World Class Bodybuilding's

ALDACTONE

ANABOLICUM VISTER

ANADROL Oxymethylone

ANADUR nandrolone hexyloxyphenylpropionate

ANAPOLAN

ANDRIOL testosterone undecanoate

ANDRODERM

ANDROSTANOLONE

ARATEST 250-500-2500

CLENBUTEROL HYDROCLORIDE

CLOMID clomiphene citrate

CYCLOFENIL

CYTRADREN aminoglutethimide

CYTOMEL T-3

DANOCRINE danazol

DECA nandrolone decanoate

DETECTION TIMES

DIANABOL methandrostenlone - methandienone

DNP (2,4-Dinitrophenol)

DURABOLAN nandrolone phenylpropionate

DYNABOLAN

EPHEDRINE

EQUIPOSE- boldenone undecylenate

ESCICLINE formebolone

ESTANDRON

FINAPLIX

GHB gamma-hydroxybutyrate

HALOTESTIN fluoxymesterone

HCG human chorionic gonadotropin

HGH- HUMAN GROWTH HORMONE

INSULIN

L-THYROXINE T-4/ liothyronine sodium

LASIX Furosemide

LAURABOLAN nandrolone laurate

MASTERON

MEGAGRISEVIT clostebole acetate

METHANDRIOL methylandrostenediol dipropionate

METHYLTESTOSTERONE

MIOTOLAN furazabol

NAXEN naproxen

NELIVAR norethandrolone

NOLVADEX tamoxifen citrate

NUBIAN

OMNADREN-250

ORABOLAN

ORAL TURINABOL

OXANDRALONE

PARABOLAN trenbolone hexahydrobencylcarbonate

PRIMOBOLAN methenolone acetate

PROVIRON mesterlone

SPIRONOTHIAZ spironolactone/hydrochlorthiazide

STEN

STENBOLONE ACETATE

STENOX-HALOTESTIN

SUSTANON 250

TESLAC

TESTOSTERONE CYPIONATE

TESTOSTERONE ENANTHATE

TESTOSTERONE HYTHELATE

TESTOSTERONE PROPIONATE

TESTOSTERONE SUSPENSION

TESTOVIRON

TRENBOLONE ACETATE

TRIACANA

WINSTROL DEPOT- stanazolol- {INJECTABLES}

WINSTROL- stanazolol-orals

ALDACTONE

Remark: Internationally, numerous other compounds containing the substance spironolactone are available. Due to limited space they are not listed here. Aldactone is a diuretic and belongs to the subgroup of potassium--sparing diuretics. Aldactone is an aldosterone antagonist. It influences the body's own hormone, aldosterone, which accelerates the excretion of potassium and reduces the excretion of sodium and water. Simplified, aldosterone regulates the endogenous water household. The higher the aldosterone level, the more water is stored in the body. The use of Aldactone results in a significant reduction in the aldosterone level so that an increased excretion of sodium and water occurs while, at the same time, potassium is reabsorbed. This also explains why Aldactone is called a potassium-sparing diuretic since it does not cause a loss of potassium like thiazides and furosemides (lasix) do. Athletes must strictly observe that during the use of Aldactone no additional potassium is taken since this would cause a life-threatening increase in the serum potassium level. Potassium--sparing diuretics have relatively low diuretic effects so that Aldactone can be called a mild diuretic. It is interesting to note that Aldactone is also an antiandrogen since it reduces the androgen level. Female athletes take advantage of this characteristic by using it to minimize the virilization symptoms during steroid treatment or the symptoms after treatment. For this purpose Aldactone is normally taken daily for 10 to14 days, usually in a dose of 50 mg/day. In men this could cause problems since the relationship of the androgen level to the estrogen level changes in favor of the latter. Thus, common side effects in men include pain in the nipples and breast swelling (gynecomastia). Bodybuilders use Aldactone almost exclusively during the last week before a competition. Since this causes neither a dramatic nor an immediately noticeable draining effect, it is usually taken over 5-6 days in a dosage of 2 tablets of 50 mg daily. Both male and female athletes take it. The main problems in men consist of gynecomastia and possible impotence. Other side effects can be low blood pressure, muscle spasms, dizziness, gastrointestinal pain, vomiting, irregular pulse rate, and fatigue.

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ANABOLICUM VISTER

Substance: quinbolone Anabolicum Vister is an oral steroid produced only in Italy. It is administered in an unusual form since it is either taken as a capsule or in drops. The latter type of administration is not used by athletes. In schools of medicine Anabolicum Vister is used primarily in treating of the elderly, in particular women after menopause, and for the treatment of general diseases and symptoms of old age. This is due to the fact that AnabolicumVister is a very weak androgenic steroid which is well-tolerated. It has mainly an anabolic effect which stimulates the protein synthesis and has the welcome characteristic that it only slightly aromatizes. It also causes only a low retention of water and salt. In addition, the substance is not I 7-alpha alkalifying and consequently, not liver-toxic. However, all these positive characteristics make Anabolicurn Vister a very weak steroid which does not help athletes achieve significant improvements. Women, older athletes, and steroid novices may gain some advantages while the more advanced will be disappointed by its effect. Men usually need very high doses in the range of 80-120 mg/day to feel anything at all, while some women react with a small muscle gain and a nice strength gain by taking only 30-40 mg/day. As mentioned earlier, the side effects are minimal and usually occur in persons taking high doses and showing sensitivity to the androgenic residual effect. Thirty capsules come in a glass bottle with a screw cap, pack-aged in a matching box. Anabolicum Vister is rarely found on the black market since there are very few requests from athletes.

