Benzodiazepines

may also have other actions. For example, diazepam has been shown to counteract the cardiovascular toxicity of chloroquine. It is thought that diazepam increases the urinary clearance of chloroquine by improving electrocardiographic and hemodynamic function.

Clenbuterol is a widely used bronchodilator in many parts of the world. It is most often prepared in 20mcg tablets (see: Spiropent), but Clenbuterol is also available in syrup and injectable form (see: Spasmobronchal). This drug belongs to a broad group of drugs knows as sympathomimetics. Clenbuterol affect that sympathetic nervous system in a wide number of

ways, largely mediated by the distribution of adrenoceptors.

If testosterone is the most powerful mass builder, then gram for gram this is the most powerful testosterone. Suspension is pure testosterone and has no ester attached, and thus no ester calculated in the weight. Where 100 mg of a testosterone ester equals 100 mg minus the weight of the ester, 100 mg of testosterone suspension contains an actual 100 mg of the steroid. Very potent and very powerful. Although it is a rather crude compound, it is without a doubt very, very effective. Suspension is not only not esterified, its not even dissolved in oil the

way esters are. Instead it is an aqueous suspension, much like the injectable forms of Winstrol/Stromba (stanazolol). Since a steroid, made of cholesterol, is somewhat lipophillic, it does not readily dissolve in water either. Just as with Winstrol, we will note that the steroid accumulates at the bottom, separated from its water environment if the vial is left sitting for a while. So before use a vial should be shaken, which will provide an even distribution, and then drawn out of the vial. It probably couldn't hurt to shake the syringe again before injecting as well.

The effect of dianobol promotes the protein

synthesis, thus it supports the build up of muscle.

Absolute change in total fat mass (A) and trunk fat (B) by dual-energy X-ray absorptiometry from baseline to study week 12 (solid bars) and from baseline to study week 24 (open bars) in the placebo (n = 12) and the oxandrolone (n = 20) study groups. Values are means ± SE. *Significant decrease from baseline, P < 0.001. Significant difference between study groups for change in fat mass from 0 to 12 wk, P < 0.001.

Proviron cycle. Most athletes actually prefer to use both Proviron and Nolvadex, especially during strongly estrogenic cycles.

Proviron and Nolvadex attack estrogen at a different angle, side effects are often greatly minimized.

Carcinogenesis - Phenols in general are reputed to be carcinogenic. Although 2,4-dinitrophenol has never been implicated in a cancer diagnosis, some are nonetheless concerned, and understandably so. In addition to the inherent carcinogenic potential caused by its status as a phenol, production of free radicals and the release of various compounds stored in adipose tissue stores during DNP's rapid oxidation of fat may also potentially be harmful.

The use of all drugs carries some risk along with potential

or perceived benefits, whether used for legitimate medical reasons or for other purposes. Insulin carries some risk even when used by an insulin dependent diabetic, as demonstrated by the observation that some diabetics run into difficulties with their treatment from time to time and often require assistance to restabilize their medical condition and insulin requirements. If used by a healthy non diabetic person in whom there is no natural deficiency in insulin production or reduced insulin sensitivity and in the absence of medical advice and monitoring, the risks may be substantially increased.

 - If you

have very high blood fats (cholesterol or triglycerides).

During a typical Testosterone Propionate cycle one will see action that is consistent with a testosterone. Users sensitive to gynecomastia may therefore need to addition an antiestrogen. Those particularly troubled may find that a combination of Nolvadex and Proviron works especially well at preventing/halting this occurrence. Also unavoidable with a testosterone are androgenic side effects like oily skin, acne, increased aggression and body/facial hair growth. Those who may have a predisposition for male pattern baldness may also find that propionate

will aggravate this condition. To help combat this we also have the option of adding Proscar, which will reduce the buildup of DHT in many androgen target tissues. This will help minimize related side effects (particularly hair loss) although it offers us no guarantees. And as with all testosterone products, propionate will also suppress endogenous testosterone production. The use of a testosterone stimulating drug like HCG and/or Clomid is therefore almost a requirement in order to avoid enduring a post-cycle crash.

