Equipoise

Equipoise Buy Equipoise Equipoise (Boldenone Undeclynate), or "EQ" is one of the most widely used compounds by athletes today. Even though it is a vetrinary steroid, the quality of production is quite high due to its use in rather expensive animals. It is one of the safest and most effective steroids used today, by athletes, power lifters and bodybuilders. It can effect slow and continuous muscle mass and strength gains over a prolonged period, and generally cycles with this drug tend to be quite long because of this fact. Gains on a cutting cycle including Eq tend to be high quality lean mass, while bulking cycle gains with Eq aren't as "clean" but still have a very nice quality about them. This could be due to Eq's resistence to being converted to Estrogen, as well as DHT (technically, it converts to Dihydroboldenone). Equipoise has become much more popular in recent years since dosages hit 200mg/ml Men get good results from a 300-600mg weekly total. In the past, this included utilizing an every other day (EOD) injection schedule, because Eq was only available in very low concentrations (50-100mgs/ml). Recently, companies like British Dragon have begun offering Boldenone in a much higher concentration (200mgs/ml) making injections much easier. Women have made excellent progress with dosages of 50-100mg total weekly doses, and this usually means a 1 injections weekly schedule. Women as a rule, seem to prefer less scar-tissue build up than men are comfortable with. In this dose range, women almost never report virilizing side effects, and usually only experienced an elevated libido. Increased hair growth on face and legs is, of course, possible (though not probable).. Liver toxicity is not an issue with Boldenone, and it can be used for long times on either a bulking or cutting cycle, very safely. It has a reputation for appetite and red blood cell production stimulating effects, and this makes it very nice for a bulking cycle. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport, making less food become more efficient...a very nice effect for a cutting cycle. Athletes generally stacked Boldenone with testosterone and Anadrol for mass cycles. Dianabol, due to it's close resemblance to Eq chemically, is not usually used interchangably with Anadrol in cycles containing EQ (a rare exception). Cutting, or pre-contest cycles including Boldenone often include Trenbolones, Winstrol. With the afforementioned drugs, an anti-estrogen is generally not necessary. Reported Characteristics Boldenone Undeclynate 1,4-androstadiene-3-one-17b-ol Cutting/Bulking:Both Anabolic Rating: 100 Active-Life: 7-9 days Drug Class: Anabolic /Androgenic steroid (for injection) Average Reported Dosage: Men 300-600mg weekly Women 50-100mg weekly Acne: Rare Water Retention: Low High Blood Pressure: Rare Aromatization: About 50% of testosterone Liver Toxic: No DHT Conversion: No (*converts to DHB) Decreases HPTA function: Yes Average Price: $150/10ml bottle Trade Names EQUIPOISE 200MG/ML (British Dragon) ULTRAGAN 100 100MG/ML BOLDEBAL-H 50MG/ML EQUIPOISE 25MG,50MG, /ML ULTRAGAN 50 50MG/ML GANABOL 25MG, 50MG/ML PACE 25MG/ML VENBOL 25MG/ML

Anavar (oxandrolone)

Anavar (oxandrolone) Quick overview: Active Life: 8-12 hoursDrug Class: Anabolic/Androgenic Steroid (Oral)Average Dose: Men 20-50 mg/day......Women 5-15 mg/dayAcne: Only in higher dosesWater Retention: RareHigh Blood Pressure: RareLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low doses, toxicity is low to mediumAromatization: NoneDHT Conversion: LowDecrease HPTA function: Dose depandant Anavar was the old U.S. brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer Searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. As the opinions surrounding steroids began to change in the 1980's, prescriptions for oxandrolone began to drop. Lagging sales probably led Searle to discontinue manufacture in 1989, and it had vanished from U.S. pharmacies until recently. Oxandrolone tablets are again available inside the U.S. by BTG, bearing the new brand name Oxandrin. BTG purchased rights to the drug from Searle and it is now manufactured for the new purpose of treating HIV/AIDS related wasting syndrome. Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (DHT). Although one might think that this would make it a more androgenic steroid, it in fact creates a steroid that is less androgenic because it is already "5-alpha reduced". In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent "dihydro° form. It is a simple matter of where a steroid is capable of being potentiated in the body, and with oxandrolone we do not have the same potential as testosterone, which is several times more active in androgen responsive tissues compared to muscle tissue due to its conversion to DHT. It essence oxandrolone has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances. This steroid works well for the promotion of strength and duality muscle mass gains, although it's mild nature makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results. It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone. In this case the androgen really helps to harden up the muscles, while at the same time making conditions more favorable for fat reduction. Some athletes do choose to incorporate oxandrolone into bulking stacks, but usually with standard bulking drugs like testosterone or Dianabol. The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol, Primobolan or Durabolin. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup. Studies using low dosages of this compound note minimal interferences with natural testosterone production. Likewise when it is used alone in small amounts there is typically no need for ancillary drugs like Clomid/Nolvadex or HCG. This has a lot to do with the fact that it does not convert to estrogen, which we know has an extremely profound effect on endogenous hormone production. Without estrogen to trigger negative feedback, we seem to note a higher threshold before inhibition is noted. But at higher dosages of course, a suppression of natural testosterone levels will still occur with this drug as with any anabolic/androgenic steroid and therefore require post cycle therapy to restore the HPTA. Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that will put stress on the liver. It is important to point out however that dispite this alteration oxandrolone is generally very well tolerated. While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not usually a problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. One study comparing the effects of oxandrolone to other agents including as methyltestosterone, norethandrolone, fluoxymesterone and methAndriol clearly supports this notion. Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among all the alkylated orals tested. 20mg of oxandrolone in fact produced 72% less BSP retention than an equal dosage of fluoxyrnesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during longer cycles than most of other orals with this distinction. Although this may very well be true, the chance of liver damage still cannot be excluded, especially with hogher dosages. At one time oxandrolone was also looked at as a possible drug for those suffering from disorders of high cholesterol or triglycerides. Early studies showed it to be capable of lowering total cholesterol and triglyceride values in certain types of hyperlipidemic patients, which initially this was thought to signify potential for this drug as a hypo-lipid (lipid lowering) agent. With further investigation we find however that while use of this drug can be linked to a lowering of total cholesterol values, it is such that a redistribution in the ratio of good (HDL) to bad (LDL) cholesterol occurs, usually moving values in an unfavorable direction. This would of course negate any positive effect that the drug might have on triglycerides or total cholesterol, and in fact make it a danger in terms of cardiac risk when taken for prolonged periods of time. Today we understand that as a group anabolic/androgenic steroids produce very unfavorable changes in lipid profiles, and are really not useful in disorders of lipid metabolism. As an oral c17 alpha alkylated steroid, oxandrolone is probably even more risky to use than an injectable esterified injectable such as a testosterone or nandrolone in this regard.

