You will receive an additional 10% discount on this cycle...

7x Proviron 25mg/20 Tablet
1x Decabolon 200
100 Tablet Winstrol and 3x Tamoxsifene box

Product Presentation: Proviron 25mg/20 Tablet

Proviron© is the Schering brand name for the oral androgen mesterolone (1 methyl-dihydrotestosterone). Just as with DHT, the activity of this steroid is that of a strong androgen which does not aromatize into estrogen. In clinical situations Proviron© is generally used to treat various types of sexual dysfunction, which often result from a low endogenous testosterone level. It can usually reverse problems of sexual disinterest and impotency, and is sometimes used to increase the sperm count. The drug does not stimulate the body to produce testosterone, but is simply an oral androgen substitute that is used to compensate for a lack of the natural male androgen.

Although this steroid is strongly androgenic, the anabolic effect of it is considered too weak for muscle building purposes. This is due to the fact that Proviron© is rapidly reduced to inactive metabolites in muscle tissue, a trait also characteristic of dihydrotestosterone, The belief that the weak anabolic nature of this compound indicated a tendency to block the androgen receptor in muscle tissue, thereby reducing the gains of other more potent muscle building steroids, should likewise not be taken seriously. In fact due to its extremely high affinity for plasma binding proteins such as SHBG, Proviron© may actually work to potentate the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes Proviron© is primarily used as an antiestrogen. It is believed to act as an antiaromatase in the body, preventing or slowing the conversion of steroids into estrogen. The result is somewhat comparable to Arimidex© (though less profound), the drug acting to prevent the buildup of estrogen in the body. This is in contrast to Nolvadex©, which only blocks the ability of estrogen to bind and activate receptors in certain tissues. The anti-aromatization effect is preferred, as it is a more direct and efficient means of dealing with the problem of estrogenic side effects. A related disadvantage to Nolvadex© is that if discontinued too early, a rebound effect may occur as high serum estrogen levels are again free to take action. This of course could mean a rapid onset of side effects such as gynecomastia and water retention. Most athletes actually prefer to use both Proviron© and Nolvadex©, especially during strongly estrogenic cycles. With each item attacking estrogen at a different angle, side effects are often greatly minimized.

The anti-estrogenic properties of Proviron© are not unique to this compound. A number of steroids have in fact demonstrated similar activity. Dihydrotestosterone and Masteron (2methyl-dihydrotestosterone) for example have been successfully used as therapies for gynecomastia and breast cancer due to their strong anti-estrogenic effect. It has been suggested that nandrolone may even lower aromatase activity in peripheral tissues where it is more resistant to estrogen conversion (the most active site of nandrolone aromatization seems to be the liver). The antiestrogenic effect of all of these compounds is presumably caused by their ability to compete with other substrates for binding to the aromatase enzyme. With the aromatase enzyme bound to the steroid, yet being unable to alter it, and inhibiting effect is achieved as it is temporarily blocked from interacting with other hormones.

This drug is also favored by many during contest preparations, when a lower estrogen/high androgen level is particularly sought after. This is especially beneficial when anabolics like Winstrol©, oxandrolone and Primobolan© are being used alone, as the androgenic content of these drugs is relatively low. Proviron© can supplement a wellneeded androgen, and bring about an increase in the hardness and density of the muscles. Women in particular find a single 25mg tablet will efficiently shift the androgen/estrogen ratio, and can have a great impact on the physique. Since this is such a strong androgen however, extreme caution should be taken with administration. Higher dosages clearly have the potential to cause virilization symptoms quite readily. For this reason females will rarely take more than one tablet per day, and limit the length of intake to no longer than four or five weeks. One tablet used in conjunction with 10 or 20mg of Nolvadex© can be even more efficient for muscle hardening, creating an environment where the body is much more inclined to burn off extra body fat (especially in female trouble areas like the hips and thighs).

