$30.00
It is obtained from human origin and is obtained from women who are in their first few months of pregnancy.
While it won’t have a huge effect on the FSH. It does, however, have a great effect on stimulating the LH which in turn can help the Leydig cells found in the testes to start creating testosterone.
Human Chorionic Gonadotropin is mainly prescribed for women, yet it does have some medical uses for men. For teens who have issues with their testicles not dropping during puberty, HCG is prescribed to help. It is also prescribed for men with low testosterone.
Having first been in manufacture since 1920 and has been a prescribed medication since the 1930s. It has had much clinical use and thousands of trials, which is why it is quite trusted in the bodybuilding world.
HCG Dose and Availability
HCG is available in pharmaceutical grade. It comes as a power puck which you will need to mix with sterile water.
Once reconstituted the doses range from 1500iu 2500iu to 5000iu and 10000iu. The general price is between £25 – £35 per box.
Human Chorionic Gonadotropin has been a staple as a part of a PCT for many, many years. It has solidified its place in the bodybuilding world by being one of the most effective treatments to boost natural testosterone production in men.
After a cycle, a user’s natural production of testosterone has been significantly slowed or completely shut down. The difference between those who keep some gains and those who lose everything is usually a good PCT and how quickly the natural testosterone production can recover.
Human Chorionic Gonadotropin works by stimulating the Leydig cells inside the testes to being making testosterone again. Thanks to its ability as a fertility drug it is very effective.
HCG is usually injected two-three times a week for around three weeks from the start of the PCT. FDA approved protocols involve 500 – 1000iu being injected three times a week for a three-week cycle.
Most users will feel the benefit of using 1500iu three times a week for three weeks.
Human Chorionic Gonadotropin isn’t injected like steroids are. It follows a similar injection technique to that of HGH or Insulin.
Once prepared in your insulin pin you grab some fat in the lower abdomen and inject the Human Chorionic Gonadotropin into the fat under the skin, this is referred to as a subcutaneous injection.
Insulin pins are also much, much smaller than steroid injections and are extremely easy and painless to do.
HCG is usually a very tolerable drug and not many people will experience side effects from using it. However, there are some side effects to be aware of including; headaches, irritability, restlessness, fatigue, depression and gynecomastia.
Human Chorionic Gonadotropin should only be used while also running Nolvadex to protect the user from any gynecomastia symptoms
Clomid (Clomiphene Citrate) is a powerfully effective anti-estrogen officially classified as a Selective Estrogen Receptor Modulator (SERM). In many ways, it is very similar to another popular SERM in Nolvadex (Tamoxifen Citrate). Clomid first gained worldwide attention in the early 1970’s as a strong fertility aid and is still used for that purpose today. It is also one of the most commonly used SERM’s by anabolic steroid users. No, it is not an anabolic steroid but can be used to combat estrogenic side effects sometimes caused by anabolic steroids. It can also be used as a Post Cycle Therapy (PCT) medication in order to stimulate suppressed testosterone production due to anabolic steroid use. PCT use of Clomid is the most common purpose and most beneficial point of use for the anabolic steroid user.
Clomiphene Citrate is a SERM that is specifically used as a fertility aid due to its ability to enhance the release of gonadotropins. Clomid has the ability to oppose the negative feedback of estrogens on the Hypothalamic-Pituitary-Ovarian-Axis. This will increase the release of Luteinizing Hormone (LH) and Follicle Stimulating Hormone (FSH) significantly. By increasing gonadotropin release, this can lead to the egg being released, thereby increasing the chance of conception.
Clomid also carries strong anti-estrogen properties that could be used therapeutically, but its anti-estrogen properties are most commonly associated with anabolic steroid use. Testosterone and many testosterone derived steroids have the ability to convert to estrogen through testosterone’s interaction with the aromatase enzyme. As estrogen levels rise, this can lead to gynecomastia and excess water retention. Heavy water retention can also promote high blood pressure. By supplementing with Clomid during anabolic steroid use, the SERM will bind to the estrogen receptors, therefore inhibiting the estrogen hormone from binding. This can be very useful in combating gynecomastia, as when Clomid binds to the receptor it prevents estrogen from stimulating the mammary tissue. It can also have a positive impact on water retention, but as it won’t actively reduce serum estrogen levels it’s sometimes not enough.