A first time user should not exceed 40 mcg the first day. Increase by one tablet until the side

effects are not tolerable.

On the black market, Cytomel® is readily available. 100 tablets (50 mcg) will sell for approximately $50. This price is considerably reduced when purchasing this drug from a variety of mail-order sources. Even lower in price is the Cynomel brand in Mexico. The pharmacy price for 100 25mcg tablets is only a few U.S. dollars.

Sustanon is a very popular steroid which is highly appreciated by its users since it offers several advantages when compared to other testosteron compounds. Sustanon is a mixture of four different testosterones which, based on the well-timed composition, have

a synergetic effect.These substances are: Testosterone propionate 30 mg, Testosterone phenylpropionate 60mg, Testosterone isocaporate 60 mg, Testosterone decanoate 100 mg.

Change in vaginal discharge, chills, fever, hoarseness, lower back or side pain, pain or feeling of pressure in pelvis, pain, redness, or swelling in your arm or leg, painful or difficult urination, rapid shallow breathing, skin rash or itching over the entire body, sweating, vaginal bleeding, wheezing, absent, decrease in amount of urine, feeling of warmth redness of the face, neck, arms and occasionally, upper chest, menstrual changes, nausea,

vaginal bleeding, weight changes, white or brownish vaginal discharge.

Usually 50-100 mg will suffice, the lower end is preferred for maximal results since estrogen plays a key role in gains, but those more worried about estrogen should opt for a higher dose. For those worried about androgenic side-effects (hair loss, prostate hypertrophy, deepening of voice), one can utilize the hair loss treatment finasteride. This blocks the 5-alpha-reductase enzyme and stops the conversion of testosterone to the more androgenic compound DHT. I'm not a big fan of this, because DHT reduces estrogenic bloat, increases free levels

of testosterone and is a very potent androgen that is 3-4 times stronger than testosterone. Those worried about hair loss however, may want to opt for arimidex as their anti-aromatase, since Proviron is a form of DHT after all.

Halotestex (fluoxymesterone) is an oral derivative of the male hormone testosterone. Unlike testosterone, halotestex does not convert to estrogen. Therefore, estrogen-related side effects such as fat deposition, water retention, and gynecomastia do not occur. Halotestex has powerful androgenic properties. It is particularly noted for increased strength without significant additional

weight gain. Side effects include aggression, oily skin, and virilization. Halotestex is considered to be very toxic to the liver, and thus must be used with caution and for short durations only.

During a typical Testosterone Propionate cycle one will see action that is consistent with a testosterone. Users sensitive to gynecomastia may therefore need to addition an antiestrogen. Those particularly troubled may find that a combination of Nolvadex and Proviron works especially well at preventing/halting this occurrence. Also unavoidable with a testosterone are androgenic side effects like oily skin, acne, increased

aggression and body/facial hair growth. Those who may have a predisposition for male pattern baldness may also find that propionate will aggravate this condition. To help combat this we also have the option of adding Proscar, which will reduce the buildup of DHT in many androgen target tissues. This will help minimize related side effects (particularly hair loss) although it offers us no guarantees. And as with all testosterone products, propionate will also suppress endogenous testosterone production. The use of a testosterone stimulating drug like HCG and/or Clomid is therefore almost a requirement in order to
avoid enduring a post-cycle crash.

Minor side effects with diazepam include:

CIALIS ® 20mg / TADALAFIL

This drug is a potent nonsteroidal anti-estrogen. It is indicated for use in estrogen dependent tumors, i.e. breast cancer. Steroid users take Nolvadex C&K to prevent the effects of estrogen in the body. This estrogen is most often the result of aromatizing steroids. Nolvadex C&K can aid in preventing edema, gynecomastia, and female pattern fat distribution, all of which might occur when a man's estrogen levels are too high. Also, these effects can occur when androgen levels are

too low, making estrogen the predominant hormone. This can occur when endogenous androgens have been suppressed by the prolonged use of exogenous steroids. Nolvadex C&K works by competitively binding to target estrogen sites like those at the breast.

