Anadrol (Oxymetholone)

Anadrol  is the strongest and, at the same time, also the most effective oral steroid. Anadrol has an extremely high androgenic effect which goes hand in hand with an extremely intense anabolic component. For this reason, dramatic gains in strength and muscle mass can be achieved in a very short time. An increase in body weight of 10 - 15 pounds or more in only 14 days is not unusual. Water retention is considerable, so that the muscle diameter

quickly increases and the user gets a massive appearance within record time. Since the muscle cell draws a lot of water, the entire muscle system of most athletes looks smooth, in part even puffy. Anadrol does not cause a qualitative muscle gain but rather a quantitative one which in the off-season is quite welcome. Anadrol "lubricates" the ANADROL-OXYMETHOLONE IH 50mgjoints since water is stored there as well. On the one hand this is a factor in the enormous increase of strength and, on the other hand, it allows athletes with joint problems a painless workout. Powerlifters in the higher weight classes are sold on Anadrol. A strict diet, together with the simultaneous intake of Nolvadex and Proviron, can significantly reduce water retention so that a distinct increase in the solid muscles is possible. By taking Anadrol the athlete experiences an enormous "pump effect" during the workout in the exercised muscles. The blood volume in the body is significantly elevated causing a higher blood supply to the muscles during workout. Anadrol increases the number of red blood cells, allowing the muscle to absorb more oxygen. The muscle thus has a higher endurance and performance level. Consequently, the athlete can rely on great power and high strength even after several sets. The highly androgenic effect of Anadrol stimulates the regeneration of the body so that the often feared "overtraining" is unlikely. Although Anadrol is not a steroid used in preparation for a competition, it does help more than any other steroid during dieting to maintain the muscle mass and to allow an intense workout. Many bodybuilders therefore use it up to about one week before a competition, solving the problem of water retention by taking antiestrogens and diuretics so that they will appear bulky and hard when in the limelight.

HOW TO USE ANADROL: Anadrol is unfortunately also the most harmful oral steroid. Its intake can cause many considerable side effects. Since it is I 7-alpha alkylated it is very liver toxic. Most users can expect certain pathological changes in their liver values after approximately one week. An increase in liver values of both the enzymes GOT and GPT also called transaminases, often cannot be avoided. Elevated GOT and GPT values are indications of hepatitis, i.e. a liver infection. Those who discontinue oxymetholone will usually show normal values within two months. Longer intake and/or higher doses can cause a yellow discoloration of fingernails, eyes, or skin jaundice). This is because oxymetholone induces an increase of biliburin in the liver, producing a bile pigment which causes the yellow discoloring of the skin. The liver enzyme gamma-GT also reacts sensitively to the oxymetholone, causing it to elevate. If high dosages ofANADROL-OXYMETHOLONE 50mg Anadrol are taken over a long period, there is an increased risk that the described liver changes could end up damaging the liver. During the intake of Anadrol, the liver values, GOT, GPT, bilirubin, gamma-GT and alkaline phosphatase (AP), as well as the LDH/HBDH quotient, should always be checked by a competent physician. Anadrol (representing all oxymetholone containing steroid products) is the only anabolic/androgenic steroid which was linked with liver cancer.

The compound oxymetholone easily converts into estrogen. This causes signs of feminization (e.g. gynecomastia) and the already mentioned water retention which in turn requires the intake of antiestrogens (e.g. Nolvadex and Proviron) and an increased use of diuretics (e.g. Lasix) before a competition. The increased water retention, in addition to the aesthetical problems, can be further detrimental since it may cause high blood pressure. In extreme cases the intake of an antihypertensive drug, e.g. Catapresan, may be necessary. Oxymetholone doesn't convert to DHT. However, it is a potent androgen. Bodybuilders who experience severe steroid acne caused by Anadrol can get this problem under control by using the prescription drug Accutane.

Other possible side effects may include headaches, nausea, vomiting, stomach aches, lack of appetite, insomnia, and diarrhea. The athlete can expect a feeling of "general indisposition" with the intake of Anadrol which is completely in contrast to Dianabol which conveys a "sense of wellbeing". The increased aggressiveness is caused by the resulting high level of androgen and occurs mostly when large quantities of testosterone are "shot" simultaneously with the Anadrol. The body's own production of testosterone is considerably reduced since Anadrol has an inhibiting effect on the hypothalamus, which in turn completely reduces or stops the release of GnRH (gonadotropin releasing hormone). For this reason the intake of testosterone stimulating compounds such as HCG and Clomid is absolutely necessary to maintain the hormone production in the testes.

