Bad:

High G.I. carbohydrates (e.g. sweets, soft drinks and ice-cream)

will raise your blood sugar quickly and prevent early hypoglycemia. Low G.I. carbohydrates (e.g. white pasta, high amylose rice, softened whole grain breads and instant noodles) are metabolized more slowly and will keep your blood glucose level up over a more extended period of time, when the medium acting insulin preparations begin to take effect;

Not a rapid mass builder, instead Equipoise® will be looked at to provide a slow but steady gain of strength and quality muscle mass. The most positive effects of this drug are seen when it is used for longer cycles, usually lasting more than 8-10 weeks in duration.

The muscle gained should not be the smooth bulk seen with androgens, but very defined and solid. Since water bloat is not contributing greatly to the diameter of the muscle, much of the size gained on a cycle of Equipoise® can be retained after the drug has been discontinued. It is interesting to note that structurally Equipoise® and the classic bulking drug Dianabol are almost identical. In the case of Equipoise® the compound uses a l7beta ester (undecylenate), while Dianabol is 17 alpha alkylated. Aside from this the molecules are the same. Of course they act quite differently in the body, which

goes to show the 17-methylation effects more than just the oral efficacy of a steroid.

The third reason for the popularity of Anavar is that oxandrolone does not influence the body's own testosterone production.

Reductil works like other appetite suppressants on the market by increasing the amount of serotonin and catecholamine in the brain. Serotonin and catecholamine are two important chemicals that control mood and appetite. When levels of serotonin and catecholamine are raised, your appetite decreases.

Additional comments:

Day 4: 100 mcg

Generic Name: Orlistat

KEEP THIS PRODUCT out of the reach of children.

IMPORTANT NOTE: The following information is intended to supplement, not substitute for, the expertise and judgment of your physician, pharmacist or other healthcare professional. It should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. Consult your healthcare professional before using this drug. SIDE EFFECTS: Fatty / oily stool, oily spoting, intestinal gas with discharge, bowel movement urgency, poor bowel control or headaches may occur. If these efects persist or worsen, notify your doctor promptly. Intestinal

side effects {e. g. oily stool} may increase in intensity if you exceed your daily dietary fat allowance. If you notice other effects not listed above contact your doctor or pharmacist.

References:

  1. Anat Histol Embryol. 2003 Apr;32(2):70-9.
  2. J Lab Clin Med. 1995 Mar;125(3):326-33.
  3. Zhonghua Nan Ke Xue. 2003;9(4):248-51
  4. J Clin Endocrinol Metab. 2003 Apr;88(4):1478-85
  5. J Clin Endocrinol Metab. 2004 Feb;89(2):718-26.
  6. Am J Physiol. 1998 Jun;274(6 Pt 1):C1645-52.
  7. Biochim Biophys Acta. 1995 May 11;1244(1):117-20.
  8. Am J Physiol Endocrinol Metab. 2001 Dec;281(6):E1172-81.
  9. Health
    Psychol. 1990;9(6):774-91.
  10. Fertility and Sterility 33.

It is also interesting to note that methandrostenolone is structurally identical to boldenone, except that it contains the added c17 alpha alkyl group discussed above. This fact makes clear the impact of altering a steroid in such a way, as these two compounds appear to act very differently in the body. The main dissimilarity seems to lie in the tendency for estrogenic side effects, which seems to be much more pronounced with Anabol. Equipoise® is known to be quite mild in this regard, and users therefore commonly take this drug without any need

to addition an antiestrogen. Anabol is much more estrogenic not because it is more easily aromatized, as in fact the 17 alpha methyl group and c1-2 double bond both slow the process of aromatization. The problem is that methandrostenolone converts to l7alpha methylestradiol, a more biologically active form of estrogen than regular estradiol. But Anabol also appears to be much more potent in terms of muscle mass compared to boldenone, supporting the notion that estrogen does play an important role in anabolism. In fact boldenone and methandrostenolone differ so much in their potencies as anabolics that the two are

rarely though of as related. As a result, the use of Anabol is typically restricted to bulking phases of training while Equipoise® is considered an excellent cutting or lean-mass building steroid.

