Sustanon + Winstrol – a muscle mass gaining combination

If you are interested in quality of the results, rather than in quantity, then we recommend you to pay attention to Sustanon and Winstrolcombination for weight gain.

Effects of the combination

  • Significantly increasesstrength
  • Induces the growth of high quality muscle mass
  • Increases working capacity
  • Speeds up protein synthesis in muscle fibers
  • Reduces recovery period after intensive workouts

Characteristics of the drugs

Sustanon 250

It is a composite anabolic mixture, which consists of four testosterone esters. Since they have different life-time, Sustanonprovides both quick and long-term effect on the organism. Due to the dual nature of this compound, there is no need for frequent injections.
Like many other AAS,Sustanonwas created for medical purposes.But nowadays it one of the most popular steroids among athletes, which are eager to increase strength and gainmass.

Winstrol (Stanozolol)

This is an anabolic steroid, which significantly increases strength and endurance. It is suitable for gaining of muscle massonly in combination with other steroids. Today we are going to talk about advantages of such combination (Winstrol + Sustanon).

  • First of all, this combination produces synergistic effect and greatly improves the quality of muscles. Besides both drugs rarely cause side effects and can be considered safe. At the same time, they mutually eliminate some negative features of each other.
  • Absence of aromatization. Winstrolis not an aromatizable steroid. Moreover, there are scientific reports that it can suppress estrogenic activity of other steroids.
  • Flexible dosing, which is suitable both for beginners and professional athletes.
  • High efficiency. Winstrol is one of the best steroids. You can use it both for cutting cycle and for gaining mascle mass (in combinations with other steroids).

Clomid

It is an auxiliary drug, which accelerates the recovery of an organism after the cycle.

Dosage and Usage

The following doses are suitable for athletes whose weight does not exceed 90 kg. The duration of a cycle is six weeks. If necessary, you can extend your cycle up to two months.

We suggest a classical scheme for Sustanon and Winstrol usage. Injectable stanozolol- 50 mg every day. Alternatively, you can do 0.1 gram every other day. However, in the first case, you are sure to avoid hormonal jumps.

Do not underestimate this fact, as any changes in hormonal levels may negatively affect the whole organism. Thus, we advise you to take Winstrol (Stanozolol) every day.

The dosage of Sustanon 250 should be 250mg/week. You can do injection once a week, but we recommend you to divide the weekly dosage and do two injections. This is necessary to smoothen your hormonal background.
Start PCT in two weeks since last injection. The duration of PCT should be 2-3 weeks. During this period take 1 tablet of Clomid daily.

If your body is prone to aromatization, then include Proviron (Masterlone) or Exemestaneinto your cycle. Androgenic side-effects are very rare for this combination, however if you have high activity of 5-alpha-reductase enzyme, then take Finasteride.

Don’t forget about proper diet and intensive training if you want to achieve optimal results.

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Saizen – HGH (Somatropin)

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Saizen (HGH, Human Growth Hormone) [Somatropin]

Saizen click.easy, is a recombinant human growth hormone (rHGH) for injection. It is a liquid consisting of the identical sequence of 191 amino acids of human growth hormone. The molecular formula is C990H1528N262O300S7. Its molecular weight is 22,125 Daltons.

As with no other doping drug, growth hormones are still surrounded by an aura of mystery. Some call it a wonder drug which causes gigantic strength and muscle gains in the shortest time. Others consider it completely useless in improving sports performance and argue that it only promotes the growth process in children with an early stunting of growth. Some are of the opinion that growth hormones in adults cause severe bone deformities in the form of overgrowth of the lowerjaw and extremities. And, generally speaking, which growth hormones should one take the human form, the synthetically manufactured version, recombined or genetically produced form and in which dosage? All this controversy about growth hormones is so complex that the reader must have some basic information in order to understand them.

The growth hormones is a polypeptide hormone consisting of 191 amino acids. In humans it is produced in the hypophysis and released if there are the right stimuli (e.g. training, sleep, stress, low blood sugar level). It is now important to understand that the freed HGH (human growth hormones) itself has no direct effect but only stimulates the liver to produce and release insulin-like growth factors and somatomedins. These growth factors are then the ones that cause various effects on the body. The problem, however, is that the liver is only capable of producing a limited amount of these substances so that the effect is limited. If growth hormones are injected they only stimulate the liver to produce and release these substances and thus, as already mentioned, have no direct effect.