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ANADROL Oxymethylone

Substance: oxymetholone

Anadrol 50 is the strongest and, at the same time, also the most effective oral steroid. The compound has an extremely high androgenic effect which goes hand in hand with an extremely intense anabolic component. For this reason, dramatic gains in strength and muscle mass can be achieved in a very short time. An increase in body weight of 10 - 15 pounds or more in only 14 days is not un-usual. Water retention is considerable, so that the muscle diameter quickly increases and the user gets a massive appearance within record time. Since the muscle cell draws a lot of water, the entire muscle system of most athletes looks smooth, in part even puffy. Anadrol does not cause a qualitative muscle gain but rather a quantitative one which in the off-season is quite welcome. Anadrol "lubricates" the joints since water is stored there as well. On the one hand this is a factor in the enormous increase of strength and, on the other hand, it allows athletes with joint problems a painless workout. Powerlifters in the higher weight classes are sold on Anadrol. A strict diet, together with the simultaneous intake of Nolvadex and Proviron, can significantly reduce water retention so that a distinct increase in the solid muscles is possible. By taking Anadrol the athlete experiences an enormous "pump effect" during the workout in the exercised muscles. The blood volume in the body is significantly elevated causing a higher blood supply to the muscles during workout. Anadrol increases the number of red blood cells, allowing the muscle to absorb more oxygen. The muscle thus has a higher endurance and performance level.

Consequently, the athlete can rely on great power and high strength even after several sets. The highly androgenic effect of Anadrol stimulates the regeneration of the body so that the often-feared "overtraining" is unlikely. Although Anadrol is not a steroid used in preparation for a competition, it does help more than any other steroid during dieting to maintain the muscle mass and to allow an intense workout. Many bodybuilders therefore use it up to about one week before a competition, solving the problem of water retention by taking anti-estrogens and diuretics so that they will appear bulky and hard when in the limelight.

As for the dosage, opinions differ. A dosage sufficient for any athlete would be 0,5 - 0,8 mg per pound of body weight/day. This corresponds to 1-4 tablets; i.e. 50-200 mg/day. Under no circumstances should an athlete take more than four tablets in any given day. We are of the opinion that a daily intake of three tablets should not be exceeded. Those of you who would like to try Anadrol 50 for the first time should begin with an intake of only one 50 mg tablet. After a few days or even better, after one week, the daily dosage can be increased to two tab-lets, one tablet each in the morning and evening, taken with meals. Athletes who are more advanced or weigh more than 220 pounds can increase the dosage to 150 mg/day in the third week. This dos-age, however, should not be taken for periods longer than two to three weeks. Anadrol 50 should not exceed six weeks. After discontinuing Anadrol, it is important to continue steroid treatment with another compound since, otherwise, a drastic reduction takes place and the user, as is often observed, within a short period looks the same as before the treatment. No other anabolic/androgenic steroid causes such a fast and drastic loss in strength and mass as does Anadrol 50. Athletes continue their treatment with injectable testosterone such as Sustanon 250 or Testosterone enanthate for several weeks. Body-builders often combine Anadrol with Deca-Durabolin or Testosterone to build up strength and mass. A very effective stack which is also favored by professionals consists of Anadrol 100 mg +/day, Parabolan 228 mg +/week, and 5ustanon 500 mg +/week. This stack quickly improves strength and mass but it is not suitable for and steroid novices. Anadrol 50 is to be taken seriously and the prevailing bodybuilder mentality "more is better" is out of place.

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

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

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

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

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ANADUR nandrolone hexyloxyphenylpropionate

Substance: nandrolone hexyloxyphenylpropionate

Anadur is one of many steroids which contain the compound nandrolone. Although available in many countries athletes do not use it often. Since its effect is similar to Deca-Durabolin's most people see no reason to take Anadur. This product does, however, have a few characteristics which make it different from "Deca" and therefore an interesting drug. Anadur is the longest lasting nandrolone. After only one injection the substance remains active in the body for four weeks. Anadur, above all, has an anabolic effect which stimulates the protein synthesis and, as with all nandrolones, requires a high protein intake. Anadur is not a steroid to be used to achieve rapid gains in weight and strength but is a classic, basic anabolic steroid which can be stored in the body, allowing a slow but solid muscle gain and an even strength gain. Athletes using Anadur report less water retention than with Deca. For this reason some bodybuilders prefer Anadur when preparing for a competition. It must be observed, however, that in this phase usage of Anadur should be combined with stronger androgenic steroids such as Parabolan or Testosterone propionate. Because of its slow, even, and compatible effect it is mostly used during steroid treatments which last for several months. For the most part, progress made during this period usually remains after discontinuing the product. When taking 50-100 mg every 10 days some women normally show no virilization symptoms but it has been shown that only a few weeks of such use will result in some irreversible virilization for some women. They like to combine Anadur with Winstrol tablets, Primobolan S-tablets, or Oxandrolone. Men do not have to take anti-estrogens since Anadur aromatizes only lightly and only in rare cases does it lead to gynecomastia.