Dianabol

Dianabol is one of the most highly effective mass building steroids ever created. It was, in fact, created specifically for athletes to use to improve performance (although it was claimed to have theraputic ability). It provideds highly impressive weight and strength gains for most users. Experiencing a 2-3kg weight gain per week is not unheard of, especially in novices. It must be noted that alot if this is water weight, and that with higher dosages gynecomastia (bitch tits), high blood pressure, and acne could occur. Dianabol (Methandrostenlone) when taken orally becomes active very rapidly, but only remains active for less than half a day. Often, for this reason, dosages were spread through the day. Ciba, the original makers of Dianabol claimed that 10 mgs of the product was enough for full androgen replacement in a man, and this dose increased androgen anabolic activity roughly 5 times over normal and provided a reduction in natural cortisol activity of between 50-70%. Despite this, many athletes take 50-100mgs daily. It would appear that over 50mgs/day, there is a point of diminishing return. Dianabol is most commonly found in tablet form Since Dianabol (often called D-bol by athletes) is a 17aa compound, side effects such as increased liver values (toxicity) are to be expected, although they generally return to normal quickly after the athlete stops taking the product. In addition, as previously noted, gyno, heavy water retention (and raised blood pressure as a result), and acne were all commonly reported side effects of D-bol use. Interestingly, some users note a sense of well being during use of this drug, which is quite pronounced. This is the exact opposite of Anadrol, which is noted for an "unwell" feeling in users. This product is also available in an injectable form from both British Dragon (in oil) as well as under the Reforvit-B name (which has the addition of B vitamins) which is suspended in water and is quite frankly a very painful injection, and not often used for this reason. TRADE NAMES NAPOSIM 5MG TABS METHANDO (Akrihin) METHANABOL (British Dragon) AVERBOL 25 injectable, 25mg/ml British Dragon ANABOL TABS 5MG TABS ANABOLIN 5MG TABS ANDOREDAN 5MG TABS BIONABOL 2,5MG TABS DIALONE 5MG TABS DIANABOL 5MG ENCEPHAN 5MG TABS METANABOL 1,5MG TABS METHANDROSTENOLONUM 5MG TABS NEROBOL 5MG TABS PRONABOL-5 5MG TABS STENOLON 1,5MG TABS TRENERGIC 5MG CAPS NAPOSIM 5MG TABS D-BOL 10MG CAPSVETERINARY: ANABOLIKUM 2.5% 25MG/ML;50ML METANDIOBOL 25MG/ML;50ML D-BOL INJECTION 25MG/MLReported Characteristics Pharmaceutical Name:Methandrostenolone Chemical Structure:17a-methyl-17b-hydroxy-1,4-androstadien-3-one Cutting/Bulking:Bulking Anabolic Rating:90-210 Active-Life: 6-8 hours (24 for injectable) Drug Class: Anabolic/androgenic steroid Average Reported Dosage: Men 25-50 mg daily Acne: Possible Water Retention: Yes High Blood Pressure: Aromatization: Yes Liver Toxic: Yes DHT conversion: No Decreases HPTA function: Inhibitory Average Price: .50cents-$1 per 5-10mg tab

Winstrol (stanozolol)

Winstrol (stanozolol) 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.

IGF-1

IGF-1 stands for insulin-like growth factor. It is a natural substance that is produced in the human body and is at its highest natural levels during puberty. During puberty IGF is the most responsible for the natural muscle growth that occurs during these few years. There are many different things that IGF does in the human body; I will only mention the points that would be important for physical enhancement. Among the effects the most positive are increased amino acid transport to cells, increased glucose transport, increased protein synthesis, decreased protein degradation, and increased RNA synthesis.
When IGF is active it behaves differently in different types of tissues. In muscle cells proteins and associated cell components are stimulated. Protein synthesis is increased along with amino acid absorption. As a source of energy, IGF mobilizes fat for use as energy in adipose tissue. In lean tissue,
IGF prevents insulin from transporting glucose across cell membranes. As a result the cells have to switch to burning off fat as a source of energy.
IGF also mimic's insulin in the human body. It makes muscles more sensitive to insulin's effects, so if you are a person that currently uses insulin you can lower your dosage by a decent margin to achieve the same effects, and as mentioned IGF will keep the insulin from making you fat.
Perhaps the most interesting and potent effect IGF has on the human body is its ability to cause hyperplasia, which is an actual splitting of cells. Hypertrophy is what occurs during weight training and steroid use, it is simply an increase in the size of muscle cells. See, after puberty you have a set number of muscle cells, and all you are able to do is increase the size of these muscle cells, you don't actually gain more. But, with IGF use you are able to cause this hyperplasia which actually increases the number of muscle cells present in the tissue, and through weight training and steroid usage you are able to mature these new cells, in other words make them grow and become stronger. So in a way IGF can actually change your genetic capabilities in terms of muscle tissue and cell count. IGF proliferates and differentiates the number of types of cells present. At a genetic level it has the potential to alter an individuals capacity to build superior muscle density and size.
There is a lot of talk about the similarity between IGF and growth hormone. The most often asked question is simply which is more effective. GH doesn't directly cause your muscles to grow, it works very indirectly by increasing protein synthesis capabilities, increasing the amount of insulin a person can use effectively, and increasing the amount of anabolic steroids a person can use effectively. GH also indirectly causes muscle growth by stimulating the release of IGF when it (the GH) is destroyed in the human body. So one way you could look at it as GH being a precursor to IGF. So to put it simple IGF is more effective at directly causing muscle growth and density increases. IGF is also much more cost effective.
IGF can also be effectively used by itself and gains will still be easily noticeable. With growth hormone you need to use high amounts of anabolics and often insulin to see any gains at all, this is not the case with IGF. IGF can be used by itself and is often used by bodybuilders who bridge between cycles, during this bridge is a good time to use IGF since it has no effect on natural testosterone production so it will therefore allow you to return to normal in terms of hormone levels. A stack of IGF, PGF2a, HCG, and clomid would be a good bridge stack and would allow your body to return to normal and still allow you to retain and make new gains.
IGF is a research drug, it hasn't been approved by the FDA for use as a pharmaceutical and it is currently being researched for nerve tissue repair, possible burn victims, and also as a possible aid in muscle wasting for AIDS patients. There are many different analogs of IGF available, instead of mentioning them all, I will simply mention the two most common and the most effective. Regular recombinant IGF is one of the two, it is also the more expensive and the least effective. Regular IGF only has a half-life of about 10-20 minutes in the human body and is quickly destroyed, it can be combined with certain binding proteins to extend the half-life, but it is not a very simple procedure and there is a more effective and less expensive version available. The most effective form of IGF is Long R3 IGF-1, it has been chemically altered and has had amino acid changes which cause it to avoid binding to proteins in the human body and allow it to have a much longer half life, around 20-30 hours. "Long R3 IGF-1 is an 83 amino acid analog of IGF-1 comprising the complete human IGF-1 sequence with the substition of an Arg(R) for the Glu(E) at position three, hence R3, and a 13 amino acid extension peptide at the N terminus. This analog of IGF-1 has been produced with the purpose of increasing the biological activity of the IGF peptide."
"Long R3 IGF-1 is signifacantly more potent than IGF-1. The enhanced potency is due to the decreased binding of Long R3 IGF-1 to all known IGF binding proteins. These binding proteins normally inhibit the biological actions of IGF's."
It is also not as expensive since a media grade version is available which is sufficient for bodybuilding use. There is also a receptor grade available but it is VERY expensive and the only noticeable difference between the two would only be able to be noticed in a laboratory setting. The price on the black market for Long R3 IGF-1 can be seen anywhere from $300-$500 per milligram depending on the source, be wary of black market dealers of any IGF since it is a VERY difficult item to obtain. As mentioned IGF is a research product and is only available from a few laboratories in the world and is only available to research companies and biotechnology institutions. For the rest of this article when I say IGF I am now referring to Long R3 IGF-1 for simplicity sake.
There is no such product made anywhere in the world and even if there were real IGF ever present in the vial it would all be dead by the time you receive it. IGF is a very delicate peptide and must be diluted by yourself, where you have access to a refrigerator and freezer. There has also been a lot of talk by certain sources claiming to have IGF made by the Eli Lilly company, to clear things up Lilly is a pharmaceutical company and as stated IGF is a research drug and has not yet been approved, Lilly does not and never has manufactured research drugs for retail sale.
The dilutents you will need for the IGF are a weak concentration of hydrochloric acid and a sterile buffer(sterile water or bacteriostatic water) the procedure for diluting the IGF is not very difficult, the dilutents can be obtained from most local chemical suppliers and a good source of IGF would also be able to supply the necessary dilutents.
The most effective length for a cycle of IGF is 50 days on and 20-40 days off. The most controversy surrounding Long R3 IGF-1 is the effective dosage. The most used dosages range between 20mcg/day to 120+mcg/day. IGF is only available by the milligram, one mg will give you a 50 day cycle at 20mcg/day, 2mg will give you a 50 day cycle at 40mcg/day, 3mg will give you a 50 day cycle at 60mcg/day, 4mg will give you a 50 day cycle at 80mcg/day and so on. The dosage issue mainly revolves around how much money you have to spend, plenty of people use the minimum dosage of 20mcg/day and are happy with the results, and in fact several top bodybuilders use the 20mcg/day dosage and are pleased with the results. IGF is most effective when administered subcutaneously and injected once or twice daily at your current dosage. The best time for injections is either in the morning and/or immediately after weight training.
Another frequently asked question of IGF refers to the real world results, in terms of pure weight gain don't expect to gain 5 lbs. a week like you may off of anadrol or a similar steroid. The only weight you will gain from IGF use is pure lean muscle tissue, with steroids most of the weight gained is water weight. With an effective dosage you can expect to gain 1-2 lbs of new lean muscle tissue every 2-3 weeks and these effects can be increased with the use of testosterone, anabolic steroids, and insulin use. Increased vascularity is also very common, people report seeing veins appear where they never have before. And yet another effect reported is the ability to stay lean while bulking with heavy dosages of steroids and TONS of food while on an IGF cycle, this is perhaps the most pleasing effect. Increased pumps are also noticeable almost immediately, the pumps can almost become painful, pumps are even noticeable when doing cardio.
Overall, IGF is a very exciting drug due to its ability to alter ones genetic capabilities. If you can find a trustworthy source and you use it correctly it can be a VERY useful tool in your bodybuilding drug arsenal.