ANADROL-OXYMETHOLONE IP 50mgAnadrol is not recommended for women since it causes many and, in part, irreversible virilizing symptoms such as acne, clitorial hypertrophy, deep voice, increased hair growth on the legs, beard growth, missed periods, increased libido, and hair loss. Anadrol is simply too strong for the female organism and accordingly, it is poorly tolerated.

ANADROL DOSAGE: As for the dosage, opinions differ. A dosage sufficient for any athlete would be 0,5 - 0,8 mg per pound of body weight/day. This corresponds to 1-4 tablets; i.e. 50-200 mg/day. Under no circumstances should an athlete take more than four tablets in any given day. We are of the opinion that a daily intake of three tablets should not be exceeded. Those of you who would like to try Anadrol for the first time should begin with an intake of only one 50 mg tablet. After a few days or even better, after one week, the daily dosage can be increased to two tablets, one tablet each in the morning and evening, taken with meals. Athletes who are more advanced or weigh more than 220 pounds can increase the dosage to 150 mg/day in the third week. This dosage, however, should not be taken for periods longer than two to three weeks. Anadrol should not exceed six weeks. After discontinuing Anadrol, it is important to continue steroid treatment with another compound since, otherwise, a drastic reduction takes place and the user, as is often observed, within a short period looks the same as before the treatment. No other anabolic/androgenic steroid causes such a fast and drastic loss in strength and mass as does Anadrol. Athletes continue their treatment with injectable testosterone such as Sustanon or Testosterone enanthate for several weeks. Bodybuilders often combine Anadrol with Deca-Durabolin or Testosterone to build up strength and mass. Anadrol is to be taken seriously and the prevailing bodybuilder mentality "more is better" is out of place.

Anavar (Oxandrolone)

Oxandrolone represent a 17-alpha alkylated anabolic steroid that is widely known as being mild steroid.It is often chosen by sportsmen because it promotes protein anabolism and side effects appear seldom. Oxandrolone is much less toxic than other supplements that have the same positive effects on the body.Oxandrolone is a DHT derivative and is considered to be easy on the liver. This compound is also a good choose for bodybuilders/athletes because it dose not aromatize. That mean it doesn’t convert to estrogen and side effects as water retention and gyno will be avoided as well as anti-estrogens are rarely needed.Another not less important thing about Oxandrolone is the fact that it was approved for orphan drug status by the Food and Drug Administration (FDA) in treating such diseases alcoholic hepatitis, Turner’s syndrome, and weight loss caused by HIV, anemia and hereditary angioedema.In most cases Oxandrolone is taken to promote strength and muscle hardness. The gain is obtained not quickly but instead of this sportsmen have quality muscle and strength gains.Oxandrolone is often chosen by those bodybuilders/athletes who are in their pre-contest period, in order to keep their muscles hardness without gaining additional weight.Also Oxandrolone is considered to be an excellent fat burner and it is often taken in cutting cycles.Because of its extremely mild nature Oxandrolone is popular supplement amongst female sportsmen.As we noticed earlier side effects are rarely with this steroid in case bodybuilders/athletes will not exceed the dose. It can include oily face and acne.

Clenbuterol

Clenbuterol is a selective beta-2 agonist/antagonist. Its primary medical use in many parts of the world is as a bronchodialator, although it is not prescribed for human use in North America. It is however still in use in veterinary medicine, being utilized for various treatments and purposes.

In terms of the use of clenbuterol for strength athletes and bodybuilders, its function as a beta-2 agonist can help to increase lipolysis (1). This is accomplished via an increase in basal metabolic rate, as well as increased heat production in the mitochondria which serves to increase body temperature and therefore increasing thermogenesis (1). Additionally, it has been shown that clenbuterol is able to directly stimulate fat cells and accelerate the breakdown of triglycerides, thus forming free fatty acids. All of this is accomplished while clenbuterol has a minimal effect on the user cardiovascularly. This, as stated previously, is due to the drug being a selective beta-2 agonist/antagonist and having a minimal impact on the beta-1 receptors. This should cause less negative side effects, at least cardiovascularly, for the user.