In his book, Anabolics 2002, Bill Llewellyn says that Cytomel is not a drug to start off on, and that use of milder drugs like T4 (Synthroid) or triacana can help ease a person into the use of T3. I'm inclined to disagree here however. Triacana is weak compound and I find of little use. Its not easily found anymore and not cheap either. T4 is basically similar

to Cytomel except that its weaker. Something that users normally compensate with higher doses and sends them down a similar lane as simply using cytomel. Agreed, cytomel is NOT a drug for beginners, but with adequate research, experience with diet and some self-control, I don't see why cytomel shouldn't be the first thyoid compound used. But for recreational users looking for a fatburner, I still suggest using clenbuterol over cytomel for all intents and purposes. Cytomel is much more powerful, but clenbuterol is a lot safer for use. The results are easier to maintain with clenbuterol as well. Negative feedback in the thyroid

may decrease natural levels of T3 in the body, causing a decrease of metabolic rate after coming off a cycle of T3. That can cause a rebound effect during which a lot of weight is gained back.

Severe hypoglycemia or a combination of alcohol and other drugs, particularly drugs which suppress the central nervous system, can cause a person to stop breathing and their heart to stop beating. Remember, it only takes a few minutes for someone to suffer permanent brain damage or to die, once they stop breathing.

Clomid comes as a tablet containing 50 mg clomiphene citrate, to take by mouth. Impediments to achieving

pregnancy must be excluded or adequately treated before beginning Clomid therapy.

Although Dianabol has many potential side effects, they are rare with a dosage of up to 20 mg/day. Since Dianabol is 17-alpha alkylated it causes a considerable strain on the liver. In high dosages and over a longer period of time, Dianabol is liver-toxic. Even a dosage of only 10 mg/day can increase the liver values; after discontinuance of the drug, however, the values return to normal. Since Dianabol quickly increases the body weight due to high water retention, a high blood pressure and a faster heartbeat can occur, sometimes

requiring the intake of an antihypertensive drug such as Catapresan. Additive intake of Nolvadex and Proviron might be necessary as well, since Dianabol strongly converts into estrogens and in some athletes causes gynecomastia ("bitch tits") or worsens an already existing condition. Because of the strongly androgenic component and the conversion into dihydrotestosterone, Dianabol, in some athletes, can trigger a serious acne vulgaris on the face, neck, chest, back, and shoulders since the sebaceous gland function is stimulated.

Example of a first cycle:

Do not use this medicine for other health conditions.

Keep this medicine out of the reach of children and pets. If using this medicine for an extended period of time, obtain refills before your supply runs out.

Example of a second cycle:

But the degree in which HGH actually works for an athlete has been the topic of a long running debate. Some claim it to be the holy grail of anabolics, capable of amazing things. Able to provide incredible muscle growth and unbelievable fat loss in a very short period of time. Since it is used primarily by serious competitors who can afford such an expensive drug, a great body of myth further surrounds HGH discussion (among

those personally unfamiliar). Many will state with the utmost confidence that the incredible mass of the Olympian competitors each year is 100% due to the use of HGH. Others have crossed bodybuilding materials claiming it to be a complete waste of money, an ineffective anabolic and barely worthwhile for fat loss. With its high price tag, certainly an incredibly poor buy in the face of steroids. So we have a very wide variety of opinions regarding this drug, whom should we believe?

Trinabol is a combination of three esters of trenbolone. The presence of the acetate ester allows trinabol to display a rapid initial

physiological response. The other two esters, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duation of the injection life-cycle. Trinabol has a great effect on promoting protein synthesis, as well as creating a positive nitrogen balance. It is an appetite stimulant and improves the conversion of proteins. In laboratory tests, it has been demonstrated that trenbolone acetate increases protein and decreases fat deposition. It has proven to be an excellent product for promoting size and strength in the presence of adequate protein and calories, promotes body
tissue building processes, and can reverse catabolism.

