Stanozolol is one of the most popular and recognized anabolic steroid among bodybuilders, that’s why most of steroid manufacturers make use of this opportunity and has this drug in their production. An exception is not Platinum Biotech, which during years have proved that they can offer to users high quality steroids.
For stanozolol, Platinum Biotech uses the branded name Stanabolic-10. As you realized, the active component of Stanabolic-10 is Stanozolol and it is 10 mg per tablet. It is sold by 100 tablets in a sterile sachet.
The main reason why this steroid is so popular is maybe because it does not convert to estrogen and an anti estrogen drug is not needed while using stanozolol. Also it does not give water retention and not giving gynecomastia.
The daily dosage of Stanabolic-10 is usually 35 – 75 mg. Most often it is not taken alone, usually it is taken in combination with other steroids depending on desired goals. Testosterone, D-bol or Oxymetholone is added for bulking purposes. In this case stanozolol will balance out the cycle a bit, giving good anabolic effect with lower estrogenic activity. The result of this combination should be a gain in muscle mass with a low level of water and fat retention.
Stanabolic-10 can be used in combination with Trenbolone or Halotestin. Such combination is usually for contests and dieting phases. The result should be a strongly defined and hard look of muscularity.
SIDE EFFECTS:
Stanozolol is a 17-alpha-alkylated, that’s why for those who take this steroid for a long period of time and in high doses, liver toxicity should be a concern. Due to the liver toxicity it is recommended to those who take this steroid to limit their cycles to six weeks or less. If you decided to run Stanabolic-10 for a longer period of time, you should monitor your liver values via blood test to ensure that no damage occurs.
Other side effects are: acne, prostate enlargement and aggravation of male pattern baldness. As i said earlier, to avoid dramatic side effects the dosage and the time of using should be strictly monitored.
Oxandrolone is popular among bodybuilders because of its fabulous effects. It was a shame if EURO-MED with its reputation wouldn't make its own Oxandrolone. Oxandrolone by EURO-MED is called Anavar. Its strength is 10 mg per tablet and it is sold by 30 tablets. This steroid is ideal for bulking purposes and it is commonly used during cutting phases of training. Who used this steroid probably know that it has two major advantages: it does not aromatize and it does not influence the body’s testosterone production. These two things are very, very important for body's health. No less importantly is that Anavar does not retain liquid in the joints and the muscles.
This steroid is commonly used by bodybuilders, weightlifters and powerlifters. Weightlifters and powerlifters likes this steroid because it causes fabulous gains in strength without gaining body weight. This is very important for them because they don’t want to end up in higher weight class. Anavar itself does not cause noticeable muscle growth and strength. It can be combined with many steroids, like Deca Durabolin, Dianabol and various testosterone compounds. A combination that has been proven to be very effective is Oxandrolone and Halotestin 20 - 30 mg per day. The same effect will have Oxandrolone with 120 – 140 mcg of Clenbuterol daily. A good gain in muscle mass and strength is 200 mg of Deca Durabolin per week, 500 mg of Testosterone Enanthate per week and Anavar 25 mg daily.
SIDE EFFECTS: Anavar is slightly toxic and shows only few side effects, but should not forget that as almost oral steroids it is 17-alpha-alkylated and the usage in high dosage and for a long period of time it can put stress on liver.
50mg - 100mg per day
Anabol 10 is the branded name of British Dispensary. This lab is new on the market, but in a short period of time became well known by bodybuilders from all over the world because of its high quality products. The active substance in Anabol 10 is Methandienone, which is 10 mg per tab, also it is sold by 500 tabs per pack. This kind of drug is also known among bodybuilders as D-bol, Anabol, Methan, Methanabol, Anabol 10 etc.
Anabol 10 it is an oral steroid, which has a great effect on protein metabolism and its androgenic effect manifests itself in buildup of muscle mass and strength. Often it is called a "mass steroid", because in the first six weeks it is normal to gain 2 – 4 pounds of body weight per week. It is important to know that this steroid manifests itself in a noticeable retention of water and aromatizes easily. To avoid these effects it is recommended to take Nolvadex and Proviron.
The dosage should be coordinated with individual goals, for experienced bodybuilders the daily dose should be around 40 – 60 mg. Novices do not need to take more than 20 – 40 mg per day.
After eight weeks when the effect begins to slow down and you want to continue the cycle, the dosage of Anabol 10 should not be increased, it is enough to add such injectable steroids as Deca Durabolin or Primobolan. If you’ll choose Deca Durabolin, the dosage should be 200 mg per week, if Primobolan the same dosage of 200 mg per week should be enough. If you are either impatient or more advanced, you can start taking Anabol 10 20 – 30 mgs daily and Deca Durabolin 200 – 400 mg per week.
If you are more interested in strength and less in body mass, than you can combine Anabol 10 with Oxandrolone or Stanozolol tablets.
SIDE EFFECTS:
As many other steroids, Anabol 10 has many potential side effects, but they are rare when the daily dosage is up to 20 mg. This steroid is I 7-alpha-alkylated, so it can be toxic to liver when it is taken in high dosage and for a long period of time. Anabol 10 strongly converts into estrogens and in some athletes causes gynecomastia. To avoid such effects it is recommended to take such drugs as Nolvadex and Proviron. Because of androgenic component the sebaceous gland is stimulated and it can cause acne vulgaris on the face, neck, chest, back and shoulders.
40 - 60mg per day.
Methandienone 10mg is the branded name of LA Pharma. This lab is new on the market, but in a short period of time became well known by bodybuilders from all over the world because of its high quality products. The active substance in Methandienone 10mg is Methandienone, which is 10 mg per tab, also it is sold by 100 tabs per pack. This kind of drug is also known among bodybuilders as D-bol, Anabol, Dianabol, Methan, Methanabol, Methandienone 10mg etc.
Methandienone 10mg it is an oral steroid, which has a great effect on protein metabolism and its androgenic effect manifests itself in buildup of muscle mass and strength. Often it is called a "mass steroid", because in the first six weeks it is normal to gain 2 – 4 pounds of body weight per week. It is important to know that this steroid manifests itself in a noticeable retention of water and aromatizes easily. To avoid these effects it is recommended to take Nolvadex and Proviron.
The dosage should be coordinated with individual goals, for experienced bodybuilders the daily dose should be around 40 – 60 mg. Novices do not need to take more than 20 – 40 mg per day.
After eight weeks when the effect begins to slow down and you want to continue the cycle, the dosage of Methandienone 10mg should not be increased, it is enough to add such injectable steroids as Deca Durabolin or Primobolan. If you’ll choose Deca Durabolin, the dosage should be 200 mg per week, if Primobolan the same dosage of 200 mg per week should be enough. If you are either impatient or more advanced, you can start taking Methandienone 10mg 20 – 30 mgs daily and Deca Durabolin 200 – 400 mg per week.
If you are more interested in strength and less in body mass, than you can combine Methandienone 10mg with Oxandrolone or Stanozolol tablets.
SIDE EFFECTS:
As many other steroids, Methandienone 10mg has many potential side effects, but they are rare when the daily dosage is up to 20 mg. This steroid is I 7-alpha-alkylated, so it can be toxic to liver when it is taken in high dosage and for a long period of time. Methandienone 10mg strongly converts into estrogens and in some athletes causes gynecomastia. To avoid such effects it is recommended to take such drugs as Nolvadex and Proviron. Because of androgenic component the sebaceous gland is stimulated and it can cause acne vulgaris on the face, neck, chest, back and shoulders.
