Steroid Newbie Thread (Help Build It Vets!)

Training
141

Omnadren 250

Quick overview:

Active Life: Approx. 18 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: 250-1000 mg/week (males only)
Acne: Yes
Water Retention: Yes
High Blood Pressure: Yes
Liver Toxic: Low
Aromatization: Yes
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Omnadren 250 is an oil-based injectable containing a blend of four different testosterone esters: Testosterone propionate, phenylpropionate, isocaproate and caproate. Being as it is a four-ester testosterone, Omnadren is most commonly compared to Sustanon. While it does contain Testosterone propionate, testosterone phenylpropionate and isocaproate in the same strength as Sustanon, the last ester is different. Please note however, that the older versions of Omnadren list isohexanoate and hexanoate as the final two ingredients. Hexanoate is simply another word for caproate, so the last ester (decanoate) is the only Sustanon constituent missing from Omnadren.

One of the only noticeable differences between Sustanon and Omnadren seems to be the speed in which estrogen buildup occurs. In comparison, the process appears to be slightly more pronounced with Omnadren. This is of course just a matter of timing, as the slowest releasing ester in Omnadren (caproate) is a little faster acting than enanthate. Blood testosterone levels will therefore peak much faster with this compound, not having the same gradual release time imposed by testosterone decanoate. Users likewise report water retention much earlier into a cycle.

While water retention may lead to a more rapid buildup of size and strength, it can become pronounced enough to cause a very smooth and watery look to develop (hiding muscle definition). In addition, the excess estrogen is likely to cause the development of gynecomastia. This effect is especially pronounced with Omnadren, usually presenting itself quickly after a cycle has been started.

Estrogen can also be responsible for increases in body fat storage during treatment, resulting in a further loss of definition. Individuals who are sensitive to the effects of estrogen, yet still seek the power of a testosterone, would therefore need to add an anti-estrogen such as Nolvadex and/or Proviron. Arimidex,Femara, or Aromasin, 3 powerful anti-aromatase, are another option available to us. These three drug works much more efficiently than any other anti-estrogen. They would have great use with such a strong item as Omnadren, as the standard remedies would not be quite as effective.

Being a testosterone, you can also expect the typical set of androgenic side effects. Oily skin, acne, body/facial hair growth and increased aggression are all very common with this product. It can also bring out or aggravate a condition of male pattern baldness. We do however, have the option to addition Proscar (finasteride).

This is a drug that can effectively prevent testosterone from converting into DHT (dihydrotestosterone) in certain androgen target tissues. Since DHT is the primary culprit with testosterone’s androgenic side effects, adding Proscar to the cycle should allow it to be much more comfortable.

Omnadren is also likely to suppress endogenous testosterone production rather quickly. It is therefore a necessity to add a testosterone stimulating drug like HCG and/or Clomid/Nolvadex when concluding therapy.

Being a powerful, long acting testosterone blend, the effect of Omnadren is of course quite comparable to that of Sustanon (except that its release time is closer to cypionate or enanthate). It is similarly a powerful androgen, capable of providing great gains in mass and strength.

Due of the high level of water retention associated with testosterone, Omnadren is really only applicable for bulking purposes. While it is very effective alone, it is also combined often with a number of other steroids depending on the desired result.

Many athletes prefer to combine Omnadren with a strong anabolic like Deca-Durabolin or Equipoise for example, in an attempt to lower the overall testosterone dosage and run a more quality mass building cycle. On the other hand, power-lifters and those looking for dramatic gains in mass and strength (regardless of quality) may stack Omnadren with heavy orals such as Anadrol or Dianabol. Here of course the strength and weight gain should be even more extreme, although androgenic/estrogenic side effects are expected to be as well.

Although Omnadren stays active in the body for about two weeks, it is generally injected on a weekly or bi-weekly basis. A dosage of 250-750mg per week is more than sufficient to achieve great results. Some take advantage of the very low price of Omnadren (Europe) and take excessively large amounts. Beyond 750mg or 1000mg weekly added side effects will no doubt be greatly outweighing growth, so there is usually little need for such excess. With this drug we really don’t want to mistake water bloat for muscle growth.

And while a number of adventurous women do experiment with testosterone products, Omnadren is probably not a good choice. The long action of this compound, mixed with the highly androgenic nature of testosterone, makes a poor combination. Virilization symptoms can develop quite easily with a strong androgen, making a long acting product like Omnadren notably dangerous should problems become evident. Testosterone propionate is a much better choice should an androgen like this be absolutely necessary, as it will give the user much greater control over her blood testosterone level.

Due to the extremely low price for this drug in Poland, Omnadren is made readily available on the black market. Among bodybuilders, Omnadren is generally considered to be inferior to Sustanon however. Price may have something to do with this belief, as this drug is usually much cheaper than Sustanon. Counterteits are not a major concern, so it is considered a trustworthy item.

Don’t be alarmed if your Omnadren seems to have a different look than or you remember from previous experience. The packaging of this product seems to change quite often. For starters, the company name changed officially in 1991 from “Polfa” to “Jelfa”, although for years after the older version boxes could still be found in circulation.

The color of the boxes also varies, and has included pink & white, green & white, gray, and gray & blue. What is constant is that each box contains five ampules, protected in a white paper or plastic holder. The old ampules are clear glass, and are imprinted with red or black ink that will rub off easily. The newer version is identified by a paper ampule label, which currently bears black print.

142

Primobolan Depot (methenolone enanthate)

Quick overview:

Active Life: 10-14 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 200-400 mg/week…Women 50-100 mg/week
Acne: Yes, mainly in higher doses
Water Retention: Low
High Blood Pressure: Rare
Liver Toxic: Low
Aromatization: None
DHT Conversion: None
Decrease HPTA function: Yes

Primobolan? Depot is the injectable version of the steroid methenolone. It is the same compound as the one in Primobolan Orals (methenolone acetate), both produced by Schering. In this injectable version, an enanthate ester is added to the steroid, which makes for a slow and gradual release from the site of injection. Its length of activity would thus be quite similar to Testosterone enanthate, with blood levels remaining elevated for approximately two weeks. Methenolone itself is a long acting anabolic, with extremely low androgenic properties. It’s anabolic effect is also quite mild, its potency is considered to be slightly less than DecaDurabolin (nandrolone decanoate) on a milligram for milligram basis.