Product Description

Greater cardiac output

HGH Basics

Perhaps the most interesting and potent effect IGF has on the human body is its ability to cause hyperplasia, which is an actual splitting of cells. Hypertrophy is what occurs during weight training and steroid use, it is simply an increase in the size of muscle cells. See, after puberty you have a set number of muscle cells, and all you are able to do is increase the size of these muscle cells, you don't actually gain more. But, with IGF use you are able to cause this hyperplasia

which actually increases the number of muscle cells present in the tissue, and through weight training and steroid usage you are able to mature these new cells, in other words make them grow and become stronger. So in a way IGF can actually change your genetic capabilities in terms of muscle tissue and cell count. IGF proliferates and differentiates the number of types of cells present. At a genetic level it has the potential to alter an individuals capacity to build superior muscle density and size.

Virormone Veterinary: 100 mg/ml; Paines & Byrne GB

Sustanon is a fairly safe steroid but it is probably

wise to use an antiestrogen such as Nolvadex (tamoxifen citrate) or Proviron (mesterolone). Athletes interested in rapid size and strength gains find that Sustanon stacks extremely well with orals such as Anadrol (oxymetholone) and Dianabol (methandrostenlone). On the other hand, Sustanon also stacks well with Parabolan (trenbolone hexahydrobencylcarbonate), Masteron (drostanolone propionate), and Winstrol (stanozolol) for athletes seeking the hard, ripped look.

Testosterone propionate is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of

the natural hormone. In a healthy male organism, androgens are formed by the testes and adrenal cortex. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, it also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.

Generic Name: methenolone enanthate

Dianabol (17-alpha-methyl- -17beta-hydroxil-androsta- -l.4dien-3-on) is a new, orally applicable steroid with a great effect on the protein metabolism. The effect of Dianabol promotes the protein synthesis, thus it supports the buildup of protein. This effect manifests itself in a positive nitrogen balance and an improved well-being. The calcium balance is positively influenced as well: Dianabol promotes the calcium deposits in the bones. Dianabol is indicated in the treatment of all diseases and conditions in which an anabolic(protein-buildup promoting) effect and a generally roborizing (entire organism

strengthening) effect can be obtained.

Clenbuterol can cause sudden death at very high dosages.

Usage: Average dose is 50-100 mg a day.

Testosterone cypionate is a long acting ester of testosterone which is increasingly difficult to find.Before the scheduling of anabolics in the U.S., this was the most common form of testosterone available to athletes. Cyp had gained a reputation as being slightly stronger than enanthate and became the testosterone of choice for many. Now that anabolics are controlled, this is an almost impossible find. In general, the only versions you\'ll find on the black market

are Sten from Mexico, which contains 75mg cyp with 25mg propionate along with some DHEA, and Testex from Leo in Spain which contains 250mg cypionate is a light resistant ampule. All versions of Upjohn and Steris in multi-dose vials should be looked at with extreme caution as they are very difficult to get on the black market. Counterfeits are quite easy to obtain. Real Steris products have the inking STAMPED into the box and the labels cannot be removed from the bottle. Any variation of that is definitely counterfeit. A running dosage of test cypionate is generally in the range of 200-600mg per week. When this was available
for $20 per10ml bottle, many users would take a whopping 2000mg per week. This kind of dosage however, is unsafe, generally not needed and in today's day and age too costly.

The potential side effects of Oral Turanabol usually depend on the dosage level and are gender-specific. in women, depending on their predisposition, the usual virilization symptoms occur and increase when dosages of more than 20 mg per day are taken over a prolonged time. In men the already discussed reduced testosterone production can rarely be avoided. Gynecomastia occurs rarely with Oral Turanabol Since the response of the water

and electrolyte household is not overly dis-tinct athletes only rarely report water retention and high blood pressure. Acne, gastrointestinal pain, and uncontrolled aggressive behavior are also the exception rather than the rule with Oral Turanabol An increased libido is reported in most cases by both sexes. Since the substance chlordehydromethyltestosterone is 17-alpha alkylated the manufacturer in its package insert recommends that the liver func-tion be checked regularly since it can be negatively affected by high dosages and the risk of possible liver damage cannot be excluded. Thus Oral Turanabol is also a steroid

that can be taken without interruption for long intervals. Studies of male athletes who over a period of six weeks were given 10 mg Oral Turanabol/day did not show any indications of health-threatening effects.