20mg - 60mg per day
BOLDEN-300 is destinated for intramuscular injection and is made by Global Anabolic. This steroid drug contains Boldenone Undecylenate, and it is also known as Equipoise. Boldenone Undecylenate is a derivative of testosterone, with strong anabolic and moderately androgenic properties. Athletes who are taking Equipoise often report a slow, but constant and quality muscle growth.
Boldenone Undecylenate was created while attemptiing to make a drugsimillar to D-bol, but more long acting. But what was created was a steroid that wasn't like D-bol. A simple way to think of Equipoise is simply as Dianabol without the 17-alpha-methyl group.
Usually BOLDEN-300 is compared with Deca Durabolin, but water retention with BOLDEN-300 would be slightly higher than that with Deca Durabolin, but less than with Testosterone.
The benefit of taking BOLDEN-300 is that this steroidincreases protein synthesis in the muscle cells. This effect is verysimilar while taking such steroids like Anavar. Equipoise gives slowerbut higher quality gains in muscles, more quality than taking steroid based on Testosterone.
BOLDEN-300 is not a rapid mass builder, this steroid provide slow but steady gains in strength a muscles. Better effects are seen when this steroidis taken for long cycles, usually 10 weeks in length. The musclesshould be very defined and the look should be very solid. The avantageof this steroid is that the size of the muscles gained during the cyclecan be retained after the drug is discontinued. As was mentionedearlier structurally Equipoise is very identing with bulking drug Dianabol.
Depending on the desired results, BOLDEN-300 can be combinated with other steroids. For exemple, for mass, it can be combinated with Anadrol or injectableTestosterone. The effect should be incredible gains of muscles andstrength, without the same intensity of side effects if using this steroid alone. In cutting phases, to mentain and to improve the hardness and density of the muscles it is advised to combine BOLDEN-300 with a non-aromatizable steroid such as Trenbolone Acetate, Halotestin, or Winstrol.
The compound of this steroid drug, BOLDEN-300 or Equipoise, increase red blood cell production. These proprieties are characteristic for anabolic or androgenic steroids.Athletes inject BOLDEN-300 ( Equipoise) at least once a week and the dosage of this steroid drug should be in range: for men 400 - 600 mg per week; for women the dosage should be in range 50 - 150 mg per week. When this drug is used for longer cycles, are seen the most positive effects. The duration of the cycle should be more than 8 - 10 weeks.In cutting phases, to improve density and hardness of the muscles, BOLDEN-300 drug can be combined with non-aromatizable steroids, such as GP Halotest, Trenbolone Acetate, or Stanozolol.
BOLDEN-300 is not an ideal steroid for athletes. This steroidhas the tendency to produce detectable metabolites in the urine monthsafter use. This effect is associated and with Deca Durabolin. This isof course due to the high oil solubility of long chain esterifiedinjectable steroids, a property which enables the drug toremain deposited in fatty tissues for extended periods of time. Whilethis will reliably slow the release of steroid into the bloodstream, it also allows small residual amounts to remain present in thebody far after the initial injection. The release of stubborn stores ofhormone would no doubt also be enhanced around contest time, a periodwhen the athlete drastically attempts to mobilize unwanted body fat. Ifenough were used in the off-season, the athlete may actually fail adrug screen for boldenone although many months may have past since thedrug was last injected.
SIDE EFFECTS:
Side effects of BOLDEN-300 ( Equipoise) are very mild, even when the dose of this drug is up to a gram per week. Side effects can be related when BOLDEN-300 with its compound - Boldenone Undecylenate is used in very high doses. Typically are related: incidences of oily skin, acne, increased aggression and hair loss.
At a low dosage, BOLDEN-300can produce distinct androgenic side effects. Possible side effects areoily skin, acne, increased aggression and hair loss. Women find thisdrug quite comfortable, virilization symptoms usually unheard of whentaken at low doses.
BOLDEN-300 has a depressive effect on endogenous testosterone levels, therefore a proper post cycle therapy HCG and Clomid is needed at the conclusion of each cycle.
Deca Dura 300 is destinated for intramuscular injection and is made by Platinum Biotech, Europe. This steroid drug contains Nandrolone Decanoate.
Deca Dura 300 is a brand name of Platinum Biotech, the manufacturer of the drug containing the substance Nandrolone Decanoate. Although Nandrolone Decanoate is still contained in many generic compounds, almost every athlete connects this substance with Nandrolone Decanoate. Most common are the administrations of 50 mg/ml and 100 mg/ml. Deca Dura 300 is the most widespread and most commonly used injectable steroid. Its popularity is due to the simple fact that it exhibits many very favorable properties. Structurally Nandrolone is very similar to Testosterone.
Deca Dura 300 is a favorite to thousands of steroid users. In our recent survey, it was revealed that Nandrolone Decanoate is the most widely used anabolic steroid. It is easy on the liver and promotes good size and strength gains while reducing body fat.
Deca Dura 300 causes the muscle cell to store more nitrogen than it releases so that a positive nitrogen balance is achieved. A positive nitrogen balance is synonymous with muscle growth since the muscle cell, in this phase, assimilates (accumulates) a larger amount of protein than usual. The same manufacturer, however, points out on the package insert that a positive nitrogen balance and the protein building effect that accompany it will occur only if enough calories and proteins are supplied. One should know this since, otherwise, satisfying results with Deca Dura 300 cannot be obtained.
The highly anabolic effect of Deca Dura 300 is linked to a moderately androgenic component, so that a good gain in muscle mass and strength is obtained. At the same time, most athletes notice considerable water retention which, no doubt, is not as distinct as that with injectable testosterones but which in high doses can also cause a smooth and watery appearance.
Since Deca Dura 300 also stores more water in the connective tissues, it can temporarily ease or even cure existing pain in joints. This is especially good for those athletes who complain about pain in the shoulder, elbow, and knee, they can often enjoy pain-free workouts during treatment while using Deca Dura 300. Another reason for this is that it blocks the cortisone receptors thus allowing less cortisone to reach the muscle cells and the connective tissue cells. Athletes use this steroid, depending on their needs, for muscle buildup and in preparation for a competition.
It is suitable, even above average, to develop muscle mass since it promotes the protein synthesis and simultaneously leads to water retention. The optimal dose for this purpose lies between 200 and 600 mg per week. Scientific research has shown that best results can be obtained by the intake of 2 mg per pound of body weight. Those who take a dose of less than 200 mg per week will usually feel only a very light anabolic effect which, however, increases with a higher dosage.
The anabolic and consequent buildup effect of Deca Dura 300, up to a certain degree, depends on the dosage. In the range of approx. 200 to 600 mg per week, the anabolic effect increases almost proportionately to the dosage increase. If more than 600 mg per week are administered, the relationship of the positive to the negative effects shifts in favor of the latter.
In addition, at a dosage level above 600 mg per week, the anabolic effect no longer increases proportionately to the dosage increase, so that 1000 mg per week do not guarantee significantly better results than 600 mg per week.
Most male athletes experience good results by taking 400 mg per week. Steroid novices usually need only 200 mg per week.
