Oxandrolone (also known as Anavar) is believed to be a mild oral anabolic steroid. Oxandrolone was first introduced in 1962. Oxandrolone was designed to be as safe as possible for women and children. The same is true in clinical practice, with men, women, and children showing high tolerance. With extensive clinical success, Oxandrolone has been used to promote postoperative lean weight gain, trauma treatment, glucocorticoid disorders, bone mineral density in patients with osteoporosis, and slow development in childhood and adolescence. Welcome to buy Oxandrolone powder from getraws.com.
Oxandrolone is derived from DHT. It is designed to have very strong anabolic and androgen dissociation without significant estrogen or progesterone activity. Oxandrolone is classified as an anabolic steroid of c17-aa, but the effect is not extreme (Oxandrolone was administered at 20mg per day for 12 weeks and no significant effect on liver values was observed). Short-term and low Oxandrolone use does not significantly affect endogenous testosterone production. (the study showed that 80mg per day over 12 weeks inhibited endogenous testosterone production by only 67 percent.)
Most importantly, Oxandrolone increases the ability to retain nitrogen in muscles, reduces sex hormone-binding globulin (SHBG), and inhibits glucocorticoids. An increase in nitrogen retention promotes anabolic capacity, since lowering nitrogen retention levels usually results in catabolic states. A reduction in SHBG will produce higher levels of free testosterone in the body, promoting the free or unbound state of all circulating anabolic steroids. In short, it makes steroid use more effective.
Cortisol is the best known for glucocorticoid suppression. Such a hormone can promote the increase of fat, but also can destroy lean muscle tissue. Oxandrolone also boosts the number of red blood cells, which increases muscle endurance.
Some studies have even shown that Oxandrolone directly promotes fat breakdown. It is thought by many to bind firmly to androgen receptors, reduce the ability of thyroid-binding globulin, and increase the number of thyroxine-binding pro-endogenous proteins. This effect leads to greater utilization of the T3 hormone.
Oxandrolone has been described as a good agent for promoting strength and increasing muscle mass, although the mild nature of the compound makes it less desirable for bloating purposes. Among bodybuilders, the most commonly used is training during the cutting phase. Oxandrolone can be combined with synthetic metabolites such as Methenolone, Stanozolol, and Mesterolone to achieve a stronger, more defined appearance. This combination is very popular.
We cannot call Oxandrolone a very powerful anabolic steroid. However, we can call it a very beneficial anabolic steroid. When we consider its generally good tolerability, it makes it one of the most valuable anabolic steroids of all time. It’s critical that we understand Oxandrolone, know what it can do, and implement it into your plan to get it right.
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Proviron can actually enhance the activity of other steroids by replacing them with a free unbound state, leading to higher use of other steroids. In athletes, Proviron is used primarily to increase androgen levels during dieting or preparation for the competition, and as an anti-estrogen due to its intrinsic ability to antagonize aromatase. Welcome to buy Proviron powder from us.
History of Proviron
Schering developed testosterone in 1934, which is a very old drug for anabolic steroids. It was the first drug to be used in clinical practice to treat “hormone-related diseases”. Proviron has a long history of clinical efficacy and safety and is still widely used today. Men are generally prescribed for the treatment of physical and mental impairment caused by age and subnormal androgen levels, low sexual desire caused by inadequate androgen levels, hypogonadism, and infertility (Proviron improves sperm quality and quantity).
The use of Proviron as a fertility aid may be one of the most controversial indications for the drug. Because it is an effective androgen, it provides minimal inhibition of gonadotropin in normal therapeutic doses, not because it increases LH output. Lacking gonadotropin inhibition, drugs can supplement the androgens necessary for sperm production. Androgen is known to directly stimulate spermatogenesis and to influence sperm transport and maturation through its effects on the epididymis, tubular structures, and seminal vesicles. So the effects of these hormones are not completely inhibited. Proviron appears to have a uniquely positive effect on fertility in some men because its potential stimulation of sperm quantity and quality is not offset by gonadotropin suppression.