The typical dosage for men is one to four 25 mg per tablets per day. This is a sufficient amount to prevent gynecomastia, the drug often used throughout the duration of a strong cycle. As mentioned earlier, it is often combined with Nolvadex© (tamoxifen citrate) or Clomid© (clomiphene citrate) when heavily estrogenic steroids are being taken (Dianabol, testosterone etc.). Administering 50mg of Proviron© and 20mg Nolvadex© daily has proven extremely effective in such instances, and it is quite uncommon for higher dosages to be required. And just as we discussed for women, the androgenic nature of this compound is greatly welcome during contest preparation. Here again Proviron© should noticeably benefit the hardness and density of the muscle, while at the same time increasing the tendency to burn off a greater amount of body fat. Proviron© is usually well tolerated and side effects (men) are rare with dosages under 100 mg per day. Above this, one may develop an excessively high androgen level and encounter some problems. Typical androgenic side effects include oily skin, acne, body/facial hair growth and exacerbation of a male pattern baldness condition, and may occur even with the use of a moderate dosage. With the strong effect DHT has on the reproductive system, androgenic actions may also include an extreme heightening of male libido. And as discussed earlier, Women should be careful around Proviron©. It is an androgen, and as such has the potential to produce virilization symptoms quite readily. This includes, of course, a deepening of the voice, menstrual irregularities, changes in skin texture and clitoral enlargement.

Proviron© is also not a c17 alpha alkylated compound, an alteration commonly used with oral anabolic/androgenic steroids. Not using this structure in the case of Proviron© removes the notable risk of liver toxicity we normally associate with oral dosing. We therefore consider this a "safe" oral, the user having no need to worry about serious complications with use. This steroid in fact utilizes the same 1-methylation we see present on Primobolan© (methenolone), another well tolerated orally active compound. Alkylation at the one position also slows metabolism of the steroid during the first pass, although much less profoundly than 17 alpha alkylation. Likewise Proviron© and Primobolan© are resistant enough to breakdown to allow therapeutically beneficial blood levels to be achieved, although the overall bioavailability of these compounds is still much lower than methylated oral steroids.

The popularity of Proviron© amongst bodybuilders has been increasing in recent years. Many experienced bodybuilders have in fact come to swear by it, incorporating it effectively in most markedly estrogenic cycles. Due to high demand Proviron© is now very easy to obtain on the black market. Most versions will be manufactured by Schering, and should cost about $1-$2 per 25 mg tab. In many instances this item is obtained via mail order, and here can sell for less than .50 per tab. This drug is packaged in both push-through strips and small glass vials, so do not let this alarm you. There is currently no need to worry about authenticity with this drug, as no counterfeits are known to exist. If money and availability does not prevent it, Arimidex© is actually a much better choice than Proviron© though. This drug was designed specifically as an antiaromatase, and works much more effectively than anything else we have available. Since this item is extremely expensive however, Nolvadex© and Proviron© will no doubt remain to be the "standard" antiestrogen regimen among athletes.

Product Presentation: Nandrolone Decanoate 200mg/ml, 10 ml Glass Vials

Nandrolone is a modification of testosterone (carbon atom removed from the 19th position) With an Anabolic/Androgenic ratio: 125:37, meaning it is highly anabolic (muscle building) and moderately androgenic (male characteristics). Due to nandrolones chemical structure it only aromatizes (converts to estrogen) slightly, at about 20% the rate of testosterone when it interacts with the aromatase enzyme. Ergo, estrogenic effects are not a major concern with its use. Of note, however, is that nandrolone is a progestin with a binding affinity of 20% to the progesterone receptor (PgR), so side effects are still possible, though rare. The development of breast tissue in males (gynecomastia) has been reported in some steroid.com users. One of the most popular anabolic steroid used in bodybuilding cycles, nandrolone is also (medically) used to treat severe debility or disease states and refractory anemias. It promotes tissue building processes, reverses catabolism (muscle destruction) and stimulates erythropoiesis (red blood cell production). This makes it a very useful drug to treat wasting disorders such as advanced H.I.V. , and also, makes it highly sought after by bodybuilders and athletes. Nandrolone is most commonly found with a cypionate, undecaonate, decanoate or plenylpropionate ester. Briefly explained, the ester determines how much of the given hormone is released over a period of time. Longer esters such as decanoate peak slowly and can keep stable blood plasma levels up to ten days, shorter esters such as the phenylpropionate peak more rapidly but the half-live is shorter. Shorter esters usually release much more active hormone per mg than longer esters, and of course, allow the drug´s effects to leave your system more quickly.. Nandrolone in general, has a number of benefits for athletes; it increases levels of serotonergic amines in the brain, these chemicals contribute to aggressive behavior, this could help athletes to train harder and improve speed and power.4 Nandrolone also increases levels of IGF-1 in muscle tissues. This may be another way that makes nandrolone highly anabolic. Nandrolone also benefits the athlete by increasing the number of androgen receptors (AR) one study showed that nandrolone given to rats at a dosage of 6mg/kg of bodyweight combined with muscle functional overload (muscle functional overload gives a similar effect to resistance training) had a 1,300% (!) increase in AR protein concentrations. There is a direct link to muscle growth and AR levels. Also seems to be a promising fat loss agent, men given the drug had reduced levels of subcutaneous (under skin) adipose(fat) tissue, visceral (gut) fat loss was not as good however. The fat loss effect seems though to be dose dependant, in one study Nandrolone at a daily dose of 1, 4, or 10mg per kg of bodyweight the 10mg dose had the greatest effect on fatloss, thus displaying a dose respondant curve with Nandrolone . The more you use, the more results you´ll get, with regards to this drug. Nandrolone is used to treat anemia by stimulating red blood cell production, and an increase in RBC count can improve endurance during exercise via better lactic acid clearing and oxygen delivery. The blood is also better enabled to carry nutrients to muscle tissue to aid in repair, administration also increases the rate of muscle glycogen repletion after exercise helping the athlete dramatically improve recovery after strenuous physical exercise. Athletes who require a high level of endurance in their chosen sport can benefit from the use of Nandrolone. A favorite with bodybuilders who suffer with sore joints, Nandrolone can also improve collagen synthesis (10), which may improve joint function and alleviate joint pains. Dosage : Standart dosage of Nandrolone is 2 mg per pound of body weight. For Example , 90 kg( 200pound) athlete should take 400 mg per week. Maximum dosages can be as high as 1000-1500 mg per week.