In the human body growth hormone is produced by the pituitary gland. It exists at especially high levels during adolescence when it promotes the growth of tissues, protein deposition and the breakdown of subcutaneous fat stores. Upon maturation endogenous levels of GH decrease, but remain present in the body at a substantially lower level. In the body the actual structure of growth hormone is a sequence of 191 amino

acids. Once scientists isolated this hormone, many became convinced it would exhibit exceptional therapeutic properties. It would be especially effective in cases of pituitary deficient dwarfism, the drug perhaps restoring much linear growth if administered during adolescence.

Pharmaceutical Name: Testosterone (as Cypionate)

Ephedrine is similar in structure to amphetamines, because of this. It mimics some of the effects of "speed" such as dampening the appetite and raising blood pressure. It Is however, much weaker and far less toxic than amphetamines (although It is banned as a stimulant

by most athletic organizatlons). The effect of ephedrine Is called a "futile energy cycle." Ephedrine stimulates the conversion of thyroid into Its most active form. T-3 in peripheral tissue. This stimulates the metabolism and burns up calories quicker. Caffeine and aspirin stimulate the thermogenic effects of ephedrine. In fact It has recently become quite commonplace for pre-contest bodybullders to forgo the use of dangerous thyroid drugs and instead use a combination of ephedrine, aspirin and caffeine for cutting up. A usual dose for fat loss has been in the area of 100 mg caffeine. 50 mg ephedrine and
one aspirin tablet, three times dally. I've seen athletes get totally shredded on this stack without losing any muscle! Recent studies on humans found that combining ephedrine with caffeine and aspirin enhances calorie-dissipating. Caffeine and aspirin are thought to help by suppressing agents that would normally further block release of norepinephrine. The long term effects of combining these three OTC drugs Is largely untested though. While It appears they are safe, in large dosages they could be dangerous, particularly the ephedrine.

The strong androgen component will generate good strength increases with

little body weight gain.

Andriol, is a unique version of testosterone undecanoate developed by Organon. This version of testosterone is based in oil and is sealed in a capsule to be taken orally. According to the manufacturer, this method bypasses the liver and enters the body as a fat through the lymphatic system. In theory this seems quite interesting, however, athletes find Organon's claims don't hold up well. In doses of less than 240mg per day effects are generally non-existent. With higher doses, effects are small at best. This leads one to think most of the steroid is not making it to circulation.

Generally, steroid users experienced with any strong anabolics will be disappointed with Andriol's results. Combined with other anabolics it may lend some effectiveness but should be questioned.

If you take too much

Wrinkle removal

Do not treat yourself for coughs, colds or allergies without asking your doctor or pharmacist for advice. Some ingredients can increase possible side effects.

Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that will put stress on the liver. It is important to point out however that dispite this alteration oxandrolone is generally

very well tolerated. While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not usually a problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. One study comparing the effects of oxandrolone to other agents including as methyltestosterone, norethandrolone, fluoxymesterone

and methAndriol clearly supports this notion. Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among all the alkylated orals tested. 20mg of oxandrolone in fact produced 72% less BSP retention than an equal dosage of fluoxyrnesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during longer cycles than most of other orals with this distinction.
Although this may very well be true, the chance of liver damage still cannot be excluded, especially with hogher dosages.

Faster wound healing

It is also important to note that while Women may receive some small benefit from the drug (although testosterone is really not a steroid for females), they must be very careful with it. Those who are, or might become pregnant, should never take or even handle a Proscar / Propecia tablet. The DHT blocking action can cause severe developmental problems to an unborn fetus, even in very small amounts. Since the drug can be absorbed through the skin, handling

a broken tablet may be all that is needed for such an occurrence. Since women generally stay away from testosterone, and the design of Proscar/Propecia has been strictly for men, as of yet there is little to report on the effectiveness of this compound for combating virilization symptoms.