The structural characteristics of Proviron
Proviron is a modified form of DHT. The difference is that methyl groups are added to carbon 1, which helps protect the hormone from liver metabolism during oral administration. The same structural modification is also used in oral (methyl phenol) tablets. Alkylation at one site slowed liver metabolism during the first pass of the steroid, although it was much less significant than c-17 alkylation. Although overall bioavailability remains much lower than that of c-17 alpha-alkylated oral steroids, testosterone is resistant enough to achieve therapeutic beneficial blood levels. Proviron also has a very strong binding affinity for sex hormone-binding globulin.
Proviron is not aromatic and is not a measurable estrogen. Anti-estrogen is not required when using this steroid because the drug cannot induce breast development, water retention or other estrogen-related side effects in men.
Proviron is thought to act as an anti-aromatase in the body, preventing or slowing the conversion of steroids to estrogen. The results are somewhat similar to Arimidex, though not as profound. Proviron’s anti-estrogen properties are not unique, and many other steroids have been shown to have similar activity. Dromostanolone, for example, has been successfully used as a treatment for male breast development and breast cancer because of its strong androgen and potential anti-estrogen effect. Proviron can even reduce aromatase activity in peripheral tissues, where it is more resistant to estrogen conversion. The anti-estrogen effect of all these compounds may be caused by their ability to compete with other substrates to bind to aromatase. Because aromatase binds to steroids, it cannot be changed because it is temporarily blocked and does not interact with other hormones to achieve inhibition.
Proviron is classified as an androgen steroid. Androgen side effects are common with this substance, especially at higher doses. This can include oily skin, acne, and episodes of body/facial hair growth. Anabolic/steroids/may also aggravate male pattern hair loss. Women are also warned of the potential masculine effects of anabolic/steroid /. These can include deepening of the voice, irregular periods, changes in skin texture, facial hair growth, and enlargement of the clitoris.
Proviron is not c17-alpha alkylated and no hepatotoxic effects have been reported.
Anabolic steroids/may have harmful effects on serum cholesterol. This includes a tendency to lower HDL (good) cholesterol levels and increase LDL (bad) cholesterol levels, which may shift HDL in favor of a greater risk of atherosclerosis. The relative effects of anabolic/androgen steroids on serum lipids depend on the dose, route of administration (oral or injectable), type of steroid (aromatized or not), and level of resistance to liver metabolism. Proviron is an oral non-aromatic androgen and is expected to have significant negative effects on lipids.
To help reduce cardiovascular stress, it is recommended to maintain an active cardiovascular exercise program throughout active AAS administration and to minimize saturated fat, cholesterol, and simple carbohydrates. Supplementation with fish oil (4 grams per day) and natural cholesterol/antioxidant formula, such as Lipid Stabil or with a similar composition of products is also recommended.
Proviron has a very weak inhibitory effect on gonadotropin and serum testosterone. Studies have shown that no significant inhibition of testosterone levels occurs when given at moderate doses (150mg/d or less). With higher doses (300 mg/day or more), serum testosterone will be strongly inhibited.
Usage of Proviron
To treat androgen deficiency, Proviron is usually administered three times a day (25mg) at the beginning of treatment. The drug is then continued at a lower maintenance dose, which usually consists of taking one tablet (25mg) once or twice a day. A similar dose is used to support male fertility, usually in conjunction with other fertility drugs such as injectable FSH. The usual dose for male athletes is 50mg to 150mg of testosterone per day, or two to six 25mg tablets. Medications are usually administered in cycles of 6 to 12 weeks, which is usually enough time to notice the benefits of the medication.