Deca Dura 300 works very well for muscle buildup when combined with Dianabol (D-bol) and Testoviron Depot. The famous Dianabol (D-bol)/Deca Dura 300 stack results in a a fast and strong gain in muscle mass. Most athletes usually take 15 - 40 mg Dianabol (D-bol)/day and 200-400 mg Deca Dura 300 per week. Even faster results can be achieved with 400 mg Deca Dura 300 per week and 500 mg Sustanon per week. Athletes report an enormous gain in strength and muscle mass when taking 400 mg Deca Dura 300 per week, 500 mg Sustanon per week, and 30 mg Dianabol per day. Deca Dura 300 is a good basic steroid which, for muscle buildup, can be combined with many other steroids. Although it is not an optimal steroid when preparing for a competition, many athletes also achieve good results during this phase. Since Deca Dura 300 is a long-term anabolic, there is risk that with a higher dosage, the competing athlete will retain too much water. A conversion into estrogen, that means an aromatizing process, is possible with deca durabolin but usually occurs only at a dose of 400 mg per week.
During competitions with doping tests Deca Dura 300 must not be taken since the metabolites in the body can be proven in a urine analysis up to 18 months later. Those who do not fear testing can use Deca Dura 300 as a high-anabolic basic compound in a dosage of 400 mg per week. The androgens contained in 400 mg per week also help to accelerate the body's regeneration.
SIDE EFFECTS:
Side effects with this steroid are relatively low with dosages of 400 mg per week, androgenic caused side effects can occur. Most problems manifest themselves in high blood pressure and a prolonged time for blood clotting, which can cause frequent nasal bleeding and prolonged bleeding of cuts, as well as increased production of the sebaceous gland and occasional acne. Some athletes also report headaches and sexual overstimulation. When very high dosages are taken over a prolonged period, spermatogenesis can be inhibited in men, the testes produce less testosterone. The reason is that Deca Dura 300, like almost all steroids, inhibits the release of gonadotropins from the hypophysis.
Women with a dosage of up to 100 mg per week usually experience no major problems with Deca Dura 300. At higher dosages androgenic-caused virilization symptoms can occur, including deep voice (irreversible), increased growth of body hair, acne, increased libido, and possibly clitorishypertrophy. Since most female athletes get on well with Deca Dura 300 a dose of 50 mg per week is usually combined with Anavar 10 mg per day. Both compounds, when taken in a low dosage, are only slightly androgenic so that masculinizing side effects only rarely occur. Deca Dura 300, through its increased protein synthesis, also leads to a net muscle gain and Anavar, based on the increased phosphocreatine synthesis, leads to a measurable strength gain with very low water retention. Other variations of administration used by female athletes are Deca Dura 300 and Winstrol tablets, as well as Deca Dura 300 and Primobolan.
MAST-100 is an injectable steroid made by Global Anabolic, its active substance is Drostanolone Propionate.
MAST-100 is perhaps one of the more exotic androgenic / anabolic steroids that may be used by an athlete. Originally it was developed and used as an anti-estrogen for the treatment of breast cancer. It was largely used in combination with the SERM (Selective Estrogen Receptor Modulator) Tamoxifen (Nolvadex) for the treatment of breast cancer, and did give a significant decrease in estrogen levels in women undergoing such treatment. It is not much used these days for such purposes, for varying reasons, however for many athletes including competitive bodybuilders in particular, MAST-100 remains a rather unsung favourite of AS medicines.
The fact that MAST-100 was being used as an anti-estrogen goes to suggest quite a lot about some properties MAST-100 possesses. MAST-100 is a derivative of DHT (dihydrotestosterone) and does not convert to estrogen through means of aromatisation. It is thought that the anti-estrogenic properties of MAST-100 may be in part to do with either an inhibition in some way of the aromatase enzyme or an interaction with estrogen itself in a way which blocks receptor binding of the estrogen. Either way, this would put MAST-100 as a useful tool for the AS user who uses compounds that convert to estrogen (which most AS users do, considering testosterone is the main basis of most cycles). By inhibiting the aromatase enzyme, MAST-100 would be in effect blocking the conversion of free testosterone to estrogen by the aromatisation pathway. This would not only serve to marginally increase the amounts of active free testosterone in circulation, but it would also negate the side-effects that result from high levels of estrogen due to aromatisation. Such side effects include the development of gynecomastia and water retention/bloating. Conversely, if MAST-100 actually blocks the binding of estrogen to the estrogen receptor (ER) in some way, although aromatisation of testosterone may occur, its effects would be limited due to the inability of the estrogen to bind to the ER. Thus through this mechanism, the effects of excess estrogen production through aromatisation would also be limited by use of this steroid.
Although MAST-100 contains such anti-estrogenic properties, it also (being a DHT derivative) has anabolic and androgenic properties. Although in theory and on paper it may be seen to be not a very strong androgen, in fact MAST-100 does give higher androgenic effects than one may expect. The use of MAST-100, as it is an AAS, will shut down natural testosterone production and so despite having anti-estrogenic effects again, one must not think that MAST-100 could be used as an option in post cycle therapy as it will inhibit recovery.
There are two forms of Masteron that are generally available for use – Drostanolone Propionate and Drostanolone Enanthate. The propionate version is usually dosed at 50-150mg/ml and is the fast acting version of Masteron, needing to be injected every other day. The enanthate version of Masteron is dosed normally at around 200mg/ml and needs only to be injected twice per week as the ester attached to the drostanolone is longer thus giving a slower release of hormone.
Due to the effects of MAST-100 on estrogen related side effects, MAST-100 is a very useful tool (especially in competitive bodybuilding) when cutting. As higher levels of estrogen result in water retention, MAST-100 inhibits water retention, and many users claim that their muscles feel very full and tight on MAST-100, with it giving them amazing muscle pumps in the gym. Use of MAST-100 (in combination with other appropriate meds) at low body fat levels results in the user seeing fine detail of the muscles being accentuated, such as striations and the fine details of the muscle. MAST-100 helps draw out the water from between the skin and the muscle giving this very cut look (at low body fat levels). Not many other AS medicines can give such effects on muscle detail as those seen with MAST-100.
Despite these effects of this steroid, it is a rather weak AS in itself. One would hardly benefit at all from use of MAST-100 on its own, and furthermore use of MAST-100 alone may result in loss of libido due to shutdown of the body's natural testosterone production. For these reasons, it is always recommended to stack MAST-100 with other steroids.
It is said by many that using MAST-100 is a waste when the user has a body fat percentage higher than 10-12%. I can understand the reasoning, and the user must understand that at higher body fat levels the detail to the muscle will not be seen in such a way as described, however I do not see it as a waste due to its anti-estrogenic properties. Such properties may allow one to not use other ancillaries on cycle that would have other undesirable side effects, and in addition MAST-100 may work in a synergistic fashion with other AS medicines to amplify their effects (for example with testosterone as described above). MAST-100 would however not be recommended for beginner use as it is not needed at this starting out level.
SIDE EFFECTS:
As discussed, MAST-100 possesses anti-estrogenic properties which results in the elimination of many of the unwanted side effects that AS users may experience, such as gynecomastia, water retention and dangerous increases in blood pressure. Although MAST-100 is a weak steroid and on paper it has low androgenic properties, it has already been mentioned that in practice the androgenic properties appear to be slightly higher than in theory, and secondly MAST-100 is a DHT derivative.
Briefly however, the side effects that may occur with use of MAST-100 include hair loss (if prone to male pattern baldness), aggression and acne. If a user does experience acne with other androgens such as testosterone, then it is a real possibility that they may experience it with the use of MAST-100. I know of people who experience only a few spots with the use of testosterone however when using MAST-100 they experience many more spots. On the other hand, there are users who seem to experience less spots on MAST-100 than they do on Trenbolone.
