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There are several best intensity cycles.
The first and best strength stack is Anadrol. Anadrol is a combination of DHT based compounds so it can increase the strength by a very large amount and they can get to people who are on steroids very quickly. In most cases, this happens within two weeks of a person taking the steroid. It is common for a person to have some water retention.
The second most effective method is testosterone suspension. This is because one has the ability to obtain large amounts of muscle in a short time with higher doses. The suspension helps the body produce enough testosterone to build muscle. So that’s one of the main reasons why this is one of the best intensity cycles. There are many different mechanisms that help produce testosterone to increase a person’s muscle mass.
The third best strength stack is Halotestin. It’s a little more expensive than some steroids, but it’s very effective. One of the main components of this superimposed strength is an androgen called Vida. Vida is 19 times more powerful than testosterone, which is one reason it is a little more expensive. But most of the anabolic properties are not shown in this drug so it’s more effective when it’s a pure drug.
The fourth largest is Methyltrienolone. This is a methylated trenbolone, which is one of the best strength stacks known on the market. It has a good reputation as a power builder because many people say it’s more powerful than anything they use to increase their power. People will have to take higher doses to get the best results, but they usually have no problem with this solution.
The fifth best strength overlay is Trenbolone. People take it when they want to exercise or any other strength related activity. This version is not methylated like previous steroids. Its androgen level is about 500, which is very high for steroids. So one should be able to see the great results of this steroid. Of course, it depends on the individual, because some people may have to change their diet, maybe everyone has different goals.
The sixth best strength cycle is Superdrol, one of the newest steroids on the market, which came out in 2005. But for a short time, it managed to maintain its lead for several years. Most of the time, a person will gain 15 to 20 pounds of muscle from these steroids. This is great for steroids, which have just entered the superdrug market.
Masteron for muscle building
Masteron is used by those interested in increasing muscle stiffness and density, and is almost always used in fitness competitions. The drug is considered ideal for many reasons.
Characteristic of Masteron
Masteron is reduced by 5-alpha, and cannot form estrogen after interaction with aromatase, but still shows a high affinity. Because it absorbs a lot of the aromatase, but because it’s structurally impossible to actually use it, it reduces the amount of estrogen that forms from other steroids. Because these compounds have fewer aromatase enzymes that are used to form estrogen. For that reason alone, however, most people will find drostanolone too expensive to use, especially when compounds such as Proviron can be used for the same purpose at much lower cost.
Masteron increases the stiffness and density of muscles, giving individuals a more complete look when competing on stage. This is the effect of many pure male hormones. But all of this requires you to have already fairly low body fat levels to be fully functional. If you do, drostanolone can increase your strength while keeping your body fat the same or even lowering it, and some things can help prevent muscle loss while dieting. This can also allow strength athletes or those who are at a weight level in the sport to improve their performance without the risk of being elevated to a higher weight level or increased quality that could hamper performance.
Usage of Masteron
Masteron is primarily considered a pre-competition drug for bodybuilders. To fully appreciate its effects, users must have a very low body fat content. If the user is not aware of the effect, the “hardening” of the muscles that many people expect when using the compound will not be achieved. This, combined with the fact that drostanolone is unlikely to make much money, should serve as a reminder to individuals that unless they are well-placed, they may be disappointed with their results.
As mentioned earlier, it has been suggested that strength athletes or competitive athletes can benefit from drostanolone because it increases strength without adding too much mass or weight to the user. However, there are countless other compounds that are more effective and better suited for this purpose, so using Masteron seems unnecessary for such purposes.
Because propionate is almost always used with Masteron, it is necessary for users to give the drug daily or at least every other day to maintain a stable level of the drug in the blood. Most users take 50 to 100 milligrams daily or every other day, with a total of 300 to 500 milligrams of the compound each week doing well. More experienced drug users may use higher doses, but since compounds should be mixed with other drugs to maximize their effectiveness, large doses are largely unnecessary.
