Testosterone has a profound

ability to protect your hard earned muscle from the catabolic (muscle wasting) glucocorticoid hormones (11), and increase red blood cell production (12), and as you may know, a higher RBC count may improve endurance via better oxygenated blood. The former trait increases nitrogen retention and muscle building while the latter can improve recovery from strenuous physical activity, as well as increase endurance and tolerance to strenuous exercise.

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/or Clomid - Nolvadex are a must when discontinuing a cycle.

Molecular weight of base: 650.9776

The following is a list of the most common side effects:

For athletes using anabolic steroids, 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.

Finasteride that is a specific inhibitor of 5a-reductase. Proscar is the enzyme responsible for converting testosterone into DHT (dihydrotestosterone). Proscar can efficiently reduce the serum concentration of DHT, therefore Proscar minimizes the unwanted androgenic effects that result from its presence. Propecia is the same drug but the tablet contains only 115 of the Proscar dosage. Scientists have long believed that DHT was the main culprit in many cases of male hair

loss (along with genetic factors), so there was little doubt after the release of Proscar that Finasteride would eventually be used for this purpose.

Those who are more interested in strength and less in body mass can combine Dianabol with either Oxandrolone or Winstrol tablets. The additional intake of an injectable steroid does, however, clearly show the best results. To build up mass and strength, Sustanon, Testosterone enanthate,Testosterone cypionate at 250 mg per week and/or Deca-Durabolin at 200 mg/week are suitable. To prepare, for a competition, Dianabol has only limited use since it causes

distinct water retention in many athletes and due to its high conversion rate into estrogen it complicates the athlete's fat breakdown. Those of you without this problem or who are able to control it by taking Nolvadex or Proviron, in this phase should use Dianabol together with the proven Parabolan, Winstrol Depot, Masterject, Oxandrolone, etc.

Drive (boldenone/methylandrostenediol blend)

What Is VIAGRA?

Although Sustanon does not aromatize excessively when taken in a reasonable dosage many people, in addition, also take an antiestrogen such as Nolvadex and/or Proviron to prevent possible estrogen-linked

side effects.

Estrogenic Activity: low Progestational Activity: moderate.

Prescription Phentermine Drug Information

It is important to note however, that this drug does not directly convert to estrogen in the body. Oxymetholone is a derivative of dihydrotestosterone, which gives it a structure that cannot be aromatized. As such, many have speculated as to what makes this hormone so troublesome in terms of estrogenic side effects. Some have suggested that it has progestational activity, similar to nandrolone, and is not actually estrogenic at all. Since the obvious side effects of both estrogens

and progestins are very similar, this explanation might be a plausible one. However we do find medical studies looking at this possibility. One such tested the progestational activity of various steroids including nandrolone, norethandrolone, methandrostenolone, testosterone and oxymetholone. It reported no significant progestational effect inherent in oxymetholone or methandrostenolone, slight activity with testosterone and strong progestational effect inherent in nandrolone and norethandrolone. With such findings it starts to seem much more likely that oxymetholone can intrinsically activate the estrogen receptor itself, similar
to but more profoundly than the estrogenic androgen methAndriol. If this is the case we can only combat the estrogenic side effects of oxymetholone with estrogen receptor antagonists such as Nolvadex or Clomid, and not with an aromatase inhibitor. The strong anti-aromatase compounds such as Arimidex, Femara, or Aromasin would prove to be totally useless with this steroid, as aromatase is not involved.

They will give you advice on what to do, which might include:

The main difference between propionate, cypionate, and enanthate is the respective duration of effect. In contrast to the long-acting enanthate