Primobolan-100 is an injectable steroid made by Platinum Biotech Europe, this steroid contains Methenolone Enanthate.
Primobolan-100 is the injectable version of the steroid methenolone and, although it produces a weaker effect than Deca Durabolin it is a very good basic steroid whose effects are predominantly anabolic. The fact that an enanthate ester is added to this steroid enables a slow and gradual release from the injection site. This addition allows for a longer half-life of approx 14 days (similar to Testosterone Enanthate) although most athletes prefer to administer it on a weekly basis.
Primobolan-100 popularity stems from the fact that it is the only steroid that seems to work well on a low calorie diet (making it a pre-contest drug of choice) and side effects are rarely a problem since it is relatively non toxic, low in androgens and it does not convert to estrogen (aromatize) therefore estrogen related side effects are not an issue. In addition to this it seems to have a positive effect on the immune system (thus its popular use in Aids patients) and the fact that it adds primarily lean mass leads to a strengthening of the whole body system.
Primobolan-100 is commonly used by those who wish to keep oestrogen and androgenic related side effects to a minimum. Primobolan-100 is also a popular choice for cutting cycles due its mild anabolic properties which may be best suited for sustaining muscle tissue under strict pre-content dieting. Excessive subcutaneous fluids will also not be a concern due to Primobolan-100 being a non-aromatising steroid. The compound could also be added to bulking cycles to heighten the anabolic nature of the cycle whilst minimising adding to the overall oestrogen and androgenic side effects.
Androgenic related side effects are usually only confined to the sensitive individuals, or those who opt to take the larger dosages of the product. Primobolan-100 is often regarded as a safe steroid in comparison to other products, and it is a very sought after product which reflects in its cost. A dose of 400 mg a week has been shown to provide decent gains, but higher doses are common, with many claiming 600 - 800 mg a week will provide a much better yield in muscle size whilst not causing too much in terms of side effects. As we rise the dose we can expect the androgenic side effects to become more pronounced, so its down to the user to see what dose provides fruitful when weighing up the side effects to net positive gains.
Primobolan-100 is often stacked with other steroids to provide more pleasing results to the user. During a cutting cycle the product could be stacked with a non-aromatising androgen to aid muscle hardness whilst keeping a very defined look with little water retention. Others may find primobolan a nice compound to add to their usual Testosterone course to add to the anabolic nature of the cycle, whilst not adding too much to side effects. This may be useful for those who have found their tolerance dosage with Testosterone but wish to add another compound to their stack to aid gains.
Primobolan-100 displays many favorable characteristics, most which stem from the fact that methenolone does not convert to estrogen. Estrogen linked side effects should therefore not be seen at all when administering this steroid. Sensitive individuals need not worry about developing gynecomastia, nor should they be noticing any water retention with this drug. The increase seen with Primobolan-100 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 - 200 mg weekly, Primobolan-100 should also not interfere with endogenous testosterone levels as much as when taking an injectable nandrolone or testosterone. This is very welcome, as the athlete should not have to be as concerned with ancillary drugs when the steroid is discontinued (a less extreme hormonal crash). At higher doses strong testosterone suppression may be noticed however, as all steroids can act to suppress testosterone production at a given dosage. Here of course an ancillary drug regimen may be indicated.
It is most popular for male bodybuilders to stack Primobolan-100 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 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-100 is also used effectively during bulking phases of training. The addition of testosterone, Dianabol or Anadrol 50 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-100 should allow the user to take a much lower dosage of the more "toxic" drug and still receive acceptable results.
SIDE EFFECTS:
Side effects in general are usually not much of a problem with Primobolan-100. There is a chance to 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. Primobolan-100 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 - 200 mg per week, a level that should produce at least some noticeable muscle growth.
Sustanon 375 is an injectable steroid, this drug is also known as Sustanon and is made by LA-PHARMA.
Sustanon 375 in essence it is a mixture of testosterone cypionate, testosterone phenylpropionate, testosterone isocaproate and testosterone decanoate. The different proportions of the esterified mixtures provide different half lives. This provides for a continuous release of testosterone from the injected site. Sustanon was widely used for the treatment of a few medical disorders in Europe. The drug was useful to treat infertility and administered once a month. While Sustanon has been heavily touted by athletes and bodybuilders as a drug of choice, a single formulation of Testosterone Enanthate or Cypionate can do the same thing. The combination of esters is better suited for the treatment of medical disorders and not for bodybuilders. One negative aspect about Sustanon 375 is that it does remain in the body for a very long time and can be easily detected in the urine.
Besides being an anabolic agent, Sustanon 375 also has the ability to increase the production of red blood cells. This results in more oxygen carrying capacity and hence more exercise endurance.
Sustanon 375 has been used widely by bodybuilders in the past. Why this testosterone formulation is preferred by some is not well understood. Some claim that there is less water retention and more muscle build up. However, like all testosterone products, Sustanon 375 is converted to estrogen in the body and can cause gynecomastia and water retention. To get rid of the water many builders also use diuretic medications.
Many bodybuilders use a combination of Sustanon 375, growth hormone or thyroxin during the stacking phase.
Sustanon 375 is taken for 4 weeks and then a wash out phase is undertaken. During the wash out phase, some athletes take Clomiphene, Tamoxifen or Arimidex. Because the Sustanon 375 suppresses the hypothalamic pituitary axis, a profound suppression of testosterone synthesis in the body occurs. For this reason it is important to taper off the drug slowly. It is recommended that one take 1-2 injections a month and then stop for a month. During the wash out phase, a mild anabolic steroid can be used, or one can use growth hormone/thyroxin.
The weight gain is gradual but significant. Most builders can expect weight gain of at least 15 - 25 lbs in 2-3 cycles (months). The other aspect of Sustanon 375 which has been observed is that it can significantly increase exercise endurance and provides for spontaneous bursts of energy. This has been linked to its effect on the red blood cells and the increased oxygen carrying capacity. Others claim that Sustanon can also increase the recovery time following an injury.
Sustanon 375 is only administered via an intramuscular injection. It is typically injected in the buttock area every week. The dose of Sustanon 375 usually starts off at 250 mg/week and gradually increased during each cycle. Some athletes use doses as high as 1000 mg/week. Once injected, Sustanon 375 remains in the body for about a month. For the majority of bodybuilders, a dose of 250-500 mg/week should be sufficient.
Although Sustanon 375 does not aromatize excessively when taken in a reasonable dosage many people, in addition, also take an antiestrogen such as Nolvadex and/or Proviron to prevent possible estrogen linked side effects. Since Sustanon 375 suppresses the endogenous testosterone production the intake of HCG and Clomid must be considered after six weeks or at the end of treatment. It is recommended that women not take depot testosterones since the androgen level would strongly increase and virilization symptoms could result. Despite this, it is not uncommon for female competing athletes in the higher weight classes to take testosterone since it helps in remaining "competi-tive." Women who use "Testo" or who would like to try it should limit its use to either only Testosterone Propionate or inject a maxi-mum of 250 mg Sustanon 375 every 10-14 days over a period of no longer than six weeks. At this point we would like to emphasize once more that steroid novices should stay away from all testosterone compounds since, at this time, they simply do not need them. The side effects of Sustanon 375 are similar to those of Testosterone Enanthate only that they are usually less frequent and less severe.Depending on the predisposition and dosage, the user can experience the usual androgenic linked side effects such as acne, aggressiveness, sexual overstimulation, oily skin, accelerated hair loss, and reduced production of the body's own hormones. Water retention and gynecomastia are usually within limits with the "Sustas" or are not as massive as with enanthate and cypionate. Liver damage is unlikely with Sustanon 375; however, in very high dosages, elevated liver values can occur which, after discontinuing use of the compound, usually go back to normal.