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Nandrolone is currently one of the most popular anabolic steroids. This is because the compound has a high anabolic affinity but is relatively mild in androgen side effects. By attaching phenylpropionate to nandrolone, the compound provides all the advantages of nandrolone and allows it to reach blood concentrations faster than the more popular decyl ester.
Benefits of Nandrolone Phenylpropionate
Like most anabolic steroids, nandrolone phenylpropionate can treat anemia by increasing red blood cell production. However, nandrolone responds faster than most drugs. An increase in the number of red blood cells helps improve performance. This is done by eliminating lactic acid more quickly and efficiently, and also improving the delivery of oxygen to muscles. This increase in red blood cells also causes muscles to recover more quickly, because after physical exertion, the blood can more quickly replenish muscle glycogen and carry other components that help the muscle repair.
In medicine, nandrolone is now often used to treat AIDS patients who suffer from muscular dystrophy. However, because of its short active life, it is not a very effective ester. In most cases, longer – acting esters are preferable.
Another benefit of nandrolone is that it promotes collagen synthesis. This can help improve joint pain and their ability to function. Many users typically just run nandrolone during their cycles to achieve this particular effect. However, users should note that nandrolone has relatively little ability to heal or repair severe joint injuries and should not be used for this purpose. In fact, it may simply allow the user to cause further damage to the joints that will not be felt until much later. If the compound is used to improve joint health, make sure it does not replace appropriate medical treatment.
Due to the active life of the compound, most users will be given daily or every other day. However, as long as the compound was injected every four days, blood levels of the drug did not change significantly. Nandrolone phenylpropionate can be used in swelling or cutting cycles. The drug lacks water retention, which is especially beneficial for those who don’t want to develop bloating when taking anabolic steroids.
Most inexperienced male users used 300 to 500mg of the compound per week for the first cycle. Of course, depending on the experience of users in anabolics, these Numbers can rise quite high. Women can also use Nandrolone phenylpropionate, because the potential and effectiveness of the masculine effects associated with the drug are relatively low if the dose remains modest. The weekly dose reportedly ranges from 50 to 200 milligrams, but clearly it could be higher.
Mesterolone is an oral androgen used primarily to treat male sexual dysfunction, loss of libido, or impotence. To a lesser extent, it has also been used with varying degrees of success to try to increase the number of sperm in some individuals. It can run for a long time because it’s not a 17-alkylated compound. This makes it less toxic, because it’s not alkylated in the same way, but at the number one site, which reduces liver damage. However, Mesterolone’s anabolism is not strong enough to be used for muscle-building purposes.
Since Mesterolone is not used for anabolism in most cases, there must be other reasons for using this compound. First, there is evidence that when the compound is used to circulate testosterone, it may actually increase its potency. The results showed that mesterolone attached to sex hormone binding globulin (SHBG) and albumin. This leaves more free testosterone for anabolism.
Mesterolone can also be used as an anti-aromatase enzyme. Because of this, many users use it when stacking other compounds that may be partially converted to estrogen. Mesterolone binds to the aromatase enzyme. This in turn does not allow other steroids to interact with this enzyme to form estrogen.
Function of Mesterolone
Some competitive gym-goers will add the mesterolone to their workouts because many believe it will improve muscle density and stiffness. This may be due to the compound’s ability to reduce water retention and reduce the amount of circulating estrogen in the body, similar to many other male compounds. However, as discussed earlier, there are several other drugs that are more effective in this regard than mesterolone.
Many steroid users who have adverse reactions to testosterone or do not wish to use testosterone in their circulation often add mesterolone to their circulation, allowing it to increase the user’s libido. Typically, when users don’t include testosterone or don’t have enough testosterone compared to other compounds he USES, libido is reduced, and mesterolone can help alleviate the condition. Clearly, the compound’s dihydrotestosterone effect plays a key role in this process.
Proviron for use and dose
Most men who use Proviron find that 25 to 100 milligrams a day is enough to get the desired effect. Women typically consume about 25 milligrams a day, but many consume much more. Because of the active life of the compound, it is beneficial to divide the drug dose into two parts and take it twice a day, but the effect of the compound should be maintained for 24 hours, so it is not completely necessary.
