. Many breast cancers have estrogen receptors and growth of these tumors can be stimulated by estrogens. In post-menopausal women, the principal source of circulating estrogen (primarily estradiol) is conversion of adrenally-generated androstenedione to estrone by aromatase in peripheral tissues, such as adipose tissue, with further conversion of estrone to estradiol. Many breast cancers also contain aromatase, the importance of tumor-generated estrogens is uncertain. Treatment of breast cancer has included efforts to decrease estrogen levels by ovariectomy premenopausally and by use of anti-estrogens and progestational agents both pre- and post-menopausally, and these interventions lead to decreased tumor mass or delayed progression of tumor growth in some women. Anazole is a potent and selective non-steroidal aromatase inhibitor. It significantly lowers serum estradiol concentrations and has no detectable effect on formation of adrenal corticosteroids or aldosterone.
Anazole is the first in a new class of third-generation selective oral aromatase inhibitors. It acts by blocking the enzyme aromatase, subsequently blocking the production of estrogen. Since many forms of breast cancer cells are stimulated by estrogen, it is hoped that by reducing amounts of estrogen in the body the progression of such a disease can be halted. This is the basic premise behind Nolvadex, except this drug blocks the action and not production of estrogen. The effects of Anazole can be quite dramatic to say the least. A daily dose of one tablet can produce estrogen suppression greater than 80 % in treated patients. With the powerful effect this drug has on hormone levels, it is only to be used (clinically) by post-menopausal women whose disease has progressed following treatment with Nolvadex (tamoxifen citrate). Side effects like hot flushes and hair thinning can be present, and would no doubt be much more.
For the steroid using male athlete, Anazole shows great potential. Up to this point, drugs like Nolvadex and Proviron have been our weapons against excess estrogen. These drugs, especially in combination, do prove quite effective. But Anazole appears able to do the job much more efficiently, and with less hassle. A single tablet daily, the same dose use clinically, seems to be all one needs for an exceptional effect (some even report excellent results with only 0.25 mg daily). When used with strong, readily aromatizing androgens such as Dianabol or testosterone, gynecomastia and water retention can be effectively blocked. In combination with Propecia (finasteride), we have a great advance. With the one drug halting estrogen conversion and the other blocking 5-alpha reduction , related side effects can be effectively minimized. Here the strong androgen testosterone could theoretically provide incredible muscular growth, while at the same time being as tolerable as nandrolone. Additionally the quality of the muscle should be greater, the athlete appearing harder and much more defined without holding excess water.
In the majority of users, 5 mgs per day should be enough to prevent any estrogen related side effects related to anabolic steroid use. Even when doses were increased to 1 mg per day there was no change in the amount of estrogen that was able to be reduced as compared to doses of 5 mgs per day. This would seem to indicate that raising your dosage will show no further results if estrogenic side effects continue to be a problem at a dosage of 5 mgs. If symptoms persist the user may have to try a more potent compound such as femara.
Having said all of this however, most users will be able to reduce any water retention that they may have, or other estrogen related side effects, with dose less than 5 mgs per day. Anecdotally users have reported that doses in the range of 25 mgs per day or 5 mgs every other day are enough to acheive this result. It is possible to administer Anazole every other day due to it's active life of 48 hours.
For users using Anazole during their post cycle therapy the same dosages should apply. There is no need to increase or decrease dosages. It can be run throughout the post cycle period with no ill effects.
Blood levels of the compound should stabilize and reach their peak at about 7 - 10 days after first administering the drug. Therefore it is unlikely that a user would need to frontload with Anazole or begin taking it before they start administering the anabolics that they plan on taking.
SIDE EFFECTS:
Anazole is seemingly very mild on blood lipids (cholesterol) and has not been shown to affect them adversely. However it should be noted that in theory if one was to consistently suppress your natural estrogen levels for a long period of time, this would negatively impact your health (including your cholesterol). Despite this there is no scientific evidence that Anazole can be dangerous for healthy individuals to use, even for extended periods of time.
It would seem then that Anazole has little in the way of negative side effects associated with it's use. It is by far one of the safest compounds that an athlete can use.
0.5mg - 1mg per day