Anavar (oxandrolone)

Anavar (oxandrolone)
Quick overview:
Active Life: 8-12 hoursDrug Class: Anabolic/Androgenic Steroid (Oral)Average Dose: Men 20-50 mg/day......Women 5-15 mg/dayAcne: Only in higher dosesWater Retention: RareHigh Blood Pressure: RareLiver Toxic: Yes, c17-alfa-alkylated steroid. Due to low doses, toxicity is low to mediumAromatization: NoneDHT Conversion: LowDecrease HPTA function: Dose depandant
Anavar was the old U.S. brand name for the oral steroid oxandrolone, first produced in 1964 by the drug manufacturer Searle. It was designed as an extremely mild anabolic, one that could even be safely used as a growth stimulant in children. One immediately thinks of the standard worry, "steroids will stunt growth". But it is actually the excess estrogen produced by most steroids that is the culprit, just as it is the reason why women stop growing sooner and have a shorter average stature than men. Oxandrolone will not aromatize, and therefore the anabolic effect of the compound can actually promote linear growth. Women usually tolerate this drug well at low doses, and at one time it was prescribed for the treatment of osteoporosis. As the opinions surrounding steroids began to change in the 1980's, prescriptions for oxandrolone began to drop. Lagging sales probably led Searle to discontinue manufacture in 1989, and it had vanished from U.S. pharmacies until recently. Oxandrolone tablets are again available inside the U.S. by BTG, bearing the new brand name Oxandrin. BTG purchased rights to the drug from Searle and it is now manufactured for the new purpose of treating HIV/AIDS related wasting syndrome.
Anavar is a mild anabolic with low androgenic activity. Its reduced androgenic activity is due to the fact that it is a derivative of dihydrotestosterone (DHT). Although one might think that this would make it a more androgenic steroid, it in fact creates a steroid that is less androgenic because it is already "5-alpha reduced". In other words, it lacks the capacity to interact with the 5-alpha reductase enzyme and convert to a more potent "dihydro° form. It is a simple matter of where a steroid is capable of being potentiated in the body, and with oxandrolone we do not have the same potential as testosterone, which is several times more active in androgen responsive tissues compared to muscle tissue due to its conversion to DHT. It essence oxandrolone has a balanced level of potency in both muscle and androgenic target tissues such as the scalp, skin and prostate. This is a similar situation as is noted with Primobolan and Winstrol, which are also derived from dihydrotestosterone yet not known to be very androgenic substances.
This steroid works well for the promotion of strength and duality muscle mass gains, although it's mild nature makes it less than ideal for bulking purposes. Among bodybuilders it is most commonly used during cutting phases of training when water retention is a concern. The standard dosage for men is in the range of 20-50mg per day, a level that should produce noticeable results. It can be further combined with anabolics like Primobolan and Winstrol to elicit a harder, more defined look without added water retention. Such combinations are very popular and can dramatically enhance the show physique. One can also add strong non-aromatizing androgens like Halotestin, Proviron or trenbolone. In this case the androgen really helps to harden up the muscles, while at the same time making conditions more favorable for fat reduction. Some athletes do choose to incorporate oxandrolone into bulking stacks, but usually with standard bulking drugs like testosterone or Dianabol. The usual goal in this instance is an additional gain of strength, as well as more quality look to the androgen bulk. Women who fear the masculinizing effects of many steroids would be quite comfortable using this drug, as this is very rarely seen with low doses. Here a daily dosage of 5mg should illicit considerable growth without the noticeable androgenic side effects of other drugs. Eager females may wish to addition mild anabolics like Winstrol, Primobolan or Durabolin. When combined with such anabolics, the user should notice faster, more pronounced muscle-building effects, but may also increase the likelihood of androgenic buildup.
Studies using low dosages of this compound note minimal interferences with natural testosterone production. Likewise when it is used alone in small amounts there is typically no need for ancillary drugs like Clomid/Nolvadex or HCG. This has a lot to do with the fact that it does not convert to estrogen, which we know has an extremely profound effect on endogenous hormone production. Without estrogen to trigger negative feedback, we seem to note a higher threshold before inhibition is noted. But at higher dosages of course, a suppression of natural testosterone levels will still occur with this drug as with any anabolic/androgenic steroid and therefore require post cycle therapy to restore the HPTA.
Anavar is also a 17alpha alkylated oral steroid, carrying an alteration that will put stress on the liver. It is important to point out however that dispite this alteration oxandrolone is generally very well tolerated. While liver enzyme tests will occasionally show elevated values, actual damage due to this steroid is not usually a problem. Bio-Technology General states that oxandrolone is not as extensively metabolized by the liver as other l7aa orals are; evidenced by the fact that nearly a third of the compound is still intact when excreted in the urine. This may have to do with the understood milder nature of this agent (compared to other l7aa orals) in terms of hepatotoxicity. One study comparing the effects of oxandrolone to other agents including as methyltestosterone, norethandrolone, fluoxymesterone and methAndriol clearly supports this notion. Here it was demonstrated that oxandrolone causes the lowest sulfobromophthalein (BSP; a marker of liver stress) retention among all the alkylated orals tested. 20mg of oxandrolone in fact produced 72% less BSP retention than an equal dosage of fluoxyrnesterone, which is a considerable difference being that they possess the same liver-toxic alteration. With such findings, combined with the fact that athletes rarely report trouble with this drug, most feel comfortable believing it to be much safer to use during longer cycles than most of other orals with this distinction. Although this may very well be true, the chance of liver damage still cannot be excluded, especially with hogher dosages.
At one time oxandrolone was also looked at as a possible drug for those suffering from disorders of high cholesterol or triglycerides. Early studies showed it to be capable of lowering total cholesterol and triglyceride values in certain types of hyperlipidemic patients, which initially this was thought to signify potential for this drug as a hypo-lipid (lipid lowering) agent. With further investigation we find however that while use of this drug can be linked to a lowering of total cholesterol values, it is such that a redistribution in the ratio of good (HDL) to bad (LDL) cholesterol occurs, usually moving values in an unfavorable direction. This would of course negate any positive effect that the drug might have on triglycerides or total cholesterol, and in fact make it a danger in terms of cardiac risk when taken for prolonged periods of time. Today we understand that as a group anabolic/androgenic steroids produce very unfavorable changes in lipid profiles, and are really not useful in disorders of lipid metabolism. As an oral c17 alpha alkylated steroid, oxandrolone is probably even more risky to use than an injectable esterified injectable such as a testosterone or nandrolone in this regard.