and cypionate depot steroids, propionate has a distinctly lower duration of effect. Testosterone proprionate has a duration of effect of 1 to 2 days. A noticable difference is that the athlete get a lot less water retention with propionate. Since propionate is quickly effective, often after only one or two days, the athlete experiences an increase of his training energy, a better pump, an increased appetite, and a slight strength gain. As an initial dose most athletes prefer a 50-100 mg injection. This offers two options: First, because of the rapid initial effect of the propionate ester one can initiate a several week long steroid
treatment with Testosterone Enanthate. Those who cannot wait until the depot steroids become effective inject 250 mg of Testosterone Enanthate and 50 mg of Testosterone propionate at the beginning of the treatment. After two days, when the effect of the propionates decreases, another 50 mg is injected. Two days after that, the elevated testosterone level caused by the propionate begins to decrease. By that time, the effect of the enanthates in the body would be present; no further propionate injections would be necessary. Thus the athlete rapidly reaches and maintains a high testosterone level for a long time due to the
depot testo. This, for example, is important for athletes who with Anadrol 50 over the six week treatment have gained several pounds and would now like to switch to testosterone. Since Anadrol 50 begins its "breakdown" shortly after use of the compound is discontinued, a fast and elevated testosterone level is desirable.

Harifin side effects

Diazepam is classified as pregnancy category D because it can cause harm to the fetus when administered to pregnant women. Positive evidence of human fetal risk exists based on investigational, marketing, or human studies, but the potential benefit to the mother may

outweigh the potential risks to the fetus. Diazepam is distributed into breast milk and can cause sedation, feeding difficulties, and weight loss in the nursing infant. The use of diazepam during breast-feeding is generally not recommended.

The steroid dianobol a.k.a. Anabol has a very strong androgenic and anabolic effect which manifests itself in an enormous build up of strength and muscle mass. Dianabol is simply a mass building steroid that works quickly and reliably. A weight gain of 2-4 pounds per week in the first six weeks is normal with dianobol.

In May 2005, the U.S. Food and Drug Administration

found that tadalafil (along with other PDE5 inhibitors) could lead to vision impairment in certain patient groups, including diabetics. An investigation is currently ongoing.

For the bodybuilder, the water retention that goes hand in hand with Testosterone enanthate cuts both ways. Certainly, one gets rapidly massive and strong; however, one's reflected image after a few weeks often shows completely flat, watery, and puffy muscles. The muscles appear as if they have been pumped up with air to new dimensions, yet during flexing nothing happens. Those who do not believe this should bother to go visit the so-called "bodybuilding

champions" during the OFF-season when these exaggerated quantities of "Testo" come in. A look at the now defunct bodybuilding magazine WBF makes it even clearer. An additional problem when taking Testosterone enanthate is that the conversion rate to estrogen is very high. This, oil one hand, leads the body lo store more fat; on the other hand, feminization symptoms (gynecomastia) are not unusual. However, it must be clearly stated that this depends on the athlete's predisposition. By all means, there are athletes who even with 1000 mg+/week do not show feminization symptoms or fat deposits and who suffer very low water
retention. Others, however, develop pain in their nipples by simply looking at a Testoviron-Depot ampule. Yet the additional intake of Nolvadex and Proviron should be considered at a dosage level of 1000 mg+/week. As already mentioned, Testo is effective for everyone, whether a beginner or Mr. Olympia. Testosterone enanthate also strongly promotes the regeneration process. This leads to distinctly shorter overcompensation phases, an increased feeling of well-being, and a distinct energy increase. This is also the reason why several athletes are able to work out twice daily for several hours six times a week and continue to build

up mass and strength. Those who can work out again ,two hours after a hard leg workout know that testo works. Athletes who take Testosterone enanthate report an excessively strong pump effect during training. This "steroid pump" is attributed lo an increased blood volume with a higher oxygen supply and a higher quantity of red blood cells. Those who take mega doses of Testosterone enanthate will already feel an enormous pump in their upper thighs and calves when climbing stairs. Despite this we recommend that steroid novices stay away from all testosterone compounds. To make it very clear: Those who have never taken steroids

do not yet need any testosterone and should wait until later when the "weaker" steroids begin to have little effect. For the more advanced, Testosterone enanthate can either be taken alone or in combination with oilier compounds.

Formula: C20 H24 O3

The body's own production of testosterone 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.

Propecia is for men only. Women who are or may potentially be pregnant must not use Propecia because of the risk that the finasteride may cause a specific kind of birth defect. Likewise, women should avoid handling tablets that are crushed or broken. Propecia tablets are coated to prevent contact with the active ingredient during normal handling.