Since many other compounds are more effective than metosterone for the same purpose, there seems no need to increase the dose to more than 100 milligrams a day. On the contrary, if the desired effect is not achieved, it is best to try a more effective drug.
Exemestane for pct cycle
Exemestane is a steroidal aromatase inhibitors/suicide irreversible aromatase inactivator, by blocking aromatase reduces the production of estrogen in the body. The drug, which is structurally similar to formestan, is used in the treatment of estrogen-dependent breast cancer, are most aromatase inhibitors. It is popular among bodybuilders when it was used to the post pct-cycle.
The function of Exemestane
For strength athletes and bodybuilders, Exemestane several useful features. First of all, Exemestane estrogen can be 85% lower. Doing so will certainly help prevent estrogen-related side effects from aromatase steroids. The drug also boosts users’ testosterone levels, which may be beneficial if used during post-cycle therapy. In addition, there is evidence that Exemestane is likely to raise the level of insulin growth factor of IGF.
Effects of Exemestane
Like other aromatase inhibitors, the effects of Exemestane lipid/cholesterol to the users, there are conflicting information and research. Some studies have shown that Exemestane lipid/cholesterol almost has no impact to the user, and the influence of other research shown that it can be rather serious.
After oral 25 milligrams, Exemestane2 hours peak plasma concentration. The effective life of this medicine is between 24 and 30 hours. This is important because it is much shorter than nsaids. Single oral 25 milligrams Exemestane will result in plasma and urine estrogen levels decline in a relatively long time, about 2 to 3 days after taking a maximum inhibition, and last about 4 to 5 days.
Research shows that 25 milligrams of Exemestane improves the level of testosterone and estrogen as welll as levels of IGF is basically as effective as 50 mg. Therefore, a daily dose of more than 25 milligrams is not necessary. Due to the activity of Exemestane, it is suggested taking it about every 24 hours.
The only negative effect of the compound from the dose plan is that it takes about seven days to reach stable plasma levels. However, this is not the main barrier to its use. It simply needs a week before the users fully realize the effect of compound Exemestane came into use.
Side effects when using Exemestane
Exemestane under the dose of 600 mg/day is no significant drug toxicity. Most users are well tolerated and the maximum tolerable dose of toxicity has not been determined. Adverse side effects associated with the use of this compound are usually very mild and may include transient gastrointestinal reactions, hot flashes, nausea and/or fatigue. As noted earlier, the effect of esimetan on lipids/cholesterol is unknown and should therefore be monitored when the compound is used.
Exemestane is a relatively safe in aromatic steroid inhibitors, due to the compound has a moderate negative side effects, should be used under the guidance.
Oral Turinabol is a steroid that has a reputation among bodybuilders. It was originally developed by east German scientists for use by their Olympic athletes. The success of those athletes proves its effectiveness. In fact, it is widely used to improve athletic performance, which means that it has been affected by many experiments, and the documented results are very impressive.
Characteristic of oral Turinabol
It really gives the muscles a good workout. While muscle strength and gain are not as dramatic as other compounds, they are unlikely to be accompanied by water retention. That means you’re more likely to hold on to whatever gains you get at the end of a cycle. In addition, oral Turinabol does not produce estrogen-related side effects (such as male breast development). Although it is alkylated with 17-alpha, this means it is toxic to the liver. Therefore, it is advisable to use some form of liver support in circulation (e.g., Silymarin, Dandelion, NAC).
Oral Turinabol is described as a derivative of Dianabol, although its androgen activity is much lower. This means it won’t make you look as puffy as those who use Dianabol. In fact, many users have already compared it to Anavar in terms of results.
Side effects of Turinabol
The substance has few side effects and usually the result of too long a cycle or too high a dose leads to side effects. The above risk of hepatotoxicity and reduced blood clotting capacity are the only things to note. It’s also associated with a natural drop in testosterone levels, but it’s usually dose-related. It has been reported that women suffer more side effects when using the substance than men, but these reactions are more common in women. Why? They take almost twice as much as men, so they certainly have more side effects.