In the U.S.A. dianabol was introduced in the 1960s by Ciba Giegy. The patent expired on the product and this is how a number of rival brands emerged with the same chemical constituents. Dianabol is a brand name and not a chemical name, therefore any product containing methandrostenolone, is now called dianabol (including Anabol).

Liver Toxic: Yes

Film-Coat: lactose monohydrate, hypromellose,

triacetin, titanium dioxide (E171), iron oxide yellow (E172), talc.

Side effects that may occur while taking this medicine include headache, flushing, stomach upset, heartburn, nasal stuffiness, diarrhea, dizziness, or lightheadedness. Vision changes such as increased sensitivity to light, blurred vision, or impaired blue/green color discrimination may also occur. If these continue or are bothersome, check with your doctor or pharmacist.

Somatotropin HGH / 10vials / original box Description Somatotropin hgh by EuroHormones

How Reductil works

HGH is responsible for everything, which

goes on in our body. This is why, HGH is often called the "fountain of youth". Human Growth Hormone (HGH) plays a significant role in:

Primobol is a mild oral anabolic with extremely low androgenic activity, meaning that there is only a minimal chance of typical steroid side-effects. It does not convert to estrogen and, therefore, estrogen-caused water retention and fat deposition will not occur from using it. Methenolone increases the conversion of protein to lean muscle tissue through its anabolic activity. Because primobol has virtually no androgen (i.e., masculinizing) effects, it can generally be used safely

by women.

What does this mean?

Structurally stanozolol is not capable of converting into estrogen. Likewise an antiestrogen is not necessary when using stanozolol, gynecomastia not being a concern even among sensitive individuals. Since estrogen is also the culprit with water retention, instead of bulk produces a lean, quality look to the physique with no fear of excess subcutaneous fluid retention. This makes Winstrol a favorable steroid to use during cutting cycles, when water and fat retention are a major concern. This drug is also very popular among athletes in combination strength/speed sports such

as Track and Field. In such disciplines one usually does not want to carry around excess water weight, and may therefore find the raw muscle-growth brought about by Winstrol quite favorable over the lower quality mass gains of more estrogenic agents.

Effective Dose: 4-10 caps/day.

100 mg Primobolan Depot/week, combined with 50 mg Winstrol Depot/week, is usually an effective stack for many women and is tolerated well so that virilization symptoms are rarely observed. To avoid an undesired accumulation of androgens in the body women should pay attention that there are three to four days in between the relative

injections. For competing female athletes this stack, however, is too weak.

• It improves on wrinkle disappearance (51%)

What is more interesting to me is the role of NO on muscles during resistance training. JE Anderson found that NO appears to be a vital signal in the activation of muscle satellite cells in response to damage. Satellite cell activation is the key first step in the repair and hypertrophy of muscle cells after heavy training. Viagra may therefore enhance the hypertrophy response to exercise, working at the most basic and primary level of the process.

A combination of

100 mg Virormone (Testosterone propionate) every 2 days, either 50 mg Winstrol Depot/day or 76 mg Parabolan every 2 days, and 25 mg Oxandrolone/day help achieve this goal and are suitable for building up "quality muscles." Women especially like propionate since, when applied properly, an-drogenic-caused side effects can be avoided more easily The trick is to increase the time intervals between the various injections so that the testosterone level can fall again and so there is an accumulation of androgens in the female organism. Women therefore take propi-onate only every 5-7 days and obtain remarkable results
with it. The, androgenic effect included in the propionate allows better regeneration without virilization symptoms for hard-training women. The dosage is usually 25-50 mg/injection. Higher dosages and more frequent intervals of intake would certainly show even better re-sults but are not recommended for women. The duration of intake should not exceed 8-10 weeks and can be supplemented by taking mild and mostly anabolic steroids such as, for example, Primobolan, Durabolin, and Anadur in order to promote the synthesis of pro-tein. Men who do not fear the intake of testosterone or the possible side effects should go ahead

and give propionate a try. The side ef-fects of propionate are usually less frequent and are less pronounced. The reason is that the weekly dose of propionate is usually much lower than with depot testosterones.