While low estrogen and high androgen levels are ideal, many bodybuilders like to use Proviron during the diet or in preparation for competition. When these drugs are relatively low in androgen, this is particularly beneficial if synthetic metabolites such as Methenolone are used alone. Proviron can be used to regulate the ratio of androgens to estrogens, resulting in increased muscle stiffness and density, supporting sexual desire and general well-being and increasing the tendency to burn body fat. When used in combination with Nolvadex, usually 10-20mg per day, it prevents breast development in both men and women. Not recommended for women.
Nandrolone Phenylpropionate is an injectable form of the anabolic steroid Nandrolone. The properties of this drug are very similar to those of Nandrolone Decanoate. The main difference between the two preparations is the rate at which nandrolone is released into the bloodstream. Nandrolone Decanoate provides about three weeks of Nandrolone release at the injection site, while Nandrolone Phenylpropionate provides only one week. So Nandrolone Decanoate can be given clinically every two or three weeks, while Nandrolone Phenylpropionate is given clinically once a week. On the other hand, the two drugs are actually interchangeable. Like Nandrolone Decanoate, drugs such as Phenylpropionate, which enable athletes and bodybuilders to increase muscle strength and lean muscle mass, are valuable and do not have significant estrogen or androgen side effects.
Nandrolone Phenylpropionate first appeared in 1957. It soon became a prescription drug marketed by the international pharmaceutical giant Organon (now Merck/MSD) under the brand name Nandrolone Phenylpropionate. When first introduced in the United States, Nandrolone Phenylpropionate was used for the retention of sperm quality before and after surgery, osteoporosis, advanced breast cancer, weight loss due to convalescence or disease, geriatric diseases (general weakness and weakness), burns, severe trauma, ulcers, anemia, and developmental retardation in children. In the 1970s, the FDA began to modify the use of the drug, and its use quickly declined significantly. After a while, the drug was used primarily to treat advanced metastatic breast cancer and as an adjunct therapy for postmenopausal osteoporosis in the elderly.
Nandrolone Phenylpropionate has been Organon’s focus for less than a decade. When Nandrolone Decanoate was introduced in the 1960s, drugs with short-term effects, such as Phenylpropionate, were still available but began to decline. At the time, Nandrolone Phenylpropionate had not been abandoned by Organon, in part because some countries had slightly different therapeutic USES and thus remained profitable for some time. As the anabolic steroid market continued to grow in the 1970s and 1980s, it caught the attention of other drug manufacturers, and many drug companies have begun to make their own Nandrolone Phenylpropionate. Today, however, the drug is almost non-existent. The current owners of Organon (Merck/MSD) will sell Nandrolone Phenylpropionate, which is nearing the end of production.
Nandrolone Phenylpropionate is circulating in some human drug markets. The composition and dosage may vary from country to country and manufacturer, but usually contains 25 mg/mL or 50 mg/mL of steroids dissolved in oil.
Nandrolone Phenylpropionate is a modified form of Nandrolone in which a carboxylate (Phenylpropionate) has been attached to a 17-beta-hydroxyl group. Esterified steroids have less polarity than free steroids and are absorbed more slowly in the injection area. Once in the blood, the ester is removed to produce a free (active) nandrolone. Esterified steroids are designed to extend the therapeutic window after administration, allowing less frequent injections than free (unesterified) steroids. Nandrolone Phenylpropionate peaked at release 24 to 48 hours after deep intramuscular injection and dropped to near baseline within a week.
Side effects (estrogen)
Nandrolone’s estrogen conversion is low, estimated at about 20 percent of testosterone. This is because although the liver converts Nandrolone to estradiol, the estrogen-related side effects of nandrolone are much lower in other, more active, steroid-aromatizing sites, such as adipose tissue. However, elevated estrogen levels at high doses are still noticeable and can cause side effects such as increased hydration, body fat, and breast development in men. Anti-estrogens such as clomiphene or tamoxifen may be necessary to prevent the occurrence of estrogenic side effects. People can also use aromatase inhibitors, such as anastrozole, which control estrogen more effectively by preventing its synthesis. However, compared to anti-estrogen, aromatase inhibitors can be quite expensive and may have negative effects on blood lipids.