The side effects of Anadur are even less than those of Deca-Durabolin. Liver damage can be excluded so that it can even be taken by people with liver disease. Virilization symptoms such as acne, hoarseness, deep voice, hirsutism, and increase in libido only occur, if at all, in very sensitive women. A higher blood pressure, due to a low water and salt retention, cannot be excluded but rarely occurs. The use of testosterone stimulating compounds such as HCG or Clomid is not necessary since Anadur influences the hypothalamohypophysial testicular axis only slightly so that the endogenous testosterone production is not significantly reduced and the risk of a spermatogenic inhibition is minimal. Anadur is a very compatible steroid which improves the general condition and well-being of its user. Some athletes mention an improved psychological well being. As for the dos-age, good results can be obtained with 200 mg every 10 days. On the U.S. black market, one large ampule costs approx. $13 to $15. A U.S pharmaceutical product does not exist. The Belgian and Turkish Anadur, the French Anador, and the Greek version Anadurin are individually packed and costs approx. $10-15 per 50 mg/ampule on the black market. Insufficient availability on the black market forces athletes to use the more readily available Deca-Durabolin. Unlike Deca, there are no fakes of Anadur.

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ANAPOLAN

Anapolon has been the strongest, oral steroidal compound, which is a derivative of dihydrotestosterone, which has been currently only available for institutional use in Mexico. Clinically, Anapolon had been often prescribed in efforts to treat anemias that had been caused by deficient red cell production. The androgenic and high anabolic properties of Anapolon have been substandard of Testosterone, which had been perinined this compound to have also been a dramatic muscle-building product. Many athletes had claimed the strength and weight increases had been very substantial within is a relatively short period of time. This characteristic had allowed the compound of Anapolon to be a very popular choice of oral steroidal compounds amongst many athletes, primarily those of the male gender. Most athletes had frequently experienced a general weight increase of approximately 10 to 15 lbs or more, within two weeks with the administration of this compound. This of course, had been largely attributed to the tremendous amount of water retention which had immediately increased the muscle diameters, which in turn, had permitted a rapid increased size appearance. Consequently, this retained amount of water in the muscle cells and joints had also additionally provided a smooth appearance, as the size increase had been quantitative, not qualitative. An advantageous effect of the water retention however, had been the ability to eliminate, or having soothed associated joint problems, which had been due to this side effect's subsequent lubricating quality. This had often been appreciated by most athletes, as this characteristic had frequently allowed for intense workouts, which had often been previously somewhat restricted, due to associated aggravated pain in the joints.

The Anapolon oral steroidal compound had further increased the number of red blood cells, which in turn, had enabled the muscles to absorb more oxygen. This had generally resulted in the muscle being able to have endured more physical stress, which had been due to the significant increase in blood volume. A "pump" effect had often been experienced when training particular muscles, and had even become somewhat painful to the extent, that the performed exercise had frequently been required to have been abandoned, in order to have alleviated this sensation.

However, this perception of increased strength and power had commonly been desired by all athletes who had practiced the self-administration of this compound, as this sensation had usually been indicative that the compound of Anapolon had indeed, been performing to it's full capacity. Several athletes had also claimed that another distinguishing trait of Anapolon, had been the increased training duration's, as this compound had been able to have stimulated the regeneration of the body, which often had enabled further muscle-building progress, and had stalled the possibility of overtraining.

However, although the substance of Anapolon had been powerful, it unfortunately, also had imposed the highest threat for serious adverse reactions out of any oral or injectable steroids compounds. A few athletes had experienced excessive water retention which had sometimes resulted in high blood pressure. Anapolon had very high DHT levels, and had been very toxic to the liver, due to the characteristics of being C-17 alphaallrylated steroid. Although the Anapolon steroidal compound had been known for quick strength and mass gains, it's utilization had not been suitable for novices, and had only been used by some athletes after a certain development had been achieved; or consequently, the prior us of weaker steroid compounds had been experienced.

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ANDRIOL testosterone undecanoate

Substance: testosterone undecanoate

Andriol is a revolutionary steroid because, besides methyltestosterone, it is the only effective oral testosterone compound. Testosterone itself, if taken orally, is ineffective since it is reabsorbed through the portal vein (1) and immediately deactivated by the liver. The substance testosterone undecanoate contained in Andriol, however, is reabsorbed from the intestine through the lymphatic system, thus bypassing the liver and becoming effective. The liver function is not affected by this. Andriol aromatizes only minimally, meaning that only a very small part of the substance can be converted into estrogen, since the dihydrotestosterone does not aromatize. The users of Andriol therefore do not experience feminization symptoms such as gynecomastia or increased body fat. Andriol's non-aromatizing quality consists of the fact that the body's own hormone production is only affected after a long-term administration of very high dosages. Andriol should be the perfect steroid; however, this is not the case.