The use of these STH (somatotropic hormone) compounds offers the athlete three performance-enhancing effects. STH has a strong anabolic effect and causes an increased protein synthesis which manifests itself in a muscular hypertrophy (enlargement of muscle cells) and in a muscular hyperplasia (increase of muscle cells.) The latter is very interesting since this increase cannot be obtained by the intake of steroids. This is probably also the reason why STH is called the strongest anabolic hormone. The second effect of STH is its pronounced influence on the burning of fat. It turns more body fat into energy leading to a drastic reduction in fat or allowing the athlete to increase his caloric intake. Third, and often overlooked, is the fact that STH strengthens the connective tissue, tendons, and cartilages which could be one of the main reasons for the significant increase in strength experienced by many athletes. Several bodybuilders and powerlifters report that through the simultaneous intake with steroids STH protects the athlete from injuries while inereasing his strength.

You will say that this sounds just wonderful. What is the problem, however since there are still some who argue that STH offers nothing to athletes? There are, by all means, several athletes who have tried STH and who were sadly disappointed by its results. However, as with many things in life, there is a logical explanation or perhaps even more than one:
1. The athlete simply has not taken a sufficient amount of STH regularly and over a long enough period of time. STH is a very expensive compound and an effective dosage is unaffordable by most people.

2. When using STH the body also needs more thyroid hormones, insulin, corticosteroids, gonadotropins, estrogens and what a surprise androgens and anabolics. This is also the reason why STH, when taken alone, is considerably less effective and can only reach its optimum effect by the additive intake of steroids, thyorid hormones, and insulin, in particular. But we must point out in this case that STH has a predominantly anabolic effect. There are three hormones which are needed at the same time in order to allow for maximum anabolic effect. These are STH, insulin, and an LT-3 thyroid hormone, such as, for example, Cytomel T3. Only then can the liver produce and release an optimal amount of somatomedin and insulin-like growth factors. This anabolic effect can be further enhanced by taking a substance with an anticatabolic effect. These substances are-everybody should probably know by now-anabolic/androgenic steroids or Clenbuterol. Then a synergetic effect takes place.`Are you still wondering why pro bodybuilders are so incredibly massive but, at the same time, totally ripped while you are not. Most athletes have tried STH during preparation for a competition in that phase when the diet is calorie-reduced.

The body usually reacts by reducing the release of insulin and of the L-T3 thyroid hormone. And, as was described under point 2, this is not an advantageous condition when STH is expected to work well. Well, we almost forgot. Those who combine Clenbuterol with STH, should know that Clenbuterol (like Ephedrine) reduces the body`s own release of insulin and L-T3. True, this seems a little complicated and when reading it for the first time it might be a little confusing; however it really is true: STH has a significant influence on several hormones in the human body; this does not allow for a simple administration schedule.

As said, :ST: is not cheap and those who intend to use it should know a little more about it. If you only want to burn fat with STH you will only have to remember user information for the part with the L-T3 thyroid hormone as is printed by Kabi Pharmacia GmbH for their compound Genotropin:

“The need of the thyroid hormone often inereases during treatment with growth hormones.”

3. Since most athletes vho want to use STH can only obtain it if prescribed by a physician, the only supply source remains the black market. And this is certainly another reason why some athletes might not have been very happy with the effect of the purchased compound. How could he, if cheap HCG was passed off as expensive STH?

Since both compounds are available as dry substances, all that would be needed is a new label of Serono`s Saizen or Lilly`s Humatrope on the HCG ampule. It is no longer fun when somebody is paying $200 for 5000 I.U. of HCG, only worth $ 12, and thinking that he just purchased 4 I.U. of STH. And if you think this happens only to novices and to the ignorant, ask Ben Johnson. “Big Ben,” who during three tests within five days showed an above-limit testosterone level, was not a victim of his own stupidity but more likely the victim of fraud. According to statistics by the German Drug Administration, 42% of the HGH vials confiscated on the North American black market are fakes. In addition to a display of labels in the Dutch or Russian language the fakes are distinguished from the original product, in sofar as the dry substance is not present as lyophilic but present as loose powder. The fakes confiscated so far use the name “Humatrope 16” under the name of Lilly Company (with Dutch denomination) or “Somatogen” (in Russian).” Nowhere can this much money be made except by faking STH. Who has ever held original growth hormones in his hand and known how they should look?