Molecular Weight (base): 288.429

Nolvadex C&K is also useful during a diet since it helps in the burning of fat. Although tamoxifen has no direct fatburning effect its antiestrogenic effect contributes to keeping the estrogen level as low as possible. Nolvadex C&K should especially be taken together with the strong

androgenic steroids Dianabol and Anadrol , and the various testosterone compounds.

Street Price: $.50 - 1.00 / tab. Fairly inexpensive in Mexico though. Spiropent is currently going for about $7.50/box, Novegam for $5.25/box, and Oxyflux for about $3.30/box.

Packaging: 1000 mg in 10 ml.

SEROSTIM BASICS: (Somatotropin / HGH)

Cialis ® comes as yellow film-coated tablets. They are in the shape of almonds and have "C 20" marked on one side. These tablets are available in blister packs containing 2, 4 or 8 tablets.

After a cycle, mainly due to the high aromatization

and increased levels of estradiol in the blood after discontinuing, natural testosterone levels will be severely suppressed. This means steps need to be taken to assure the quick return of natural testosterone, or we stand to lose a lot of the gains we made while using testosterone. Since it's a non-toxic, potent mass-builder its mostly used in long 10-12 week cycles. So some testicular shrinkage will have occurred too. Its very important that people see that HCG and Nolvadex/clomid are essential as a post-cycle therapy, and that both are equally important in achieving our goal. HCG injections should be started the last
week of the cycle and continued for 3-4 weeks, using 1500-3000 IU every 5-6 days. HCG will act as an alternative to LH and start the endogenous testosterone cycle, thereby increasing testicle size once again. Then about 2 weeks after the last shot of testosterone is given, Nolvadex/Clomid cycle should be started. 40 mg of Nolva or 150 mg of Clomid per day for two weeks, followed by two more weeks with either 20 mg of Nolva or 100 mg of Clomid per day should be adequate. Always remember that HCG is suppressive of natural testosterone itself and should be discontinued at least 2 weeks prior to finishing Nolvadex/Clomid.

Those who are not bothered by frequent injections will find that propionate is quite an effective steroid. It is of course of powerful mass drug, capable of producing rapid gains in size and strength. At the same time the buildup of estrogen and DHT (dihydrotestosterone) will be pronounced, so typical testosterone side effects are to be expected. Some do consider Testosterone Propionate to be the mildest testosterone ester, and the preferred form of this hormone for dieting/cutting phases of training. Some will go so far as to say that propionate will harden the physique. while giving the user less water and fat

retention than one typically expects to see with a testosterone. Realistically however, this is nonsense. The ester is removed before testosterone is active in the body, and likewise the ester cannot alter the activity of the parent steroid in any way, only slow its release. We can say that propionate might be the favored testosterone among female bodybuilders (for those who insist on testosterone use!) as blood levels are easier to control with it compared to other esters. Should virilization symptoms develop, one would not wish to wait the weeks needed for testosterone concentrations to fall after a shot of enanthate
for example.

OMFG I am so tired of all the misinformation floating around on IGF-1. Look at the length of this post. Did you read all of it? You should, you know.

by Bill Roberts - Parabolan is trenbolone cyclohexylmethylcarbonate. The half-life of a steroid ester is mostly dependent on its ratio of fat solubility to water solubility: the longer chain the ester, the higher this ratio, and the longer the half-life. This particular carbonate could be most closely compared with an enanthate ester; the half-life is probably a little less than week.

Does KAMAGRA automatically cause an erection?

Individual variation: two different people can respond in a very different way to a given dose of insulin, even if they are of a similar height, weight and other personal characteristics. The fact that a certain dose does not seem to cause a problem for one person does not mean this will be so for another. In addition, the response to insulin will also vary greatly within any one individual over time, according to changes in one or more of the above noted factors.