The disadvantage of Andriol is that it only becomes effective if taken in high doses. Even if a dose of 200 mg of Andriol/day is taken, the testosterone level in the blood is still too low for a bodybuilder to gain strength and muscle growth. The capsules, therefore, are effective for only a few hours so that 6-7 capsules, that is 240- 280 mg (minimum), must be taken daily to achieve good results comparable to those of injectable compounds. This, however, puts the athlete in a dosage range which begins to influence the hormone production and the compound now more readily converts into estrogen. Such a dose can also manifest itself in a higher retention of sodium and water. This is one factor which competing athletes must consider. Another disadvantage is Andriol's high price. A package with 60 capsules costs approximately $80 and the minimum daily dose of 6-7 capsules thus costs almost $8. For those athletes who would like to try Andriol 8 capsules (320 mg daily) should be taken. The capsules should be taken three times daily (approximately every 8 hours) after meals so that the substance can be properly reabsorbed. However, even this high dosage does not guarantee satisfactory results. Those of you who believe that you need even higher doses should then consider that it might be more sensible to switch to the injectable testosterone. The Andriol/ Oxandrolone stack gives athletes who do not yet have much experience with steroids a fairly large strength increase and also often substantial muscle growth. Andriol is quickly eliminated by the body it should also be considered for use before competitions requiring doping tests. Women should avoid Andriol since the androgenic component-common with testosterone-is also strongly developed in this compound. Andriol intake can occasionally lead to high blood pressure, retention of fluids, acne, sexual overstimulation, and, in women, the well-known virilization symptoms.

Andriol should be stored in a cool place (6 - 15 C), preferably in the refrigerator. Since the capsules are extremely sensitive to heat they can easily melt into an indefinable shape if left in direct sunlight, e.g. in a car.

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ANDRODERM

Androderm is a transdermal patch, designed to release testosterone over a 24-hour period, in a natural pattern resembling that of a healthy young man. This product is being used primarily by older men who have reached an age in which there body no longer produces sufficient amounts of testosterone ("Andropause"). Each patch contains 12.2 gm of testosterone, but according to the paperwork only about 2.5 mg is dispersed in each 24- hour application. Two patches are most commonly used, and are applied to the abdomen, back, thigh, or upper arm. Athletes would no doubt find this dosage insufficient, and will likely avoid this product all together. Quite a number of patches would have to be used for a strong effect, making it much easier to use an injectable testosterone instead

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ANDROSTANOLONE

Substance: androstanolone
Trade Names:
Andractim 2.5% gel Besins-Iscovesco FR; Piette B
Apeton 5 mg, 25 mg tab.; Fujisawa. Japan
Apeton Depot 2%, 5% inj. solution,- Fujisawa. Japan
Gelovit 2.5% gel Berenguer Infall ES

Androstanolone is identical to the body's own dihydrotestosterone which, as we know, is formed by the peripheral conversion of testosterone. Some therefore call Androstanolone a synthetic d1hydrotestosterone. This steroid has a predominantly androgenic effect and, due to its structure, cannot be converted into estrogen. For a fast buildup of power and muscle mass Androstanolone is of little value. It used to be the athlete's favorite competition steroid since it helped to obtain a harder muscle through a lower fat content by increasing the androgen level without aromatizing. Numerous athletes used Androstanolone during work-outs for doping tested championships since the substance remains in the body for only a short time and the testosterone/epitestosterone value is not influenced. Another positive characteristic is that the injectable version is not liver-toxic. Today, however, Androstanolone is rarely used by athletes. One reason for this is that almost all European and American compounds are no longer commercially available. The other reason is that most athletes use the still readily available Masteron which has similar effects. Neither the original nor a fake of Androstanolone is available on the black market.

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ARATEST 250-500-2500

Aratest2500 (ENANTHATE 200mg, PROPIONATE50mg /ml)
Aratest500 (TESTOSTERONE PROPIONATE 50mg)
Aratest250 (TESTOSTERONE PROPIONATE 25mg)

ARATEST is a new Mexican veterinarian steroid that has been getting a lot of attention from steroid users everywhere. There are three types: Aratest 2500, 500, and 250. Aratest 2500 is the most popular of the three containing 200mg of enanthate and 50 mg propionate per ml. This mixture comes in a 10ml vial and is manufactured by Lab Aranda. This new steroid makes a great mass builder when stacked with Dbol or Anadrol and when stacked with Deca, Winstrol, Equipoise, etc.
it has the benefits of good strength gains with low water retention. As a first time user you can easily gain 10-25lbs of good mass and has been compared to the gains of Sustanon 250. As a matter of fact some users report that the Aratest is a better product and costs much less! The black market prices range from $75-$100. It is a good idea to use Nolvadex, HCG, and Clomid when using Aratest because of the testosterone, especially at higher dosages. Be careful when buying Aratest on the black market because this steroid is new and is a good target to be faked. For more information on the Aratest 500 and 250
please see Testosterone Propionate in the "Drug Profiles" section.