Like all anabolic steroid, Sustanon 375 also has side effects. Even though the side effects are rare, most builders will develop them when the drug is used for a long time. The most common side effects include: general fatigue; mood changes- depression, anger, anxiety, insomnia; gynecomastia; hair loss; impotence; retention of water; changes in liver enzymes; liver masses; testicular atrophy; acne, oily skin.
The majority of these side effects reverse when the drug is stopped. It is important that all individuals who use anabolic steroids have a follow up with a physician to monitor their liver. Rare cases of liver failure and cancers have been reported.
375 - 1000mg per week.
TC-200 is made by Global Anabolic. This drug contains 250 mg of hormone Testosterone Cypionate per ml.
Testosterone Cypionate is a white or creamy white crystalline powder, odorless or nearly so and stable in air. It is insoluble in water, freely soluble in alcohol, chloroform, dioxane, ether, and soluble in vegetable oils.
Testosterone is the primary male sex hormone, and is largely responsible for some of the physical and psychological development of men. TC-200 promotes sex drive, as well as both muscle gain and fat loss. Testosterone Cypionate is simply testosterone which has undergone 17beta-estrification, to allow for a steady release over the course of about a week. Besides this difference (the ester), this form of testosterone will do what all others do.
Testosterone Cypionate is very similar to tesosterone enanthate. Although half lives and active life periods are different, they are similar. Injections are normally less frequent for cypionate. TC-200 is the king of all mass builders and for this purpose is also fairly cost effective. It works well either alone or stacked to create a great bulking cycle. It has a high risk of side effects due to its conversion to DHT and has the potential to form estrogen, causing gynecomastia. These characteristics also cause it to have such excellent mass building tendencies. Due to some other side effects, such as water retention, it may not be the best used alone for lean mass gains, but with bulking comes the addition of a lot of muscle as well as some gains in fat and water weight. This is typical and a natural part of the enhanced bodybuilder's bulking regiment.
TC-200 is a long acting, single ester testosterone product. It has a length of 8 carbons, and is stored mostly in the adipose tissue when injected intra-muscularly. It is slowly and steadily released in the body after it is injected. The blood levels of cypionate peak 24-48 hours after injection and then decline slowly. The blood levels reach a steady point 12 days after initial injection and stay there for over three weeks. Cypionate is normally injected once a week, which makes the very lowest dose higher than half the peak dose at any given time. Any testosterone, as the king of mass builders, are cost effective products and important for any steroid stack. Used alone, the user can expect to see some significant gains. The long acting nature of cypionate allows the user to inject less frequently while maintaining stable blood levels.
TC-200 is a good choice for the first time steroid user. A simple cycle consisting of 500 mg of cypionate weekly for 10 weeks, with ancillaries on hand, and standard post cycle therapy makes a good first cycle and can create some excellent gains in muscle mass. Along with those gains will come some gains in fat as well as water rentention, but that is a standard part of bulking up and should be expected. Enanthate or Cypionate are also normally preferred over sustanon for a first cycle, due to the inability to maintain stable blood levels of Sustanon while at the same time minimizing injection frequency. For maximum efficiency, every day or every other day injections of sustanon are normally administered. This is unnecessary while using cypionate due to its extreme length of action.
Doses of 200 - 100 mg a week are common using TC-200, with excellent results found midway at about 500 mg or less for the first time user and between 500 - 1000 mg weekly for the more advanced athlete. Testosterone stacks well with anything and is also great when used alone. When stacked with another anabolic-androgenic steroid, distinct androgenic effects may be seen. Using TC-200 will improve regenerative capacity as well as training aggressiveness which results in significant increases in overall strength during the course of the cycle.
A long acting testosterone ester will be very helpful for your bulking needs, and TC-200 is a product which is more simple than some of the other steroids out there. Not to say it is without its share of complications, but it's a good choice, especially for those new to enhanced bodybuilding. Discontinuing the product is not an option in case side effects occur, because it will continue to aggravate these side effects over extended periods of time due to the long length of action of this steroid. Ancillary drugs such as Nolvadex, Proviron, Clomid and HCG may help, both during cycle and post cycle to help restore natural testosterone production. TC-200 does aromatize slightly more than Sustanon, but when using either drug, one should be familiar with anti-estrogens such as Nolvadex or Clomid and use one of them when symptoms of gyno occur.
Any form of testosterone will be longer acting and at times difficult to control. Having ancillary drugs on hand is considered very important due to the possibility of side effects. However, these potential side effect risks do not come without a benefit - and that benefit is that testosterone is the most powerful mass builder there is and stacks well with just about anything. The added benefit of TC-200 is that the long acting ester only requires a single weekly injection to elicit great gains. This makes TC-200 especially attractive for the first time user, who will likely have no prior experience with self administrations of intra-muscular agents and will want to minimize those injections.
Weekly totals of 250 - 1000 mg weekly are frequently used, and sometimes more for the highly advanced athlete. Due to the relatively long half life of TC-200, injections are usually administered once per week. This will allow stable blood levels to be maintained. When the level of steroid tapers down, a new injection is made, keeping everything fairly level. This is unlike Sustanon, which requires more frequent injections for the same effect. For a first cycle, 500 mg alone of TC-200, shot once weekly (Monday and Thursday for example), for 10 weeks along with standard post cycle therapy would be very sufficient for good gains.
Testosterone being the most effective mass builder there is, stacks well with virtually everything and can be used alone for significant increases in both muscle mass and strength. If used in combination with other anabolic-androgenic steroids, items of choice include Dianabol, Primobolan, Equipoise and Deca Durabolin. The testosterone using athlete should be familiar with a variety of ancillary drugs in case estrogen related side effects such as gyno take place. Nolvadex, Clomid, and HCG are items which you will likely want to keep on hand, either to use during your cycle, or for post cycle therapy.
SIDE EFFECTS:
The downside of a long acting ester like Cypionate is that it can lead to more water retention (although this can be somewhat alleviated by ensuring adequate water consumption and keeping a check on your intake of carbohydrates). Testosterone is also metabolized in the body to the female hormone estrogen by the aromatize enzyme. This can result in gynecomastia (the growth of breast tissue in men) some fat gain, testicular shrinkage and an increase in blood pressure. Hair loss and possible swelling of the prostate are also potential side effects.
TDT-Extend is an injectable steroid made by Platinum Biotech, its active substance is Testosterone Enanthate 100mg, Drostalone Enanthate 100mg, Trenbolone Enanthate 100mg.
Composition Each ml contains: Testosterone Acetate 30mg; Testosterone Propionate 55mg; Testosterone Phenylpropionate 55mg; Testosterone Cypionate 85mg; Testosterone Decanoate 100mg
Presentation: 325mg/ml, 10ml multidose vial with purple fliptop cap
Storage: Keep out of the reach of children; protect from light; store at room temperature; do not refrigerate or freeze
Manufactured by: Global Anabolic
Product Description:
TMIX-325 is a combination of five of testosterones. The presence of the acetate ester allows the testosterone to display a rapid initial physiological response. The other four esters, which release at slower rates, prolong the physiological response with a relatively flat absorption curve over the duation of the injection life-cycle. Testosterone is a male sexual hormone with pronounced, mainly androgenic action, possessing the biological and therapeutic properties of the natural hormone. It is normally produced in women in small physiological quantities. In addition to the specific action that determines the sexual characteristics of the individual, testosterone also has a general anabolic action, manifested in enhancement of protein synthesis. Under the effect of testosterone, body weight increases and urea excretion is reduced. High doses suppress the production of hypophyseal gonadotropin, while low doses stimulate it. It has an antitumor effect on mammary gland metastases.