Arimidex

Arimidex

Arimidex is an aromatase inhibitor (sometimes called an AI). It is usually provided in 1MG tabs or in liquid form. The drug works in a non-steroid form by inhibiting the aromatase enzyme which convertstestosterone and other androgens into estrogen. This means that there is less estrogen tocause female pattern fat deposits, gyno, and water retention. In medicine, Arimidex isutilized to treat prostate cancer. In sports chemistry, the drug has been employed as ameans of preventing excessive estrogenic side effects during AAS use and to aid increating a harder appearing musculature for competitive bodybuilders. Unlike Nolvadex,which simply block estrogen receptor-sites, this drug prevents or reduces estrogenproduction. Though some estrogen presence is noted as necessary for AAS to reach fulleffectiveness, too much can cause a layer of fat, water retention, and breast tissue growthpotentially with tumors called gynecomastia or bitch tits. Arimidex has a 75-85%aromatization inhibition rate. Males who experienced excessive aromatization of AAS or who were extremelyestrogen sensitive usually utilized a dosage of 0.5-3.0 mg daily. In fact, most realizedexcellent estrogen control with only 0.5mg/d (mg daily). Women usually showedexcellent lean appearances (even in their legs) with 0.5-1.0 mg daily. Arimidex has a veryshort active-life so 0.5 mg dosages were often taken 2-6 times daily at equal intervals.Stacking 10-30 mg of Nolvadex with 1.0 mg of Arimidex has resulted in a near "0"estrogen activity situation regardless of the AAS protocol utilized. Directly following anAAS cycle, estrogen control has also become a problem (during periods intended for reestablishingHPTA function). In this case, the dosage was reduced from a higher startingdosage to a low dosage that was continued for 7-14 days after AAS discontinuance. Thisprotocol was considered necessary to assure clearing of AAS induced estrogen build-up.

Reported Characteristics
Active-Life: 4-6 hours Drug Class: Aromatase inhibitor (Oral) Average Reported Dosage: 0.5-3.0 mg daily Acne: No Water Retention: None Liver Toxic: Yes dosage dependent Decreases HPTA function: Increases it.

TRADE NAMES:
ARIMIDEX .25 MG TABS (International Pharmaceuticals) ARIMIDEX 1mg TABS (British Dragon)

Nolvadex (Tamoxifen Citrate)

Nolvadex (Tamoxifen Citrate)
Buy Nolvadex (Tamoxifen Citrate)
Nolvadex is a drug commonly referred to as an anti-estrogen. This would suggestless or no estrogen is produced due to the drug's actions as in the case of Teslac. Actually,Nolvadex is an estrogen antagonist, meaning it competes with estrogen at estrogenreceptor- sites. This prevents the active estrogen from entering its receptor and creatingan estrogenic complex capable of activity. Since many AAS aromatize (covert toestrogen) to some degree, the control of feminizing side effects (males should payattention here) is important. Males normally have a very low estrogen level. During AAScycles, due to aromatization, estrogen levels rise considerably. This elevated estrogenlevel can cause feminizing side effects such as increased fat deposits, water retention, andgynecomastia (growth of breast gland tissue and painful tumors under the nipple). As arule, it is more the ratio of androgens-to-estrogens than the simple increase in estrogenthat actually initiates feminizing side effects.
It is important that the reader realizes that Nolvadex does not decrease estrogenproduction and that it simply blocks estrogen receptors. For this reason the suddendiscontinuance of Nolvadex will allow the increased level of circulating estrogen tomerge with the newly freed receptors and do feminine things to the body.
"Enter Proviron". At the end of a steroid cycle, the body's natural testosteroneproduction can be impaired. Due to the aromatization of the AAS estrogen levels aresignificantly higher than normal and Nolvadex only helps by blocking the estrogenreceptors. If an athlete abruptly ends an AAS protocol without regeneration of the HPTAunder these conditions, much of the hard earned gains would disappear due to estrogenbecoming the dominant hormone. So what did the boys (that didn’t want to be a girl) do?
Proviron is an anti-estrogen (*See "Proviron" for more info) that helps to preventestrogen production while elevating androgen levels. During the last week of an AAScycle, some male bodybuilders began a HCG protocol (*See HCG) and administered 25-mg Proviron/10-20-mg Novladex 1-2 times daily. This was commonly noted to almostcompletely suppress post-cycle estrogen and its activity. Since Nolvadex increases thebody's own testosterone production, as does HCG, much of the cycle gains were retainedquite well. Nolvadex has a direct effect on the hypothalamus and therefore increases therelease of Gonadotropic hormones to a minor degree. (The hormones that tell the Leydigcells in the testes to produce androgens such as testosterone are refereed to asGonadotropics) Many added Clomid (*See Clomid) to their post-cycle stacks beginning6-10 days after HCG and continued for the average reported two week duration. In mostcases the result was athletes with normal (or above) sex drive and androgen production!
* High dosage use of Nolvadex can inhibit natural testosterone production. This is due toinhibition of enzymes needed for testosterone production by the testes.
Nolvadex was normally layered into any protocol utilizing high aromatizing steroids suchas testosterone, Dianabol, or those that are progesterone receptor stimulators such asAnadrol-50. Those who were prone to high fat deposits, water retention, and gynoconsistently reported inclusion of Nolvadex. Many are were to obtain excellent estrogenicactivity suppression with only 10-mg daily while others noted the need for as much as60-mg daily (20mg 3 times daily). The best results and guidelines were obtained bystarting low and increasing dosages only when necessary.
It is important for the reader to realize that AAS must have some estrogen presentin order to achieve their full positive potential effectiveness and provide the bestcommonly desired results. This is why many AAS lose their anabolic qualities whencombined with anti-estrogens. It is also why Methandriol magnifies the effects of thesame AAS. Those who used high anabolic/moderate-low androgenic steroids such asnandrolones, Primobolan, or Winstrol, and did not combine them with high aromatizingsteroids (such as testosterone) often considered not using Nolvadex during cycles the bestchoice when increased mass was the primary intent.
Women who used Nolvadex usually did so because it aids in fat loss due to lessestrogenic activity. I have yet to see a female compete whom was able to achieve trulycut legs with out it. Women athletes often combined 10-20mg of Nolvadex with 50-75mgProviron daily for the last few weeks of dieting. Due to availability of Clenbuterol,Proviron dosages were reported lower as of late, at least in female fitness competitors.Women should be aware that birth control is an estrogen and Novladex will block itseffectiveness. Women have note irregular menstrual cycles, weaker menstrual bleeding,and sometimes skip periods all together during Nolvadex use. I know several women whouse Nolvadex for this reason and can not say I disagree with their choice. After all, theuse of progestin type birth control as a means of regulating or even stopping menstruationis becoming accepted in the medical circles at last.
A few athletes have experienced a paradox when using high dosages of Nolvadex.Instead of lowering estrogenic activity, it increased it. What happened was that theAdrenal glands went into over drive producing a pro-hormone called DHEA. DHEA isactually an adrenal androgen normally secreted in lower levels. As circulating levelsincreased enzymic factors came into play. Research shows DHEA readily converts intoandrostenedione, and to some extent, estrogens in males. (That sucks!) The femaleendocrine system usually favors testosterone production from converted DHEA orandrostenedione. The newly formed estrogen then overwhelmed the estrogen receptorsblocking the intended qualities of Novladex. In this case, Proviron, and especially Teslacwhere notably better choices.
*Gyno that fails to react to these drugs normally must be removed by surgery. DHTderivatives can cause increases endogenous estrogen production also in some individuals.Cytadren was a commonly co-administered drug with Nolvadex.