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CLENBUTEROL HYDROCLORIDE

Substance: Clenbuterol hydrochloride

Remark: 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. 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 Clenbuterol is its distinct fat-burning effect. Clenbuterol burns fat without dieting because it increases the body temperature slightly, forcing the body to burn fat for this process. Due to the higher body temperature Clenbuterol magnifies the effect of anabolic/androgenic steroids taken simultaneously, since the protein processing is increased. 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. The compound is usually taken over a period of 8-10 weeks. Since Clenbuterol 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 per-spiration, 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, 70¢-$120 each.

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CLOMID clomiphene citrate

Substance: clomiphene citrate

Clomid is not an anabolic/androgenic steroid. Since it is a synthetic estrogen it belongs, however, to the group of sex hormones. In school medicine Clomid is normally used to trigger ovulation. Clomid also has a strong influence on the hypothalamohypophysial testicular axis. It stimulates the hypophysis to release more gonadotropin so that a faster and higher release of FSH (follicle stimulating hormone) and LH (luteinizing hormone) occurs. This results in an elevated endogenous (body's own) testosterone level. Clomid is especially effective when the body's own testosterone production, due to the intake of anabolic/androgenic steroids, is suppressed. In most cases Clomid can normalize the testosterone level and the spermatogenesis (sperm development) within 10- 14 days. For this reason Clomid is primarily taken after steroids are discontinued. At this time it is extremely important to bring the testosterone production to a normal level as quickly as possible so that the loss of strength and muscle mass is minimized. Even better results can be achieved if Clomid is combined with HCG or when Clomid is used after the intake of HCG.

Paradoxically, although Clomid is a synthetic estrogen it also works as an antiestrogen. The reason is that Clomid has only a very low estrogenic effect and thus the stronger estrogens which, for example, form during the aromatization of steroids, are blocked at the receptors. These would include those that develop during the aromatizing of steroids. This does not prevent the steroids from aromatizing but the increased estrogen is mostly deactivated since it cannot attach to the receptors. The increased water retention and the possible signs of feminization can thus be reduced or even completely avoided. Since the antiestrogenic effect of Clomid is lower than those found in Proviron, Nolvadex, and Teslac it is mainly taken as a testosterone stimulant. Clomid is a medication that promotes the production of the body's own stimulating hormone, gonadotropin, which in turn increases the testosterone level. It is, for example, administered to women as a so-called antiestrogen to trigger ovulation (ovulation stimulator).

Side effects of Clomid are very rare if reasonable dosages are taken. Possible side effects are climacteric hot flashes and occasional visual disturbances which can manifest themselves in blurred vision, giving flickering or flashing. Should visual disturbances occur, the manufacturer recommends discontinuing Clomid treatment. Inadequate liver functions cannot be excluded; however, they are very unlikely. In women enlargement of the ovaries and abdominal pain can occur since Clomid stimulates the ovaries. When taking Clomid multiple pregnancies are possible as well. As for the dosage, 50-100 mg/day (1 -2 tablets) seems to be sufficient. The tablets are usually taken with fluids after meals. If several tablets are taken it is recommended that they be administered in equal doses distributed through-out the day. The duration of intake has been rumored to not be taken for longer than 10-14 days. This is incorrect. Clinical studies with male patients have shown clomid to be used for up to a year or longer. Most athletes begin with 100 mg/day, taking one 50 mg tablet every morning and evening after meals. After the fifth day the dosage is often reduced to only one 50 mg tablet per day It is normally not necessary to take the compound for more than ten days in order to increase the endogenous testosterone production. Clomid is relatively expensive. A package with 10 tablets costs approx. $35 - 45 on the black market.

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CYCLOFENIL

Substance: cyclofenil

Cyclofenil is not an anabolic/androgenic steroid. Cyclofenil works as an antiestrogen and, at the same time, increases the body's own testosterone production. Since Cyclofenil itself is only a very weak and mild estrogen it occupies, the estrogen receptors, and prevents the stronger estrogens from bonding with the receptors thereby becoming active. As a matter of fact, this works so well that some athletes take Cyclofenil during the steroid treatment in order to maintain a low estrogen level. The result is a lower water retention produced by the steroids and less gynecomastia. The athlete has a harder appearance, making this is a compound that can potentially be taken during the preparation for a competition. Bodybuilders, however, use it less frequently since they prefer the more readily available Nolvadex and Proviron compounds.

Based on our experience, the dosage lies between 400 and 600 mg/day. Lower dosages usually do not show satisfying results. Cyclofenil, for this purpose, is either used during steroid treatment, after the treatment, before competitions with doping tests, or by "natural bodybuilders". Like HCG and Clomid, Cyclofenil is ineffective in women since it has a positive influence on the male hormone system. Even in men, the increased testosterone level attributed to the effect of Cyclofenil is not high enough to speak of drastic improvements; however, strength gains, a slight gain in body weight, a noticeable increase in energy, and a higher regeneration are possible. These results are noticeable particularly in advanced athletes who have little or no experience with steroids. Cyclofenil needs a response time of approximately one week before it becomes effective.