ANASTROL-1 is an post cycle steroid, its active substance is Anastrozole and is made by Global Anabolic.
ANASTROL-1 is a potent and selective non-steroidal aromatase inhibitor indicated for the treatment of advanced breast cancer in post-menopausal women with disease progression following tamoxifen therapy. Many breast cancers have estrogen receptors and growth of these tumors can be stimulated by estrogens. In post-menopausal women, the principal source of circulating estrogen (primarily estradiol) is conversion of adrenally-generated androstenedione to estrone by aromatase in peripheral tissues, such as adipose tissue, with further conversion of estrone to estradiol. Many breast cancers also contain aromatase, the importance of tumor-generated estrogens is uncertain. Treatment of breast cancer has included efforts to decrease estrogen levels by ovariectomy premenopausally and by use of anti-estrogens and progestational agents both pre- and post-menopausally, and these interventions lead to decreased tumor mass or delayed progression of tumor growth in some women. ANASTROL-1 is a potent and selective non-steroidal aromatase inhibitor. It significantly lowers serum estradiol concentrations and has no detectable effect on formation of adrenal corticosteroids or aldosterone.
ANASTROL-1 is the first in a new class of third-generation selective oral aromatase inhibitors. It acts by blocking the enzyme aromatase, subsequently blocking the production of estrogen. Since many forms of breast cancer cells are stimulated by estrogen, it is hoped that by reducing amounts of estrogen in the body the progression of such a disease can be halted. This is the basic premise behind Nolvadex, except this drug blocks the action and not production of estrogen. The effects of ANASTROL-1 can be quite dramatic to say the least. A daily dose of one tablet can produce estrogen suppression greater than 80 % in treated patients. With the powerful effect this drug has on hormone levels, it is only to be used (clinically) by post-menopausal women whose disease has progressed following treatment with Nolvadex (tamoxifen citrate). Side effects like hot flushes and hair thinning can be present, and would no doubt be much more.
For the steroid using male athlete, ANASTROL-1 shows great potential. Up to this point, drugs like Nolvadex and Proviron have been our weapons against excess estrogen. These drugs, especially in combination, do prove quite effective. But ANASTROL-1 appears able to do the job much more efficiently, and with less hassle. A single tablet daily, the same dose use clinically, seems to be all one needs for an exceptional effect (some even report excellent results with only 0.25 mg daily). When used with strong, readily aromatizing androgens such as Dianabol or testosterone, gynecomastia and water retention can be effectively blocked. In combination with Propecia (finasteride), we have a great advance. With the one drug halting estrogen conversion and the other blocking 5-alpha reduction , related side effects can be effectively minimized. Here the strong androgen testosterone could theoretically provide incredible muscular growth, while at the same time being as tolerable as nandrolone. Additionally the quality of the muscle should be greater, the athlete appearing harder and much more defined without holding excess water.
In the majority of users, 0.5 mg per day should be enough to prevent any estrogen related side effects related to anabolic steroid use. Even when doses were increased to 1 mg per day there was no change in the amount of estrogen that was able to be reduced as compared to doses of 0.5 mg per day. This would seem to indicate that raising your dosage will show no further results if estrogenic side effects continue to be a problem at a dosage of 0.5 mg. If symptoms persist the user may have to try a more potent compound such as femara.
Having said all of this however, most users will be able to reduce any water retention that they may have, or other estrogen related side effects, with dose less than 0.5 mg per day. Anecdotally users have reported that doses in the range of 0.25 mg per day or 0.5 mg every other day are enough to acheive this result. It is possible to administer ANASTROL-1 every other day due to it's active life of 48 hours.
For users using ANASTROL-1 during their post cycle therapy the same dosages should apply. There is no need to increase or decrease dosages. It can be run throughout the post cycle period with no ill effects.
Blood levels of the compound should stabilize and reach their peak at about 7 - 10 days after first administering the drug. Therefore it is unlikely that a user would need to frontload with ANASTROL-1 or begin taking it before they start administering the anabolics that they plan on taking.
SIDE EFFECTS:
ANASTROL-1 is seemingly very mild on blood lipids (cholesterol) and has not been shown to affect them adversely. However it should be noted that in theory if one was to consistently suppress your natural estrogen levels for a long period of time, this would negatively impact your health (including your cholesterol). Despite this there is no scientific evidence that ANASTROL-1 can be dangerous for healthy individuals to use, even for extended periods of time.
It would seem then that ANASTROL-1 has little in the way of negative side effects associated with it's use. It is by far one of the safest compounds that an athlete can use.
Aroma-25 is an post cycle steroid, it is also known as Aromasin and is made by Platinum Biotech.
Aroma-25 is a steroidal suicide aromatase inhibitor, which means that it lowers estrogen production in the body by blocking the aromatase enzyme, the enzyme responsible for estrogen synthesization.
Exemestane was developed to fight breast cancer in post-menopausal women, who need a particularly aggressive therapy, and for whom first line defenses such as SERMS (Tamoxifen) have not worked. This should be our first clue in inferring that this stuff is pretty strong, or at least stronger than some of the other compounds which are used to fight breast cancer.
Aroma-25 averages an 85% rate of estrogen suppression, so it´s clearly a very effective agent for bodybuilders and other athletes wanting to avoid estrogen related side effects such as gyno, acne, or water-retention brought on by aromatizing steroids. Specifically, Aroma-25 dose this by selectively inhibiting aromatase activity in a time-dependent and irreversible manner.
As with most of the compounds in this class, it also causes a reasonable rise in testosterone levels, and as you may have guessed, this rise in testosterone means that Aroma-25 can also cause androgenic sides. As you can see from the chart below, exemestane is very effective at both lowering estrogen (estradiol) and raising testosterone: Estrogen and androgen plasma levels after 10 d of daily exemestane (25 or 50 mg) in healthy young males. To convert to Systeme International units: estradiol, picomoles per liter; estrone, picomoles per liter; androstenedione, nanomoles per liter; and testosterone, nanomoles per liter.
So we can see that 25 mgs is a very effective dose from that chart, right? As an added benefit, exemestane not only increases testosterone and lowers estrogen, but it also increases IGF levels. Additionally Worth noting is that Aroma-25 may possibly be less harsh on blood lipids than some of the other (similar) compounds we use in the world of bodybuilding or athletics. It also has, at best no effect on IGF, and at worst could lower it. AI´s are very tricky with regards to inconsistencies in IGF levels.
Unfortunately, you need to take Exemestane for a week to reach steady blood plasma levels of it, and exemestane has a half life of 27 hours.
The ability of exemestane to lower estrogen levels by the aforementioned 85% makes it a very nice choice for use in any cycle where aromatizing steroids are used. In addition, since it´s not too harsh at all on blood lipid profiles, it´s a very good choice for longer cycles. It´s ability to raise both testosterone levels also seem to suggest that it would be a very nice addition to a Post-Cycle-Therapy (PCT).