A second benefit to the administration of clenbuterol for athletes is an increase in strength as well as a possible increase in muscle size/lean body mass. It has been repeatedly demonstrated in animal studies that clenbuterol contributes to an increase in muscle mass, weight and protein content (2). The exact mechanism by which this takes place has still not been definitively identified but it can be concluded that it is far different then the response produced by anabolic steroids.

Like other beta-2 agonists, clenbuterol has also been shown to increase muscular strength (3,4,5). Again, these results were achieved in animal studies but there is little reason to believe would not be transferable to human users. These gains are made over time and not a result of any type of stimulatory effect of the drug. Again however, the exact mechanism by which these results are achieved with clenbuterol is not known. It is not the same as anabolic steroids but more research needs to be done before a full understanding of this mechanism is known. Clenbuterol does increase muscle protein synthesis (6) so this is likely to contribute but is unlikely to be the only cause.


Use Dosing:
In terms of a dosing schedule for clenbuterol, most users would be well served to split their dosages into two or three evenly spaced doses throughout the day. The first can be taken upon rising and then the one or two others throughout the rest of the morning and/or afternoon. This is due to the half-life of the drug being approximately seven to nine hours. Using this as a guide, frequent dosing is unnecessary. The only caution is that one should avoid taking a dose too late in the day to help and reduce the impact the drug will have on the sleep pattern of a user. For some, sleep interruption may be inevitable with the use of clenbuterol but if the user is able to limit their use of it later in the day. Most users anecdotally report that by taking their last dose six to nine hours before they expect to sleep, the drug has less of a negative on their ability to rest. However the user will have to experiment to determine their own tolerance of the compound.

Prior to the start of administering clenbuterol the user should monitor his or her body temperature to obtain a “normal” reading. Throughout the use of clenbuterol the user should continue to monitor their body temperature to determine the effectiveness of the dose used, as well as when to increase it. Many believe that simply going by “feel” and/or the presence of noticeable side effects is enough to determine whether or not the compound is accomplishing what the user desires. This is simply not true. The only accurate way to do this is to constantly monitor one’s body temperature.

As for the specific doses needed, most users would be well served to begin using about 20mcgs per dose initially. This is applicable to both male and female users. This dosage should be enough to produce an increase in body temperature while not producing side effects that could be overly detrimental to the user. However if one does have an adverse reaction a reduction in the dosage used should be completed immediately or else the administration of the drug should be ceased.

Once the administration of the drug has begun body temperature should be the determining factor in when a user should increase his or her doses. These increases should be slow and incremental as not to suffer from large increases in the severity of possible side effects. Doses ranging from sixty to higher then two hundred micrograms are not abnormal for many users, but as with most compounds, the smaller amount a user is able to use usually the less likely they are to experience negative side effects. For the most part it is recommended that users keep their daily dose of clenbuterol to well under two hundred micrograms.

Due to the fact that clenbuterol is a beta-2 agonist/antagonist the downregulation of the cardiac, pulmonary and central nervous system beta-adrenergic receptors is an issue that users must combat when using this compound (3). A proven method to help alleviate this effect and ensure that the clenbuterol remains effective throughout its use is via the administration of ketoifen (7). Ketoifen is a prescription anti-histamines that acts to reduce beta-2 receptor activity. By reducing this activity, the receptor function is restored to nearly its original capability and the potency of the clenbuterol remains in effect. Doses of two to ten milligrams of ketoifen have been used by users of clenbuterol, but most would be well served to start at lower doses. It is unlikely that many will need doses higher then 5 milligrams per day. Taking ketoifen for seven days every two to three weeks should be enough to maintain well functioning beta-2 receptors and ensure that the clenbuterol maintains its effectiveness.

An alternative to ketoifen may be diphenhydramine, commonly referred to as Benedryl. Benadryl is a cationic ampiphylic drug, with this fact being significant because cationic ampiphylic drugs have the ability to inhibit phospholipase A2 and therefore upgrade beta-2 receptors (8). The inhibition of the enzyme phospholipase A2 is key due to it being responsible for methylated phospholipids. It is thought that by reducing and/or ending this action this allows the phospholipid membrane to remain relatively intact and the beta-adrenoreceptors will be able to remain functioning at their full capacity, or near to it, for much longer. For most, an effective dose would be 50-100mgs per day for seven days every three weeks while running clenbuterol. Users would be well served to take this dosage just prior to going to sleep as it will likely cause drowsiness.