Reported Characteristics
Active-Life: Less than 24 hours Drug Class: Anti-estrogen/estrogen antagonist (Oral) Average Reported Dosage: 10-30-mg daily Acne: None Water Retention: No High Blood Pressure: Rare (not normally attributed to the drug itself) Liver Toxic: Yes

Equipoise

Equipoise
Buy Equipoise
Equipoise (Boldenone Undeclynate), or "EQ" is one of the most widely used compounds by athletes today. Even though it is a vetrinary steroid, the quality of production is quite high due to its use in rather expensive animals. It is one of the safest and most effective steroids used today, by athletes, power lifters and bodybuilders. It can effect slow and continuous muscle mass and strength gains over a prolonged period, and generally cycles with this drug tend to be quite long because of this fact. Gains on a cutting cycle including Eq tend to be high quality lean mass, while bulking cycle gains with Eq aren't as "clean" but still have a very nice quality about them. This could be due to Eq's resistence to being converted to Estrogen, as well as DHT (technically, it converts to Dihydroboldenone).

Equipoise has become much more popular in recent years since dosages hit 200mg/ml Men get good results from a 300-600mg weekly total. In the past, this included utilizing an every other day (EOD) injection schedule, because Eq was only available in very low concentrations (50-100mgs/ml). Recently, companies like British Dragon have begun offering Boldenone in a much higher concentration (200mgs/ml) making injections much easier. Women have made excellent progress with dosages of 50-100mg total weekly doses, and this usually means a 1 injections weekly schedule. Women as a rule, seem to prefer less scar-tissue build up than men are comfortable with. In this dose range, women almost never report virilizing side effects, and usually only experienced an elevated libido. Increased hair growth on face and legs is, of course, possible (though not probable)..

Liver toxicity is not an issue with Boldenone, and it can be used for long times on either a bulking or cutting cycle, very safely. It has a reputation for appetite and red blood cell production stimulating effects, and this makes it very nice for a bulking cycle. Obviously with increased red blood cell count an increase in oxygen transport was also realized, as was improved nutrient transport, making less food become more efficient...a very nice effect for a cutting cycle.
Athletes generally stacked Boldenone with testosterone and Anadrol for mass cycles. Dianabol, due to it's close resemblance to Eq chemically, is not usually used interchangably with Anadrol in cycles containing EQ (a rare exception). Cutting, or pre-contest cycles including Boldenone often include Trenbolones, Winstrol. With the afforementioned drugs, an anti-estrogen is generally not necessary.

Reported Characteristics
Boldenone Undeclynate 1,4-androstadiene-3-one-17b-ol Cutting/Bulking:Both Anabolic Rating: 100 Active-Life: 7-9 days Drug Class: Anabolic /Androgenic steroid (for injection) Average Reported Dosage: Men 300-600mg weekly Women 50-100mg weekly Acne: Rare Water Retention: Low High Blood Pressure: Rare Aromatization: About 50% of testosterone Liver Toxic: No DHT Conversion: No (*converts to DHB) Decreases HPTA function: Yes Average Price: $150/10ml bottle

Trade Names
EQUIPOISE 200MG/ML (British Dragon) ULTRAGAN 100 100MG/ML BOLDEBAL-H 50MG/ML EQUIPOISE 25MG,50MG, /ML ULTRAGAN 50 50MG/ML GANABOL 25MG, 50MG/ML PACE 25MG/ML VENBOL 25MG/ML

Masteron (Drostanolone Propionate)

Masteron (Drostanolone Propionate)
Buy Masteron (Drostanolone Propionate)
Masteron is a highly androgenic injectable steroid that is derived from DHT (dihydrotestosterone). DHT does not aromatize to estrogen (and in fact may combat estrogenic sides), and as a result, there was no noted water retention during administration nor gynocomastia. Masteron is almost exclusively used during the last 4-5 weeks before a bodybuilding show at a dose of 100-mg every second day. Additionally, according to available literature, Masteron is not much of a mass drug, and it's always used for cutting, from what I've seen reported. Masteron has a receptor binding ability above that of testosterone, due to it's being DHT-derived, which should impart lypolytic (fat-burning) effects above that of testosterone, and also give it a nice strength building component.
Pictured above is British Dragon's MASTABOL
Masteron can bind to Sex-Hormone-Binding-Globulin, which prevents AAS from merging with their receptors. Masteron can stop this from happening. This may mean that it enhances cycles, by letting other steroids work more effectively. Proviron, which is often called "oral masteron" (*correctly) does this very well also. Usually, Masteron would be stacked with Testosterone Propionate and possibly Trenbolone Acetate, which would be administered all at once, every second or third day in the same injection.
Reported Characteristics
Chemical Name:Drostanolone Pharmaceutical Name:2-alpha-methyl-androstan-3-one-17beta-ol Cutting/Bulking:Cutting Anabolic Rating: 62 Active Life: 2-3 days Drug Class: Androgenic/Anabolic steroid (For injection) Average Reported Dosage: Men 300-500-mg weekly Women 100-350mg weekly Acne: Yes Water Retention: None High Blood Pressure: Rare Liver Toxic: None Aromatization: None Noted Comments: High Androgenic/Moderate Anabolic/Moderate anti-estrogenic DHT Conversion: DHT-derived Decreases HPTA Function: Low if any
Trade Names:
MASTABOL 100MG/ML (British Dragon) MASTERIL 100-MG/2-ML MASTERON 100-MG/2-ML

Insulin

Insulin, by itself, is not an effective anabolic. (If it were, diabetics such as Mary Tyler Moore would be huge.)
Insulin, in combination with androgen and resistance exercise, may trigger maturation of satellite cells (small, more or less useless cells that are held in reserve, which do not contribute to muscular strength) into mature muscle cells. The advanced steroid user may have plateau'd in that respect, and adding insulin can give new gains.
I don't think anyone knows whether short or long acting is more effective for building muscle. They seem to be about equally effective. A problem with long acting appears if it would continue acting while asleep: one might die if insufficient carbs had been taken.

Winstrol (stanozolol)

Winstrol (stanozolol)
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.

Cytomel ( liothyronine sodium )

Cytomel ( liothyronine sodium )
Cytomel (liothyronine sodium)
Quick overview:
Drug Class: Synthetic thyroid hormone Average Dose: 25-100 mcg/dayComments: Significant suppression of Thyroid function during use
Cytomel is the popularly recognized brand name for the drug liothyronine sodium. This is not an anabolic steroid but a thyroid hormone. It is used medically to treat cases of thyroid insufficiency, obesity, certain metabolic disorders and fatigue. Specifically this drug is a pharmaceutical preparation of the natural thyroid hormone triiodothyronine (T-3). When administered, T3 increases the patient's metabolism. The result is an increased rate of cellular activity (noted by a more rapid utilization of carbohydrates, fats and proteins). Bodybuilders are particularly attracted to this drug for its ability to burn off body excess fat. Most often utilized during contest preparation, one can greatly decrease the amount of stored fat without being forced to severely restrict calories. To this end Cytomel is commonly used in conjunction with Clenbuterol and can produce extremely dramatic results. This combination has become very popular in recent years, no doubt responsible for many "ripped" on-stage physiques. It is also noted by many that when thyroid hormones are taken in conjunction with steroids, an increased anabolic effect can be seen (noticeably greater than if the steroids are used alone). This is likely due to faster utilization of proteins by the body, increasing the rate for new muscle accumulation.
Caution should be taken if one is considering using this drug. Cytomel comes with an extensive list of warnings and precautions which are not to be ignored. Side effects include, but are not limited to, heart palpitations, agitation, shortness of breath, irregular heartbeat, sweating, nausea, headaches, and psychic/metabolic disorders. It is a powerful hormone, and one that could potentially alter the normal functioning of the body if misused. When taking Cytomel, one must remember to increase the dosage slowly. Generally one 25mcg tablet is taken on the first day, and the dosage is thereafter increased by one tablet every three of four days for a maximum dosage of 100mcg. This will help the body adjust to the increased thyroid hormone, hopefully avoiding any sudden "shock" to the system. The daily dose should also be split evenly throughout the day, in an effort to keep blood levels steadier. Women are more sensitive to the side effects of Cytomel than men, and usually choose not to take no more than 50mcg daily.
It is important to stress that a cycle should last no longer than 6 weeks and it should never be halted abruptly. As slowly as the dosage was built up it should also be lowered, one tablet every 3-4 days. Taking Cytomel for too long and/or at too high a dosage can result in a permanent thyroid deficiency. After doing such, one might need to be treated with a drug like Cytomel for life. It is also a good idea to first consult your physician and have your thyroid function tested. An undiagnosed hyperfunction would not mix well with the added hormone. An athlete should also be sure never to purchase an injectable form of the drug. It is generally an emergency room product, much too powerful for athletic use. Since T-3 is the most powerful thyroid hormone athletes are using, this is generally not the starting point for a beginner. Before using such a powerful item, it is a good idea to become familiar with a weaker substance. The highly popular Triacana is very mild, allowing the user much more latitude (from severe side effects) than Cytomel. An in-between point is Synthroid (synthetic T-4), still weaker in action than Cytomel. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.