Manufacturer: Cattle implants, British Dragon, Various

The undesired effect of growth hormones, the so-called side effects, are also a very interesting and hotly-discussed issue. Above all it must be said: STH has none of the typical side effects

of anabolic/androgenic steroids including reduced endogenous testosterone production, acne, hair loss, aggressiveness, elevated estrogen level, virilization symptoms in women, and increased water and salt retention. The main side effects that are possible with STH are an abnormally small concentration of glucose in the blood (hypoglycemia) and an inadequate thyroid function. In some cases antibodies against growth hormones are developed but are clinically irrelevant. What about the horror stories about acromegaly, bone deformation, heart enlargement, organ conditions, gigantism, and early death? In order to answer this question
a clear differentiation must be made between humans before and after puberty. The growth plates in a person continue to grow in length until puberty. After puberty neither an endogenous hypersection of growth hormones nor an excessive exogenous supply of STH can cause additional growth in the length of the bones. Abnormal size (gigantism) initially goes hand in hand with remarkable body strength and muscular hardness in the afflicted; later, if left untreated, it ends in weakness and death. Again, this is only possible in pre-pubescent humans who also suffer from an inadequate gonadal function (hypogonadism). Humans who suffer

from an endogenous hypersecrehon after puberty and whose normal growth is completed can also suffer from acromegaly. Bones become wider but not longer. There is a progressive growth in the hands and feet and enlargement of features due to the growth of the lower jaw and nose. What the authorities like to do now is to present extreme cases of athletes suffering from these malfunctions in order to discourage others and to drum into athletes the fact that with the exogenous supply of growth hormones they would suffer the same destiny. This, however, is very unlikely, as reality has proven. Among the numerous athletes using STH comparatively
few are seven feet tall Neanderthalers with a protruded lower jaw, deformed skull, claw like hands, thick lips, and prominent bone plates who walk around in size 25 shoes. In order to avoid any misunderstandings, we do not want to disguise the possible risks of exogenous STH use in adults and healthy humans, but one should at least try to be openminded. Acromegaly, diabpetes, thyroid insuficiency, heart muscle hypertrophy, high blood ressure, and enlargement of the kidneys are theoretically possible if STH is used excessively over prolonged periods of time; however, in reality and particularly when it comes to the external
attributes, these are rarely present. Some athletes report headaches, nausea, vomiting, and visual disturbances during the first weeks of intake. These symptoms disappear in most cases even with continued intake. The most common problems with STH occur when the athlete intends to inject insulin in addition to STH. The substance somatropin is available as a dried powder and before injecting it must be mixed with the enclosed solution-containing ampule. The ready solution must be injected immediately or stored in the refrigerator for up to 24 hours. It is usually recommended that the compound be stored in the refrigerator. With

the exception of the remedy Saizen the biological activity of growth hormones is usually not impaired when storing the dry substance at 15-25 C (room temperature); however, a cooler place (2-8° C) is preferable. It is noted that for the U.S.-American growth hormones compounds, the substance content is not given in I.U.(International Units) but in mg (milligrams). Since l mg corresponds to exactly 2.7 I.U. the 5mg solution of the compound Humatrope by Lilly contains exactl 13.5 I.U. of Somatropin. The 10 mg solution of the Protropin compound by the Genentech therefore contains 27 I.U. of Somatropin. In American powerlifting

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

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

*  = Integral component

of DNP program

Anabolic steroids are not recommended during pregnancy. They may cause the development of male features in the female fetus and premature growth and development of male features in the male fetus. Be sure you have discussed this with your doctor.

Each 10 ml multidose vial contains 250 mg per ml.

Proviron has four distinct uses in the world of bodybuilding. The first being the result of its structure. It is 5-alpha reduced and not capable of forming estrogen, yet it nonetheless has a much higher affinity for the aromatase enzyme (which converts testosterone to estrogen) than testosterone does.

That means in administering it with testosterone or another aromatizable compound, it prevents estrogen build-up because it binds to the aromatase enzyme very strongly, thereby preventing these steroids from interacting with it and forming estrogen. So Mesterolone use has the extreme benefit of reducing estrogenic side-effects and water retention noted with other steroids, and as such still help to provide mostly lean gains. Its also been suggested that it may actually downgrade the actual estrogen receptor making it doubly effective at reducing circulating estrogen levels.