Having said this, there is much more anecdotal feedback in regards to the effectiveness of ketoifen in relation to clenbuterol then there is Benedryl simply because ketoifen has been used much longer by strength athletes and bodybuilders for this purpose. As well, there is seemingly more direct research that indicates that ketoifen is effective while only a few studies suggest the same of Benedryl. That is not to say that Benedryl is ineffective, just that there is less “real world” feedback as to its use with clenbuterol.

This prevention of the downregulation of the beta-2 receptors is important since it appears that clenbuterol gains effectiveness and produces its best results if it is run for six weeks or longer. This is true of fat loss and muscle mass gain it appears. For this reason most users will want to run clenbuterol for at least six weeks and ensure that they use some protection against receptor downregulation so that the clenbuterol remains effective throughout.

Side Effects:
Clenbuterol has an array of potential negative side effects that are indicated in the available research, most of which has been performed using animals. The problem with this is the fact that animals have quite different beta-2 receptor reactions then humans in some cases as well as having a larger quantity of these receptors in the relevant tissues. This obviously could lead to differing reactions in humans then those found in various animals. However due to the lack of research available conducted with human subjects, we are left to decipher the applicability of the animal research that has been conducted.

The most commonly reported side effects associated with clenbuterol are tremors, increased heart rate, increased sweating, restlessness, headaches, and loss of appetite. The only way to prevent or reduce such symptoms from occurring is to either reduce the dosing being administered or ceasing to use the drug completely.

Like most drugs however, it is the side effects that are least noticeable initially that can be the most dangerous for the user. One such example is the apparent detrimental effect clenbuterol has on the fragility of bones (9, 10). In one study, even after only six weeks of administering clenbuterol there was a significant decline in the bone mineral density of the rats that were used to conduct the study (9). This finding may be of significant interest to women or those with family histories of bone diseases such as osteoporosis.

Along with this, heart damage as attributed to the use of clenbuterol is seemingly a regular occurrence in animal research. Most of this centers around such things are cardiac hypertrophy, including enlargement of ventricles, and cardiac necrosis (11). Along with this, blood pressure should be monitored constantly when using clenbuterol. Due to the mechanism by which clenbuterol works, some users will undoubtedly suffer from hypetension when using it. A reduction in dosage or complete cessation from the drug may be necessary to correct this side effect. It should be noted again however that some of the studies which have indicated that heart damage is likely to occur with clenbuterol use were using extremely large doses and in animals that have a far greater number of beta-2 receptors in the heart muscle. This is not too say that clenbuterol is safe for human use, but rather that the research is far from definitive in this and other areas.

It has also been demonstrated that clenbuterol like other beta-2 agonists can deplete
the levels of the amino acid taurine in the serum and the heart of users (12, 13). This is a similar trait of other beta agonists. Many users will supplement with taurine to counteract this effect. It is believed that when the body is depleted of taurine, muscle cramps are more likely to occur, although there is no real scientific research that supports this assertion. However due to the depletion of taurine and the fact that your body requires it, supplementing is beneficial.

There is contradictory research as to the effect that clenbuterol has on the hepatic function of users as well. For the most part there have been little in the way of research that has indicated that even long-term use of clenbuterol at heavy doses would cause liver damage or distress, with some studies even going so far as claiming to demonstrate that use clenbuterol could in fact help protect the liver against some types of damage (14). However in a small number of studies there is some evidence that clenbuterol, when taken at heavy doses can cause some liver damage (15). As always, users should be aware that there may exist a chance that liver damage could occur with use of clenbuterol, even if the research seemingly indicates that this chance is a small one.

It should also be noted that there are some studies which have indicated that beta agonists, of which clenbuterol is one, can impair cardiovascular endurance and/or performance (16). However they have also been shown to help increase performance. Obviously like all situations where contradictory research exists, users will have to experiment with the drug themselves and see exactly how they react to the compound.