4. In a few very rare cases the body reacts by developing antibodies to the exogenous STH, thus making it ineffective. The question of the right dosage, as well as the type and duration of application, is very difficult to answer. Since there is no scientificresearch showing how STH should be taken for performance improvement, we can only rely on empirical data, that is experimental values. The respective manufacturers indicate that in cases of hypophysially stunted growth due to lacking or insuffieient release of growth hormones by the hypophysis, a weekly average dose of 0.3 I.U/ week per pound of body weight should be taken. An athlete weighting 200 pounds, therefore, would have to inject 60 I.U. weekly. The dosage would be divided into three intramuscular injections of 20 I.U. each. Subcutaneous injections (under the skin) are another form of intake which, however would have to be injected daily, usually 8 I.U. per day. Top athletes usually inject 4-16 I.U./day. Ordinarily, daily subcutaneous injections are preferred. Since STH has a half life time of less than one hour, it is not surprising that some athletes divide their dail dose into three or four subcutaneous injections of 2-4 I.U. each.

Application of regular small dosages seems to bring the most effective results. This also has its reasons: When STH is injected, serum concentration in the blood rises quickly, meaning that the effect is almost immediate. As we know, STH stimulates the liver to produce and release somatomedins and insulin like growth factors which in turn effect the desired results in the body. Since the liver can only produce a limited amount of these substances, we doubt that larger STH injections will induce the liver to produce instantaneously a larger quantity of somatomedins and insulin-like growth factors. It seems more likely that the liver will react more favorably to smaller dosages. If the STH solution is injected subcutaneously several consecutive times at the same point of injection, a loss of fat tissue is possible.

Therefore, the point of injection, or even better, the entire sisde of the body should be continuously, changed in order to avoid a loss of local fat tissue (lipoathrophy) in the injection cell. One thing has manifested itself over the years: The effect of STH is dosage-dependent. This means either invest a lot of money and do it right or do not even begin. Half-hearted attempts are condemned to failure Minimum effective dosages seem to start at 4 I.U. per day. For comparison: the hypophysis of a healthy; adult, releases 0.5-1.5 I.U. growth hormones daily.

The duration of intake usually depends on the athlete`s financial resources. Our experience is that STH is taken over a prolonged period, from at least six weeks to several months. It is interesting to note that the effect of STH does not stop after a few weeks; this usually allows for continued improvements at a steady dosage. Bodybuilders who have had positive results with STH have reported that the build-up strength and, in particular, the newly-gained muscle system were essentially maintained after discontinuance of the product. It remains to be clarified what happens with the insulin and LT-3 thyroid hormone.

Athletes who take STH in their build-up phase usually do not need exogenous insulin. It is recommended, in this case, that the athlete eats a complete meal every three hours, resulting in 6-7 meals day. This causes the body to continuously release insulin so that the blood sugar level does not fall too low. The use of LT-3 thyroid hormones, in this phase, is carried out reluctantly by athletes. In any case, you must have a physician check the thyroid hormone level during the intake of STH. Simultaneous use of anabolic /androgenic steroids and/or Clenbuterol is usually appropriate. During the preparation for a competition the use of thyroid hormones steadily inereases. Sometimes insulin is taken together with STH, as well as with steroids and Clenbuterol.

Apart from the high damage potential that exogenous insulin can have in non-diabetics, incorrect use will simply and plainly make you “FAT! Too much insulin activates certain enzymes which convert glucose into glycerol and finally into triglyceride. Too little insulin, especially during a diet, reduces the anabolic effect of STH. The solution to this dilemma? Visiting a qualified physician who advises the athlete during this undertaking and who, in the event of exogenous insulin supply, checks the blood sugar level and urine periodically.