Clomid also possess functioning traits that are beneficial to the anabolic steroid user post anabolic steroid use. Specifically we’re referring to Post Cycle Therapy (PCT). In men, Clomid also has the ability to stimulate the pituitary to release more LH and FSH, which will in turn stimulate enhanced natural testosterone production. This is extremely beneficial to the anabolic steroid user post cycle as natural testosterone levels will be very low due to suppression caused by anabolic steroid use.
In a therapeutic setting as a fertility aid, the effects of Clomid are simple. The woman is having difficulty becoming pregnant, Clomid enhances the chance of conception and pregnancy occurs. It doesn’t always work and we’ll look at the process in the administration section, but it will greatly increase the odds of conception and is fairly successful.
As an anti-estrogen for on cycle steroid use, Clomid is fairly effective at staving off gynecomastia. It will not reduce estrogen levels or inhibit the aromatization process, but in many cases, binding to the receptors is enough protection for many men. In fact, while there are stronger protective agents, many men would be surprised as to how well a SERM like Clomid can work if they would give it a chance. More importantly, when using Clomid for this purpose it can also have a positive impact on cholesterol levels. While an anti-estrogen, Clomid actually acts as estrogen in the liver, which in turn will promote healthier cholesterol levels. This can be very beneficial to the anabolic steroid user as anabolic steroid use is notorious for promoting unhealthy cholesterol levels.
For many men, especially hardcore anabolic steroid users, Clomid is not enough for estrogenic protection. In this case, an Aromatase Inhibitor (AI) like Arimidex (Anastrozole) or Femara (Letrozole) will be needed. AI’s actively inhibit the aromatase process and will see serum estrogen levels reduced. By far they are the most effective at combating gynecomastia and will have more success in combating water retention. In fact, SERM’s like Clomid often do very little to combat water retention. However, in many cases, many performance athletes would do a better job controlling water retention if they did a better job controlling their diet. In off-season bulking plans this requires excess calories to grow. However, many take it too far, especially carbohydrate consumptions, and this will cause you to hold water with or without anabolic steroid use. Add in aromatizing steroids to the equation and water retention will be even greater. Further, AI’s while effective will have a negative impact on cholesterol, which leads us to only one sane conclusion. Control your diet and if you can control gynecomastia with a SERM like Clomid it should be your first choice.
Then we’re left with the effects of Clomid as they pertain to PCT. When we supplement with anabolic steroids, this will suppress natural testosterone production. The rate of suppression will be dependent on the steroids being used and to a degree the total dosing, but it will generally be substantial. For this reason, most men will always include exogenous testosterone in their steroid cycles. In fact, it’s not uncommon for it to be the only steroid used. This will protect the individual from a low testosterone condition while on cycle. Unfortunately, once steroid use comes to an end natural testosterone levels will be very low. Natural testosterone production will begin again on its own, but it will take a significant amount of time for levels to reach their previous high state. In fact, total recovery can take months to even a year. Further, natural testosterone recovery is dependent on no prior low testosterone condition existing and assumes that no severe damage was done to the Hypothalamic-Pituitary-Testicular-Axis (HPTA) through improper anabolic steroid use.
Due to natural testosterone levels being low post cycle, most men are encouraged to implement a PCT program. This will stimulate natural testosterone production greatly and shorten the total recovery time. It will not return your levels to normal on its own; there is no PCT plan on earth that can do this. However, a solid PCT plan will ensure you have enough testosterone for proper bodily function while your levels continue to naturally rise. Clomid is an excellent choice for this purpose and one of the most commonly used PCT medications. Highly successful PCT programs will often include Clomid and Nolvadex as well as the powerful peptide hormone HCG (Human Chorionic Gonadotropin).
Those who forgo Clomid therapy post cycle or any type of PCT plan and are going to be off cycle for an extended period of time will rest in a low testosterone condition for an extended period of time. Not only is this an extremely unhealthy state, it can come with all the traditional low testosterone symptoms. Many will find cortisol levels greatly increase as testosterone levels are low, and as a result, body fat levels go up and strength and muscle mass decrease. If you’re going to be off cycle for an extended period of time, 8 weeks or more there is no reason for forgoing a PCT program. If you are going to be off cycle for less than 8 weeks or bridging with a low dose of exogenous testosterone, which is very common in hardcore bodybuilding circles, this is the only time a PCT would be counterproductive.
Clomid is one of the most well-tolerated SERM’s and anti-estrogens on the market, and this applies to both men and women. While it carries a very high threshold of toleration, side effects of Clomid do exist and are possible. However, “possible” is the key word and a very important one. Anytime anabolic steroids are discussed as well as non-steroidal items used by anabolic steroid users, many seem to enjoy implying side effects are assured. This is not the case; in fact, most should be able to use Clomid side effect free.