SIDE EFFECTS:
All medicines may cause side effects, but many people have no, or minor, side effects. Check with your doctor if any of these most COMMON side effects persist or become bothersome when using Exemestane: anxiety; back, joint, muscle, or limb pain; constipation; coughing; diarrhea; dizziness; fatigue; flu-like symptoms; hair loss; headache; hot flashes; increased or decreased appetite; increased sweating; joint pain; nausea; stomach pain or upset; tiredness; trouble sleeping; weight gain; vomiting.
Composition Each ml contains: Mesterolone 100mg
Presentation: 100mg/ml, 10ml multidose vial with maroon fliptop cap
Storage: Keep out of the reach of children; protect from light; store at room temperature; do not refrigerate or freeze
Manufactured by: Global Anabolic
Product Description:
Mesterolone is generally well liked nonetheless as it delivers very few side-effects in men. In high doses it can cause some virilization symptoms in women. But because of the high level of deactivation and pre-destination in the system (albumin, SHBG, 3bHSD, aromatase) quite a lot of it, if not all simply never reaches the androgen receptor where it would cause anabolic effects, but also side-effects. So its relatively safe. Doses between 25 and 250 mg per day are used with no adverse effects. 50 mg per day is usually sufficient to be effective in each of the four cases we mentioned up above, so going higher really isn’t necessary. Unlike what some suggest or believe, its not advised that Proviron be used when not used in conjunction with another steroid, as it too is quite suppressive of natural testosterone, leading to all sorts of future complications upon discontinuation. Ranging from loss of libido or erectile dysfunction all the way up to infertility. One would not be aware of such dangers because Proviron fulfills most of the functions of normal levels of testosterone.
TAMO-20 is an post cycle steroid and is made by Global Anabolic. The active substance is TAMO-20 Citrate.
TAMO-20 is probably the most popular ancillary drug for male steroid users who wish to avoid the estrogen like effects caused by the use of anabolic steroids. TAMO-20 Citrate binds to estrogen receptors thus blocking the hormones action on target tissues and achieving an anti-estrogenic effect.
Also worth noting is the fact that TAMO-20 is an estrogen agonist in the liver and is capable of mimicking estrogen in this organ. At first glance you may wonder why this could be considered a good thing, however, when you realize that estrogen positively effects HDL (good) cholesterol values in the liver its value in this instance becomes obvious. As you know, steroid use tends to suppress HDL levels and raise LDL levels significantly leading to increased cholesterol levels and cardiac risk. Adding TAMO-20 may therefore form a protective function in this case, although it certainly does not save the liver from all the other hazards involved with the use of c-17 alpha alkylated orals.
TAMO-20 Citrate is a selective estrogen receptor modulator. Selective estrogen receptor modulators can act as estrogen receptor agonists or antagonists. This activity of TAMO-20 Citrate is tissue selective, effecting those estrogen receptors located in the liver, breast, and bone. When the TAMO-20 molecule binds to this receptor, the estrogen is blocked and can not have any influence, thereby remaining inactive in that tissue. By doing so, an "anti-estrogenic" effect is achieved. The drug was developed and still used to treat breast cancer. It is often used as a first option due to its mild nature in comparison to aromatase inhibitors. Of course one would want to use the mildest compound possible when dealing with estrogen levels in women, but one could afford to be more aggressive in dealing with male strength athletes or bodybuilders.
In terms of its use in steroid users, TAMO-20 can help in two ways. Firstly due to the binding affinity of the compound it is able to help in the prevention of gynocomastia. TAMO-20 will compete with estrogen for the estrogen receptors in certain tissues, including the breast, and if it can bind to the receptor estrogen will not have an opportunity to interact with receptor and therefore gynocomastia should not be able to develop. When using anabolic steroids that can convert to estradiol (estrogen) this protection against gynocomastia can be invaluable. However it should be noted that TAMO-20 Citrate will not eliminate the estrogen or disallow the conversion to occur. Instead it attempts to counteract the effects of circulating estrogen in the body in those tissues that the drug effects. Therefore there is no evidence that TAMO-20 has any effects counteracting etrogenic side effects that are unrelated to the tissues that are not in the breast, liver or bone. Namely there is no real causal connection to any reduction in water retention and acne in users that begin taking TAMO-20 citrate as it relates to estrogen.
The second, and possibly more beneficial, aspect of TAMO-20 for steroid users is its ability to increase the production of luteinizing hormone and follicle stimulating hormone, and therefore increasing testosterone. This ability is why it is often used by steroid users during their post-cycle therapy. There are numerous studies that indicate that TAMO-20 Citrate can increase the levels of these hormones quite dramatically. TAMO-20 does this by blocking the negative feedback inhibition caused by estrogen at the hypothalamus and pituitary, and this in turn will help to increase the production of these hormones. Unlike clomiphine citrate, TAMO-20 citrate has also been shown to increase luteinizing hormone responsiveness to gonadotropin releasing hormone. Clomiphine Citrate can lower this responsiveness over time.
In terms of dosing for combating gynocomastia that has begun to form, there is very little research. The limited research that does exist does point to the fact that doses of 20-40 mgs per day are effective in treating the existing condition. However, anecdotally users have reported sometimes using doses of 60-80 mgs per day. These doses may have more to do with users impatience rather than the need for higher doses, as no research indicates that such doses are needed. It should be noted as well however that TAMO-20 may have no effect on existing gynocomastia in some individuals. Many users have indicated that the compound will only help alleviate symptoms if the gynocomstia has not been apparent for a long period of time. Of course, this is all subjective and the effectiveness of the drug can only be determined on a trial and error basis.
For use during post-cycle therapy users have anecdotally indicated that doses ranging between 20 and 40 mgs per day are average. These doses have been shown to significantly raise levels of testosterone, luteinizing hormone and follicle stimulating hormone. Most users have reported when using TAMO-20 for their post-cycle therapy they will administer the drug for a minimum of three weeks. A maximum length has not necessarily been established due to the few side effects associated with the compound. In this case, this compound can be run for as long as wanted with little to no concern being needed to be paid to potential side effects. See the below section for more details.
Some users have used TAMO-20 for the purpose of helping raise their HDL (good) cholesterol values. In theory it is thought that since the compound is an estrogen agonist in the liver and therefore is capable of activating the estrogen receptor and mimicking the actions of the hormone in the organ that it may help improve cholesterol levels as estrogen does. However this effect is rather slight and won’t significantly improve a user’s HDL levels very noticeably at all. This is especially true when one factors in the dramatic effect that most anabolic steroids have on these levels. For this reason, TAMO-20 should not be relied upon for this purpose.
SIDE EFFECTS:
One of the possible side effects associated with use of TAMO-20 is the possible reduction of insulin-like growth factor levels. If these levels are reduced this could suppress the gains an individual can make slightly. However this reduction, if it actually exists, would not be overly significant with gains in muscle mass only being marginally reduced for the most part.
Another effect of use of TAMO-20 may be vision problems. Recently, there has been some information from researchers that indicates corneal, retinal and optic nerve abnormalities seen in patients using the drug could be related to its use. Anecdotally a small number of steroid users have reported that they have suffered from visual problems while using this drug as well. After discontinuation of the drug these symptoms seemingly dissipate. However there is simply not enough research on the subject to know whether permanent damage could occur. More research needs to be conducted.
Other than these concerns, there is little in the way that long-term use of TAMO-20 could cause damage to in the human body. It is seemingly safe in terms of possible effects to the body’s hormonal production, other than the one relating to insulin-like growth factor, and endocrine system. For the vast majority of users the compound is relatively side effect free and well tolerated.
Clomifin-50 is an post cycle steroid, this drug is also known as Clomid and is made by Platinum Biotech.