For this reason, Primobolan is most commonly used during cutting cycles when a mass increase is not the main goal. Some athletes do prefer to combine a mild anabolic like “Primo” with bulking drugs such as Dianabol, Anadrol, or testosterone however, presumably to lower the overall androgen dosage and minimize uncomfortable side effects. When choosing between Primobolan versions, the injectable is preferred over the oral, as it is much more cost effective.

Since Primobolan does not convert to estrogen, it displays many favorable characteristics. Estrogen related side effects should therefore not be seen at all when using this steroid. Sensitive individuals need not worry about developing gynecomastia, nor should they be noticing any water retention with this drug. The gains seen with Primobolan will be only quality muscle mass, and not the smooth bloat which accompanies most steroids open to aromatization.

During a cycle the user should additionally not have much trouble with blood pressure values, as this effect is also related (generally) to estrogen and water retention.

At a moderate dosage of 100-200mg weekly, Primobolan should also not interfere with endogenous testosterone levels as much as when taking an injectable nandrolone or testosterone. At higher dosages strong testosterone suppression will be noticed, as all steroids can act to suppress testosterone production at a given dosage. Here of course a proper post cycle therapy is a must.

Side effects in general are usually not much of a problem with Primobolan Depot. There is a chance one will notice a few residual androgenic effects such as oily skin, acne, increased facial/body hair growth or an aggravation of male pattern baldness condition. This steroid is still very mild however, and such problems are typically dose related.

Women will in fact find this preparation mild enough to use in most cases, observing it to be a very comfortable and effective anabolic. If both the oral and injectable were available for purchase, the faster acting oral should probably be given preference however. This is simply due to the fact that blood hormone levels are more difficult to control with a slow acting injectable, the user also having to wait many days for steroid levels to diminish if side effects become noticeable.

Overall, Primobolan Depot is actually considered to be one of the safest anabolic steroids available. Steroid novices, older athletes or those sensitive to side effects would undoubtedly find it a very favorable drug to use. The typical “safe” dosage for men is 100-200mg per week, a level that should produce at least some noticeable muscle growth.

In European medicine it is not uncommon for Primobolan to be used safely at such a dosage for extended periods of time. Among athletes, men may respond to weekly doses of 200mg but regular users will often inject much higher doses looking for a stronger anabolic effect. It is not uncommon for a bodybuilder to take as much as 600 or 800mg per week, a range which appears to be actually quite productive. Of course androgenic side effects may become more pronounced with such an amount, but in most instances it should still be quite tolerable.

In addition, it is most popular for male bodybuilders to stack Primobolan with other steroids in order to obtain a faster and more enhanced effect. During a dieting or cutting phase, a non-aromatizing androgen like Halotestin or trenbolone can be added. The strong androgenic component should help to bring about an added density and hardness to the muscles.

On the other hand (or in addition) we could add Winstrol, another mild anabolic steroid. The result of this combination should again be a notable increase of muscle mass and hardness, but in this case the gain should not be accompanied by greatly increased side effects.

As mentioned earlier, Primobolan Depot is also used effectively during bulking phases of training. The addition of testosterone, Dianabol or Anadrol would prove quite effective for adding new muscle mass. Of course we would have to deal with estrogenic side effects, but in such cases Primobolan should allow the user to take a much lower dosage of the more “toxic” drug and still receive acceptable results.

Women respond well to a dosage of 50-100mg per week, although (as stated above) the oral should usually be given preference. Additionally, some choose to include Winstrol Depot or Oxandrolone and receive a greatly enhanced anabolic effect. Remember though, androgenic activity can be a concern and should be watched, particularly when more than one anabolic is used at a time.

If stacking, it would be best to use a much lower starting dosage for each drug than if they were to be used alone. This is especially good advice if you are unfamiliar with the effect such a combination may have on you. A popular recommendation would also be to first experiment by stacking with oral Primobolan, and later venture into the injectable if this is still necessary.

143

Primobolan Tablets (methenolone acetate)

Quick overview:

Active Life: 4-6 hours
Drug Class: Anabolic/Androgenic Steroid (Oral)
Average Dose: Men 50-150 mg/day…Women 50-75 mg/day
Acne: Rare
Water Retention: No
High Blood Pressure: Rare
Liver Toxic: Very low and only in very high dosages
Aromatization: None
DHT Conversion: No
Decrease HPTA function: Low
Comments: Moderately Anabolic/Low Androgenic

This section refers to the oral Primobolan? preparation, which contains the drug methenolone acetate. It is very similar in action to the injectable Primobolan? Depot (methenolone enanthate), but obviously here the drug is designed for oral administration.

At one time Schering was in fact also manufacturing an injectable methenolone acetate (Primobolan? acetate, out of manufacture since 1993), which proved to be very useful for pre-contest cutting purposes. This steroid is now gravely missed, as it was once a favorite among European competitors. Although we still have the acetate in oral form, it is a close, but not equal substitute (injection is a much more efficient form of delivery for this steroid).

Methenolone regardless of the ester is a very mild anabolic steroid. The androgenic activity of this compound is considerably low, as are its anabolic properties. One should not expect to achieve great gains in muscle mass with this drug. Instead, Primobolan? is utilized when the athlete has a specific need for a mild anabolic agent, most notably in cutting phases of training. It is also a drug of choice when side effects are a concern.

A welcome factor is that Primobolan? is not c17 alpha alkylated as most oral steroid are. Due to the absence of such an alteration, this compound is one of the few commercially produced oral steroids that is not notably stressful to the liver.

While liver enzymes values have been affected by this drug in some rare instances, actual damage due to use of this substance is not a documented problem. Unfortunately the 1 alkylation and 17-beta esterification of Primobolan? do not protect the compound very well during first pass however, so much of your initial dose will not make circulation. This is obviously why we need such high daily dose with the oral version of Primobolan?.