It is recommended that men take 20-40 milligrams a day and women 5-10 milligrams a day. In real life, however, male bodybuilders generally prefer 0.4 milligrams per pound.
One interesting aspect of oral Turinabol is that it lowers SHBG. It binds to other steroid hormones, causing the body to release more testosterone. For this, many athletes find it an important adjuvant to any cycle? Especially those who use testosterone. The fact that oral Turinabol is not associated with aromatization (that is, conversion to estrogen) also adds to its appeal.
In short, when you consider that it produces few annoying side effects (at reasonable doses) and that muscle mass improves over time with high quality, oral Turinabol is definitely worth considering as it is part of an effective circulation. Even when used alone, it is sure to yield significant improvements in quality and strength. This increase would not be surprising, but it would be easier to maintain because the improvement in oral Turinabol was not an illusion of water weight.
Sustanon 250 profile
Sustanon 250 is primarily used for hormone replacement therapy, a mixture of testosterone esters that is thought to provide long-term testosterone release. It is thought that by using short, medium and long acting esters, the stable flow of the compound can be maintained and very infrequent injections will be required. However, this theory turned out to be wrong, because over time, the complex peaks in the blood decreased rapidly and slowly. To maintain stable blood levels, the drug must be injected as often as other short esters.
Sustanon 250 composition
Sustanon 250 was mixed with esters of testosterone in doses of 30mg propionic acid, 60mg phenylpropionic acid, 60mg isopropionic acid and 100mg decanoic acid. It should also be noted that there is a Sustanon 100. It is: 20mg propionic acid, 40mg phenylpropionic acid and 40mg isopropionic acid. Since Sustanon 100 does not contain decanoate, the active life of the compound is shorter than that of Sustanon 250. Apart from this difference, the compounds are quite similar.
Compared to other testosterone steroid
Sustanon 250, in addition to the ester compounds, has no distinct advantage over other testosterone compounds. The effect should be much the same as that of any testosterone compound. In terms of the effect of esters, Sustanon 250 appears to be the most detrimental. Many users have complained of water-retention problems with long-acting esters, but the compound should be injected regularly due to the presence of long-acting esters. This leads many users to choose another testosterone ester that is better designed for their target.
Testosterone promotes strength and muscle growth through a number of mechanisms. First, testosterone promotes the retention of nitrogen in muscles, which allows them to store more protein and promote the repair and growth of these muscles. Secondly, testosterone binds to androgen receptors, promoting receptor-dependent mechanisms of muscle growth and fat loss. Testosterone also helps increase the concentration of androgen receptors in cells, which are essential for muscle growth and repair.
As mentioned earlier, testosterone plays a role in promoting fat loss. Testosterone binds to androgen receptors in fat cells. This breaks down body fat and prevents the formation of new fat. Of course, since testosterone promotes muscle growth, it also indirectly promotes fat loss, since any excess calories could be used to build muscle rather than as body fat.
Like most anabolic steroids, testosterone increases the production of red blood cells. An increase in the number of red blood cells in the blood can improve endurance through better oxygenated blood, as well as the user’s ability to recover after strenuous exercise. It should be noted, however, that there are other steroids and compounds that are much more adept at this function.
Other mechanisms by which testosterone helps promote anabolism include its role in promoting the growth of insulin factor 1 and inhibiting the release of catabolic hormones in the body. Testosterone also has many advantages when it comes to improving performance. That is, it has the ability to increase the number of muscle motor neurons, which improves muscle contraction. Like many other anabolic steroids, testosterone promotes glycogen synthesis. This, of course, helps increase the user’s endurance and strength by providing more fuel for high-intensity exercise.
Like other testosterone compounds, the drug dose a user takes depends largely on the user’s experience and goals. Testosterone users with doses as low as 200-250 mg/week reported good results, with experienced users taking several grams of testosterone per week. It is widely used. That includes women taking testosterone. Since some of the esters in Sustanon 250 have a longer active life, it is not recommended that women take Sustanon 250 or other long-acting formulations.