Ephedrine (ephedrine hydrochloride)

Ephedrine (ephedrine hydrochloride)
Ephedrine (ephedrine hydrochloride)
Ephedrine is a stimulant drug, belonging to a group of medicines known as sympathomimetics. Specifically it is both an alpha and beta adrenergenic agonist (you may remember Clenbuterol is a selective beta-2 agonist). In addition, ephedrine enhances the release of norepinephrine, a strong endogenous alpha agonist. The action of this compound is notably similar to that of the body's primary adrenergic hormone epinephrine (adrenaline), which also exhibits action toward both alpha and beta receptors. When administered, ephedrine will notably increase the activity of the central nervous system, as well as have a stimulatory effect on other target cells. This will produce a number of effects beneficial to the athlete. For starters, the user's body temperature should rise slightly as more free fatty acids are produced from the breakdown of triglycerides in adipose tissue (stimulating the metabolism). This should help the user shed subcutaneous body fat stores, enhancing the look of definition in the physique. The anabolic effectiveness of steroids may also be increased with this substance (mildly), as the metabolic rate is a measure of fat, protein and carbohydrate conversion by the body. An enhanced metabolic state could clearly hasten the deposit of new muscle mass.
This stimulant effect of this drug will also increase the force of skeletal muscle contractions. For this reason ephedrine is commonly used by powerlifters before a competition, as the resultant (slight) strength and energy increase can clearly improve the weight totals on major lifts. It may also provide a notable mental edge, as the user is more energetic and better able to concentrate on the tasks ahead. Many recreational weight lifters find this effect particularly welcome, and use 25-50mg of this stimulant as a regular adjunct to their training sessions. The user often feels capable of attacking the weights with much more intensity while taking ephedrine, and leaves the gym knowing they will have had a more productive workout. It is important that this compound not be used continuously for this purpose, as its effect will diminish as the body becomes accustomed to the drug. In most instances the user will take the drug only two or three times per week, usually on those days personally "important" (like chest day). The athlete is also wise to take a break (one to two months) from ephedrine treatment after several weeks have past, so as to continue receiving the optimal effect from this drug. While the strength boosting effect of this drug is noteworthy, the primary application for ephedrine remains to be as a cutting agent. The athlete will generally take this drug a few times daily during dieting phases of training, at a dosage of 25 to 50mg per application. The widely touted stack of ephedrine (25-50mg), caffeine (200mg) and aspirin (300mg) is shown to be extremely potent for fat loss. In this combination, the ephedrine and caffeine both act as notable thermogenic stimulants. The added aspirin also helps to inhibit lipogenesis by blocking the incorporation of acetate into fatty acids. The athlete will be sure this stack is working by noticing an increase in body temperature, usually a degree or so (not an uncomfortable raise). This combination is taken two to three times daily, for a number of consecutive weeks. It is discontinued once the user's body temperature drops back to normal, a clear sign these drugs are no longer working as desired. At this point increasing the dosages would not prove very efficient. Instead a break of several weeks should be taken, so that this stack may once again work at an optimal level.
Ephedrine can produce a number of unwelcome side effects that the user should be aware of. For starters, the stimulant effect can produce shaky hands, tremors, sweating, rapid heartbeat, dizziness and feelings of inner unrest. Often these effects subside as the user becomes more accustomed to the effect of this drug, or perhaps the dosage is lowered. In general, those negatively impacted by caffeine would probably not like the stronger effects of ephedrine. The mental and physical state produced by this drug is also quite similar to that seen with Clenbuterol, so those who find little discomfort with this treatment should (presumably) be fine with this item (and vice versa). While taking this drug one may also endure a notable loss of appetite, usually a welcome effect when dieting. Ephedrine is in fact a popular ingredient in combination (prescription) appetite suppressants. The user may further notice headaches and an increase in blood pressure with regular use of ephedrine. Those suffering from thyroid dysfunctions, high blood pressure or cardiac irregularities should also not be taking this drug, as it will certainly not mix well with such conditions.
As of late there is much discussion about the future availability of ephedrine. This is due to that fact that ephedrine tablets are used as the primary base for the manufacture of methamphetamine. This is you know is an illegal drug, made and sold illicitly. The structure of these two compounds is notably similar, as only a few chemicals are needed to change ephedrine into "meth". Since ephedrine is currently an over-the-counter product, underground manufacturers can easily obtain it. A trend involving large volume retail purchases for OTC ephedrine products has been developing, and many states are taking notice of it. With the widespread increase of amphetamine addiction (and related crime) ephedrine may soon join the list of federally controlled substances. While some states have already taken action to restrict the sale of this stimulant, federal action would probably be required in order have a major impact on availability. Even if a particular state is aggressively preventing the sale of these products, a thriving mail-order market still exists to fill the demand. Thumbing through the back pages of many national magazines should make this clear, as we notice advertisements for companies which ship Ephedrine tablets out by the thousand.

Deca-Durabolin

Deca-Durabolin
Buy Deca-Durabolin
Nandrolone Decanoate is a very anabolic and slightly androgenic form of 19-nortestosterone A very prominent positive nitrogen balance is realized with administration of this product. And since nandrolone promotes nitrogen storage, growthand repair in hard-trained muscles will bemore pronounced than normal. In addition, a noted effect by many athletes polled was that most of them experienced a joint healing effect during Deca cycles. Since aromatization was low, in 400-600-mg weekly dosages, and fatburning was high due to the high affinity to the androgen recepror that Deca has, anti-estrogens were not typically necessary to avoid gyno and other estrogen induced side effects.
British Dragon's Nandrolone Decanoate 200mg/ml 10ml bottle. Quickly becoming a best seller according to many bodybuilders
Commonly used doses for men were in the area of 400-600mg weekly, and dosages over 400 mgweekly caused more water retention, while women seemed to do well with 100mgs/week. In fact, women have consistently reported very respectable lean mass and strength gains at dosages of only 50-100 mg weekly. Virilizing effects usually were avoided by single weekly injections of 50-100 mg nandrolone decanoate. Men, however would need to stack Deca with testosterone in order to have more appreciable weight gains, and avoid sexula dysfunction. Unfortunately, this compound is detectable for up to a year and a half after administration, so drug tested athletes should avoid it.