Primobolan? will also not aromatize, so estrogen related side effects are of no concern. This is very useful when leading up to a bodybuilding contest, as subcutaneous water retention (due to estrogen) can seriously lessen the look of hardness and definition to the muscles.

Non-aromatizing steroids are therefore indispensable to the competitor, helping to bring about a tight, solid build the weeks leading up to a show. And of course without excess estrogen there is little chance of the athlete developing gynecomastia. Likewise there should never be a need for anti-estrogen use with this steroid. Primobolan? is also said to have a low impact on endogenous testosterone production. Although this may well be true in small clinical doses, it will not hold true for the bodybuilder.

For example, in one study more than half of the patients receiving only 30-45 mg noted a suppression of gonadotropin levels of 15% to 65% a. This is a dose far less than most bodybuilders would use, and no doubt increasing it would only lead to worse suppression. One would therefore still need a testosterone stimulating drug like HCG or Clomid?/Nolvadex? when concluding a low-dose Primobolan? cycle, unless a deliberately small dose were being used.

It is also important to note that although the androgenic component of Primobolan? is low, side effects are still possible. One may therefore notice oily skin, acne and facial/body hair growth during treatment. Men with a predisposition for hair loss may also find it exacerbates this condition, and wish to avoid this item (nandrolone injectables are a much better choice).

While always possible, side effects rarely reach a point where they interfere with the progress of cycle. Primobolan? is clearly one of the milder and safer oral steroids in production. Female athletes, older or more sensitive individuals and steroid beginners will no doubt find this a comfortable steroid to experiment with.

The dosage for men is somewhere in the range of 75-150mg daily. This can obviously be tedious (and costly) if one can only obtain the 5mg tablets from Mexico and S. America. A mild anabolic such as Primobolan? is often used in conjunction with other steroids for optimal effect, so some users find a slightly lower dose effective when stacking.

During a dieting or cutting phase, thought to be its primary application, a non-aromatizing androgen like Halotestin? or trenbolone can be added for example. Such combinations would enhance the physique without water retention, and help bring out a harder and more defined look of muscularity. Non-aromatizing androgen/anabolic stacks like this are in fact very popular among competing bodybuilders. This compound is also occasionally used with more potent androgens during bulking phases of training.

The addition of testosterone, Dianabol or Anadrol 50? would prove effective for instance, although the gains are likely to be accompanied by some level of smoothness due to the added estrogenic component.

Among women, Primobolan? is one of the most popular steroids in use. At a dosage of 50-75mg daily, virilization symptoms are extremely uncommon. One would of course not expect a tremendous amount of muscle mass with this drug, and instead should expect a slow and steady (quality) increase.

Some women choose to further add-in other anabolics such as Winstrol? or oxandrolone, in an effort to increase the muscle building effectiveness of a cycle. While both of these compounds are quite tolerable to women, one must be sure not to use too high an accumulated dosage. Troublesome androgenic side effects are always a possibility with steroid use, even with very mild substances. Taken at too high a dosage, these weak anabolics can become a formidable danger to femininity.

It would therefore be the best advice not to use the normal dosage range of both, but instead start with a much lower dosage of each steroid to compensate for the other. On the black market Primobolan? orals are popular, but still much less commonly found than the injectable. This is due to the higher cost effectiveness of the injectable, which uses the same active compound but with 100% bioavailability due to the form of administration.

144

Proviron (mesterolone)

Quick overview:

Active Life: 8-12 hours (effects last about 24 hours)
Drug Class: Androgenic Steroid/Anti- Aromatization (Oral)
Average Dose: Men 25-100 mg/day…Women 25-50 mg/day
Acne: Rare
Water Retention: No
High Blood Pressure: Rare
Liver Toxic: Low
Aromatization: None
DHT Conversion: No, it is a derivative of DHT
Decrease HPTA function: No

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 increase the activity of other steroids by displacing a higher percentage into a free, unbound state. Among athletes Proviron is primarily used as an anti-estrogen. It is believed to act as an anti-aromatase 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 direct 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. Another disadvantage of 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. Most 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 reduced.

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 anti-estrogenic 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 well needed 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 is often used throughout the entire 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 drugs. It is therefore considered 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. 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, Femara, or Aromasin ares actually a much better choice than Proviron though. These drugs were designed specifically as an anti-aromatase, and works much more effectively than anything else we have available.

145

Sustanon 250

Quick overview:

Active Life: Approx. 21 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: 250-1000 mg/week (males only)
Acne: Yes
Water Retention: Yes
High Blood Pressure: Yes
Liver Toxic: Low
Aromatization: Yes
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Sustanon 250? is an oil-based injectable testosterone blend, developed by Organon. It typically contains four different testosterone esters: Testosterone propionate (30 mg); testosterone phenylpropionate (60 mg); testosterone isocaproate (60mg); and testosterone decanoate (100 mg), although a lower dosed version is also produced. An intelligently “engineered” testosterone, Sustanon is designed to provide a fast yet extended release of testosterone. 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 about two and three weeks (respectively).

As with all testosterone products, Sustanon is a strong anabolic with pronounced androgenic activity. It is mainly used as a bulking drug, providing good gains in strength and muscle mass. Although it does convert to estrogen, as is the nature of testosterone, this injectable is noted as being slightly more tolerable than cypionate or enanthate. Such observations are only issues of timing however. With Sustanon, blood levels of testosterone are building more slowly, so side effects do not set in as fast. For equal blood hormone levels however, testosterone will break down equally without regard to ester. Also correlating with estrogen, water retention would be noticeable with Sustanon, unless steps were taken to minimize estrogen.
Many individuals like to use a combination of Nolvadex & Proviron, while others use an anti-aromatase like Arimidex, Femara, or Aromasin, to help control estrogen related side effects.