Deca Durabolin (Nandrolone Decanoate)

Nandrolone is by far one of the most popular anabolic steroids available. This is due to the compound's affinity for being highly anabolic but relatively mild in terms of androgenic side effects. Nandrolone is the base steroid 19Nor-testosterone, meaning that it is like testosterone in appearance except for the absence of a carbon atom in the 19th position. This small change makes a major difference in the characteristics of the compound (1). Notably, this change makes nandrolone a less potent agonist of the androgen receptor. This of course reduces the chance that a user will experience androgenic side effects. Instead of forming dihydrotestosterone when encountering the 5 alpha reductase enzyme like testosterone does, nandrolone will form dihydronandrolone. Dihydronandrolone is extremely mild in terms of it's antagonizing the androgen receptor. Therefore androgenic side effects should be far less likely to occur with nandrolone than with testosterone.

It is of note however that nandrolone is believed to have some activity as a progestin in the body. Although progesterone is a c-19 steroid, removal of this group as in 19-norprogesterone creates a hormone with greater binding affinity for its corresponding receptor. The compound will stimulate the progesterone receptor, along with progesterone. Side effects associated with this activity are similar to some of those related to estrogenic ones including water retention, acne, and gynecomastia among others. However these side effects are fairly rare in comparison to more androgenic compounds.

Now, with the reduced chance of negative side effects associated with the use of nandrolone one would assume that the gains in lean body mass that a user could expect to make would also be reduced. This is not true however. Nandrolone is 2.4 times as anabolic as testosterone when compared gram for gram (1). This does not mean that a user will gain 2.4 times as much muscle if using nandrolone instead of testosterone however. It is not that easy. It does show how powerful this drug is and how it can help a user make serious gains in muscle mass.


Use/Dosing :
Due to the active life of the compound, users would only need to administer nandrolone decanoate once per week to maintain fairly stable of the drug. However, since the vast majority of users will stack nandrolone with testosterone (for reasons that will be discussed later in the Side Effects/Risks section of this profile) and the most commonly used esters need to be injected more frequently most will simply injected it when it is convenient, such as twice a week with their testosterone enanthate or cypionate.

Anecdotally most users report that the full benefits of nandrolone decanoate will not be felt until the fifth, sixth or even seventh week of using the compound. This necessitates that users run the drug for at least eleven or twelve weeks for a cycle of the compound to have the results that a user expects. Of course, since nandrolone decanoate is a relatively mild drug many users have run it for extremely lengthy cycles with little in the way of serious side effects.

Most inexperienced male users will start using about 400mgs of nandrolone decanoate during their first cycles of the compound. Like most drugs users have used quite large doses of the compound, with diminishing returns being seen as these doses go higher and higher.

Females also have found that nandrolone can be quite effective while offering relatively mild side effects. Doses ranging from about 50 to 150mgs per week seem to be the norm for most first time users of the compound, again with these doses increasing as users try to achieve more and more with the compound.


Side Effects:
Estrogenic effects are not a major concern with use of nandrolone due to it's low rate of aromatization. However it can cause progesterone-like effects in some users. Commonly reported sides effects associated with nandrolone are such things as acne/oily skin, insomnia, diarrhea, and nausea. These of course are coupled with the common side effects most often associated with anabolic steroids including testicular atrophy, gynecomastia (including lactation in some cases), and sexual dysfunction.

To combat sexual dysfunction most users will stack testosterone with nandrolone. The obvious choice to be used with nandrolone decanoate is testosterone enanthate or cypionate due to the length of the esters being similar. How much testosterone one would need to take to ward off side effect associated with use of nandrolone and lack of natural testosterone production varies from individual to individual. Some have anecdotally reported that a low dose similar to 200mgs per week is enough. Others state that they need to run several hundreds more milligrams per week of testosterone than nandrolone to combat the effects. There is a small minority of individuals that also report having no sexual dysfunction from the drug even while running it without any type of testosterone. This variance again demonstrates that individuals will react to a compound differently than others.

This effect also points to the fact that nandrolone is extremely suppressive to a user's natural testosterone production. Even at relatively small doses, much smaller than those that would be used by those wanting to reap the anabolic effects that the compound can offer, nandrolone can suppress the natural production of testosterone of a user so much that it can take up to thirty days after the drug cycle is complete for it to fully recover (2). For this reason it is imperative that a user run a well planned post cycle therapy after using nandrolone.