When it comes to the possible side effects of Clomid, we will find most are fairly rare. Some women who have used the SERM as a fertility aid have experienced ovarian enlargement, but again this is very rare. Other possible side effects of Clomid use include:
The side effects of Clomid are also well noted for including possible visual disturbances. Data shows that approximately 1.5% of all those who use Clomid may experience some type of visual disturbance normally in the form of blurred or hazy vision. If this occurs, use should be discontinued and alternative medications should be examined. In most all cases, once use is discontinued vision will shortly return to normal. However, there have been a few reported cases over the years of visual disturbances that did not remedy post discontinuation. Normally, such cases have been linked to long term and extremely high dose use. Again, if visual disturbances occur, discontinue use immediately and choose another SERM to meet your needs.
A final note on the side effects of Clomid, some may experience acne. This appears to be most common when the SERM is used as part of a PCT program. In this case, it’s not really the SERM that’s causing the issue but rather the high influx of natural testosterone that is now being produced. Most should not have an issue, but those who are already genetically sensitive to acne may find a few pimples appear on their back, shoulders or chest.
For the purpose of fertility aid, Clomid doses will normally be at 50mg per day. The process is very simple; five days into the menstrual cycle a daily 50mg dose is administered every day once a day for five straight days. If this doesn’t result in conception, the dose is sometimes increased to 100mg per day. This cycle will be repeated 5-6 times over the course of the woman’s menstrual cycles until pregnant. If conception does not occur after 5-6 cycles of therapy, alternative treatments will need to be examined.
For the anabolic steroid user, standard Clomid doses for on cycle estrogenic protection will normally be 50mg per day throughout the duration of the cycle. If this doesn’t do the trick it’s unlikely any amount of Clomid will work. If this does not provide the protection you need, keep in mind many have reported greater success with the SERM Nolvadex for on cycle protection. However, you may very well need an AI like Arimidex.
Then we’re left with PCT Clomid use. Standard PCT Clomid doses will normally start at 100-150mg per day for 1-2 weeks. From here the dose will drop to 50-100mg per day for 1-2 weeks and finish with 1-2 weeks at 50mg per day. Total Clomid therapy should last 4-6 weeks, so dosing should be based and considered on that total schedule. Most will also be far more successful in their PCT recovery by including Nolvadex and HCG. Timing is also important when planning your Clomid PCT use, and this timing factor will vary depending on the inclusion of HCG:
Deca Durabolin is an extremely popular anabolic steroid comprised of the steroidal hormone Nandrolone and is attached to the large Decanoate ester. The Nandrolone hormone first appeared in 1960 and developed for commercial use in 1962 by Organon under the trade name Deca Durabolin. Since that time numerous Nandrolone Decanoate versions have hit the market, but Deca Durabolin remains the most recognized. This was not the first Nandrolone compound ever created, that would belong to Organon’s Durabolin, which is specifically Nandrolone Phenylpropionate. The Phenylpropionate version is much faster acting with a less active duration, and while Phenylpropionate forms are popular, Deca Durabolin has largely dominated the Nandrolone marketplace.
Deca Durabolin is one of the most commonly used anabolic steroids among performance enhancing athletes. It is well known for being a tremendously beneficial off-season mass steroid, but it’s also a favorite in many athletic circles for its therapeutic benefits. Due to its tremendous therapeutic benefits, the Nandrolone hormone is one of the most beneficial anabolic steroids in medical practice. However, due to years of anabolic steroid controversy such use has been quite limited in the U.S. for many years. Outside the U.S. Deca Durabolin remains a bit more popular in therapeutic treatment plans that can cover a host of areas.
Deca Durabolin is officially classified as a 19-nortestosterone (19-nor) anabolic androgenic steroid. The 19-nor classification refers to its direct structural nature, which is the testosterone hormone lacking a carbon atom at the 19th position. While this is only a slight change in structure from the testosterone hormone, this slight change gives us a unique anabolic steroid. As a Nandrolone base, Deca Durabolin is attached to the large Decanoate ester, which controls the hormone’s releasing activity slowing it down tremendously. This allows the individual to make use of the Nandrolone hormone without the need for frequent injections. Once injected, as the Decanoate ester begins to detach there will be a sharp spike in Nandrolone released within the body during the first 24-48 hours. From this point, the hormone will continue to release into the body for approximately 2-3 weeks.