Being a strong androgen, we can expect the typical side effects. This includes oily skin, acne body/facial hair growth and premature balding. The addition of Proscar/Propecia should be able to minimize such side effects, as it will limit the conversion of testosterone to DHT (dihydrotestosterone) . Sustanon will also suppress natural testosterone production rather quickly. The use of HCG and/or Clomid/Nolvadex are necessary at the conclusion of a cycle in order to avoid a hormonal crash. Remember though, Sustanon will remain active in the body for up to a month after your last injection was given. Beginning you post cycle drug therapy immediately after the steroid has been discontinued will not be very effective. Instead, HCG or Clomid/Nolvadex should be delayed three weeks, until you are near the point where blood androgen levels have dropped significantly.

Although Sustanon remains active in the body for approximately three weeks, injections are taken at least every 10 days. An effective dosage ranges from 250mg (one ampule) a week, to 1000mg (four ampules) weekly. Some athletes do use more extreme dosages of this steroid, but this is really not a recommended practice. When the dosage rises above 750-1000mg per week, increased side effects will no doubt be outweighing additional benefits. Basically you will receive a poor return on your investment, which with Sustanon can be substantial. Instead of taking unnecessarily large amounts, athletes interested in rapid size and strength will usually opt to addition another compound. For this purpose we find that Sustanon stacks extremely well with the potent orals Anadrol and Dianabol. On the other hand, Sustanon may work better with trenbolone or Winstrol if the athlete were seeking to maintain a harder, more defined look to his physique.

Sustanon 250 is probably the most sought after injectable testosterone. I must however emphasize that this is not due to an unusual potency of this testosterone combination however (remember esters only effect the release of testosterone), but simply because a “stack” of four different esters is a very good selling point. In many instances you will get a lot more for your money with enanthate, so don’t let the fancy stack fool you. Sustanon is however still very abundant on the U.S. black market, and doesn’t stay long on dealer’s shelves. In fact the high demand for this steroid has stirred new interest in its manufacture, particularly by veterinary companies in Mexico.

146

Testosterone cypionate

Quick overview:

Active Life: 15-16 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 250-1000 mg/week
Acne: Yes
Water Retention: Yes, high
High Blood Pressure: Yes
Liver Toxic: Low, except in mega dosages
Aromatization:Yes, high
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

American athletes have a long and fond relationship with Testosterone cypionate. While Testosterone enanthate is manufactured widely throughout the world, cypionate seems to be almost exclusively an American item. It is therefore not surprising that American athletes particularly favor this testosterone ester. But many claim this is not just a matter of simple pride, often swearing cypionate to be a superior product, providing a bit more of a “kick” than enanthate. At the same time it is said to produce a slightly higher level of water retention, but not enough for it to be easily discerned. Of course when we look at the situation objectively, we see these two steroids are really interchangeable, and cypionate is not at all superior. Both are long acting oil-based injectables, which will keep testosterone levels sufficiently elevated for approximately two weeks. Enanthate may be slightly better in terms of testosterone release, as this ester is one carbon atom lighter than cypionate (remember the ester is calculated in the steroids total milligram weight). The difference is so insignificant however that no one can rightly claim it to be noticeable (we are maybe talking a few milligrams per shot). Regardless, cypionate came to be the most popular testosterone ester on the U.S. black market for a very long time

As with all testosterone injectables, one can expect a considerable gain in muscle mass and strength during a cycle. Since testosterone readliy converts to estrogen, the mass gained from this drug is likely to be accompanied by quite a bit of water retention. The resulting loss of definition of course makes cypionate a very poor choice for dieting or cutting phases. The excess level of estrogen brought about by this drug can also cause one to develop gynecomastia rather quickly. Should one notice an uncomfortable soreness, swelling or lump under the nipple, an ancillary drug like Nolvadex should be added immediately. This will minimize the effect of estrogen greatly, making the steroid much more tolerable to use. The powerful anti-aromatases Arimidex, Femara, or Aromasin are yet a better choice. Those who have a known sensitivity to estrogen may find it more beneficial to use ancillary drugs like Nolvadex and Proviron from the onset of the cycle, in order to prevent estrogen related side effects before they become apparent.

Since testosterone is the primary male androgen, we should also expect to see pronounced androgenic side effects with this drug. Much intensity is related to the rate in which the body converts testosterone into dihydrotestosterone (DHT). This, as you know, is the devious metabolite responsible for the high prominence of androgenic side effects associated with testosterone use. This includes the development of oily skin, acne, body/facial hair growth and male pattern balding. Those worried that they may have a genetic predisposition toward male pattern baldness may wish to avoid testosterone altogether. Others opt to add the ancillary drug Proscar/Propecia, that prevents the conversion of testosterone to dihydrotestosterone. This can greatly reduce the chance for running into a hair loss problem, and will probably lower the intensity of other androgenic side effects. Although active in the body for much longer time, cypionate is injected on a weekly or bi-weekly basis in order to maintain stable blood levels. At a dosage of 250mg to 800mg per week we should certainly see dramatic results. It is interesting to note that while a large number of other steroidal compounds have been made available since testosterone injectables, they are still considered to be the dominant bulking agents among bodybuilders. There is little argument that these are among the most powerful mass drugs. When taking dosages above 800-1000mg per week there is little doubt that water retention will come to be the primary gain, far outweighing the new mass accumulation. The practice of “megadosing” is therefore inefficient, especially when we take into account the typical high cost of steroids today.

It is also important to remember that the use of an injectable testosterone will quickly suppress endogenous testosterone production. It is therefore mandatory to complete a proper post cycle therapy, constisting of HCG and Clomid or Nolvadex at the conclusion of a cycle. This should help the user avoid a strong “crash” due to hormonal imbalance, which can strip away much of the new muscle mass and strength. This is no doubt the reason why many athletes claim to be very disappointed with the final result of steroid use, as there is often only a slight permanent gain if anabolics are discontinued incorrectly. Of course we cannot expect to retain every pound of new bodyweight after a cycle. This is especially true whenever we are withdrawing a strong (aromatizing) androgen like testosterone, as a considerable drop in weight (and strength) is to be expected as retained water is excreted. This should not be of much concern; instead the user should focus on ancillary drug therapy so as to preserve the solid mass underneath. Another way athletes have found to lessen the “crash”, is to first replace the testosterone with a milder anabolic like Deca-Durabolin. This steroid is administered alone, at a typical dosage (200-400mg per week), for the following month or two. In this “stepping down” procedure the user is attempting to turn the watery bulk of a strong testosterone into the more solid muscularity we see with nandrolone preparations. In many instances this practice proves to be very effective. Of course we must remember to still administer ancillary drugs at the conclusion, as endogenous testosterone production will not be rebounding during the Deca therapy.