Nandrolone is relatively safe in terms of a user's lipid profile and cholesterol. In some studies it has even been shown to actually improve HDL cholesterol levels (4). A major increase in a user's blood pressure or their liver toxicity should not be noticed with this compound either. Nandrolone is relatively mild in these respects.

Since nandrolone is a progestinic anabolic steroid (3,4). Some special precautions need to be taken to ensure that side effects do not get out of control as a result of a rise in prolactin levels. Using compounds such as bromocriptine, cabergoline and/or vitamin b6 have all been shown and reported to help lower prolactin levels. The drug Femara (letrozole) is also effective for use with nandrolone as it will regulate the progesterone and estrogen receptors in the body, therefore preventing some of the negative side effects associated with the compound.

A word of caution also for those that may plan on stacking nandrolone with trenbolone. Trenbolone is a strong progestin, much stronger than even nandrolone. By running these two compounds concurrently the user will suffer from extremely high levels of prolactin. This in turn will force the user to pay special attention to progesterone-like side effects and using compounds to prevent them, as well as having to run a particularly aggressive post-cycle therapy due to severe suppression of the hypothalamus pituitary testicular axis. Some users have anecdotally reported that they have suffered no ill effects of running the two compounds together, but it is a definite risk. One must weigh the costs versus the benefits.

Dianabol (Methandrostenolone)

Methandienone (Dianabol) is an orally applicable steroid with a great effect on protein metabolism. Methandienone is a derivative of testosterone and has a very strong anabolic and androgenic properties. It has a great effect on protein metabolism and protein synthesis Promotes. This effect manifests itself in by creating a positive nitrogen balance, supporting the build up of protein and, thus, skeletal muscle mass. Methandienone also induces an improved sense of well-being.

Methandienone (Dianabol) is one of the most highly http://www.steroid-europe.com/product.php?id_product=22 effective mass building steroids ever created. It was, in fact, created specifically for athletes to use to improve performance (although it was claimed to have therapeutic abilities). It provides highly impressive weight and strength gains for most users. Experiencing a 3-4lb weight gain per week is not Unheard of, Especially in Novices. It must be noted that a lot if Methandienone this is water weight, and that with higher dosages gynecomastia, high blood pressure, and acne could occur. Dianabol when taken orally becomes active very Rapidly, but only remains active for less than half a day. Often, for this reason, dosages were spread through the day.It is Known that 10 mgs of the Methandienone (Dianabol) was enough for full androgen replacement in a man, and this dose increased androgen anabolic activity Roughly 5 times over normal and provided a reduction in natural cortisol activity of between 50-70%. Despite this, many athletes take 50-100mgs daily. It would appear that over 50mgs/day, there is a point of diminishing return.

However, not all effects of Dianabol are positive. One of the most known side effects of Dianabol (Methandienone) is overuse on the liver. However, these effects are short lived Methandienone and liver values ​​return to normal. Some of the other effects are estrogenic effects, the risk is minimized for Which if Dianabol (Methandienone) use is stacking with an anti-estrogen. This side effects may include gynecomastia, water and salt retention, high blood pressure, oily skin, acne and facial hair (though not very north). As a result of the mild androgenic constituent of Dianabol (Methandienone) High Doses may also lead to some hair fall in the male pattern. It may also lead to changes in disposition more like aggression and irritability or in some Methandienone cases the opposite of it, Causing the individual to go into depression.

However, most of the effects are thought to be non-androgen receptor mediated because Dianabol (Methandienone) is a very weak Androgen Receptor binder. This also execute Methandienone a the low aromatase activity of Dianabol. Dianabol (Methandienone) 's users do not have to worry about sudden decrease In their natural testosterone production since the side effects are not Considered to be androgen receptor dependent.

Dianabol aromatises easily Methandienone with that it is not a very good steroid when working out for a competition but, for those wishing to acquire raw size, it is a star among oral steroids. Dianobol has a half-life time of only 3.2 - 4.5 hours. Meaning that you should take dianobol twice a day to enjoy a rich content in the blood stream.