It is noteworthy that nandrolone has some progesterone activity in the body. Although progesterone is a c-19 steroid, the removal of this group produces a hormone with a greater binding affinity for its corresponding receptor. Because of this feature, many no-19-anabolic steroids have shown some affinity for progesterone receptors. Progesterone-related side effects are similar to estrogen, including negative feedback inhibition of testosterone and increased fat storage. Progesterone also increases estrogen’s role in stimulating breast tissue growth. There seems to be a strong synergy between the two hormones, so even without excessive estrogen levels, male breast development may even occur under the influence of progesterone. The use of anti-estrogen, which inhibits estrogen, is usually sufficient to reduce the risk of breast dysplasia in men caused by nandrolone.
Side effects (androgen)
Although classified as anabolic steroids, the substance may still have androgenic side effects, especially at higher doses. These side effects may include oily skin, acne, and episodes of body/facial hair growth. Anabolic/androgen steroids may also aggravate male hair loss. Women are also warned of the potential pathogenic effects of anabolic/androgen steroids. These may include deepening of the voice, irregular periods, changes in skin texture, facial hair growth and clitoral enlargement. Norone is a steroid with relatively low androgen activity relative to its tissue-building effects, so the threshold for androgen side effects is quite high compared to androgen drugs such as testosterone, methyltestosterone. It’s also important to point out that because of its mild androgen properties and ability to suppress endogenous testosterone, nandrolone tends to interfere with sexual desire in males when not using another androgen.
Note that in androgen responsive target tissues such as skin, scalp, and prostate, the relative masculinity of nandrolone is reduced by reduction to DHN. 5- alpha reductase is the main cause of this metabolism. Concurrent use of 5-alpha reductase inhibitors such as finasteride or rasterize interfered with the site-specific effects of nandrolone significantly increasing its tendency to produce androgenic side effects. If low androgen sex is required, use of nandrolone should avoid reductase inhibitors.
Side effects (hepatotoxicity)
Norone is not c-17 alpha alkylation and does not have hepatotoxic effects. So hepatotoxicity is unlikely.
Side effects (cardiovascular)
Anabolic/androgen steroids may have harmful effects on serum cholesterol. This includes the tendency to lower HDL (good) cholesterol levels and increase LDL (bad) cholesterol levels, which may convert HDL to LDL, leading to a greater risk of atherosclerosis. The relative effects of anabolic/androgen steroids on serum lipids depend on the dose, the method of administration (oral versus injection), the type of steroid (aromatized or not), and the level of resistance to liver metabolism. Weekly administration of 600mg Deca for 10 weeks showed a 26% reduction in HDL cholesterol levels. This inhibitory effect is slightly higher than that reported by using the same dose of actor Enanthate, which is consistent with earlier research results that Deca has a stronger negative effect on HDL/LDL ratio compared with actor Propionate. The effect of nandrolone on serum lipids was significantly weaker than that of c-17 alpha alkylated. Anabolic/androgen steroids may also adversely affect blood pressure and triglycerides, reduce endothelial relaxation, and lead to left ventricular hypertrophy, which may increase the risk of cardiovascular disease and myocardial infarction.
To help reduce cardiovascular stress, it is recommended to maintain an active cardiovascular exercise program and to consistently minimize saturated fat, cholesterol, and simple carbohydrates throughout the use of AAS. Also suggested supplementation with fish oil (4 grams per day) and natural cholesterol/antioxidant formula such as Lipid Stabil or products with a similar component.