147

Testosterone enanthate

Quick overview:

Active Life: 15-16 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 250-1000 mg/week
Acne: Yes
Water Retention: Yes, high
High Blood Pressure: Yes
Liver Toxic: Low, except in mega dosages
Aromatization:Yes, high
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Testosterone enanthate is an oil based injectable steroid, designed to slowly release testosterone from the injection site (depot). Once administered, serum concentrations of this hormone will rise for several days, and remain markedly elevated for approximately two weeks. It may actually take three weeks for the action of this drug to fully diminish. For medical purposes this is the most widely prescribed testosterone, used regularly to treat cases of hypogonadism and other disorders related to androgen deficiency. Since patients generally do not selfadminister such injections, a long acting steroid like this is a very welcome item. Therapy is clearly more comfortable in comparison to an ester like propionate, which requires a much more frequent dosage schedule.

Testosterone is a powerful hormone with notably prominent side effects. Much of which stem from the fact that testosterone exhibits a high tendency to convert into estrogen. Related side effects may therefore become a problem during a cycle. For starters, water retention can become quite noticeable. This can produce a clear loss of muscle definition, as subcutaneous fluids begin to build. The storage of excess body fat may further reduce the visibility of muscle features, another common problem with aromatizing steroids. The excess estrogen level during/after your cycle also has the potential to lead up to gynecomastia. Adding an ancillary drug like Nolvadex and/or Proviron is therefore advisable to those with a known sensitivity to this side effect. The anti-aromatase Arimidex, Femara, or Aromasin are a much better choices though. It is believed that the use of an anti-estrogen can slightly lower the anabolic effect of most androgen cycles (estrogen and water weight are often thought to facilitate strength and muscle gain), so one might want to see if such drugs are actually necessary before committing to use. A little puffiness under the nipple is a sign that gynecomastia is developing. If this is left to further develop into pronounced swelling, soreness and the growth of small lumps under the nipples, some form of action should be taken immediately to treat it (obviously quitting the drug or adding ancillaries like Nolvadex).

Being a testosterone product, all the standard androgenic side effects are also to be expected. Oily skin, acne, aggressiveness, facial/body hair growth and male pattern baldness are all possible. Older or more sensitive individuals might therefore choose to avoid testosterone products, and look toward milder anabolics like DecaDurabolin or Equipoise which produce fewer side effects. Others may opt to add the drug Proscar/Propecia, which will minimize the conversion of testosterone into DHT (dihydrotestosterone). With blood levels of this metabolite notably reduced, the impact of related side effects should also be reduced. With strong bulking drugs however, the user will generally expect to incur strong side effects and will often just tolerate them. Most athletes really do not find the testosterones all that uncomfortable (especially in the face of the end result), as can be seen with the great popularity of such compounds.

Although this particular ester is active for a much longer duration, most prefer to inject it on a weekly or bi-weekly basis in order to keep blood levels stable. The usual dosage would be in the range of 250mg-750mg a week. This level is quite sufficient, and should provide the user a rapid gain of strength and body weight. Above this level estrogenic side effects will no doubt become much more pronounced, possibly outweighing any new muscle gained. Those looking for greater bulk would be better served by adding an oral like Anadrol or Dianabol, combinations which prove to work great. If one wishes to use a testosterone yet retain a level of quality and definition to the physique, an injectable anabolic like DecaDurabolin or Equipoise may prove to be a better choice. Here we can use a lower dosage of enanthate, so as to gain an acceptable amount of muscle but keep the buildup of estrogen to a minimum.

With the proper administration of ancillary drugs, Nolva/Clomid and HCG, during post cycle recovery, much of the new muscle mass can be retained for a long time after the cycle has been stopped.

148

Testosterone propionate

Quick overview:

Active Life: 2-3 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 50-200 mg/day
Acne: Yes
Water Retention: Yes, high
High Blood Pressure: Yes
Liver Toxic: Low
Aromatization:Yes, high
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Testosterone propionate is a commonly manufactured, oil-based injectable testosterone compound. The propionate ester will slow the rate in which the steroid is released from the injection site, but only for a few days. Testosterone propionate is therefore much faster acting than other testosterone esters such as cypionate or enanthate, and requires a much more frequent dosing schedule, in order to maintain stable blood levels. While cypionate and enanthate are injected on a weekly or bi-weekly basis, propionate is usually injected every second. The propionate ester can be very irritating to the site of injection. In fact, many sensitive individuals choose to stay away from this steroid completely, their body reacting with a pronounced soreness and low-grade fever that may last for a few days.

Those who do not mind frequent injections will find propionate to be quite an effective steroid. As with all testosterones, it is a powerful mass drug, capable of producing rapid gains in size and strength. At the same time the buildup of estrogen and DHT (dihydrotestosterone) will be pronounced, so typical testosterone side effects are to be expected. Many consider propionate to be the mildest testosterone ester, and the preferred form for the dieting/cutting phases of training. Some will go so far as to say that propionate will harden the physique, while giving the user less water and fat retention than one typically expects to see with a testosterone. Realistically however, this is nonsense. The ester is removed before testosterone is active in the body, and likewise the ester cannot alter the activity of the parent steroid in any way, only slow its release. We can say that propionate might be the favored testosterone among female bodybuilders (for those who insist on testosterone use), as blood levels are easier to control with it compared to other esters. Should virilization symptoms develop, one would not wish to wait the weeks needed for testosterone concentrations to fall after a shot of enanthate for example.