Buy Methandienone is a derivative of testosterone, Exhibiting strong anabolic and moderate androgenic properties. This compound was first made available in 1960, and it quickly Became the most favored and Widely used anabolic steroid in all forms of athletics. This is likely due to the fact that it is both easy to use and extremely effective. In the U.S. Dianabol production had meteoric history, exploding for quite some time, then quickly dropping out of sight. Many were nervous in the late 80's when the last of the U.S. generics were removed from pharmacy shelves, the medical community finding no Legitimate use for the drug anymore. But the fact that Dianabol has been off the U.S. market for over 10 years now has not cut its popularity. It remains the most commonly used black market oral steroid in the U.S.

Equipoise (Boldenone Undecylenate)

Boldenone Undecylenate also known as Equipoise Max Pro represent a synthetic anabolic steroid with a chemical name of 17-hydroxyandrosta beta-1 ,4-diene-3-one.

For beginning it was developed to be used in veterinary field, Especially for treating horses. In our days of boldenone is Undecylenate Often used by athletes.

While using Equipoise automatically increases protein synthesis and red blood cell. It is also Stimulate appetite Which may cause adding in body weight. This steroid is characterized with strong anabolic effects with low androgenic effects. This characteristic make confused many athletes, who say that this steroid is acting similar as Deca. Yes, both of them are highly anabolic, moderate androgenic with propriety, both of them increase protein synthesis in the cell muscles, but it does not mean they are similar. There are a lot of differences between these two kinds of steroids: Gained muscles by using boldenone looked stronger and slowly Achieved, after usage of Deca droughts occurred more side effects as acne, oily skin, that are not noticed by using Equipoise, Deca is actually a progestin and a 19-nor derived steroid Equipoise but is more Closely related to testosterone. The difference between testosterone and boldenone Undecylenate is that the last one is half androgenic that first one.

Undecylenate boldenone can be used in both cutting and bulking cycles. For better results, athletes and bodybuilders in bulking cycles combine it with oxymetholone, methandrostenlone. In cutting phases a good chose for staking will be Winstrol.

Equipoise will help you to Achieve Your Goals slower than other steroids but Gained muscles will be harder and quality. You will not see result after first week of taking this drug. You have to take it at least 12 weeks and the first results will be seemed in about 3 weeks.

By taking boldenone Undecylenate bodybuilders report a low amount of aromitization and low water retention and it was not noticed to be toxic on liver.

These characteristics make it liked by both male and female athletes.

Average dose for bodybuilders is about 400-600 mgs per week. Women bodybuilders are recommended to take 25-50 mgs per week.

Possible side effects that can occur while taking Undecylenate boldenone (Equipoise) are gynecomastia or Possibility of growing of red blood cells. The main side effect is that this steroid stays active in the human body longer than other steroids.taht is why athletes and bodybuilders who have to pass drug test are advised not to take it.