Side effects (testosterone suppression) :
All anabolic/androgen steroids are expected to inhibit endogenous testosterone production when taken at doses sufficient to promote muscle gain. Studies on 100mg Nandrolone Phenylpropionate have shown that serum testosterone can be rapidly suppressed by a single injection. Testosterone levels dropped to 30% of their initial level on day 3 and remained there for about 13 days. Frequent use can significantly prolong the endogenous hormone recovery window. It is thought that the progestational activity of norone significantly facilitates the inhibition of testosterone synthesis during treatment. Without intervention from testosterone stimulants, testosterone levels should return to normal within 2-6 months of drug disruption. Note that hypogonadism may be secondary to steroid abuse, requiring medical intervention.
In addition to these side effects, for a more detailed discussion of potential side effects, see the steroid side effects section of this book.
For general anabolic effects, early prescribing guidelines recommend a dose of 25 to 50 mg per week for 12 weeks. Doses commonly used for physical or performance enhancement purposes range from 200 to 400mg per week and are administered over a period of 8 to 12 weeks. This level is enough for most users to see a measurable gain in lean muscle mass and strength. Note that because of the rapidity of phenylpropionate, the weekly dose is usually divided into two doses.
For general anabolic effects, early prescribing guidelines recommend a dose of 25 to 50 mg per week for 12 weeks. When used for physical or performance enhancement purposes, a dose of 50mg per week (single weekly injection) is the most common, lasting 4 to 6 weeks. Higher doses or longer duration of use are not recommended due to potential androgen side effects. Although only mildly androgenic, women occasionally face viral symptoms when taking the compound. If side effects occur, immediately discontinue phenylpropionate to prevent permanent side effects.
Normal men and women in the body of estrogen and androgens in a dynamic balance, and these two hormones in addition to the difference between the sexes, but more important is to maintain the physical health and psychological level of a number of health problems. In the anabolic steroid cycle, the term “estrogen” appears, but many friends do not want to see male breast development. Previously mentioned anti-estrogen drugs like Anastrozole, Exemestane, Tamoxifen Citrate. But there is another kind of our common estrogen drugs Letrozole (Femara).
Letrozole is an aromatase inhibitor and is approved as a treatment for breast cancer. However, in the cycle of anabolic steroids, due to the influx of high levels of androgens into the body, aromatase converts androgens into estrogen through aromatization. As the breast is stimulated by estrogen, the breast develops, forming estrogen. So what aromatase inhibitors do is they block estrogen production or they block estrogen from acting on the receptor. Letrozole inhibits estrogen synthesis through reversible competition with aromatase.
At the same time, according to fitness pioneer experience, 0.36 mg/day as the basic amount of an anabolic steroid cycle, containing the right amount of aromatic steroids, such as 200-300 mg/week of testosterone. At higher doses such as 750mg/week, this amount is usually doubled. Usually no more than 1mg/day, unless blood tests show abnormally high levels of estradiol, even at that level, which rarely happens. (the blood test here refers to the six kinds of hormones.)
Overuse of Letrozole can also cause side effects, including decreased libido, depression, and joint pain. The half-life of Letrozole (two days) should be adjusted, or a blood test should be taken. For most men, 20-29pg/ml estradiol is the ideal range, so Letrozole usage was calibrated by the above symptoms and observations, as well as data comparisons.
Arimidex (anastrozole) was patented in 1987 and approved for medical use in 1995. Anastrozole can be used as a generic drug. Arimidex (anastrozole) was the first selective aromatase inhibitor for bodybuilding and remains the most popular estrogen-control drug. It is usually taken orally in tablet and liquid form. The dose is usually 0.25,0.5 or 1.0mg per dose at a frequency of once daily or once every two days.
Estradiol, the most potent form of estrogen, is produced in the body through the aromatization of testosterone. This process occurs through aromatase. Because men need a certain level of estradiol, testosterone needs to be converted to estradiol. However, in both cases, effective aromatase inhibition can provide important benefits.
First, conversion to estradiol becomes excessive when the anabolic steroid cycle leads to very aromas steroid levels and when aromatase cannot be controlled. The resulting high estradiol may cause breast, water retention, depression and/or decreased libido in men and women. This can also make it difficult to maintain a lean state.