Anastrozole is an aromatase inhibitor. Aromatase inhibitors prevent the conversion of androgens from fat, muscle, breast and brain into estrogen. The main medical use of anastrozole is to inhibit the progression and growth of breast cancer in women by blocking aromatase. It is also used by some doctors to treat testosterone deficiency in men and in combination with testosterone replacement therapy.
For bodybuilders and strength athletes, anastrozole is used to reduce the aromatization of anabolic steroids, in part because it boosts users’ testosterone levels. By reducing the amount of estrogen in a steroid user’s body, he will be able to avoid estrogen-related side effects, such as water retention and breast development in women.
Interestingly, in addition to lowering estrogen, anastrozole also increased testosterone levels by 58 percent, as well as increasing levels of the moisturizing hormone. This is very important. Considering that anastrozole can be used in combination with other compounds, it can increase users’ natural testosterone levels in the post-cycle.
Anastrozole powder uses
In most users, 0.5 mg per day should be sufficient to prevent estrogenic side effects associated with anabolic steroid use. Even when the dose was increased to 1 mg per day there was no change in the amount of estrogen compared to 0.5 mg per day. This suggests that if estrogen side effects are still a problem at 0.5mg, increasing your dose will have no further effect. If symptoms persist, users may have to try a more potent compound, such as femara.
However, most users can reduce any water retention or other estrogen-related side effects they may have by taking a dose less than 0.5 mg per day. Interestingly, users reported that a dose of 0.25 mg daily or 0.5 mg every other day was sufficient to achieve this result. It is possible to take anastrozole every other day because it has 48 hours of activity.
The same dose of anastrozole should be used in patients who take anastrozole during the postcycle treatment period. There is no need to increase or decrease the dose. It can run the entire post-cycle without any adverse effects.
Blood levels of the compound should stabilize and peak 7 to 10 days after the first dose. As a result, it is unlikely that users will have to load anastrozole in advance or start using it before they start managing the anabolics they plan to use.
Side effects of taking Arimidex
Arimidex appears to have a mild effect on blood lipids (cholesterol) and has not been shown to have a negative effect on blood lipids (cholesterol). However, it should be noted that if a person consistently suppresses your natural estrogen levels over a long period of time, this could have negative effects on your health (including your cholesterol). Nevertheless, there is no scientific evidence that anastrozole is dangerous for healthy individuals, even in the long term.
It appears that the use of anastrozole has few side effects. It is by far one of the safest compounds available to athletes. It helps to increase natural testosterone levels.
At the end of the anabolic androgen cycle, the two most important things are:
1. Reactivate natural hormonal functions that have been suppressed during the cycle, primarily to bring testosterone back to normal levels.
2. In order to maintain the gains from the cycle, this is actively achieved when the first point is satisfied.
SERMs & AIs
In order to fully resume your natural test production, you need something to stimulate your pituitary gland to restart its regular activity. These drugs are divided into two families: SERM(selective estrogen receptor modulators) and AI(aromatase inhibitors). Common SERMs are Nolvadex (tamoxifen) and Clomid (clomiphene). The most commonly used AIs are: Femara, Arimidex, aromatin, and liquidex. Proviron is also an androgen with high e – resistance.
SERMs: these compounds bind to estrogen receptors and show good estrogen effects, which are associated with our recovery.
They are used in post-cycle therapy because they stimulate the pituitary gland to release more gonadotropins, promoting faster and higher release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH).
Both hormones make the testes produce more sperm and testosterone, allowing the body to return to normal production levels.
AIs: they’re not like SERMs, they’re not estrogen. Their role is to prevent the conversion of androgens to estrogen. At the end of a cycle, the body no longer acquires exogenous hormones, and its natural hormone production is partially inhibited. Here are the risks of any estrogen-related side effects, such as increased fat and water, male breast development, low libido, and all the others mentioned earlier.
Using artificial intelligence to suppress estrogen receptors would suppress any temptation to question them. Therefore, they are often used over a cycle to prevent the aromatization of estrogen from being tested by aromatase.
When do I start my post-cycle therapy?