Product Presentation: Stanozolol 10mg/100 tablet

Structurally stanozolol is not capable of converting into estrogen. Likewise an anti-estrogen is not necessary when usiing this steroid, gynecomastia not being a concem even among sensitive individuals. Since estrogen is also the culprit with water retention, instead of bulk Winstrol produces a lean, quality look the physique with no fear of excess subcutaneous fluid retention. This makes it a favorable steroid to use during cutting cycles, when water and fat retention are a major concern. It is also very popular among athletes in combination strength/speed sports such as Truck and Field. In such disciplines oe usually does not want to carry around excess water weight, and may therefore find the raw mucle-growth brought about by Winstrol quite favorable over the lower quality mass gains of more estrogenic agents.

Product Description: Tamoxsifene 10mg/50 Tablets

Tamoxifene citrate is a non-steroidal anti-estrogenic drug, used widely in clinical medicine. It is specifically a Selective Estrogen-Receptor Modulator (SERM) of the triphenylethylene family, and possesses both estrogen agonist and antagonist properties. As such, it may act as an estrogen in some tissues while blocking the action of estrogen in others. In breast tissue tamoxifene citrate is a astrong anti-estrogen, and as a result it is commonly used in the treatment of hormone-responsive breast cancer in women. In some cases it is even utilized as a preventetive measure, taken by women with an extreamly high familial tendency for breast cancer. In male bodybuilders and athletes, tamoxifene citrate is commonly used (of-label) to counter the side effects caused by elevated estrogenes subsequend to the use of certain anabolic-androgenic steroids. The primary worry among the athletic/bodybuilding population is gynecomastia, or the very unsightly development of female breast tissue in men. This can be first noticed by the appearance of swelling or a smal lump under the nipple. If left to progress, this can develop into a large hard tissue gynecomastia that may be irreversable occurence without surgery. The estrogen can also lead to an increase in the level of water retained in the body, resulting in a notable loss of definiton  as the muscles begin to look smooth due to the retention of subcutaneous fluid. Fat storage may also be increased as estrogen levels rise in men. In fact, differences in the estrogen/androgen ratio are one of the reasons women have a higher body fat percentage, and different fat distribution (hips/thighs), than men. Tamoxifen citrate also posseses the ability to increase production of FSH (Follicile Stimulating Hormone) and LH (Luteinazing Hormone). This is accomplished by blocking negative feedback inhibiton caused by estrogen at the hypothalamus and pituitarity hormones. Since higher release of LH can stimulate the leydig's cells in the testes (men) to produce more testosterone, tamoxifene citrate can have a positive impact on one's serum testosterone level. This "Testosterone Stimulating" effect is an added benefit when preparing to conclude a steroid cycle. Since anabolic/androgenic steroids tend to suppress endogenous testosterone production , tamoxifene citrate can help restore a balance in hormone levels. It is commonly used as part of a comprehensive post cycle recovery program.