Second, estradiol levels in some men were elevated even without anabolic steroid circulation. This will have the effect of reducing the production of natural testosterone and may cause these adverse side effects. Arimidex is perfect for solving any problem. With the right dosage, free estradiol levels can be brought to the desired range with considerable precision. When not using anabolic steroids, I recommend about 20-29 pg/mL for most men to maximize mood, performance, libido, and long-term health, and to provide excellent benefits for the production of natural testosterone. Levels can be allowed to rise a little during the steroid cycle because high androgen levels are used to counteract the adverse effects of estradiol. Sometimes slightly higher estradiol is needed to protect the walls of our blood vessels and keep them softened. Nevertheless, I suggest that estradiol levels should be kept at no more than about 40 pg/mL even during the intense anabolic cycle. Aromatase inhibitors, such as Arimidex, are usually required if aromas steroids are added.
Most medical studies on the effects of Arimidex on men have used it at 1mg/day, a dose that appears to be at its best on the effects of estradiol levels. However, real-world applications for circulating steroids or optimizing hormone levels generally use lower doses, ranging from 0.25mg every other day to about 0.5mg per day. It is generally recommended to use 0.5 mg every other day as the starting point of the steroid cycle, or half of the optimal hormone level if there is a high estrogen problem.
Excess Arimidex results in abnormally low estradiol levels and typical side effects of joint pain decreased libido, and/or gastrointestinal distress. The first two are directly caused by low estradiol. If you encounter these effects, reduce the dose. The effect on the gastrointestinal tract seems to be a side effect of Arimidex itself, but fortunately only affects a few people. If this effect occurs, I recommend letrozole as an alternative to aromatase inhibitors.
Anastrozole has a half-life of about two days. So it should be used two days before other drugs, rather than waiting weeks for them to pile up. This is done by using the first does not only as a regular dose but also for the next two days. For example, if you plan to take 0.5 mg every other day, that would be an extra 0.5 mg. Therefore, the preloading dose is 1.0 mg. This will only be done on the first day of use. With this approach, the appropriate effect can be achieved almost immediately.
The controversial pairing is the use of Arimidex for PCTS. Some argue that driving estradiol levels abnormally low in PCTS stimulates testosterone production; I’m a strong advocate of SERM like Nolvadex or Clomid because it completely blocks the aromatase function and turns testosterone into estradiol, which needs to be restored to normal levels. However, if a person needs Arimidex even aperiodically because of its naturally high aromatization, then his aperiodic dose can also be used during the PCT.
Compared to letrozole, Arimidex was the best. Both drugs are effective in aromatase control. The choice between them depends entirely on personal preference, experience, and availability.
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There are currently three versions of mixed testosterone on the market: the Sustanon 250, the Sustanon 300, and the Sustanon 350. Sustanon 250 is a combination of 30 mg of equity, 60mg of equity, 60mg of equity, isocaproate, 100 mg of equity, and the total amount of testosterone in Sustanon 250 is 250 mg/ml. Known as “super testosterone” in its early days, the Sustanon 250’s time-sharing release allows users to have a constant supply of testosterone for about 10 days. So will be at the beginning of the birth of fired to the sky-high price, with the popularization of knowledge of drugs, in fact whether Sustanon 250 or testosterone enanthate and testosterone cypionate, per milliliter of testosterone levels, are the same, just released in a different way, the former is time-sharing release, which both as slow-release release, so, the latter two is more suitable for muscle growth. Compared to the characteristic (lower level in water retention) of Testosterone Enanthate as well as Testosterone Cypionate, Sustanon 250 is much more of an all-around player, so it works for all sorts of cycles and competition.
The benzene ring in testosterone phenylpropionate in Sustanon has a certain effect on testosterone propionate. As a result, the testosterone propionate in Sustanon will have a part of the injection point, so many veterans will separately inject Sustanon into the weak part in the cycle to obtain local reinforcement.