Mesterolone is an orally active, 1-methylated

DHT. Like Masteron, but then actually delivered in an oral fashion. DHT is the conversion product of testosterone at the 5-alpha-reductase enzyme, the result being a hormone that is 3 to 4 times as androgenic and is structurally incapable of forming estrogen. One would imagine then that mesterolone would be a perfect drug to enhance strength and add small but completely lean gains to the frame. Unfortunately there is a control mechanism for DHT in the human body. When levels get too high, the 3alpha hydroxysteroid dehydrogenase enzyme converts it to a mostly inactive compound known as 3-alpha (5-alpha-androstan-3alpha,17beta-diol),

a prohormone if you will. It can equally convert back to DHT by way of the same enzyme when low levels of DHT are detected. But it means that unless one uses ridiculously high amounts, most of what is administered is quite useless at the height of the androgen receptor in muscle tissue and thus mesterolone is not particularly suited, if at all, to promote muscle hypertrophy.

Athletes also find that the injectable version is far superior to the oral. Dosages range from 3-5 ccs per week for men, 1-2 ccs in women. Oral dosages are usually in the area of 16-30 mg per day for men, 4-8 mg for women.

Side effects

are very mild, liver stress can occur.

Sodium Chloride Injection Water

In this study there was a preferential preservation of type IIb muscle fibers in aging mice. These are the fibers most sensitive to muscle hypertrophy from training and they are also the first fibers to disappear with aging. In the mice receiving the engineered virus, there was also a preservation of the motor neuron, leading to an increase in functional capacity. It is speculated that age related muscle loss is secondary to the loss of neuronal activation of type-II fibers. By preventing the degeneration of typ-II motor units, functional

capacity could be maintained into old age. This technique may also serve useful in the prevention of osteoporosis. Further study is necessary to determine wether IGF-1 is having an effect only on muscle fibers or on nervous tissues as well.

Neo-Hombreol 50 mg/ml; Organon NL

Stanozolol has some unique biochemical properties which we will discuss in a later article.

Description 4: Stanabol 50 (Winstrol Depot) (stanozolol)

Lowered blood pressure

Indications

Many athletes like to use Nolvadex C&K at the end of a steroid cycle since it increases the body's own testosterone production

and to prevent estrogenic side effects of taking anabolic steroids.

These include:

This drug information is for your information purposes only, it is not intended that this information covers all uses, directions, drug interactions, precautions, or adverse effects of your medication. This is only general information, and should not be relied on for any purpose. It should not be construed as containing specific instructions for any particular patient. We disclaim all responsibility for the accuracy and reliability of this information, and/or any consequences arising from the use of this information,

including damage or adverse consequences to persons or property, however such damages or consequences arise. No warranty, either expressed or implied, is made in regards to this information.

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. Restandol (Andriol) is often combined with Anavar since Anavar also does not suppress the production of testosterone and, in addition, does not aromatize.

The propionate and phenylpropionate esters in this product are quickly utilized, releasing into circulation within the first

four days. The remaining esters are much slower to release, staying active in the body for approximately two and three weeks (respectively). This is an improvement from standard testosterones such as cypionate or enanthate, which provide a much shorter duration of activity, and a more variable blood level. This is one of the most popular injectable testosterones because the combination of the four different esters work synergistically together, both fast acting and long lasting.

Average Dosage: Men - 20-40mg daily Women - none

Always take Cialis ® exactly as your doctor has instructed you. You should check

with your doctor or pharmacist if you are unsure.

Medications similar to testosterone that are taken by mouth for a long time may cause serious damage to the liver or liver cancer. Testosterone gel has not been shown to cause this damage. Testosterone may increase the risk of developing prostate cancer. Talk to your doctor about the risks of taking this medication. Testosterone gel may cause other side effects. Call your doctor if you have any unusual problems while taking this medication.

Durabolin is very similar to the popular Deca-Durabolin. Durabolin must be injected frequently and in regular intervals.