During a typical cycle one will see action that is consistent with a testosterone. Users sensitive to gynecomastia and water retention may therefore need to add an anti-estrogen like Arimidex, Femara or Aromasin. Those particularly troubled by gynecomastia may find that a combination of Nolvadex and Proviron works especially well at preventing/halting this occurrence. Also unavoidable with a testosterone are androgenic side effects like oily skin, acne, increased aggression and body/facial hair growth. Those who may have a predisposition for male pattern baldness may also find that propionate will aggravate this condition. To help combat this one may choose to Propecia/Proscar, which will reduce the buildup of DHT in many androgen target tissues. This will help minimize related side effects (particularly hair loss) although it offers us no guarantees. And as with all testosterone products, propionate will also suppress endogenous testosterone production. The use of a testosterone stimulating drug like HCG and/or Clomid/Nolvadex is therefore a requirement in order to avoid enduring a post-cycle crash.

The most common dosage schedule for this compound (men) is to inject 50 to 100mg, every day or 2nd day. As with the more popular esters, the total weekly dosage would be in the range of 300-700mg. 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, or Deca-Durabolin, combinations that prove to work quite well. Propionate however is sometimes also used with nonaromatizing anabolics/androgens during cutting or dieting phases of training, a time when it’s 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 (50-150mg daily) or oxandrolone (15-30mg 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). One could also add a non-aromatizing androgen like trenbolone or Halotestin, 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.

Women who absolutely must use an injectable testosterone should only use this preparation. The dosage schedule should also be more spread out for a female bodybuilder, with injections coming every 5 to 7 days. The dosage obviously would be lower as well, generally in the range of 25mg to 50mg per injection. Androgenic activity should be less pronounced with this schedule, giving blood levels time to sufficiently decrease before the drug is administered again. In order to further reduce any risks, the duration of this cycle should not exceed 8 weeks. Should a stronger anabolic effect be needed, a small amount of Durabolin (Deca-Durabolin if unavailable), Oxandrolone or Winstrol could be added. Of course the risk of noticing virilizing effects from these drugs may increase, even with the addition of a mild anabolic. Since many of the masculinizing side effects of steroid use can be irreversible, it is very important for the female athlete to monitor the dosage, duration and incidence of side effects very closely.

Some Vet companies as well as UG labs are now even producing 250mg/ml dosage vials. This dosage is more shocking than it sounds at first next to all the 250mg enanthate and now cypionate products in circulation. Testosterone propionate is less oil soluble than Testosterone enanthate or cypionate, making a high dosage more difficult to achieve. Before this the highest concentration you could find of this steroid was 100mg/ml. Reaching 250 milligrams is no doubt a result of not simply adding more steroid to one ml of oil, but increasing the alcohol content in the solution considerably as well. This makes for a much more uncomfortable solution to inject. Although admittedly the highest dose of propionate you will ever find, users have been reporting that it is also intolerably painful. Most find they have to dilute the solution with other lower dosed steroids if they are to continue using the product. This should be no a surprise I guess with a steroid that already has a reputation as being painful to inject.

149

Testosterone suspension

Quick overview:

Active Life: less than 24 hours
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 50-200 mg/day
Acne: Yes
Water Retention: Yes, high
High Blood Pressure: Yes
Liver Toxic: Low, except in mega dosages
Aromatization:Yes, high
DHT Conversion: Yes, high
Decrease HPTA function: Yes, severe

Testosterone suspension is an injectable preparation containing testosterone (no ester) in a water base. Since testosterone is not highly water soluble, the steroid will noticeably separate from the solution when the vial is left to sit. A quick shake will put the drug back into suspension, at least temporarily, so that it can be withdrawn in a consistent dosage. Although it may contain testosterone without the benefit of an ester, and contrary to popular belief, the microcrystal design of this injectable will sustain an elevated testosterone release for 2-3 days. Clearly the suspension we see today is not the basic water plus testosterone design used in the 1940’s. And since the drug will not leave circulation in a matter of hours, it is obviously useful.

Among bodybuilders, “suspension” is known to be an extremely potent mass agent. It is often ranked as the most powerful injectable steroid available, resulting in an incredibly rapid gain of muscle mass and strength. This is largely due to the very fast action of this drug, as the water-based steroid will begin to enter the blood stream almost immediately after an injection is given. Unlike longer esters such as enanthate or cypionate which take weeks for blood levels to reach maximiun theraputic levels, with suspension it is just a matter of days. Clearly the anabolic effect of this testosterone will be realized much more quickly than we would expect with an oil based (esterified) preparation.

It is also important to remember that 100mg of a testosterone ester is not equivalent to 100mg testosterone of pure testosterone (as in suspension). When an ester is present, its weight is obviously included in the preparation’s milligram total. Looking at Testosterone enanthate, 100mg of this compound equates to only 72mg of raw testosterone. So the bodybuilder who uses 400mg of enanthate weekly is really getting about 288mg of testosterone into his body each week. This is clearly a great increase over the endogenous testosterone level of the average male, which is in the range of 2.5 to 11 mg per day. But the general point is that during a cycle of Testosterone suspension we will often see a much more dramatic intake of testosterone on average than is typically utilized with oils. Following common advice, the athlete will commonly inject a full 100mg of testosterone daily, a total of 700 milligrams per week. This is up to 40 times the amount produced by a normal male. Those who have attempted such a cycle are rarely disappointed with the results, as such heavy doses of this hormone will produce nothing less than a dramatic weight gain.

The most popular practice with Testosterone suspension is to inject the drug every day. The dosage will vary greatly depending on the needs of the individual, but is most often in the range of 50mg to 100mg per shot. In most cases the results will be amazing. Although some users will complain about discomfort when injecting water-based steroids, suspension is usually well tolerated.