These 10mg tablets are yellow in colour.

Diazepam should be administered cautiously to patients with severe hepatic disease because its

elimination half-life can be prolonged, possibly resulting in toxicity. Diazepam is metabolized to an active metabolite, and patients with hepatic disease are more likely to experience adverse CNS reactions and should receive reduced initial dosages.

Parabolan is a strong, androgenic steroid which also has a high anabolic effect. Whether a novice, hard gainer, power lifter, or pro bodybuilder, everyone who uses Parabolan is enthusiastic about the results: a fast gain in solid, high-quality muscle mass accompanied by a considerable strength increase in the basic exercises. in addition, the regular application over

a number of weeks results in a well visible increased muscle hardness over the entire body without dieting at the same time. Frequently the following scenario takes place: bodybuilders who use steroids and for some time have been stagnate in their development suddenly make new progress with Parabolan. Another characteristic is that Parabolan, unlike most highly-androgenic steroids, does not aromatize. The substance trenbolone does not convert into estrogens so that the athlete does not have to fight a higher estrogen level or feminization symptoms. Those who use Parabolan will also notice that there is no water retention in
the tissue. To say it very clearly: Parbolan is the number one competition steroid. When a low fat content has been achieved by a low calorie diet, Parabolan gives a dramatic increase in muscle hardness. In combination with a protein rich diet it becomes espe-cially effective in this phase since Parabolan speeds up the metabolism and accelerates the burning of fat. The high androgenic effect prevents a possible overtraining syndrome, accelerates the regeneration, and gives the muscles a full, vascular appearance but, at the same time, a ripped and shredded look.

Tamoxifen may cause unwanted effects that may not

occur until months or years after Nolvadex C&K is used. Tamoxifen increases the chance of cancer of the uterus in some women taking it. Tamoxifen may cause blockages to form in a vein, lung, or brain. In addition, tamoxifen has been reported to cause cataracts and other eye problems.

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.

Ironically, even though Tren is an excellent contest prep drug, it lowers your thyroid level, and this raises prolactin. I recommend

taking T3 (25mcgs/day) along with your Tren to avoid elevating your prolactin too high via this route.

This product has also been researched as a possible male birth control options. Regular injections will efficiently lower sperm production, a state that will be reversible when the drug is removed. With the current stigma surrounding steroids however, it is unlikely that such an idea would actually become an adopted practice. Testosterone is a powerful hormone with notably prominent side effects. Much of which stem from the fact that testosterone exhibits a high tendency to convert into estrogen. Related

side effects may therefore become a problem during a cycle. For starters, water retention can become quite noticeable.

When discontinuing Anadrol 50, the crash can be equally powerful. To begin with, the level of water retention will quickly diminish, dropping the user's body weight dramatically. This should be expected, and not of much concern. What is of great concern is restoring endogenous testosterone production. Anadrol 50 will quickly and effectively lower natural levels during a cycle, so HCG and Clomid/Nolvadex are a must when discontinuing a cycle.

Kidney or liver disease — Higher blood

levels of benzodiazepines may result, increasing the chance that side effects will occur

If overdose of Clomid is suspected, contact your local poison control center or emergency room immediately. Toxic effects accompanying acute overdosage of Clomid have not been reported. Signs and symptoms of overdosage as a result of the use of more than the recommended dose during Clomid therapy include nausea, vomiting, vasomotor flushes, visual blurring, spots or flashes, scotomata, ovarian enlargement with pelvic or abdominal pain.