The substance nandrolone-phenylpropionate quickly gets into the blood, where it remains active for two to three days. Athletes who hope for optimal results inject Durabolin every third day, or even every two days. The dosage is around 50-100 mg per injection, or a total of 150-300 mg/week. Those who have access to the 50 mg version should take advantage of it since it is less expensive than the 25 mg version, which is normally more easily available. in addition, the 1-2 ml injections are more pleasant than the 2-4 ml. Durabolin has a distinct anabolic effect which assists the protein synthesis and allows the protein to be stored

in the muscle cell in large amounts. This is combined with a moderate androgenic component which stimulates the athlete's regeneration and helps maintain the muscle mass during a diet. It shows that Durabolin stores much less water in the body than Deca-Durabolin. For this reason, Durabolin is more suitable for a preparation for a competition while Deca should be given preference for the buildup of strength and muscle mass. Durabolin, however, can be used for this purpose as well. The gains are fewer and slower than with Deca but of a higher quality and remain, for the most part, after discontinuing the com-pound. A stack suitable

for this purpose would be, e.g. 56 mg Durabolin every 2 days, 50 mg Testosterone Propionate every days, and 20 mg Winstrol tablets every day.

Viagra is used as needed, so you are not likely to miss a dose.

The oral use of stanozolol can also have a profound impact on levels of SHBG (sex hormone-binding globulin). This is characteristic of all anabolic/androgenic steroids, however its potency and form of administration makes oral stanozolol particularly noteworthy in this regard. Since plasma binding proteins such as SHBG act to temporarily constrain steroid hormones from exerting activity, this effect would

provide a greater percentage of free (unbound) steroid hormone in the body. This may amount to an effective mechanism in which stanozolol could increase the potency of a concurrently used steroid. Proviron has an extremely high affinity for SHBG. This affinity may cause Proviron to displace other weaker substrates for SHBG, another mechanism in which the free hormone level may be increased. Adding stanozolol and Proviron to a testosterone cycle may therefore prove very useful, markedly enhancing the free state of this potent muscle building androgen.

Equipoise® is not an ideal steroid for the drug tested athlete however.

This drug has the tendency to produce detectable metabolites in the urine months after use, a worry most commonly associated with Deca-Durabolin®. This is of course due to the high oil solubility of long chain esterified injectable steroids, a property which enables the drug to remain deposited in fatty tissues for extended periods of time. While this will reliably slow the release of steroid into the blood stream, it also allows small residual amounts to remain present in the body far after the initial injection. The release of stubborn stores of hormone would no doubt also be enhanced around contest time, a period when

the athlete drastically attempts to mobilize unwanted body fat. If enough were used in the off-season, the athlete may actually fail a drug screen for boldenone although many months may have past since the drug was last injected.

Dietary Guidelines:

Anxiety, blistering, peeling, or loosening of skin and mucous membranes, blurred vision, chest pain, confusion, cough, dizziness, fainting, fast heartbeat, lightheadedness, pain or swelling in fingers, hands and legs, shortness of breath or trouble breathing, weakness or sleepiness, yellow eyes or skin.

Realistically, every cycle should contain testosterone.

Go back and read that sentence again. A beginners´ dose of testosterone (i.e. someone on their first or second cycle of AAS) would be in the 250-500mgs range. Though, realistically, I wouldn´t recommend much less than 400mgs of test per cycle for anybody, beginner or not. And guess what? The more you use the more results you get. And frequently, the more side effects too (3).

If you are (hypersensitive) allergic to tadalafil or any of the other ingredients of Cialis ®.

Clenbuterol exhibits most of its effects on the stimulation of both type 2 and 3 beta-receptors. It is effective in helping to

burn bodyfat Clenbuterol is effective in increasing muscle mass and decreasing fat loss.Clenbuterol generally come is 20mcg tablets, although it is also available in syrup and injectable form. Users will usually tailor their dosage individually, depending on results and side effects, but somewhere in the range of 2-8 tablets per day is most common, it is often stacked with cytomel.

Important information about Rohypnol

Side effects are very mild, liver stress can occur.

Sleep apnea (temporary stopping of breathing during sleep) — Benzodiazepines may make these conditions worse

HOW TO TAKE

CIALIS

Usage: 250 mg - 1000 mg weekly.