As would be expected with a strong androgen, suspension can produce a number of unpleasant side effects. As with any testosterone product there will be a high rate of estrogen conversion. Estrogen levels in fact build very quickly with Testosterone suspension, which is probably the worst testosterone to use when wishing to avoid water bloat. Gynecomastia can also develop very quickly during a cycle, and in many cases this drug will be intolerable without additionally taking an anti-estrogen. A combination of Nolvadex and Proviron is an effective way to avoid experiencing such side effects, and is often taken from the onset of a cycle in order to prevent such occurrences before they become a problem. Sensitive individuals may find an investment in the anti-aromatase Arimidex, Femara, or Aromasin to be wiser. These anti-aromatase drugs are much more effective at controlling estrogen. It is also important that the athlete monitor blood pressure and kidney functions closely during a heavy cycle, as water retention becomes more pronounced. Although testosterone puts very little strain on the liver, this drug can be harsh to the kidneys at higher dosages. Of course if the athlete is encountering noticeably high blood pressure or trouble urinating (pain or darkening of the urine), the cycle should probably be discontinued and the doctor paid a visit. Since it converts to DHT. one can therefore expect to endure oily skin, acne, increased aggression and body/facial hair growth during a typical cycle. Propecia/Proscar would be a good idea for those predisposed to male pattern baldness, as suspension is known to aggravate this condition quite easily. Men with an existing hair loss problem may actually prefer to stay far away from this steroid altogether, finding it to be just to strong an item to take risks with. The slower acting oil based injectables like enanthate or cypionate would be a much better place to start with if one still desires to use an injectable testosterone.

Endogenous testosterone production will be quickly and efficiently reduced when using suspension. This can often reach the point of severe testicular shrinkage (atrophy). Some athletes will periodically take HCG while on a cycle, in order to keep this effect to a minimum. Even if no such drug is used during, a combination of HCG and Clornid/Nolvadex should always be used as the cycle is discontinued.

Overall, suspension is an extremely powerful drug, but also one that is prone to causing many side effects. Those looking for only a potent mass agent need not look no further, Suspension will certainly get the job done.

150

Trenbolone Acetate

Quick overview:

Active Life: Around 2 days
Drug Class: Anabolic/Androgenic Steroid (for injection)
Average Dose: Men 75 mg every day or two days
Acne: Yes
Water Retention: No
High Blood Pressure: Yes
Liver Toxic: Yes,debatable
Aromatization: No
DHT Conversion: No
Decrease HPTA function: Yes, moderate to extreme

Trenbolone is a very potent androgen with strong anabolic activity. It is well suited for the rapid buildup of strength and muscle mass, usually providing the user exceptional results in a relatively short time period. The anabolic effect of this drug is often compared to popular bulking agents such as testosterone or Dianabol, with one very important difference. Trenbolone does not convert to estrogen. This is indeed a very unique compound since mass drugs, almost as a rule, will aromatize (or cause other estrogen related troubles) heavily.

When we think of taking milder (regarding estrogen) steroids we usually expect much weaker muscle growth, but not so with Trenbolone. Here we do not have to worry about estrogen related side effects, yet still have an extremely potent mass/strength drug. There is no noticeable water retention, so the mass gained during a cycle of Trenbolone will be very hard and defined (providing fat levels are low enough).

Gynecomastia is also not much of a concern, so there shouldn’t be any need to addition an anti-estrogen if trenbolone is the only steroid administered.

The high androgen level resulting from this steroid, in the absence is excess estrogen, can also accelerate the burning of body fat. The result should be a much tighter physique, hopefully without the need for extreme dieting. Trenbolone can therefore help bring about an incredibly hard, ripped physique and is an ideal product for competitive bodybuilders.

Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.

Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds). However it seems likely that much of its suppressive nature still stems from its powerful androgen action.

With the strong impact trenbolone has on endogenous testosterone, of course the use of a stimulating drug such as HCG and/or Clomid/Nolvadex is recommended when concluding steroid therapy (a combination is preferred). Without their use it may take a prolonged period of time for the hormonal balance to resume, as the testes may at first not be able to normally respond to the resumed output of endogenous gonadotropins due to an atrophied state.

Those who have used Trenbolone regularly would often claim it to be indispensable. A daily dosage of 37.5-75 mg is the most popular range when running a cycle.

While Trenbolone is quite potent when used alone, it was generally combined with other steroids for an even greater effect. During a cutting phase one could add a non-aromatizing anabolic such as Winstrol or Primobolan. Such combinations will elicit a greater level density and hardness to the muscle. One could also bulk with this drug, with the addition of stronger compounds like Dianabol or Testosterone. While the mass gain would be quite formidable with such a stack, some level of water retention would probably also accompany it.

Moderately effective anabolics such Deca-Durabolin or Equipoise would be somewhat of a halfway point, providing extra strength and mass but without the same level of water bloat we see with more readily aromatized steroids.

151

[quote]Fearmy6pak wrote:
An important consideration when planning a steroid cycle, in particular the timing of dosing to be administered, is the active half-life of the drug being employed. The half-life may be defined as the time (t) the level is half of the starting level of a given compound; at time 2t, the level is a quarter of the starting level, and at time 3t, the level is an eighth of the starting level, and so on.

This information is vital in the timing of the dosing when attempting to achieve a more stable blood concentration, which leads to greater overall results and maintenance of gains. Some fluctuations of concentration levels are acceptable, and are also mostly unavoidable, but should be kept to a minimum.

Oral steroids

Anadrol / Anapolan50 (oxymetholone) 8 to 9 hours
Anavar (oxandrolone) 9 hours
Dianabol (methandrostenolone, methandienone) 4.5 to 6 hours
Methyltestosterone 4 days
Winstrol (stanozolol)
(tablets or depot taken orally) 9 hours

Depot steroids

Deca-durabolin (Nandrolone decanate) 15 days
Equipoise 14 days
Finaject (trenbolone acetate) 3 days
Primobolan (methenolone enanthate) 10.5 days
Sustanon or Omnadren 15 to 18 days
Testosterone Cypionate 12 days
Testosterone Enanthate 10.5 days
Testosterone Propionate 4.5 days
Testosterone Suspension 1 day

  • Winstrol (stanozolol) 1 day

*Winstrol depot does not actually possess a classical half-life because it is un-esterified. Instead, the microcrystals dissolve slowly. Once they have all dissolved levels of the drug fall very rapidly. It is still an important consideration.