According to what we have heard so far, athletes usually inject intermediately-effective insulin having a maximum duration of effect of 24 hours once a day. Human insulin such as Depot-H-Insulin Hoechst is generally used. Briefly-effective insulin with a maximum duration of effect of eight hours is rarely used by athletes. Again a human insulin such as H-Insulin Hoechst is preferred. The undesired effect of growth hormones, the so-called side effects, are also a very interesting and hotly-discussed issue. Above all it must be said: STH has none of the typical side effects of anabolic/androgenic steroids including reduced endogenous testosterone production, acne, hair loss, aggressiveness, elevated estrogen level, virilization symptoms in women, and increased water and salt retention.

The main side effects that are possible with STH are an abnormally small concentration of glucose in the blood (hypoglycemia) and an inadequate thyroid function. In some cases antibodies against growth hormones are developed but are clinically irrelevant. What about the horror stories about acromegaly, bone deformation, heart enlargement, organ conditions, gigantism, and early death? In order to answer this question a clear differentiation must be made between humans before and after puberty. The growth plates in a person continue to grow in length until puberty.

After puberty neither an endogenous hypersection of growth hormones nor an excessive exogenous supply of STH can cause additional growth in the length of the bones. Abnormal size (gigantism) initially goes hand in hand with remarkable body strength and muscular hardness in the afflicted; later, if left untreated, it ends in weakness and death. Again, this is only possible in pre-pubescent humans who also suffer from an inadequate gonadal function (hypogonadism). Humans who suffer from an endogenous hypersecrehon after puberty and whose normal growth is completed can also suffer from acromegaly. Bones become wider but not longer. There is a progressive growth in the hands and feet and enlargement of features due to the growth of the lower jaw and nose. What the authorities like to do now is to present extreme cases of athletes suffering from these malfunctions in order to discourage others and to drum into athletes the fact that with the exogenous supply of growth hormones they would suffer the same destiny. This, however, is very unlikely, as reality has proven.

Among the numerous athletes using STH comparatively few are seven feet tall Neanderthalers with a protruded lower jaw, deformed skull, claw like hands, thick lips, and prominent bone plates who walk around in size 25 shoes. In order to avoid any misunderstandings, we do not want to disguise the possible risks of exogenous STH use in adults and healthy humans, but one should at least try to be openminded. Acromegaly, diabpetes, thyroid insuficiency, heart muscle hypertrophy, high blood ressure, and enlargement of the kidneys are theoretically possible if STH is used excessively over prolonged periods of time; however, in reality and particularly when it comes to the external attributes, these are rarely present.

Some athletes report headaches, nausea, vomiting, and visual disturbances during the first weeks of intake. These symptoms disappear in most cases even with continued intake.

The most common problems with STH occur when the athlete intends to inject insulin in addition to STH. The substance somatropin is available as a dried powder and before injecting it must be mixed with the enclosed solution-containing ampule. The ready solution must be injected immediately or stored in the refrigerator for up to 24 hours. It is usually recommended that the compound be stored in the refrigerator. With the exception of the remedy Saizen the biological activity of growth hormones is usually not impaired when storing the dry substance at 15-25 C (room temperature); however, a cooler place (2-8° C) is preferable.On the black market the price for 4 I.U. each of the compounds Genotropin, Humatrope, Norditropin, and Saizen, in Europpe is $80-120 for a prick-through vial including the solution ampule. As already mentioned, there are many fakes. It is noted that for the U.S.-American growth hormones compounds, the substance content is not given in I.U.(International Units) but in mg (milligrams).

Since l mg corresponds to exactly 2.7 I.U. the 5mg solution of the compound Humatrope by Lilly contains exactl 13.5 I.U. of Somatropin. The 10 mg solution of the Protropin compound by the Genentech therefore contains 27 I.U. of Somatropin.

In American powerlifting and bodybuilding circles Humatrope is usually preferred over Protropin. The reason is that Humatrope is synthesized from a chain of 191 amino acids and thus is identical to the amino acid sequence of the human growth hormones. Protropin, on the other hand, consists of 192 amino acids, one amino acid too many. This might be the explanation for why more antibodies are developed with Protropin than with Humatrope. growth hormones are on the doping list but they are not yet detectable during doping tests.