So in fact, whether it is testosterone enanthate, testosterone cypionate, or Sustanon 250 powder, is used as the basis in the cycle. The difference between them is in the muscle-enhancing dimension, using testosterone enanthate, testosterone cypionate can be used according to their own needs, and Sustanon 250 powder can be used in any cycle, but Sustanon 250 powder has a problem, that is: Sustanon 250 powder is the most painful one of all testosterone. Whether it is a local target injection or a hip injection, it will have the strongest pain relative to other testosterone. Testosterone phenylpropionate will stay for a while, testosterone propionate will also make the injection point pain.
Anti-estrogen steroids which are frequently used today’s drug industry mainly includes: Exemestane, Anastrozole, Letrozole these three, three drugs have their own advantages and disadvantages. Today we are going to compare the three drugs and how do we use them? How many? In fact, anti-estrogen is also important in the steroid cycle.
In the process of steroid cycle, due to the aromatization of some drugs (such as Dianabol and Deca), the body converts some high androgens into estrogen through aromatase, so as to obtain the balance between estrogen and androgens in the body. However, this transformation can lead to fat accumulation, decreased sexual desire, depression, and even breast cancer in men and women. Aromatase inhibitors (AI) are an effective way to solve these problems.
Anastrozole and Letrozole work style completely block aromatase, and the role of Exemestane is aromatic inactivation of enzyme in the body.
But as for anti-estrogen, what should we choose?
In general, Exemestane is 25 mg each tablet dosage for sale, and usually a dose of 12.5 mg of steroid cycle every other day, or 12.5 mg a day, the highest 25 mg per day.
However, estradiol level is not as low as possible in the whole cycle. Generally, when estradiol level is lower than 20pg/mg, symptoms such as depression, decreased libido, muscle leveling or joint pain may be caused by too low estradiol, so the dose of aromatase inhibitor (AI) should be adjusted. For example, users are injected with 250mg of testosterone per week and 750mg of non-aromatized steroids per week. Then the dose of 12.5 mg daily Exemestane can to a certain extent, inhibit estrogen. But if the user put the testosterone dose to 1000 mg every week, we don’t need to put Exemestane dose increase to 50 mg a day, usually in 25 mg is enough to cope with such a high dose of testosterone.
If you use the half-life in steroid cycle supernormal and have strong aromatization drugs such as Deca, then Exemestane in the PCT phase is preferred, rather than Exemestane or Letrozole. Because during PCT we need to naturally return estradiol levels to normal levels rather than completely blocking aromatase and artificially inhibiting it. Because the blocking aromatase accumulates, when the blocking is stopped, the aromatase erupts to some extent.
In the process of PCT, Exemestane dose should be lower than the cycles, because in the blood can aromatization of steroids will reduce a lot. Usually, 12.5mg every other day, or even every three or four days is enough.
Exemestane, Anastrozole, Letrozole that several kinds of aromatase inhibitors can very good control of estrogen transformation, if you are using one of these, then you should continue to use because you can have good control of the dosage. If you haven’t used them before, so can any of the three antiestrogens. It’s just the difference between the effects and the dose.
There are two kinds of HGH on the market, which should be exactly three kinds. One is HGH191, which is the purest HGH, one is HGH Frag 176-191, and one is HGH176.
HGH Frag 176-191 is a fragment of HGH191, which is a component of pure HGH. The tail of this HGH is cut off and can only be used to reduce fat.
HGH Frag 176-191 is the end of the 191 molecular chains of HGH (human growth hormone). The use of HGH has long been associated with fat loss, muscle growth, trauma recovery, and a range of health and anti-aging effects. While the effect of HGH Frag 176-191 is limited to fat cells, it works by reducing the effect of fat cell fluid.
HGH Frag 176-191 has been shown to be an effective reduced-fat peptide that actually inhibits the formation of lipids and fatty acids. It is also important to note that since it is only a part of the total growth hormone, high blood sugar, and other factors are not normally associated with the use of HGH Frag 176-191.