In a few cases athletes experience a light acne, increased sexual desire, and hot flashes. The first two secondary symptoms are especially indicative that the compound is actually effective. After discontinuance some athletes report a depressed mood and a slight decrease in physical strength. Those who take Cyclofenil as an anti-estrogen during steroid treatment could experience a rebound effect when the compound is discontinued

In the meantime, it is very difficult to find Cyclofenil and it is rarely found on the black market. The Mexican Fertodur by Schering contains 16 tablets of 200 mg each which are welded into aluminum foil with the name "Fertodur Tabletas" printed on top. Such a package costs $25-30 on the black market.

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CYTRADREN aminoglutethimide

Substance: aminoglutethimide

Cytadren is not an anabolic/androgenic steroid. Cytadren inhibits the buildup of androgens, estrogens, and the suprarenal cortical hormones (glucocorticoids and mineralocorticoids). Cytadren has a highly antiestrogenic effect since, on the one hand, it inhibits the body's own estrogen production and, on the other hand, it obviates the conversion of androgens into estrogens. This is especially encouraging since it helps to keep the estrogen level of bodybuilders low. The second highly interesting point is that Cytadren prohibits the buildup of adrenocortical hormones. It obviates the production of endogenous cortisone like no other compound by inhibiting the conversion of cholesterol into cortisone. For this reason, Cytadren, in school medicine, is used for the treatment of Cushing's syndrome, a hyperfunction of the adrenal glands which causes the body to overproduce cortisone. Consequently, it reduces the cortisone level, which has several advantages for the athlete. Cortisone is a catabolic hormone and catabolic is the exact opposite of anabolic. Cortisone prevents the protein synthesis in the muscle cell, resulting in a muscular atrophy by breaking down amino acids in the muscle cell.

The human body constantly releases cortisone and reacts to stress situations such as intense training by increasing its cortisone re-lease. Natural bodybuilders, therefore, after a short time, experience a stagnation in their development since the release of the body's cortisone is higher than the anabolic effect of working out. The more advanced the athlete and the harder his workout, the more his cortisone level will increase.

If the release of cortisone can be successfully obviated or at least considerably reduced the ratio of anabolic hormones to catabolic hormones in the body shifts in favor of the former. This results in an increase in muscle mass and body strength. And Cytadren achieves exactly these results; however, there is one problem. Cytadren reduces the cortisone level so effectively that the body tries to balance this by hypophysially producing more ACTH (adenocorticotropic hormone), thus stimulating the secretion of cortisone by the adrenal glands. Thus in school medicine, when treating Cushing's syndrome, a low dose of oral hydrocortisone is used to prevent the hypophysis from producing ACTH. The dose is so low that the cortisone level in the blood does not rise substantially. And this is exactly the problem. Cytadren reduces the cortisone level which the body balances by producing ACTH, thus neutralizing the effect of Cytadren. If exogenous hydrocortisone is taken no ACTH is produced; however, this also reduces the effect of Cytadren. It is therefore necessary to find an administration schedule that prevents or delays the body's own production of ACTH. Since the body does not show abrupt reactions when the cortisone level is lowered by the intake of Cytadren, the compound must be taken over several days before the body begins reacting. If Cytadren is only taken for a period of two days and then discontinued for two entire days, it seems logical that the body will not have enough time to react accordingly, thus interrupting the production of ACTH in the hypophysis. Similar to Clenbuterol, an alternating administration schedule with two days of administration and two days of abstinence is created. Another problem needs to be solved since Cytadren, as mentioned earlier, inhibits the body's own production of androgen. Cytadren, therefore, should not be used by natural bodybuilders. The solution to this problem is to take a long-term effective testosterone such as Testosterone enanthate simultaneously. Testoviron Depot 250, for example, can be considered as one such possible compound.

As for the question of dosage, we have arrived at a very interesting point. In school medicine the dosage for the treatment of Cushing's syndrome is between 2 and 7 tablets per day. Since not enough athletes~ have used this compound so far, we do not have enough experimental data. Due to the fact that the cortisone level of athletes is not as high as in persons who suffer from a hyper-function of the adrenal glands, it is probable that lower dosages are sufficient. A dose of more than 250mg/day is not recommended and should be taken very carefully. A good example of dose is: half a tab 125mg in the morning and 62.5mg (quarter tab) every six hours. Make sure to not abruptly discontinue as cortisol rebound may occur. The tablets are always taken individually, in regular intervals throughout the day, and taken best during meals. How long should it be taken? This question is difficult to answer but, considering that the body can-some-times increase the production of ACTH, it is advised that the compound is not used longer than 4-6 weeks. (We must also consider potential side effects, which we will discuss in a minute.) An-other interesting aspect: Cytadren is (as of yet) not on any doping list. We have heard from reliable informants that a combination of Cytadren, growth hormones, and a low quantity of injectable testosterone is the new hit among athletes of any field, since it allows the athlete to pass any doping test.