Mesterolone (Proviron) is a synthetic, orally effective androgen which does

not have any anabolic characteristics. Mesterolone (Proviron) is used in school medicine to ease or cure disturbances eaused by a deficiency of male sex hormones. Many athletes, for this reason, often use Mesterolone (Proviron) at the end of a steroid treatment in order to increase the reduced testosterone production. This, however is not a good idea since Mesterolone (Proviron) has no effect on the body's own testosterone production but-as mentioned in the beginning-only reduces or completely eliminates the dysfunctions caused by the testosterone deficiency. These are in particular impotence which is mostly caused by an

androgen deficiency that can occur after the discontinuance of steroids, and infertility which manifests itself in a reduced sperm count and a reduced sperm quality. Mesterolone (Proviron) is therefore taken during a steroid administration or after discontinuing the use of the steroids, to eliminate a possible impotency or a reduced sexual interest. This, however does not contribute to the maintainance of strength and muscle mass after the treatment. There are other better suited compounds for this (see HCG and Clomid). For this reason Mesterolone (Proviron) is unfortunately cunsidered by many to be a useless and unnecessary
compound.

Andriol testocaps are capsules of Testosterone Undeconoato, an orally active testosterone preperation that helps users gain muscle mass.

Usage: 250 mg - 1000 mg weekly.

If you are interested in taking clenbuterol for anything other than fat loss then you might as well stay away from this compound. There is a lot of talk as to how clenbuterol compares to ephedrine as well. Most "experts" feel that clen gives a better bang for the buck than the ECA stack. It should be noted that clenbuterol’s results and effects are much shorter lived. They work through very similar mechanisms.

Both products stimulate the beta-receptors but clenbuterol seems to be a more refined version, called a second generation beta-agonist drug, than ephedrine. Clenbuterol targets the proper receptors, being the beta-2 and 3 receptors than ephedrine more specifically which should in theory make clenbuterol more effective of a fat burner. Again, most of the so called "experts" say that clenbuterol is more effective than ephedrine. I, personally, get worse results with clen vs. the good old ECA stack. Clenbuterol also didn't blunt my hunger either and I ate more while taking it as well. I also seem to get much

better effects out of cytomel as a fat burner as well. Even better than the ECA stack or clenbuterol. But, again, that is my personal opinion.

Skip a missed dose of Phentermine if you forgot to take it and continue your regular dosing schedule. If you miss your dose of Phentermine you should not take two does at once.

Day 2: 80 mcg

Anadrol 50 is the U.S. brand name for oxymetholone, a very potent oral androgen. This compound was first made available in 1960, by the international drug firm Syntex. Since oxymetholone is quite reliable in its ability to increase red blood cell production (and effect

admittedly characteristic of nearly all anabolic/androgenic steroids), it showed particular promise in treating cases of severe anemia. For this purpose it turned out to be well suited, and was popular for quite some time. But recent years have brought fourth a number of new treatments, most notably the non-steroidal hormone Epogen (erythropoietin). This item is shown to have a much more direct effect on the red blood cell count, without the side effects of a strong androgen. Financial disinterest finally prompted Syntex to halt production of the U.S. Anadrol 50 in 1993, which was around the same time they decided to

drop this item in a number of foreign countries. Plenastril from Switzerland and Austria was dropped; following soon was Oxitosona from Spain. Many Athletes feared Anadrol 50 might be on the way out for good. But new HIV/AIDS studies have shown a new light on oxymetholone. These studies are finding (big surprise) exceptional anti-wasting properties to the compound and believe it can be used safely in many such cases. Interest has been peaked, and as of 1998 Anadrol 50 is again being sold in the United States. This time we see the same Anadrol 50 brand name, but the manufacturer is the drug firm Unimed. Syntex continues to
market & license this drug in a number of countries however (under a few different brand names).

Many athletes also claim that they enjoyed significant gains in muscle mass while using clenbuterol. There is no doubt that clenbuterol has an anabolic effect in animals but there are, though, no scientific evidence this also is true in humans. The same goes for the strong anticatabolic effect of clenbuterol, meaning it decreases the rate at which protein is reduced in the muscle cell, consequently causing an enlargement of muscle cells.

The authors of this research commented that "theoretically,

this could provide a biochemical environment conducive to accelerating the rate of muscle hypertrophy and inhibiting protein degradation". However, the writer knows of no scientific studies which support this theory.