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Ventolase

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Ventolase (Clenbuterol, Albuterol/Ventolin, Salbutamol)

Details:
hemical Name: Albuterol Sulfate
Drug Class: Beta-Agonist

Albuterol (Salbutamol) as a much better alternative to clenbuterol due to lesser side effects. Albuterol is a (relatively) selective beta-2 adrenoreceptor agonist, just like Clenbuterol. Clen is simply too harsh on most people; they get too jittery, too shaky, and too anxious. It’s a lot to go through to burn some fat.

Albuterol produces a much “cleaner” type of stimulant effect than Clenbuterol. I don’t know how to really describe this other than to say that the “Clen-shakes” just aren’t as bad with Albuterol in addition, I’m able to focus better on my work when I use Albuterol, while with Clenbuterol I’m stimulated but not really focused. But even though Albuterol produces a much cleaner stimulant-type feeling in most people, the main question is “How well does it burn fat”? As far as fat-burning stimulants go, how does it stack up to Clenbuterol? Lets face it, most people are really only concerned with the end results, right? Well, at least in me and the people I’ve worked with, Albuterol seems to produce significantly better results than Clen in terms of fat burning effects and it produces them just a bit more quickly too. This makes sense, if you think about it.

Albuterol is often thought of as a “shorter acting” version of Clen and, to draw an analogy, when we look at the steroids which are shorter acting versions (think about comparing something like Testosterone Propionate vs Cypionate, or NPP vs Deca-Durabolin) – they typically produce more dramatic results a bit quicker than their long acting cousins. I’m finding the same thing to be true with Albuterol. When we take a look at a medical study examining Clenbuterol vs. a beta-2 agonist which has an even longer half life (“Salmeterol”), we see that Clen out performs it in terms of anabolic effects. So I think it would only be logical to assume that something that was a shorter acting beta-2 agonist than Clen would likely outperform it, right? Let me just restate that, to make sure we’re all on the same page, ok? Clenbuterol outperforms longer acting beta-2 agonists, in terms of anabolic effects. Albuterol is a beta-2 agonist with a shorter acting effect than Clenbuterol. Therefore, it’s only logical that Albuterol is going to be more anabolic than Clen, right? Ok, let’s move on

To understand how Albuterol works, first we need to take a look at the Beta adrenergic system. This system is comprised of something called adrenoreceptors, and the most well known (to bodybuilders anyway) of the adrenoreceptors are the beta receptors. Beta receptors are embedded in the cell’s outer phospholipid membrane, and are stimulated by all the really popular stimulants ephedrine, Clenbuterol, etc… These receptors can further be divided into three subtypes: 1, 2, & 3, (of which we are primarily concerned with type-2, because the type-3 variety seems to primarily be less relevant in humans than in other animals, and because Albuterol doesn’t stimulate the type-1 receptor). There also exists a type of receptor known as an alpha receptor, which isn’t relevant here, but warrants a brief explanation. Alpha receptors differ from beta receptors in that they are activated at significantly lower catecholamine levels than are the beta receptors. A catecholamine is simply an organic compound that affects the sympathetic nervous system. For example, dopamine, norepinephrine and epinephrine are all catecholamines.

We are, mostly concerned with Beta-2 receptors, because those are what we see stimulated with Albuterol. It should come as no surprise to anyone who has used Clenbuterol as well as Albuterol is that when you stimulate your beta receptors, it causes something called vasodilatation (increased blood flow). Stimulation of these receptors also stimulates the break down of fatty acids into the blood stream for use as fuel, which causes a reduction in stored fat. Of course, this increased blood flow also comes with an increased heart rate. This explains how Beta-2 adrenergic stimulation can also increase your body temperature a bit however this isn’t something that’s too noticeable on a thermometer most people will feel a bit hotter, and some will even break a sweat (I fall into the latter category). Beta-agonists work to do this by increasing heat production in the cell’s owerhouse, the mitochondria, which will also increase your basal metabolic rate, and decrease your appetite. Not too many people feel hungry after a whopping dose of stimulants.