Thus the side effects of Cytadren need to be looked at and they are, unfortunately, numerous and sometimes very severe. The most common side effects are fatigue and dizziness. Lack of concentration, restlessness, depression, apathy, and sleeping disorder are less common but possible. Even rarer and mostly depending on the doses are nausea, vomiting, gastrointestinal pain, diarrhea, and headaches. A possible rash and the already-mentioned fatigue and dizziness are usually initial symptoms and these can be minimized by taking slowly increasing dosages, or they may simply disappear. The package insert of Ciba-Geigy GmbH Ger-many also states that in some cases there is an inadequate thyroid function which requires treatment. It is therefore recommended that the thyroid gland be supervised by a physician during intake of Cytadren. Another problem that can occur is liver disease. Cases of reduced counts of the white blood cells, the blood platelets, and even of all blood cells have been reported. Those who plan to try Cytadren should carefully read the package insert. It has been our experience that athletes, due to the reduced cortisone level, complain about joint pain and are also exposed to a higher risk of getting injured. There is no question that Cytadren is effective when taken according to the two-day alternating ad-ministration schedule; however, the athlete should carefully consider the cost/benefit factor prior to taking the compound. Cytadren is in U.S. pharmacies only available by prescription. A package with 100 tablets of 250 mg each costs $190.-, so that Cytadren is not a budget-priced compound. Each package contains 10 push-through strips of 10 tablets each. The tablets are indented on one side with an imprinted "G" on both the right and left of the breakage line. On the other side of the tablet the letters "CG" are punched in. Cytadren is rarely found on the black market. Back to the Top

CYTOMEL T-3

Substance: liothyronine sodium
Cytomel is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodidethyronine (L-T3). The thyroid of a healthy person usually produces two hormones, the better known Lthyroxine (L-T4) and the aforementioned L-triiodine-thyronine (L-T3). Since Cytomel is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-T3 is clearly the stronger and more effective of these two hormones. This makes Cytomel more effective than the commercially available LT4 compounds such as L-thyroxine or Synthroid. L-T3 has proven to be 4-5 times more biologically active and to take effect more quickly than L-thyroxine (L-T4)." In school medicine Cytomel is used to treat thyroid insufficiency (hypothyroidism). Among other secondary symptoms are obesity, metabolic disorders, and fatigue. Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking Cytomel, which causes a faster conversion of carbohydrates, proteins, and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means in-creased fat burning. Competing bodybuilders, in particular, use Cytomel during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of Cytomel report that by the simultaneous intake of steroids, the steroids become mote effective, most likely as the result of the faster conversion of protein.

To a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and de-fined look in photos, eat fast food and iron this out by taking Cytomel. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of Cytomel, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat. Cytomel is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given today's standards. A drastic reduction of food and calories below the 1000 caloric/day mark can often be avoided by taking Cytomel. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of Cytomel in a reasonable dosage is certainly "healthier" than an extreme hunger diet.

As for the dosage, one should be very careful since Cytomel is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25-mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100-mcg/ day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also impor-tant that Cytomel not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. Those who take high dosages of Cytomel over a long period of time are at risk of developing a chronic thyroid insufficiency. As a consequence, the athlete might be forced to take thyroid medication for the rest of his life. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and -not be ended abruptly. Those who plan to take Cytomel should first consult a physician in order to be sure that no thyroid hyperfunction exists.

Possible side effects are: heart palpitation, trembling, irregular heartbeat, heart oppression, agitation, shortness of breath, excretion of sugar through the urine, excessive perspiration, diarrhea, weight loss, psychic disorders, etc., as well as symptoms of hypersensitivity." Our experience is that most symptoms consist of trembling of hands, nausea, headaches, high perspiration, and increased heartbeat. These negative side effects can often be eliminated by temporarily reducing the daily dosage. Those who use Cytomel over several weeks will experience a decrease in muscle mass. This can be avoided or delayed by simultaneously taking steroids. For the most part, since Cytomel also metabolizes protein, the athlete must eat a diet rich in protein. L-T3 can usually be found quite easily. 100 tablets of 0.05 mg each cost approx. $40. It is unlikely that there will be fakes.

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DANOCRINE danazol

Danocrine is an antigonadotropin. In school medicine it is used to treat hormone-related disorders. One such disorder, for example, is the hormone-related breast enlargement in men, better known as gynecomastia. Bodybuilders can use Danocrine to minimize*possible feminization caused by the aromatizing of steroids. It is our experience that the daily dose should be around 400 mg. Danocrine has a mild androgenic effect but no anabolic effect. The possible side effects such as virilization symptoms, hot flashes, perspiration, in-creased libido, increased liver values, and high blood pressure through retention of fluids are highly dependent on the dose and they usually decrease again later. It is difficult to find Danocrine on the black market since it is rarely used by athletes. The official price for 100 capsules of 200 mg each is $330. Fakes are not known at this time