Deca Durabolin carries a relatively potent anabolic rating, slightly greater than testosterone. However, its total androgenic activity is much lower than testosterone, carrying an androgenic rating of only 37 compared to testosterone’s 100. The lessened androgenic activity of Deca Durabolin is due to the hormone’s ability to reduce to dihydronandrolone (DHN) rather than dihydrotestosterone (DHT). This makes Deca Durabolin a much milder steroid than testosterone, and one of the most well-tolerated anabolic steroids for healthy adult men. This tolerable nature is also evident by its low estrogenic activity. Deca Durabolin does aromatize, but only at approximately 20% the rate of testosterone. However, it does carry a strong progestin nature, and this will play into the side effects as we will see later on.
Like many anabolic steroids, Deca Durabolin has the ability to enhance protein synthesis, inhibit glucocorticoid hormones, and promote enhanced IGF-1 output. Like many anabolic steroids, Deca Durabolin also has the ability to increase nitrogen retention in the muscles, but it appears to have a stronger affect than many steroids in this regard. In fact, studies have shown that even low doses of Nandrolone can greatly enhance nitrogen retention. This is an important factor, as all muscle tissue is comprised of approximately 16% nitrogen. While that may sound like a small amount, the more we retain the more anabolic we remain. When nitrogen levels are not maintained, this can cause us to enter a catabolic (muscle wasting) state.
Deca Durabolin is also well known for carrying two traits that are extremely important and largely separate it from many anabolic steroids. Again, many other steroids will carry these traits, but Deca Durabolin does so to a higher level. The traits in question are increasing bone mineral content and enhancing collagen synthesis. Due to these traits, Deca Durabolin is well known for promoting joint relief, and for many athletes that’s the only reason they’ll use it. Due to these traits, as well as its ability to increase red blood cell count, we can begin to see what types of therapeutic advantages this steroid can hold.
Deca Durabolin has been well noted for being an excellent steroid for those suffering from muscle wasting diseases, for improving geriatric weakness and fatigue, as well as anemia. Deca Durabolin has also been used to treat certain forms of breast cancer, has been life changing for severe burn victims, and even has the ability to treat ulcers. It has also been shown effective for treating pituitary deficient dwarfism, as well as development retardation in children. While Deca Durabolin has proven beneficial in all these areas, it has truly shined is in its ability to treat osteoporosis. This isn’t surprising when we consider the bone mineral content and collagen synthesis improvements. However, in the U.S. the compound is only used to treat those suffering from HIV and anemia, but some physicians are beginning to recognize the potential for therapeutic rejuvenation plans. Undoubtedly, at a low dose this steroid could provide a positive anti-aging benefit.
While the therapeutic benefits of Deca Durabolin are easy to see simply by understanding its basic nature, what most are concerned with is off-label use. Deca Durabolin is a long standing favorite among performance enhancing athletes, and while it is tremendously beneficial it is often grossly misunderstood. The misunderstanding is that this is only a bulking steroid, and while that is a fantastic point of use it is far from the only one. In fact, some competitive bodybuilders will use Deca Durabolin during their cutting phase, and during such a phase there’s no bulking going on. However, in order to understand the effects of Deca Durabolin and the varying beneficial points of use, you must remove a flawed way of thinking held by many anabolic steroid users. This type of thinking assumes all steroid progress is based on the enhancement of lean muscle tissue; specifically building more lean muscle tissue. Undoubtedly, this is the primary purpose of anabolic steroid use, but it is not the only one. With that in mind, let’s take a look at the varying positive effects of Deca Durabolin.
As an off-season bulking steroid, Deca Durabolin will provide significant gains in lean mass, but the increase in muscle mass will come slowly. This is a large ester based steroid, and it will not be fast acting. However, the mass built with this steroid will often be higher quality mass than compared to many anabolic steroids. Water retention is possible, but it should be fairly easy to control. Most should also find their strength increases to a degree, but Deca Durabolin is not what we’d call one of the stronger strength increasing steroids. During this off-season phase, the individual will also enjoy the therapeutic relief this steroid provides, which will be more than welcomed when off-season periods of growth are normally accompanied by the heaviest periods of weight training. This individual should also be able to acquire this new growth with less body fat accumulation that would normally otherwise occur. The use of anabolic steroids is well noted for enhancing the metabolic rate. This is nothing unique to Deca Durabolin, and while it will not directly burn body fat it will aid in the maintenance of a proper level. As off-season mass gains require excess calories, consider the metabolic enhancement an added bonus.