Wrinkle removal

Use of Xenical should not continue beyond 1 year and never beyond 2 years.

This is an esterified form of the base steroid testosterone, much like enanthate, cypionate and sustanon 250. It's a superlipophillic, oil-based injectable that slows the release of the steroid into the blood stream.

Always have a source of glucose or other high G.I. food ready

at hand, in case you should begin to experience the symptoms of hypoglycemia. If this does occur, you should take this glucose or food without delay. You should eat or drink 15-20 grams of carbohydrate to begin with, which is contained in ~ 2 slices of white or brown bread, two glasses of milk, a half glass of soft drink, a tablespoon of honey or six jelly beans.

Personally I have more affinity for testosterone enanthate, but few users will note any real difference between the two products, and both remain a better buy than their popular counterpart sustanon 250, which is a poor choice of testosterone in my opinion.

It makes sense that a user simply opts for which one is most readily available at the time. They sell for roughly the same price, and are almost equally good. So most North and South-American users will usually opt for the use of a cypionate, as it is more available in those regions, whereas Europeans and Asians will probably prefer the enanthate version.

Now that the properties of trenbolone acetate have been explained we can better understand how to use it in order to maximize its advantages. Evidence suggests that trenbolone when stacked with estrogen promotes more weight gain that trenbolone alone, now

I´m not telling you to go pop some birth control with your trenbolone but the addition of aromatizing orals such as dianabol and a long estered testosterone such as cypionate or enanthate would produce great gains in a bulking cycle. For a cutting cycle trenbolone is the best choice you have; trenbolones powerful effect on nutrient shuttling allows a user to restrict calories and remain in a state of positive nitrogen balance (remember what that means?). The cortisol reducing effect and binding to the glucocorticoid receptor will greatly reduce the catabolic effects of harsh dieting and excessive amounts of cardio&

not to mention that trenbolone itself may burn fat (due to it´s strong AR-binding). A good choice to stack with tren in a cutting cycle is Winstrol. Winstrol has a low binding affinity to the AR and thus will act in your body in vastly different ways than the Tren (i.e. in non-receptor mediated action). In addition, Winstrol is a DHT-based drug and Tren is a 19-nor& throw in some Testosterone (prop), and you´ll have a cutting cycle which takes advantage of all 3 major families of Anabolic Steroids (Testosterone, 19-nor, and DHT), as well as vastly different AR-binding affinities and mechanisms of action.

Liver Toxic: Yes

The chance of finding real Parabolan on the black market is around 5%. That is the reason why we take a chance and claim that only very few of you who read this book will have ever held an original Parabolan in your hand, let alone injected one. Those who have not tried the originals simply cannot take part in this discussion. As to the effect, the difference between the real French Parabolan and the fakes circulating on the black market is gigantic.

Can I take KAMAGRA with alcohol?

Take 10 x 5mg tabs of dbol a day and 4 to 6 amps of deca a week and watch for some amazing

results in strength and size.

Before you start any treatment with KAMAGRA, be sure to ask your healthcare provider if your heart is healthy enough. If you're a man who uses nitrate drugs, like nitroglycerine, never take KAMAGRA. The combination of KAMAGRA and nitrates can make your blood pressure suddenly drop to unsafe levels. You could get dizzy, faint, or even have a heart attack or stroke. Nitrates are found in many prescription medications that are used to treat angina (chest pain due to heart disease) such as:

Anabolic steroids promote the growth of skeletal muscle and the development of male sexual

characteristics but do also have some other effects.

depression

Diazepam has reportedly decreased the elimination of digoxin in some patients. Digoxin toxicity has occurred in a patient receiving alprazolam and digoxin. The interaction between benzodiazepines and digoxin may be the result of increased protein binding of digoxin and/or an effect of benzodiazepines at the renal tubules, which decreases the elimination of digoxin. Pending further clarification of this interaction, patients receiving a benzodiazepine and digoxin concurrently should be monitored for increased serum digoxin levels.