Reported Characteristics Pharmaceutical Name:Nandrolone Decanoate Chemical Name:19-nor-testosterone Cutting/Bulking:Both Anabolic Rating: 125 Active-Life: 14-16 days Drug Class: Anabolic/Androgenic steroid Average Reported Dosage: Men 400-600mg weekly, Women 50-100mg weekly Acne: Possible Water Retention: Some Decreases HPTA function: Severe High Blood Pressure: No. Aromatization: Low, converts to less active norestrogens Liver Toxic: No DHT Conversion: No, converts to NOR- DHT Noted Comments: Highly anabolic/moderate androgenic effects Average Price: 10/amp
TRADE NAMES DECA DURABOLIN 250mg/ml (British Dragon) DECA-DURABOLIN 200mg/2ml vial (Norma Greece) DECA-DURABOLIN (Organon) ANABOLINE 50-MG/ML ANDROLONE- D 200 200-MG/ML DECA DURABOLIN 25-MG/ML DECA DURABOLIN 50-MG/ML DECA DURABOLIN "100" 100-MG/ML DECA DURABOLIN 200-MG/ML ELPIHORM 50MG/ML EXTRABOLINE 50MG/ML HYBOLIN DECANOATE 50,100MG/ML JEBOLAN 50MG/ML NANDROLONE DECANOATE 50,100, 200MG /ML NANDROBOLIC L.A. 100MG/ML NEO-DURABOLIC 100,200,/ML NUREZAN 50MG/ML RETABOLIL 25MG/ML RETABOLIL 50MG /ML DECANANDROLEN 200 200MG/ML STEROBOLIN 50MG/ML TURINABOL DEPOT 50MG/ML ANABOLICAN 25ML/ML 10, 50ML

Anadrol ( Anadrol 50 )

Anadrol
Buy Anadrol - Click Here
This is an oral, methylated (17-alpha-alkylated) steroid that is both highly androgenic as well as highly anabolic. Some novice users report weight gains of up to a pound per day fpor the first 3 weeks of administration, as well as incredible strength gains. Neither is uncommon among first-time steroid users, and this type of weight gain makes Anadrol one of the most highly coveted drugs for off season mass-building cycles. Aggressiveness often increases dramatically on this compound, and that may be due to the elevation in androgen levels it provides, it's effects on the central nervous system, and it being derived from DHT (Dihydrotestosterone), which anecdotally seems to make athletes much more agressive. This last effect is often seen by the media as a negative side effect, but in a hard training (and emotionally stable) athlete, this aggressiveness often manifests itself as a stronger drive in the gym and results in more strength gained, and ultimately, more weight. Unfortunately, users of this drug also experience the negative aspects of DHT which can include excessive water retention, acne, and hairloss.
Anadrol 50 tablets by British Dragon Many people consider Anadrol a dangerous compound, but this isn't necessarily so. Anadrol was originally produced in a whopping 50mg pill, so you don't need to take many of them to get a very high dose of Oxymetholone (the drug in Anadrol). Compare this dose to Anavar which is produced in a 2.5mg pill, or Dianabol which was produced in a 5mg pill, and you'll see why Anadrol has such a reputation for being powerful. One tab is has as many milligrams as 20 of the original Anavar tabs or 20 of the original Dianabol tabs! On a milligram for milligram basis, Anadrol is no more dangerous than most oral steroids out there. You just have to remember that you get 50mgs in each tablet, and adjust your dose accordingly. Occasionally people using Anadrol get flu-like-symptoms or a headache. I personally get both, but the headache is much worse (it is probably from my bloodpressure elevating quickly). Alot of the horror stories you hear about steroids is from people abusing this one in particulat. Chris Duffy ( a now retired IFBB professional) claimed to use ten of them every day. It's no wonder that it has been linked to prostate and liver cancer, liver disease, thyroid dysfunction, leukemia, and heart disorders, and even hepatic comas. Again, this is a powerful drug, and not to be taken lightly, but is no more dangerous than many others. It will also raise your hematocrit, and commesurately your blood pressure. to where clotting time may become an issue. Since Anadrol is derived from DHT, it can cause issues in DHT-sensitivce target tissure like the scalp, prostate, and sebaceous glands. It can also cause suppression of the Hypothalamic-Pituitary-Testicular-Axis, resulting in a low sperm count, and a lowering of Leutenizing hormone, which is what signals your testes to secrete testosterone. Anadrol therapy, therefore, will lower your testosterone levels.
Women generally steer clear of Anadrol, because of it's possible virilizing effects, including clitoral enlargement, facial hair growth, deeper voice, and missed periods..
Oxymetholone is infamous for negatively effecting liver function and increasing markers of that such as SGPT and SGOT enzymes (and others) which are all hepatic indicators (indicators of liver dysfunction). Jaundice (a yellowing of the whites of the eyes and finger nails) can even occur from extended Anadrol use. As previously stated, Anadrol is a derivative of DHT, which is itself a 5-alpha-reduced version of testosterone. Some androl users have reported gyno from its use but this is unlikely to be a result of anadrol (which doesn't convert to estrogen, nor DHT, nor can it stimulate the progesterone receptor). Users of Anadrol who experience gynocomastia (the of breast tissue by males) have probably developed this condition as a result of the concurrent use of another steroid along with their Anadrol. Oxymetholone also causes edema (water retention) which could possibly be due to enhanced retention, which often causes a smoothe appearance to muscles.
Andarol'is medical use is (as with most steroids) to treat low red blood cell production, which often manifests itself as aenemia. Therefore, during administration of Anadrol, red blood cell count is increased greatly. For the hard-training athlete, this is a great benefit bnecause it meant that there is more oxygen transported to the muscles, resulting in both an incredible muscle pump as well as increased ability to do multiple sets with very heavy weights. The time needed between sets, and ability to do more sets per workout are both increased, and a reduced need for off-days from the gym is often seen as well. This increased work capacity contributes to the athlete being able to do a great deal more productive weight training sessions per cycle, and this of course contributes to their gains immeasurably.
Advanced bodybuilders and power lifters have reported excellent results with 50-200 mg per day, taken in divided doses. It's very often the drug of choice for athletes attempting to move up a weight class in bodybuilding or powerlifting. Although myself and many others have used Anadrol alone, it's not very common to do so, and it's generally stacked with something like Testosterone, and Deca Durabolin or Equipoise. By stacking it with highly anabolic compounds like them, more high quality gains are generally seen, and less of the watery/bloated look is experienced.

Reported Characteristics
Pharmaceutical Name:Oxymetholone Chemical name:17-beta-hydroxy-2-hydroxymethylene-17 alpha-methyl-5 alpha-androstan-3-one Cutting/Bulking:Bulking Anabolic Rating:320 Active - Life: Less than 16 hours Drug Class: Highly Androgenic / Anabolic Steroid (Oral) Average Reported Dosage: Men 50-200 mg daily. Acne: Yes Water Retention: Extreme High Blood Pressure: Yes Liver Toxic: High DHT Conversions: DHT-Derived Decreases HPTA Function: Yes Aromatization: No Average Price: Up to $3/tab
TRADE NAMES
ANAPOLON 100 100mg tabs ANAPOLON 50 ANADROL-50 50 MG TABS ANAPOLON 5, 50 MG TABS HEMOGENIN 50 MG TABS SYNASTERON 50 MG TABS OXYMETHOLONE USP XXII 50 MG TABS

Human Growth Hormone (GH)