There is also some evidence that Beta-Agonists are anabolic (more properly, however, this would actually be anti-catabolic). This is because Beta-agonists also act to initiate a hormonal cascade that involves the activation of a compound called cAMP (basically: cyclic-Adenosine Monophosphate). After this, cAMP activates calpistatin that is the inhibitor of calpain. Calpain works to degrade protein in skeletal muscle (among other functions). Therefore, we already saw that how stimulation of beta 2 receptors have the ability to increase energy expenditure and free up body fat to be used as fuel, and now we have some understanding of how that stimulation can also have the potential to be anti-catabolic as well . Now that we’re all on the same page regarding the beta-adregenic system, and what sorts of effects we can expect when we stimulate it with beta-2 agonists lets take a more specific look at Albuterol, and why I think it’s such a great compound.

When we take a look at Albuterol’s ability to burn fat, it’s clear that it has the ability to aid fat loss in both normal as well as obese men . That’s not very different from Clenbuterol, in any way. However, in my personal experience with it, I think that Albuterol really outperforms Clen in areas of strength gains as well as for athletic purposes .lets take a look at my claim and see how Albuterol performs in humans In one study, subjects were given Albuterol and performed 9 weeks of isokinetic knee extensions (there was also a group who performed the same exercise routine but were not given Albuterol). The Albuterol group, predictably, had better strength gains than the non-Albuterol group (only a therapeutic dose was given). In my own experience, strength gains with Albuterol are much better and seen more quickly than I see them with Clen. In fact, while I don’t particularly experience much of a performance enhancing effect from Clen in the gym; on the other hand I see strength gains and muscular improvements within the first couple weeks of using Albuterol. Of course, this is likely a pure anabolic effect and probably not easily explained as a simple “enhanced” anti-catabolic effect, and likely can’t be explained away with the Calpain idea you read about earlier.

I still think that I can take a pretty good shot at explaining why Albuterol is anabolic, though. strong body of evidence exists to suggest that Albuterol influences the release of cAMP. As you may know, cAMP also plays an important role in mediating certain catecholamines secreted by the adrenal medulla have an inhibitory effect on muscle dependent protein degradation, but in addition, norepinephrine released from adrenergic terminals may actually increase the rate of protein synthesis(not just decrease the rate of their degradation) in oxidative muscles, thereby leading to increased protein accretion (representing a true anabolic effect). That’s most likely the way that we receive part of the anabolic effect from Beta-stimulation. Another way is perhaps through the beta-adrenergic stimulated lowering of “Interleukin-6” from fat cells (long story ). Anecdotally, Clenbuterol and ephedrine have both shown themselves capable of temporarily increasing strength, and I would bet most beta-agonists have this effect, but I don’t think has been shown as conclusively in the medical literature as it has been with Albuterol.

Albuterol has been shown to increase muscle size (3-6) as well as strength and endurance (*while people have anecdotally reported that Clen seems to lower their aerobic capacity. Clenbuterol has a disadvantage when compared with Albuterol in the area of strength gains, probably due to the act that it use-dependently inhibits action potential firing in skeletal muscle fibers, which is not directly caused by inherent Beta-2 stimulant activities . I think that’s the best quasi-scientific explanation I Again, my own personal experience and that of my research assistant(s) would also seem to strongly support this claim all of us have gotten leaner, bigger and stronger with the use of Albuterol, while with Clen, we got more ripped but not really stronger (and certainly not much bigger). Anecdotally, we’ve seen Clenbuterol fall a bit flat when people use it for anabolic effects, although in animals it would appear to be highly anabolic, though human studies are a bit shaky (ha!) in this area.

One of the things I really like about Albuterol is that it has the potential to actually be used on my cycle to make it safer by improving my lipid profile (cholesterol) or during PCT to help get my cholesterol levels back in check. This is because Albuterol shows significant benefits to cholesterol as it works to lower total cholesterol, specifically LDL (the bad stuff) while at the same time elevating HDL (the good stuff).

In my own particular case, cholesterol never seems to be an issue, but now that I’m working with Oasis for HRT, it’s certainly in my best interests to show up every three months with nice looking blood work.