Many athletes, ball players, fighters, and any athlete who could benefit from the therapeutic relief often supplement with Deca Durabolin. Such individuals commonly have no desire to build any new lean muscle mass, but the relief alone is invaluable. Further, such relief can be obtained by a very low dose. A slightly higher dose will provide relief, greatly enhance overall recovery, and enhance muscular endurance. When it comes to performance enhancement, most athletes will find this steroid is hard to beat. More importantly, the relief effects of Deca Durabolin are not masking or false; this anabolic steroid shares nothing in common with over the counter painkillers or prescription painkillers like opiates. Such painkillers only mask the pain, whereas Deca Durabolin can actually heal the body.
Then we’re left with the cutting phase, and some athletes and bodybuilders will use Deca Durabolin during this phase of steroid use. Such use will be similar to direct athletic enhancement. The individual will supplement with a rather low dose for the relief and muscular endurance it can provide. This can be very welcomed during hard diets, as a true hardcore bodybuilding cutting diet is brutal on the human body. As an added bonus, Deca Durabolin will greatly preserve the individual’s lean muscle mass that would otherwise be lost during a necessary caloric deficit. While this steroid will not provide hardening or conditioning effects like many steroids, it can serve a purpose is some cutting plans.
Deca Durabolin is one of the more side effect friendly anabolic steroids for men and can prove useful for women, but normally only in therapeutic level doses. However, side effects of Deca Durabolin most certainly exist, but as we will see they largely fall into the realm of possible rather than guaranteed. With responsible use, most men will be able to use this steroid without the first negative effect. In order to achieve this level of safe supplementation, your first step is to recognize the possible side effects of Deca Durabolin, as well as what you can do about them. For an ease of understanding, we have broken down the side effects into separate categories along with the related information you’ll need.
(Mesterolone)
Proviron represents one of the oldest anabolic androgenic steroids on the market. A product of the giant pharmaceutical company Schering, it would first appear in 1934. Officially known as Mesterolone, it has appeared under numerous brand names over the years, but the Proviron name has continually remained dominant. It has also remained one of the most misunderstood anabolic steroids among steroid users.
In many ways, Proviron is a very unique anabolic steroid. It shares some strong similarities to Masteron (Drostanolone) and to a degree Anavar (Oxandrolone) and Winstrol (Stanozolol) but in totality it is its own unique animal. In a performance capacity, Proviron is not used to promote large buildups in mass, although it can serve an important purpose during such a phase of training. We will, however, find Proviron to be far more common in cutting cycles, but once again its purpose will be somewhat unique.
As a therapeutic agent, Proviron is one of the most commonly used anabolic steroids in modern medicine. However, the Mesterolone hormone has never been approved by the U.S. FDA. It will primarily be found in European medicine, especially in Western Europe. The primary purpose of use is treating androgen deficiencies, age being the most common culprit of the condition. It is, however, also used in pre-pubescent males as well. The hormone is also used as a fertility aid in men and this alone makes it a very unique anabolic steroid as most anabolic steroids tend to have the opposite effect.
Mesterolone is a dihydrotestosterone (DHT) derived anabolic androgenic steroid. Specifically it is a structurally altered DHT hormone possessing the addition of a methyl group at the carbon one position. This allows the hormone to survive oral ingestion by protecting it from hepatic breakdown. This is one of the only oral anabolic steroids that is not C17-alpha alkylated (C17-aa) but instead carries the added methyl group. Oral Primobolan is the other most well-known oral steroid that carries this same methyl group. While the added methyl group does in fact protect it from breakdown, the total bioavailability of Proviron will be far less than most all C17-aa oral steroids. For this reason it has fallen out of popularity among many performance enhancing athletes but as we will see perhaps unjustifiably so.
Proviron carries an androgenic rating of 30-40 and an anabolic rating of 100-150. All ratings derive from and are measured against testosterone, which carries a rating of 100 in both categories. Despite having an anabolic rating that is potentially greater than testosterone, Proviron will display very low anabolic traits. This is very similar to Halotestin (Fluoxymesterone), which carries a massive anabolic rating but very little translatable anabolic activity. In the case of Proviron, while structurally very anabolic, the Mesterolone hormone converts and reduces to Diol metabolites, in turn reducing anabolic activity. However, Proviron’s androgenic rating is a different story. In fact, its translatable androgenic activity appears to commonly be higher than its structural rating would imply.