It depends on the cycle of medication use.
What is HCG and when is it used?
HCG, the human chorionic gonadotropin hormone, is recommended when your body’s sperm production needs rapid fixation. In fact, when boys are shrinking, they need nourishment.
Sometimes people find it useful to run at 500IU twice a week even in the last few weeks of a long cycle.
It should never be used alone without SERM, as it will replace the normal function of LH for a period of time and need to be supplemented again after the intake of HCG. That’s why I usually only advise when I have to.
Diet on the PCT
Don’t reduce calories when you think your body is in a highly anabolic state on PCT.
You have to maintain what you’re getting, and the PCT drugs themselves don’t work miracles, like the AAS, so keep them at high levels to maintain what you’re getting and change your diet with your goals.
Know about 17-alkylated steroids
You may have heard that 17-alkylated steroids are harder for the liver to metabolize and therefore require more effort to break them down. All 17-alkylated steroids are toxic to the liver. Non-17-alkylated steroids are not toxic to the liver. All these views are not true.
17-alkylated steroids are known to be toxic to the liver. How toxic depends on who you believe in. The media and many doctors think they are deadly, while many people online think they are actually harmless. There seems to be a lot of confusion on this topic, even among people who know a lot about steroids. The fact is that it depends how you use steroid and the actual instructions you get. Dose and duration are the main fators when it comes to steroid use. Hopefully we can dispel some rumors about how toxic substances are and how to reduce or prevent toxicity.
Toxic effect of steroid
What are the toxic effects of oral steroids? By far the most common toxicity is intrahepatic cholestasis. Generally, cholestasis is any condition in which bile ceases to flow, and oral allergy occurs in the liver. Normally, bile is released into the small intestine and its main function is to help absorb fats and lipids. This prevents bile salts from being released into the bile ducts, leading to the buildup of liver cells. This accumulation may be toxic to hepatocytes over time. Jaundice is the yellowing of the skin and eyes and is associated with cholestasis. This is because bilirubin (a product of the breakdown of red blood cells) is usually excreted through the bile. During cholestasis, the skin and eyes gradually turn yellow, a sign that something bad is happening. Jaundice is rare except in newborns, and if you notice these symptoms, you should seek professional health care. The type of cholestasis usually seen in oral steroids is clinically classified as “mild cholestasis” because there is no inflammation associated with cholestasis. This type of cholestasis is completely reversible when the pathogenic agent is stopped.
In addition to cholestasis, other reported toxic effects are cirrhosis of the liver and hepatic adenoma. Liver disease is a cavity in the liver that is filled with blood. This is a rare condition in which the theory is that cirrhosis of the liver is caused by blocked outflow of hepatic blood at the junction of the sinus vein and the lobular central vein. What causes this? It is thought to be associated with cholestasis, which causes the growth (swelling) of liver cells. In patients with AAS, obstruction may be due to prolapse of hepatocyte proliferation into the hepatic vein wall. This is good news because it means that if cholestasis can be prevented, cirrhosis can also be prevented.
Hepatic adenoma has been mentioned many times in the literature as a possible effect of oral steroids. This is extremely rare and appears to occur only after months or years of continuous use. It may also be associated with prolonged cholestasis. In my opinion, don’t worry unless someone in your family has contracted cholestasis from oral steroids (including birth control pills). The real focus of safety should be preventing cholestasis.
Function of Liver
The liver has many important functions in the body, but these include drug metabolism and excretion, and the secretion of bile salts and bicarbonates for digestion.
For 17-alkylated steroids, the conversion from 17-hydroxyl to 17-ketone steroids is prevented. That’s the key. The main difference between 17-aa and regular steroids is that the former retains a free 17-hydroxyl group in the liver, while the latter does not. The reason 17-aa is toxic is that the free hydroxyl group can combine with glucuronic acid to form d-ring 17-glucuronolactone. It is not the 17-aa steroid that is toxic to the liver, but the 17-glucan metabolite. It’s not that these steroids are harder to metabolize, it’s the way they’re metabolized that makes them toxic.