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DECA nandrolone decanoate

Deca-Durabolin is a brand name of Organon Company, the manufacturer of the drug containing the substance nandrolone decanoate. Although nandrolone decanoate is still contained in many generic compounds, almost every athlete connects this substance with Deca-Durabolin. Most common are the administrations of 5 0 mg/ml and 100 mg/ml. Deca-Durabolin is the most widespread and most commonly used injectable steroid. Deca's large popularity can be attributed to its numerous possible applications and, for its mostly positive results. Deca-Durabolin causes the muscle cell to store more nitrogen than it releases so that a positive nitrogen balance is achieved. A positive nitrogen balance is synonymous with muscle growth since the muscle cell, in this phase, assimilates (accumulates) a larger amount of protein than usual. The same manufacturer, however, points out on the package insert that a positive nitrogen balance and the protein building effect that accompany it will occur only if enough calories and proteins are supplied. One should know this since, otherwise, satisfying results with Deca cannot be obtained. The highly anabolic effect of Deca-Durabolin is linked to a moderately androgenic component, so that a good gain in muscle mass and strength is obtained. At the same time, most athletes notice considerable water retention which, no doubt, is not as distinct as that with injectable testosterones but which in high doses can also cause a smooth and watery appearance. Since Deca also stores more water in the connective tissues, it can temporarily case or even cure existing pain in joints. This is especially good for those athletes who complain about pain in the shoulder, elbow, and knee; they can often enjoy pain-free workouts during treatment with Deca-Durabolin. Athletes use Deca, depending on their needs, for muscle buildup and in preparation for a competition.

Deca is suitable, even above average, to develop muscle mass since it promotes the protein synthesis and simultaneously leads to water retention. The optimal dose for this purpose lies between 200 and 600 mg/week. Scientific research has shown that best results can be obtained by the intake of 2- mg/pound body weight. Those who take a dose of less than 200 mg/week will usually feel only a very light anabolic effect which, however, increases with a higher dosage. Most male athletes experience good results by taking 400 mg/week. Steroid novices usually need only 200 mg/week. Deca works very well for muscle buildup when combined with Dianabol and Testosterone. The famous Dianabol/ Deca stack results in a a fast and strong gain in muscle mass. Most athletes usually take 15-40 mg Dianabol/day and 200-400 mg Deca/week. Even faster results can be achieved with 400 mg Deca/week and 500 mg 5ustanon 250/week. Athletes report an enormous gain in strength and muscle mass when taking 400 mg Deca/week, 500 mg Sustanon 250/week, and 30 mg Dianabol/day. Deca is a good basic steroid which, for muscle buildup, can be combined with many other steroids.

A conversion into estrogen, that means an aromatizing process, is possible with Deca-Durabolin but occurs at a lower rate than ex: testosterone. During competitions with doping tests Deca must not be taken since the metabolites in the body can be proven in a urine analysis up to 18 months later. The risk of potential water retention and aromatizing to estrogen can be successfully prevented by combining the use of Proviron with Nolvadex. A preparatory stack often observed in competing athletes includes 400 mg/week Deca-Durabolin, 50 mg/day Winstrol, 228 mg/week Parabolan, and 25 mg/day Oxandrolone.

Although the side effects with Deca are relatively low with dosages of 400 mg/week, androgenic-caused side effects can occur. Most problems manifest themselves in high blood pressure and a pro-longed time for blood clotting, which can cause frequent nasal bleeding and prolonged bleeding of cuts, as well as increased production of the sebaceous gland and occasional acne. Some athletes also report headaches and sexual overstimulation. When very high dos-ages are taken over a prolonged period, spermatogenesis can be inhibited in men, i.e. the testes produce less testosterone. The reason is that Deca-Durabolin, like almost all steroids, inhibits the release of gonadotropins from the hypophysis.

Women with a dosage of up to 100 mg/week usually experience no major problems with Deca. At higher dosages androgenic-caused virilization symptoms can occur, including deep voice (irreversible), increased growth of body hair, acne, increased libido, and possibly clitorihypertrophy. Women who experience disturbance even at a weekly dose of only 50 mg/week of Deca-Durabolin, are often better off taking the earlier mentioned and faster-acting Durabolin. Unlike the long-acting Deca, when Durabolin is administered once or twice weekly in a dosage of 50 mg, no concentration of undesired amounts of androgens occur. Since most female athletes get on well with Deca-Durabolin a dose of Deca 50 mg +/week is usually combined with Oxandrolone 10 mg +/day Both compounds, when taken in a low dosage, are only slightly androgenic so that masculinizing side effects only rarely occur. Deca, through its increased protein synthesis, also leads to a net muscle gain and Oxandrolone, based on the increased phosphocreatine synthesis, leads to a measurable strength gain with very low water retention. Other variations of administration used by female athletes are Deca and Winstrol tablets, as well as Deca and Primobolan S-tablets.

A great disadvantage of Deca-Durabolin is its high price. In the U.S. a 50 mg ampule costs approx. $10 - 12. Deca-Durabolin in strengths of 200 mg/2 ml ampules; usually cost around $30 per ampule. Because of its great popularity and the high demand that goes along with it, there are many fakes of Deca-Durabolin