On a functional basis, Proviron carries four primary traits that largely define its mode of action. First and foremost the Mesterolone hormone has a strong binding affinity to Sex-Hormone-Binding-Globulin (SHBG). In fact, it appears to be one of the strongest anabolic steroids in this regard. By binding to SHBG, a hormone partially responsible for reducing free testosterone, binding SHBG will enhance the amount of circulating free testosterone. More importantly for the anabolic steroid user, it will make a larger percentage of the anabolic steroids used available in a free rather than bound state. A simple way to look at it is the anabolic steroids you’re taking become more powerful and potent.
Proviron also has the ability to interact with the aromatase enzyme, the enzyme responsible for the conversion of testosterone to estrogen. By binding to the aromatase enzyme, Proviron can actually inhibit aromatase activity, thereby offering protection against estrogenic side effects. It will not carry an anti-estrogenic effect near the level of power of an Aromatase Inhibitor (AI) but it will be notable. Depending on the nature of the cycle the individual undertakes it is quite possible for Proviron to take care of all your anti-estrogen needs.
The Mesterolone hormone will also carry a strong binding affinity to the androgen receptor. Once again this will promote the functionality of other steroids to a degree but more importantly promote enhanced metabolic activity through direct lipolysis. Then we’re left with the final issue that surrounds Proviron as a fertility medication. This is an anabolic steroid that does not suppress gonadotropins similarly to other anabolic steroids. With minimal suppression and its extremely strong androgenicity, this will enhance sperm production as androgens are necessary to spermatogenesis stimulation. This not only enhances the amount of sperm produced but greatly and equally important enhances the quality of the sperm. Before we go any further understand Proviron does have the ability to suppress gonadotropins, but there’s a line that has to be crossed for notable suppression to interfere with sperm production. This will make sense once we dive into the side effects section.
During a bulking phase Proviron is not going to be a foundational steroid, and for most men it will not have a place in an off-season cycle. There are exceptions and we’ll go over those here. Adding in Proviron could possibly help the individual breakthrough a sticking point during his cycle. At some point and time in all cycles the progress begins to wane, and in some cases come to a complete halt. By the way Proviron enhances the total free state of the other steroids being used in a stack, it could possibly help the individual breakthrough this sticking point. During the off-season, this is where most will use the largest amount of testosterone. Many will use large amounts during cutting cycles too, especially competitive bodybuilders but lower testosterone plans are more common during the cutting phase. However, there are those for numerous reasons who choose to run off-season cycles with limited testosterone doses. In such plans, including Proviron could give them a slight needed androgen boost. While it may not always be necessary it could prove to be beneficial.
Without question the best time to use Proviron will be during the cutting phase. This steroid has the ability to provide a bit of a hardening effect similar to Masteron, but more importantly the hardening effects of other steroids will be enhanced. Then we consider its strong binding to the androgen receptor, which will in fact enable the individual to burn body fat at a far more efficient rate. From here we must consider the anti-estrogen effect of Proviron. This will ensure the individual is less prone to water retention and as discussed, depending on the total cycle, it could negate the need for a traditional anti-estrogen. Then we’re once again left with the enhancement of circulating free testosterone. This can be a tremendous benefit when testosterone levels are often much lower during this phase of anabolic steroid use. In fact, with a low dosed testosterone cycle that includes other anabolic steroids, we can confidently say the total results will be greater for the individual who includes Proviron compared to the one who does not. In the end, the primary base benefit is the increased androgenicity of other steroids being used in order to promote a much harder and far more defined physique. It should be noted while Proviron can most certainly provide these traits they will not be noticeable unless you are lean.
There are possible side effects of Proviron use; however, this steroid carries one of the highest safety ratings among all anabolic steroids. Most men will be able to use this steroid without any negative issue, but possible side effects do exist despite a low probability. When it comes to female use, in a therapeutic or performance capacity this steroid cannot be recommended. The rate of virilization is much to high and should be avoided by females who wish to protect their femininity. In order to help you understand the possible side effects of Proviron, we have broken them down into their separate categories along with everything you need to know.
Equipoise 200mg/ml and Trenbolone Acetate 100mg/ml is another one of those compounds that delivers exactly what one would expect; dense and vascular mass. It is a great pre-contest compound, that will most definitely help you retain your size, while getting you shredded at the same time.