Boldabol 200 promotes body tissue building processes and can reverse catabolism. Specifically it is derivative of testtosterone, boldenone undecylenate which Boldabol 200 exhibits strong anabolic and moderately androgenic properties. This product boldenone undecylenate exhibits a pronounced effect on lean bodyweight, increased appetite and energy levels.Boldabol 200    (Equipoise)  (Boldenone Undeclynate)Dose = 200 - 600mg boldenone undecylenate per weekDetection time = Up to 5 monthsActive Life = 15 daysEquipoise is a staple in the bodybuilding and athletic comunity because of its incredible versatility. boldenone undecylenate  Equipoise is just as anabolic as testosterone but Boldabol 200 only half as androgenic with strength gains from the two compounds being very similar.  It is well known boldenone undecylenate for its ability to increase strength and vascularity without estrogenic side effects.  Athletes who use Equipoise report a gradual and constant buildup of quality muscle.  Because of the slow accumulation of muscle, it is recommended to run Equipoise for at least 12 weeks.  Equipoise stacks very well with any testosterone or oral steroid like Anadrol or Dianabol for a bulking cycle and stacks well with Testosterone Proprionate and either Winstrol or Masteron for a cutting cycle.Boldenone is one of the well known  boldenone undecylenate alluded brand name for the veterinary injectable steroid boldenone undecylenate.It is not a rapid mass builder, but will contribute a slow but assiduous achievement of strength and quality muscle mass. The most boldenone undecylenate accentuated effects of this drug you would see when it is used for longer cycles, usually Boldabol 200 lasting at least 12 weeks in length.More ViewsDetails Boldabol 200 (Equipoise) is an attribute of testtosterone, which attests strong anabolic and adequately androgenic properties. This product exhibits an absolute effect on lean bodyweight, increased appetite and energy levels. boldenone undecylenate  Boldabol 200 is a leader in the bodybuilding and athletic comunity as a result of its amazing diversification. It is well known for its capability to accumulate strength and vascularity without boldenone undecylenate estrogenic side effects. Athletes who use it relate a step by step and constant buildup of quality muscle. This product is admitted to go for at least 12 weeks, because of the slow increase of muscle. The most advantageous Boldabol 200  properties of this drug are greatly recognized by athletes,boldenone undecylenateBoldabol 200 being a very popular injectable in recent years. It is valued by many to be a stronger, slightly more androgenic Deca Durabolin. Actually it is cheaper, and could replace boldenone undecylenate Deca in most cycles without greatly changing the end result. Boldabol 200 aggregate very well with any testosterone or oral steroid like Anadrol or Dianabol for a bulking cycle and stacks well with Testosterone Proprionate and either Winstrol or Masteron for a cutting cycle.It is a very adjustable compound. You can create a number of drug combinations with it based on the wanted result. More ot the particulars may want to stack it with Anadrol or an injectable testosterone. The result should be an awesome increase of muscle size and strength, without the same intensity of side effects if using the androgen (at a higher dose) alone. When you boldenone undecylenate would use in a cutting cycle, muscle hardness and density can be really ameliorated when you would combine Boldabol 200 with a non-aromatizable steroid such as trenbolone acetate, Halotestin, or Winstrol. Although for a few of paticulars, even the low buildup of estrogen associated with this compound is enough to consign its use to bulking cycles only. This drug is acttualy adequate and for WOMEN too, its diversification symptoms usually unheard of when it is taken at low doses. For the support of the stable blood levels, Boldenone should be injected at least once boldenone undecylenate per week. At large, it is most used at an administration of 400-600mg per week for MEN and 50-150 mg per week for WOMEN.It is a favorite veterinary steroid boldenone undecylenate of many athletes. Its effects are strongly anabolic, and only moderately androgenic. By itself, Equipoise will provide a steady and consistent gain in mass and strength. However, best results are achieved when Equipoise is used in conjunction with other steroids. Equipoise is a favorite veterinary steroid of many athletes. Its effects are strongly anabolic, and only moderately androgenic. By itself, Equipoise will provide a steady and consistent gain in mass and strength. However, best results are achieved when Equipoise is used in conjunction with other steroids.For mass, Equipoise stacks exceptionally well with Dianabol, Anadrol or an injectable testosterone like Testoviron depot, boldenone undecylenate,  Sustanon or Testosterone cypionate. Equipoise is also highly Boldabol 200 T effective for contest preparation since it aromatizes very poorly. Muscle hardness boldenone undecylenate and density can be greatly improved when Equipoise is combined with Parabolan, Halotestin, or Winstrol.boldenone undecylenate  Average dosages of Equipoise are 200-600 mg per week. Injections are usually taken every other day.If high volume injections are made too frequently to the same injection site, an oil abscess may form. An oil abscess will often dissipate boldenone undecylenate on its own, but in extreme instances, a doctor Boldabol 200 will need to boldenone undecylenate drain it. Therefore, athletes should take caution and rotate injection sites.

Halotestin (Fluoxymesterone)

Which represent steroid fluoxymesterone is characterized with high anabolic Halotestin and androgenic proprieties that are similar to testosterone.Being Widely used by athletes this drug is not strong mass building steroid. Its main purpose is to increase strength and aggression. Often Bodybuilders take fluoxymesterone in time they are preparing for Halotestin contests.Being both anabolic and androgenic Often this drug is used to treat breast cancer, hypogonadism. It is also known because of its propriety of blocking the estrogen production, that's mean to help bodybuilders to Halotestin Avoid Such side effects as gyno or water retention. Making part of 7alpha-methylated compound, fluoxymesterone is toxic on liver. Halotestin Bodybuilders usually take 10-20 mgs per workout. Because of its powerful Halotestin androgenic proprieties women are not advised to take fluoxymesterone.After taking fluoxymesterone sportsmen report following side effects: liver damaging, increase production of the sebaceous gland, headaches, gastrointestinal pain.