With the lack of a 3-keto group, and the addition of a pentangle at the 2 and 3 positions, one could liken the structure of Danazol best to Stanozolol (Winstrol/Stromba) or Furazabol (Miotolan). But for proper understanding of this drug its best likened to Mesterolone (proviron). Its similar, but a lot less androgenic. Like mesterolone it's a steroid, but rarely regarded as such. Because of its structure its only mildly androgenic and because it binds readily in a lot of places in the body without exerting any real action, its not considered anabolic to any degree. So you can derive that the use of danazol is not that of the classic anabolic, androgenic steroid. In treatment Danazol is used as an anti-gonadotropin. Its exogenous administration gives negative feedback to the natural production of testosterone, slowing it down, but mostly it's a competitive anti-aromatase. And for that reason its sometimes employed by bodybuilders to prevent the side-effects of aromatization of certain hormones like testosterone. These side-effects include bloating through water retention, increased body-fat and gyno (growth of breast tissue in men).

I do say "sometimes" because Danazol is hard to come by these days, as is illustrated by the large number of products in the product list above that have been discontinued. On the black market too it seems the interest in this compound is relatively low, and prices considerably high. As high as 350 dollars for 100 tabs of 200 mg, and knowing the daily dose is easily 400 mg per day, that's a costly affair. That's why you won't hear much of danazol in popular literature. But in the scientific literature its still frequently used for research purposes.

Possible side-effects that can occur with use are of course very mild. Like Proviron it does not aromatize to any extent and actually prevents aromatization, and the lack of a 3-keto group amongst other things makes it a particularly poor androgen, so androgenic risk is limited. One might still note increased libido and some acne however. Perspiration, hot flashes, elevated blood pressure and liver toxicity (to a small extent, due to the high doses) can be encountered if using very high doses for extended periods of time.

Danazol may make a great alternative for Proviron, but with Proviron, arimidex, cytadren and several others available to us, the need for another mild, expensive aromatase inhibitor is limited, hence its low presence on the black market. Many governments and sports federations have also banned Danazol because of its slight androgenic effect, making things like Arimidex a much more popular choice, and selling for roughly the same on average, and those who are tied in, even a lot cheaper due to the wide-spread availability of anastrozole (Arimidex) to the underground manufacturers.

Use:

Ideally one would stack Danazol with aromatizing steroids like nandrolone, testosterone, methandrostenolone and boldenone to limit or stop them from aromatizing, and thus eliminating or reducing estrogenic side-effects. Since its an aromatase inhibitor, it would most likely be employed for continuous use. If it was merely as a short term problem-solving measure an estrogen receptor antagonist like Clomid or Nolvadex may be handier. For these purposes a dose of 200-400 mg daily is employed. The higher end being the more common. It needs to be noted that there is a downside to blocking estrogen formation as well, because estrogen increases our gains. It is (as demonstrated in the Equipoise profile) helpful in upgrading the androgen receptor, increasing natural growth hormone output and improving glucose utilization for extra energy and a sense of well-being. These are things a user needs to be aware of. Obviously a little water retention is not a big deal or you would not have chosen an aromatizing compound to begin with, so unless you are particularly sensitive to estrogenic side-effects, keeping an estrogen receptor antagonist (Nolvadex or Clomid) handy, just in case, instead of running an aromatase inhibitor throughout, will allow you to get more mass out of a cycle.

Since Danazol is an anti-gonadotropin, the post-cycle use of Clomid or Nolvadex is required, maybe even in conjunction with a preceding HCG therapy to bring natural testosterone back, but since one would only really opt for Danazol in conjunction with suppressive aromatizing steroids, you would already be doing this anyway if you know what is good for you, so surely I'm just mentioning this for no reason (although one can never be too safe). There is no real use for other ancillaries with this compound.