Human Growth Hormone (GH)
Buy Human Growth Hormone (GH) - Click Here
Human Growth Hormone (GH) has been a subject of debate since I was a kid.Natural (endogenous) GH is produced by the pituitary gland. Children produce 2 i.u."spurts" 4-7 times per day for 4-5 non-consecutive days during a 2-3 week period (duringgrowth spurts). That would equal 32-70 i.u. in only a 4-5 day span. A healthy adult'spituitary releases only 0.5-1.5 i.u. daily.
GH has quickly become a very popular product for athletes looking to reach the top level Until the mid 1980's, the only available form of exogenous (occurring outside thebody) GH was manufactured by taking the pituitary glands of dead corpses (like there area lot of "live" corpses running around?) and grinding them up. (I am not joking!). TheGH was then extracted and purified through a series of expensive procedures, packed andsold by prescription only for use by children suffering from stunted growth. About 1987,this form of GH was linked to a fatal brain disease called CREUTZFELD-JAKOBDISEASE, and removed from the market.
Enter Genetech and synthetic GH. The first synthetic GH was produced bygenetically altering transformed mouse cells /Ecoli. Natural GH has a 191 amino acidsequence where as the Protropin brand of GH produced by Genetech contains 192 aminoacids in its sequence. This may have the affect of causing the body to produce GH antibodieswhich deactivate the GH. Most synthetics now contain the normal 191 amino acidsequence, of which there are over a dozen available today.
GH has 3 effects any athlete desires: GH helps the body burn more adipose (fat)tissue by promoting the release of fatty acids to be used as energy. Normally at rest, thebody uses about an equal division of fat and carbohydrate calories. When the endocrinesystem senses a low circulatory level of glucose, the hypothalamus-pituitary-axis (HPA)reacts by releasing GH. The GH then triggers (through a series of enzymic/chemicalreactions) the release of fatty acids from adipose stores so metabolic energy requirementscan be met. This means exogenous GH administration has been well documented to dothe same.
GH has a very potent anabolic (protein synthesis/tissue building) effect. Inexerting anabolic effects, it can cause both hyperplasia (an increase in the number ofmuscle cells) and muscular hypertrophy (the enlargement of muscle cells). This change incell number is permanent and therefore means more cells to make bigger. GH also has ananabolic effect on soft tissues such as tendons, cartilage, and other connective tissue. Thismeans old injuries repair and strength increases due to stronger connective tissue… bothat an accelerated rate. It is a well known fact that GH is a powerful anti-catabolic agent(protein sparing). This effect has allowed modern bodybuilders to retain or even addsignificant lean mass tissue during calorie restricted periods (cutting phases) and becomethe shredded monsters of the new era.
When using GH many athletes were less than satisfied with their results. Mostlikely this was because they bought bogus GH. It was common to find GH for a hard-corepro bodybuilder cost about $35,000 or more, yearly. To test GH, most simply bought apregnancy test kit, mix a vial of (hopefully) GH and place a drop or two in the test area.If the test result was “pregnant”..they had been screwed. Most pregnancy test kits test forelevated gonadoltropins (which HCG is and GH is not). For those few, whose bodiesmanufactured GH anti-bodies (and GH failed to work for you) sorry about your luck. GH,used properly, has overwhelmingly been renowned as a genetic equalizer if used for thatpurpose.
Any polled athlete chose to use GH as a performance enhancing drug should havefirst understand at least the basics of its actions.
GH itself is not responsible for the majority of the effects seen from GH use.Actually GH is only a precursor to the so-called "good stuff". When GH passes throughthe liver, it is converted into INSULIN-LIKE GROWTH FACTORS (such as IGF-1).IGF-1 is a very active but unstable chemical, which is why the body waits until the lastsecond to make it naturally. The liver has a limited capacity to convert excess GH intoIGF-1 unless other chemical hormone levels are also elevated. Insulin, T-4/T-3 thyroidhormones, gonadotropins, androgens/anabolic hormones, and even estrogen andcorticosteroids all play an important role in the positive effects of GH. So they too wereoften exogenously elevated in what was considered “the correct ratios” by the largest ofthe self administering athletes. For the liver to convert high levels of GH to IGF-1 severaltimes a day and cause a high quality anabolic response, it was commonly noted that T-3thyroid hormone and insulin also needed be increased to accomplish the desired effect.
Triacana may be strong enough to increase thyroid activity, but Cytomel was consideredto be a better choice. Though some seemed to disagree, most emphatically believed that afast-acting insulin such as HUMULIN-R or Humalog was a better and safer choice ofexogenous insulin since they allowed better timing and have a much shorter effectiveperiod. This allowed the athletes to time insulin activity with the active period of GH atthe optimum absorption times such as upon waking and the first few hours after a workout.The result was less chance of fat accumulation and a heightened anabolic response.Since GH suppresses natural T-3 thyroid hormone release, the exogenous administrationof Triacana or Cytomel allowed for an elevated calorie intake that was utilized more forbuilding muscle and soft tissue than for adipose tissue storage. Many pro bodybuildersused Clenbuterol and/or ephedrine stacks with GH while dieting. Since Clenbuterol and Ephedrine both suppress natural insulin release, they usually stacked the GH and Clenbuterol /Ephedrine with a synthetic T-3 thyroid hormone and sometimes with insulinas well. The use of insulin was dependent upon whether it was a bulking or dieting phaseand depending on how their body responded to exogenous insulin use.
*I can not stress enough how dangerous insulin use can be. Comas and death are quitepossible if used wrong. If you wish to use it, please see a doctor for monitoring.AAS and/or Clenbuterol further enhance the anabolic effects of GH. From all buta few polled it was reported that excellent muscle mass gains resulted with the use of GHwhen other chosen hormone levels were also met (*also see "cycles") and one couldafford it. Also, beware of fake GH. It is more common than you may realize. It is anillegal drug and the black market is not always honest.
The question of dosage was a big one. For the purpose of stunted growthmanufacturers of GH (due to pituitary hyophysially caused stunted growth) state 0.3 i.u.weekly per LB of body weight. So for a 235 LB bodybuilder that would equal 70.5 i.u.weekly, meaning a daily total of about 10-i.u. However, even 2-3i.u. daily did producesome nice results over a 6-8 week period when the other reported hormone requirementswere met as well. Short high dosage burst cycles too were noted to create these results(which will be discussed later) by the more elite of those polled.*GH is medically administered intramuscularly or subcutaneously (under the skin).*When multiple injections were utilized, I personally noted better results withsubcutaneous administration.
*1-mg=2.7 i.u. of GH and some products are listed as such.With exception of those few whose insert states otherwise, the dry unmixed GHsubstance maybe stored at room temperature. Once the solution has been mixed with thedry GH powder, (SWIRLED, DO NOT SHAKEN) the mixture must be refrigerated andlasts for 24-hours before it begins to degrade. An interesting product has becomeavailable called DEPO-NUTROPIN that has an active-life of about a month. This wouldallow for fewer injections and a reduced price. Also, several patents run out thisyear so many overseas and less expensive GH preparation will soon be available in theU.S. by prescription only.
*Though no negative side effects were reported, the available literature does listseveral serious ones: Kidneys and heart enlargement, high blood pressure, diabetes, thyroidhormone deficiency, and acromegaly. For the most part, they are rare to say the least andusually would be from extreme dosages and lengths of cycles. But like most hormones, youjust do not know until it is a fact for you. Kind of scary, huh?When GH was utilized with an insulin protocol, it was considered important tospace injection periods between GH and insulin about an hour. Also if GH was utilizedonly twice daily, it was reported best to avoid natural high points of GH release such asfirst thing in the a.m., post-work out, and right before bed. This was if GH was utilizedwithout insulin.

Reported Characteristics
Active-Life: Varies upon injection method Drug Class: Growth Hormone/IGF-1 Precursor (For injection) Average Reported Dosage: 2-16 i.u. total daily (1mg=2.7 i.u) Acne: None Water Retention: Very rare High Blood Pressure: Very rare Liver Toxic: None Aromatization: None High Anabolic/No Androgenic Effects
Trade Names
CORPORMON 4 I.U GENOTONORM 4 I.U. GENOTROPIN 2,3,4,12 I.U. GENOTROPIN 16 I.U. GRORM 2,4 I.U HUMATROPE 4 I.U. HUMATROPE 5MG HUMATROPE 16 I.U. NORDITROPIN 12 I.U. NUTROPIN 10 MG PROTROPIN 10 MG.. SAIZEN 10 I.U. SOMATOHORM 4 I.U. ZOMACTORS 4,12 I.U.