Testosterone´s anabolic/androgenic ratio is 1:1 meaning it is exactly as anabolic as it is androgenic. Actually, testosterone is the steroid which all anabolic/androgenic ratio´s are based on. If a steroid is 2:1, then it is, compared with testosterone´s ratio, doubly as anabolic as it is androgenic. Hence, we see from testosterone´s ratio, it is both quite anabolic as well as androgenic.

Many athletes who use Clenbuterol claim that it promotes dramatic strength increases and a very noticeable reduction in body fat some athletes claim that they enjoyed significant gains in muscle mass while using Clenbuterol. Clenbuterol's most valid application seems to be as a pre-contest, cutting drug. It is not banned by any athletic committee; thus, numerous professional bodybuilders have used it for the last month of contest preparation. Athletes have used between 60-120 mcgs taken in divided doses daily. Because it causes a great deal of receptor downgrade it should not be used continually. Research

shows that using it for two days, then taking two days off prevents attenuation. Cycles range from 6-12 weeks in length. Side effects include nervousness, tremors of the hands, headaches, and insomnia. Usually these side effects are dose related. It comes in 20 mcg tablets. Clenbuterol is being counterfeited under numerous manufacturer names in the United States.

In bodybuilding Halotestin is almost exclusively taken during preparation for a competition. Since its substance is strongly androgenic while at the same time aromatizing very poorly, this substance helps the athlete obtain an elevated androgen level while

keeping the estrogen concentration low.

With the proper administration of ancillary drugs, much of the new muscle mass can be retained for a long time after the steroid cycle has been stopped. Those who rely solely on a fancy tapering-off schedule to accomplish this are likely to be disappointed. Although a common practice, this is really not an effective way to restore the hormonal balance.

Tadalafil is currently undergoing clinical trials for the treatment of pulmonary hypertension. The clinical trials are based on tadalafil's inhibitiong of PDE5. It is hoped that by inhibiting this enzyme, tadalafil

will prove effective in opening up blood vessels in the lungs, lowering pulmonary arterial resistance and pressure, and thus reducing the workload of the right ventricle of the heart.

Most athletes inject Trenabol Depot at least twice a week; some bodybuilders inject 1-2 ampules per day during the last three to four weeks be-fore a competition. Normally a dosage of 228 mg/week is used, corresponding to a weekly amount of three ampules. It is our experience that good results can be achieved by injecting a 76 mg ampule every 2-3 days. Trenabol Depot combined with Winstrol Depot works especially well and gives the

athlete a distinct gain in solid and high quality muscles together with an enormous strength gain. A very effective stack is 76 mg Trenabol Depot every 2 days combined with 50 mg Winstrol every 2 days. Athletes who are interested in a fast mass gain often also use 30 mg Dianabol/day while those who are more interested in quality and strength like to add 25 mg+ Oxandrolone/ day. Probably the most effective Trenabol Depot combination consists of 228 mg Trenabol Depot/week, 200 mg Winstrol Depot/week, and 40-50 mg Oral-Turinabol/day and usually results in a drastic gain in high quality muscle mass together with a gigantic
strength gain. Trenabol Depot also seems to bring extraordinarily good results when used in combination with growth hormones.

Aromatization: No, but it will raise testosterone levels and increased aromatization may occur.

Tiratricol is a naturally occurring metabolite of the endogenous thyroid hormone triodothyronine (T-3). The medical use for thyroid preparations is for the treatment of thyroid dysfunction and obesity. The thyroid gland in fact produces two primary hormones, identified as T-3 and T-4 (thyroxine, which Converts to T-3 in the body). Together these structures are the main regulators of

the body's metabolism. Tiratricol is a rapidly metabolised form of the T-3 hormone. When administered, this substance should markedly increase the metabolic rate. This is noted by an increase in the conversion rate of carbohydrates, proteins and fats. This basically means that the body will utilise nutrients at a much faster speed, due to increased cellular activity.