So now is the part you’ve been waiting for (*or the part you skipped to, ignoring the rest of the article whatever ). How much of this should you take, and how often? Well, I can tell you that I have found the best results by working my way up from 4mgs taken once a day, up to 4-8 mgs taken 3x a day. I know that some people will think that 24ms a day of this stuff is going to be too much (it is, after all, a stimulant). But I can tell you that I have a pretty good tolerance for stimulants (I’ve taken up to 200 mcg/day of Clenbuterol, and some other pretty hefty stimulants that I probably shouldn’t mention in polite company). Most people are going to find their sweet spot at about 4mgs of Albuterol 3x a day or so women will probably take about half that dose, and be fine with it. I think that Albuterol is about to become very popular, very soon and I, for one, am looking forward to seeing less of my old Clen article around the ‘net, and more of this one.

For oral dosage form (syrup, tablets):
Adults and children older than 12 years of age—2 or 4 milligrams (mg) taken 3 or 4 times per day.
Your doctor may increase your dose as needed up to a maximum of 32 mg per day, divided and given 4 times per day

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Clenbuterol [Clen buterol HCL tabs]

General

Clenbuterol is a β2 adrenergic agonist with some similarities to Ephedrine, but its effects are more potent and longer-lasting as a stimulant and thermogenic drug. It causes an increase in aerobic capacity, CNS stimulation, and an increase in blood pressure and oxygen transportation. It increases the rate at which fat and protein is used up in the body at the same time as slowing down the storage of glycogen. It is commonly used for smooth muscle relaxant properties. This means that it is a bronchodilator and tocolytic. It is usually used in dosages anywhere from 20-60 micrograms a day when prescribed. A dose of about 150 μg should never be exceeded in a day. It is also prescribed for treatment of horses, however, equestrian usage is usually the liquid form of Clenbuterol. It works under the PNS-sympathetic.

The substance Clenbuterol-hydrochloride is also available in various other forms of administration, including syrups, drops, liquids, dosing aerosols, injectable solutions, and granules. Since athletes usually prefer tablets, manufacturers and trade names offering this oral version are listed.

Clenbuterol is a very interesting and remarkable compound. It is not a steroid hormone but a beta-2-symphatomimetic. Its effects, however can by all means be compared to those of steroids. Similar to a combination of Winstrol Depot and Anavar, Clenbuterol can cause a solid, highly qualitative muscle growth which goes hand in hand with a significant strength gain. Clenbuterol, above all, has a strong anticatabolic effect, which means it decreases the rate at which protein is reduced in the muscle cell, consequently causing an enlargement of muscle cells. For this reason, numerous athletes use Clenbuterol after steroid treatment to balance the resulting catabolic phase and thus obtain maximum strength and muscle mass.

A further aspect of Clen is its distinet fat-burning effect. It burns fat without dieting because it inereases the body temperature slightly, forcing the body to burn fat for this process. Clenbuterol, in the meantime, is not only a favorite competition compound among professional bodybuilders. An especially intense fat-burning occurs when Clen is combined with the LT3-thyroid hormone compound Cytomel. Due to the higher body temperature Clenbuterol magnifies the effect of anabolic/androgenic steroids taken simultaneously, since the protein processing is increased. The dosage depends on body weight and can be optimized by measuring the body temperature. Athletes usually take 5-7 tablets, 100-140 mcg per day. For women 80-100 mcg/day are usually sufficient. It is important that the athlete begin by taking only one tablet on the first day and then increasing the dosage by one tablet each of the following days until the desired maximum dosage is reached. Following, there are several schedules for taking Clenbuterol.

On the one hand, emphasis is placed on the burning of fat; on the other hand, importance is placed on a balanced relationship between strength and muscle growth as well as fat reduction. The compound is usually taken over a period of 8-10 weeks. Since it is not a hormone compound it has no side effects typical of anabolic steroids For this reason it is also liked by women. Possible side effects of Clenbuterol include restlessness, palpitations, tremor (involuntary trembling of fingers), headache, increased perspiration, insomnia, possible muscle spasms, increased blood pressure, and nausea. Note that these side effects are of a temporary nature and usually subside after 8-10 days, despite continuation of the product. Throughout Europe the substance Clenbuterol hydrocloride must be prescribed by a physician. Clenbuterol is not officially available in the U.S.

 

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