Steroid esters

Formate 1.5 days
Acetate 3 days
Propionate 4.5 days
Phenylpropionate 4.5 days
Butyrate 6 days
Valerate 7.5 days
Hexanoate 9 days
Caproate 9 days
Isocaproate 9 days
Heptanoate 10.5 days
Enanthate 10.5 days
Octanoate 12 days
Cypionate 12 days
Nonanoate 13.5 days
Decanoate 15 days
Undecanoate 16.5 days

Ancillaries

Arimidex 3 days
Clenbuterol 1.5 days
Clomid 5 days
Cytadren 6 hours
Ephedrine 6 hours
T3 10 hours

A practical example is if one was to inject 100mg of testosterone propionate and allow blood levels to peak. In 4.5 days time (half-life duration from the above tables) and providing no other injections had taken place, the level would be reduced to 50mg. Again, a further 4.5 days down the line and levels would have dropped to 25mg, and the value keeps halving every 4.5 days.
[/quote]

I found this list of half-lives on this thread. But if I’m not mistaken, this half-life info may not be very accurate.

I was wondering if anyone has a more accurate list of half-lives. I can’t seem to find one.

152

Rainjack,

good point about half-lives. i checked that post with the profiles i posted, and some are quite a bit different. if i found anything i’ll throw it on here…

153

bump

154

That was some reading I just did. I just gotta say that was some awesome info Cycobushmaster
Simply great!

155

Winstrol (stanozolol)

Quick overview:

Active Life: around 48 hours
Drug Class: Anabolic/Androgenic Steroid (for injection or oral)
Average Dose: Men 50-100 mg/day…Women 25-50 mg/week
Acne: Rare
Water Retention: Rare
High Blood Pressure: Rare
Liver Toxic: Yes, it is a 17AA steroid
Aromatization: No, it is a DHT derivative
DHT Conversion: None
Decrease HPTA function: Low

Winstrol? is a popular brand name for the anabolic steroid stanozolol. This compound is a derivative of dihydrotestosterone, although its activity is much milder than this androgen in nature. It is technically classified as an anabolic steroid, shown to exhibit a slightly greater tendency for muscle growth than androgenic activity in early studies. While dihydrotestosterone really only provides androgenic side effects when administered, stanozolol instead provides quality muscle growth.

The anabolic properties of this substance are still mild in comparison to many stronger compounds, but it is still a ggod, reliable builder of muscle. Its anabolic properties could even be comparable to Dianabol, but Winstrol does not have the same tendency for water retention. Stanozolol also contains the same c17 methylation we see with Dianabol, an alteration used so that oral administration is possible. To spite this design however, there are many injectable versions of this steroid produced.

Since stanozolol is not capable of converting into estrogen, an anti-estrogen is not necessary when using this steroid, gynecomastia is not a concern even among the most sensitive individuals. Since estrogen is also the cause of water retention, instead of bulk look, Winstrol produces a lean, quality look with no fear of excess subcutaneous fluid retention. This makes it a great 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 Track and Field.

The usual dosage for men is 35-75mg per day for the tablets and 25-50mg per day with the injectable version. It is often combined with other steroids depending on the desired result. For bulking purposes, a stronger androgen like testosterone, Dianabol or Anadrol is usually added. Here Winstrol will balance out the cycle a bit, giving us good anabolic effect with lower overall estrogenic activity than if taking such steroids alone.

The result should be a considerable gain in new muscle mass, with a more comfortable level of water and fat retention. For cutting phases Winstrol can be combined with a non-aromatizing androgen such as trenbolone or Halotestin. Such combinations should help bring about the strongly defined, hard look of muscularity so sought after among bodybuilders. Older, more sensitive individuals can add compounds like Primobolan, Deca-Durabolin or Equipoise when wishing to stack this steroid. Here they should see good results and fewer side effects than with standard androgen therapies.

Women usually take around 5-10mg daily. Although female athletes usually find stanozolol very tolerable, the injectable version is usually off limits.

With the structural (c17-AA) alteration, the tablets will also place a higher level of stress on the liver than the injectable (which avoids the “first pass”). During longer or higher dosed cycles, liver values should therefore be watched closely through regular blood work. Although less common, there is still a possibility of liver damage occuring with the injectable form. While it does not enter the body through the liver, it is still broken down by it, providing a lower (but more continuous) level of stress.

Such stress would of course be increased with the addition of other c17-AA oral compounds to a cycle of Winstrol. When using such combinations, cautious users would make every effort to limit the length of the cycle (preferably 6 to 8 weeks) and take some form of liver protectants. It should also be noted that both versions of Winstrol have been linked to strong adverse changes in HDL/LDL cholesterol levels.

This side effect is common with anabolic steroid therapy, and obviously can become a health concern as the dose/duration of intake increase above normal. The oral version should have a greater impact on cholesterol values than the injectable due to the method of administration, and may therefore be the worse choice of the two for those concerned and this side effect.

The oral use of stanozolol can also have a profound impact on levels of SHBG (sex hormone-binding globulin). This is a characteristic of all anabolic/androgenic steroids, however its potency and form of administration make Winstrol 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. To further this purpose one could also addition Proviron, which has an extremely high affinity for SHBG. This affinity may cause Proviron to displace other weaker substrates for SHBG (such as testosterone), another mechanism in which the free hormone level may be increased. Adding Winstrol and Proviron to your next testosterone cycle may therefore prove very useful, markedly enhancing the free state of this potent muscle building androgen.

156

Cycobushmaster can you give me your take and opinion on Superdrol and Mag-10(I’m sure others would be interested too)
Thanks

157

nanjingldv,

i’ve never used MAG-10, but i know a lot of people had pretty good results with it. i used Superdrol at 30 mg/day for 10 days (then i got hurt and stopped it), and noticed no gains. however, i have never responded very well to prohormones…

158

OK thanks Bushmaster

159

bump.

160

Heloo everyone,
I am from India. I wnated to ask - do u know any specific indian co. which manufacturers boldenon / Equipoise.I got rest of all juice but cannot get hands on this
any help will be appreciated