Side effects experienced with Propecia are decreased libido, erectile dysfunction and ejaculation disorder, all occuring only in very few patients (<2%). Resolution of possible side effects occurs after discontinuation of Propecia.

It's of course used in other stacks with products such as methandrostenolone, boldenone and nandrolone to reduce estrogenic activity and increase muscle hardness. The addition of proviron makes boldenone a dead lock for a cutting stack and for some may even make it possible to use nandrolone while cutting, although the use of Winstrol

or a receptor antagonist in conjunction is wishful as well. The benefit of adding it to a nandrolone stack is that it may also help you reduce the decrease in libido suffered from nandrolone, since the latter is mostly deactivated by 5-alpha reductase, an enzyme that makes other hormones more androgenic.

The most common dosage schedule for Testosterone Propionate (men) is to inject 50 to 100 mg, every 2nd or 3rd day. As with the more popular esters, the total weekly dosage would be in the range of 200-400 mg. As with all testosterone compounds, this drug is most appropriately suited for bulking phases of training. Here

it is most often combined with other strong agents such as Dianabol, Anadrol 50 or Deca-Durabolin, combinations that prove to be quite formidable. Propionate however is sometimes also used with non aromatizing anabolics/androgens during cutting or dieting phases of training, a time when its' fast action and androgenic nature are also appreciated. Popular stacks include a moderate dosage of propionate with an oral anabolic like Winstrol (15-35 mg daily), Primobolan (50-150 mg daily) or Oxandrolone (15-30 mg daily). Provided the body fat percentage is sufficiently low, the look of dense muscularity can be notably improved (barring
any excess estrogen buildup from the testosterone). We can further add a non-aromatizing androgen like Trenbolone, which should have an even more extreme effect on subcutaneous body fat and muscle hardness. Of course with the added androgen content any related side effects will become much more pronounced.

Finally, it was also exciting to see muscle growth in the young mice who received the injection (15% increase in muscle mass). This means that the injection provided levels of IGF-1 far and above what the muscle normally has access to and not simply a preservation of normal levels. Remember that this was not combined

with exercise. The growth of the injected muscles happened even without an extreme mechanical stimulus. The mice were simply allowed to run around as they usually do. Because of these dramatic results, the authors expressed concern about the use of this technique to enhance performance or cosmetic appearance. Research Update is not my personal soap box so I won’t go off on the gender centered hypocrisy of cosmetic enhancement in our society. All we can hope for is that this technique will be used to treat more important diseases such as muscular dystrophy and thereby become somewhat available for other uses as well.

This is an oral steroid which is a derivative of nortesterone. It is interesting that Nilevar is produced by the same manufacturer who also introduced the well-known Anavar to the U.S. market. Nilevar, which was already sold in American pharmacies in 1956, was a precursor of Anavar which was introduced to the market in 1964 by Searle USA. It has since been voluntarily removed from the mar-ket. Thus it is not surprising that Nilevar has certain similarities to Anavar or Oxandrolone. 11ke Oxandrolone it has only a weak anabolic effect, whereas the androgenic component is distinctly stron-ger. Nilevar, even in low dosages, aromatizes easily so that the in-creased estrogen level could become a problem. The main effect of Nilevar, in part, is a considerable strength gain. This gain often goes hand in hand with a distinct water retention, especially if high dosages are taken, which also explains the gain in body weight of its users.

The manufacturer of the French and Swiss Nilevar recom-mends a daily dose of 10-30 mg. Athletes using Nilevar-usually powerlifters-take 30-40 mg/day, divided into two to three equal dosages. it is mostly used for a short period, a maximum of 4-6 weeks. Women should not take Nilevar since it can cause considerable virilization symptoms. Nilevar is I 7-alpha alkylated and there-fore potentially hepatoxic which put-, stress on the liver. Other possible side effects are acne, gynecomastia, aggressiveness, headaches, gastrointestinal pain, reduced production of the body's own hor-mones and high blood pressure. A package of thirty 10 mg tablets costs approx. $4 in the pharmacy.

Because of its price it is an interesting compound, yet Nilevar is rarely used by bodybuilders in Europe since other steroids are readily available.