There is nothing to be said about the effects of HGH Frag 176-191, other than that it directly promotes fat loss. If we use HGH only to reduce fat, is it a better option than regular HGH? This is a difficult question to answer. If fat loss is your only concern, it makes more sense to opt for HGH Frag 176-191 rather than full HGH. If HGH is difficult to control blood sugar problems, it makes sense to reapply HGH Frag 176-191. However, there are numerous benefits to using HGH Frag 176-191 if you don’t have blood sugar problems. Increased muscle fiber, wound recovery, a stronger immune system, healing, and all the related anti-aging properties will not be experienced, and on this basis, complete HGH will always be the better choice.
HGH Frag 176-191 is lyophilized. HGH Frag 176-191 is usually given subcutaneously, but can also be injected intramuscularly. Either way, all injections should be given on an empty stomach.
HGH Frag 176~191 works best twice a day. If used once a day, should be taken 30 to 60 minutes before breakfast. If taken twice a day, the second dose should be taken before bedtime and a few hours after the day’s last meal. 250 to 500 MCG per day is the most common dose range, with 500 MCG being the most common. 500 MCG per day should produce a significant fat reduction in most individuals.
Today, let’s talk about why some oral steroids can be used alone, and some steroids cannot be used alone.
As we all know: there are many kinds of oral steroids in the whole competitive sports drugs, generally the following: Mesterolone, Oxandrolone, Methenolone Acetate, Turinabol, Dianabol, Methasterone, Methyltestosterone, Parabolan, Oral Winstrol, Anadrol… They are all common oral steroids, which can be classified into single use and are not recommended for stand-alone use and are absolutely prohibited from being used alone.
Then, the steroids that can be used alone are Mesterolone, Oxandrolone, Methenolone Acetate, Turinabol;
Steroids not recommended for use alone are Dianabol, Methasterone, Methyltestosterone;
The steroids that are absolutely prohibited from being used alone are Parabolan, Oral Winstrol, Anadrol;
So what are the reasons for these distinctions?
First of all, we need to know one thing at all: any cycle or any kind of steroid needs a foundation – testosterone! Whether testosterone comes from you or is exogenous, most of the steroids will have some endogenous inhibition after entering the body. This is because our body finds that there is an exogenous androgen involved. If enough androgen is enough, it will be lazy and will be suppressed. According to the level of the androgen index of the drug, the rate of suppression of androgen is determined. The steroids that can be used alone are because these drugs have low androgen index, low suppression rate, and no low testicular symptoms. Our own testosterone is enough to support the whole process of individual use, so it can be used alone.
The steroids that are not recommended for use alone are Dianabol, Methasterone, Methyltestosterone. The inhibition rate of these steroids is higher than that of the first type of steroids. Some users will have the corresponding symptoms of the bottom test when they use this part of the drug alone, so it is not recommended to use it alone. If you must choose to take these drugs alone, it is also recommended to use Mesterolone to enhance the liberation rate of our endogenous testosterone and the utilization of androgen to support the whole process.
In the end, the drugs that were absolutely forbidden to be taken alone were Parabolan, Oral Winstrol, and Anadrol. These drugs can severely suppress endogenous testosterone. Most users will have very serious symptoms of the bottom testosterone when they use these drugs alone so that they will not want to train at all during the severe suppression period, and even affect normal sex life. These steroids generally require the completion of the entire process with the support of exogenous testosterone.
Then one of the above drugs is oral testosterone: there are two common types of exogenous testosterone in oral administration: Testosterone Undecanoate and Fluoxymesterone. The difference is that Testosterone Undecanoate has low side effects and can be used to support the entire oral Cycle. Fluoxymesterone has great liver pressure and is not recommended to support the entire Cycle. It is generally used as the final stage of the season and as a booster before the fight.