Androlic / Anadrol 50 is the strongest and, at the same time, also the most effective oral steroid. Androlic / Anadrol has an extremely high androgenic effect, which goes hand in hand with an extremely intense anabolic component - oxymetholone.

This is another one of the popular ones. Next to Deca and D-bol the third most abused substance among athletes is stanozolol, as documented by the many positive drug tests. Among them the case sprinter Ben Johnson, who was stripped of his Gold Medal in the 100 meter dash in the 1988 Olympics. But since then the number of positives has grown exponentially. In bodybuilding Shawn Ray's positive in the 1990 Arnold Schwarzenegger Classic (a brief stint the IFBB had with drug testing). Ray was the winner of that event, but Canadion pro Nimrod King was also shown to have stanazolol metabolites in his urine.

That short paragraph to illustrate what sort of an impact it has made on the world of sports. Stanozolol is commonly referred to as Winny, after its trade name as marketed by Winthrop : Winstrol. In Europe this may be a bit confusing as the most available form there is called Stromba. Winny comes in two forms, an injectable form and an oral form. Both are equally popular and both are to be used daily. The injections are the same compound as the orals, which is methylated. Due to this feat it can't be esterified for time-release. So its not quite suited for weekly injections although this is claimed on the package insert of the veterinary form of Winny. Another thing that would further add to the difficulty of time-release is that it is delivered in an aqueous solution. That would not exactly facilitate the entry into adipose tissue, needed for the esterification and storage of the substrate in the body.

The injectable version often gives more results. In similar doses there is still more breakdown upon first pass in the liver, making it difficult to get an equal amount absorbed. And on top of that it has to be mentioned that most people simply don't take an equal amount. Too many pills, lesser availability, higher cost. Many factors play a role in that. But of course an oral is to be preferred over daily injections as that gives the necessary complications as well. Think of abscesses and lumps, the searching for new injection sites due to pain and so on. Some have solved this problem by simply drinking the Winny injections. It's the same substance, also methylated to withstand the liver, the availability and price are better and its contained in water. So there really aren't many objections to this.

Of course because they are the same substance, regardless of the method of use, its not advised to use Winny for long periods of time. Slightly less hepatoxic than most 17-alpha alkylated substrates, so it can be used a bit longer, as long as 8 weeks, but longer than that is not wise. Elevation of liver values is quite common.

The specificity of Winny however, lies in how it counteracts estrogenic side-effects such as gyno and excess water retention. First of all it's a 5-alpha reduced substrate. 5-alpha reduction breaks the double bond between positions 4 and 5, which is required for conversion to estrogen via aromatase, the primary enzyme for the manufacture of estrogen in males. Because some of these compounds nonetheless show some affinity for aromatase they may have some use in blocking estrogen from other steroids they are stacked with. Wether or not Winny acts in this way is not entirely sure. What has been a popular point of discussion with stanozolol is its suggested anti-progestagenic effects. The theory goes that Winny can bind and compete for a position at the progesterone receptor much like Clomid of Nolvadex would at the estrogen receptor, thereby inhibiting progestagenic effects. Now, progesterone can aggravate estrogenic side-effects by agonizing estrogen and it does play a role in gyno.

We also discussed that certain steroids may indeed stimulate and act at the height of the progesterone receptor including nandrolone and Norethandrolone. These hormones are also altered by it inducing a decrease in libido and a sense of lethargy and such, and eventhough they aromatize in lesser rates than some other steroids, they show an equal capability to cause estrogenic side-effects, particularly when stacked with other aromatizable compounds. Now there is evidence that Winny does indeed bind to the progesterone receptor and its users do not indicate the normal characteristics of progesterone stimulation, which bodes well for these anti-progestagenic properties. There is also some clinical data that it does aid in symptoms that require progesterone suppression. Much in the way danazol was also successfully used. The one thing we shouldn't lose sight of however is in what rate it binds to the progesterone reception. There is no data on this. For all we know it couldn't bind strong enough to compete with nandrolone or norethandrolone. So its not wise to state that Winny is an anti-progestagin per se, but it does make Winny a good match for these products in stacks in any case.

Strong gains are never really made while using stanozolol (it's a weak androgen since it has no 3-keto group needed for androgen binding), but decent and fairly easy to maintain gains are possible. Its limited time of use however makes most experienced users opt for other steroids in that regard. Winny, in bodybuilding circles at least, is used mostly during cutting cycles to maintain mass. Winstrol, like a DHT compound also gives a distinct increase in muscle hardness and striations in people with a low body-fat percentage. This lends further credence that it too may be a an anti-estrogen. But most likely it has more to do with the overall lower levels of circulating estrogen. Winny is also quite effective at promoting strength because it binds very well at the androgen receptor. Short term stanozolol use can promote drastic strength, a feat often employed early in a bulking cycle (although d-bol would be more suited in that case) or late in a cutting cycle to prevent a decrease in performance. This combined with the red blood cell count-stimulating properties of its androgen affinity make it popular among track athletes as well in order to beget better results. As many, including Ben Johnson, did not take into account it can be detected for quite some time after last use so its not advisable for drug tested athletes. Many have assumed otherwise due to the short half-life, but apparently some inactive metabolites are easily esterified, so they can be found up to 5 months after the last injection.

Winny is mostly quite well-tolerated in men. Cramps, headaches, elevated blood pressure and cholesterol levels and liver damage are noted, but on a not so-frequent basis. Standard virilization symptoms associated with the stimulating of the androgen receptor, however, are a problem. Acne, prostate hypertrophy and an aggravation of male pattern baldness can occur, so use by women has to be discouraged.

Due to the frequent rate of injections, users generally have to go spotting for different sites of injection on the body. Calves, shoulders, arms and such. When doing so they noted a localized increase in mass which has given root to the myth that Winny can add muscle where it is injected. What I'm about to say goes for all compounds known to date : Steroids do not increase mass locally. The observance is noted because the injection breaks the fascia around the muscle, which possibly gives a muscle a little more room to grow. This is mostly temporary, and in the best cases very limited. Multiple injections would not increase the size in comparison. When the fascia heals, if it heals, it can lead to something called compartments syndrome, where a nerve is pinched between a muscle and its fascia. Leading to numbness quite often and in some cases to a paralysis of everything that nerve controls. This is not a frequent occurrence. This is rare, but my point was documenting that localized growth spurred by an injection is a myth.

A last note about injectable Winny is : shake before use. Its called an aqueous solution, but the Winny being a steroid is not particularly polar, meaning it doesn't dissolve in the water. When the stuff sits, it will accumulate at the bottom of the vial. A good way to recognize the real stuff as well. So shake before you draw it into a syringe or mix it before you drink it, and perhaps even stir it again once in the syringe prior to injection.

Use:

Winstrol is best used at a rate of 50 mg a day. When in an injection that amounts to a single injection every day around the same time. In orals, that'll be at least 5 tabs of a legit product.

In a mass stack Winny makes a good match for Deca and Nilevar. Whether or not its anti-progestagenic effects are for real or not, lets just say it can't hurt. In any stack with Deca the use of 25-50 mg a day for the first 6-8 weeks of the stack can kickstart it and add some strength. With Nilevar there is a practical objection because it is also 17-alpha alkylated and more toxic than Winny, so your stack would be limited to 6 weeks, which is not overly productive.

For cutting purposes Boldenone, Masteron and trenbolone are the best options. If you are employing a longer stack, then use 25-50 mg of Winny for 6 weeks or so at the end of the stack. Boldenone is the best match here as the other two do basically the same thing. They act solely or mostly at the androgen receptor. Making them poorer choices since simply upping the dose of Winny would mostly achieve similar results. Of course neither is methylated, which allows for longer use.

There is no need for an anti-estrogen as Winny may have such a property of its own and does not aromatize at any rate. The only counter-indication with Winny would perhaps be an anti-hypertensive if you use for a longer stack. Be sure to get liver values checked if you use for longer than 6 weeks on end. There is no real use for Clomid or Nolva post-cycle for Winny specifically since there is no post-cycle aromatisation to cause negative feedback. That makes whatever gains you made on Winny quite easy to maintain.