Clomiphene Citrate is not an anabolic/androgenic steroid. Since it is a synthetic estrogen it belongs, however, to the group of sex hormones. In school medicine Clomiphene Citrate is normally used to trigger ovulation. Clomiphene Citrate also has a strong influence on the hypothalamohypophysial testicular axis. It stimulates the hypophysis to release more gonadotropin so that a faster and higher release of FSH (follicle stimulating hormone) and LH (luteinizing hormone) occurs. This results in an elevated endogenous (body's own) testosterone level. Clomiphene Citrate is especially effective when the body's own testosterone production, due to the intake of anabolic/androgenic steroids, is suppressed. In most cases Clomiphene Citrate can normalize the testosterone level and the spermatogenesis (sperm development) within 10- 14 days. For this reason Clomiphene Citrate is primarily taken after steroids are discontinued. At this time it is extremely important to bring the testosterone production to a normal level as quickly as possible so that the loss of strength and muscle mass is minimized. Even better results can be achieved if Clomiphene Citrate is combined with HCG or when Clomiphene citrate is used after the intake of HCG.
Paradoxically, although Clomiphene Citrate is a synthetic estrogen it also works as an anti-estrogen. The reason is that Clomiphene Citrate has only a very low estrogenic effect and thus the stronger estrogens which, for example, form during the aromatization of steroids, are blocked at the receptors. These would include those that develop during the aromatizing of steroids. This does not prevent the steroids from aromatizing but the increased estrogen is mostly deactivated since it cannot at-tach to the receptors. The increased water retention and the possible signs of feminization can thus be reduced or even completely avoided. Since the antiestrogenic effect of Clomiphene Citrate is lower than those found in Proviron, Nolvadex, and Teslac it is mainly taken as a testosterone stimulant. Clomifin-50 is a medication that promotes the production of the body's own stimulating hormone, gonadotropin, which in turn increases the testosterone level. It is, for example, administered to women as a so-called anti-estrogen to trigger ovulation ("ovulation stimulator").
Originally developed as a female fertility aid, Clomifin-50 has been popular among steroid users for quite some time now as a post-cycle therapy compound used to help recover natural testosterone production. The compound works by partially or completely blocking the effects of estrogen in the body. This is due to the fact that it is a synthetic estrogen with both agonist and antagonist properties. With a similar structure to that of tamoxifen citrate, Clomifin-50 blocks the ability of estrogen to bind with receptors in certain tissues, these being located in the hypothalamus and being suprapituitary, although this is a somewhat contentious claim. Tamoxifen Citrate is selective to those receptors in the liver, breast, and bone. So in terms of use as a fertility drug in women, Clomifin-50 helps to eliminate the negative feedback of estrogens on the hypothalamic-pituitary-ovarian axis and increases the production of luteinizing hormone and follicle stimulating hormone. This induces ovulation.
Therefore if these results can be translated to strength athletes and bodybuilders, this ability to raise the levels of luteinizing hormone and follicle stimulating hormone should be quite impressive. An increase in these hormones will result in an increase in testosterone production in users. This of course is something that is desperately desired when coming off of anabolic steroids. If testosterone levels can be raised quickly after a cycle a user is much more likely to maintain more of his gains than if he suffered through a crash in testosterone levels and his natural production came back slowly, all the while having to combat the increased levels of estrogen and cortisol.
While it is true that Clomifin-50 has many "anti-estrogen" properties, there are a multitude of better options. It's is relatively weak in comparison to tamoxifen citrate and the anti-aromatase compounds that are available are much more potent in terms of controlling and/or eliminating estrogenic side effects that are likely to develop. The primary duty of clomiphine citrate should be left to post-cycle therapy.
Of course due to the fact that there is little research to do with the use of Clomifin-50 as it relates to steroid users, much of what we know about the dosing of it has been from anecdotal reports. For the most part users will maintain doses of the drug between 25 mgs to 150 mgs per day on a consistent basis. Often times users will "frontload" the compound using doses of between 200-300 mgs on the first day of their post-cycle therapy and then reduce the subsequent doses. However the side effects associated with large doses of the compound may hinder some individuals' abilities to do this.
Some users also advocate tapering the dose of Clomifin-50 during the last few weeks of administration. However this is more a practice that is based upon theory rather than solid medical evidence of it's productivity.
In terms of dosing length it seems that at least 3 weeks of Clomifin-50 therapy is recommended by users. Of course each has their own preferences along with individual recovery schedules. Also the types of compounds used and the duration of a cycle will of course influence the time it takes for a user to recover and the need for a lengthy post-cycle therapy. Due to the lack of serious side effects associated with the drug, as well as the fact that there is no risk of toxicity with the Clomifin-50, users are able to use the compound for months on end with seemingly no significant negative consequences.
Male users generally find that a daily intake of 50-100 mg over a four to six weeks period will bring testosterone production back to an acceptable level. This raise in testosterone should occur slowly but evenly throughout the period of intake. Since an immediate boost in testosterone is often desirable, many prefer to combine Clomid with HCG for the first week or two after the steroids have been removed. The kick-start from HCG also helps to restore the normal ability for the testes to respond to endogenous LH, which may be hindered for some time after the cycle is ended due to a prolonged state of inactivity. Once the HCG is stopped, the user continues treatment with Clomid alone. HCG should not be used for longer than two or three weeks though, as the resulting increased testosterone and estrogen levels may again initiate negative feedback inhibition at the hypothalamus. When planning your ancillary drug program, it is also important to remember that injectable steroids can stay active for a long duration. Using ancillary drugs the first week after a long acting injectable like Sustanon has been stopped may prove to be wholly ineffective. Instead, the athlete should wait for two to three weeks, to a point where androgen levels will be diminishing. Here the body will be primed and ready to restore testosterone production.
Clomid and HCG are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time. There is also no exact method for using the two drugs in this manner. Some have experimented by periodically administering small doses of HCG along with one or two tablets of Clomid, perhaps for a few days at a stretch followed by a longer break. An on/off schedule would be implemented; for fear that this combination may lose some effectiveness if used continuously for this purpose. This method of intake may prove to be effective, although it is really much more feasible to stimulate testosterone production after the cycle than to try and maintain it for the long duration during.
SIDE EFFECTS:
Despite these rather inconvenient side effects, for the most part Clomifin-50 can be run for extended periods of time with no worries of serious negative consequences. Potentially things such as hot flashes, nausea, dizziness, and headaches may occur but anecdotally users report that these symptoms are quite rare. However emotional side effects along with vision problems are frequently reported with use of this drug. Visual tracers or blurry vision are often reported by users, even some who use extremely low doses of the compound. These are often reported to become more pronounced at night. However if this symptom becomes unbearable, it quickly dissipates after administration of the compound is ceased.
In terms of the emotional side effects associated with Clomifin-50, some users complain that they become depressed, irritable or more emotional in general when using the drug. This can primarily be explained by way of Clomifin-50 being a synthetic estrogen. By introducing a type of estrogen into a user's system some effects should be expected. Coupled with the fact that the natural testosterone production of the user is already suppressed this obviously could lead to some difficulties. Of course some users find these effects much more pronounced than others, with many finding Clomifin-50 intolerable while others have little to no side effects.
Another possible effect of use of the compound is increased acne. This is a direct result in the shifting hormonal balance that a user would be experiencing while coming off of anabolic steroids and the introduction of Clomifin-50 to their system. An increase in production of seminal fluid may also be experienced by some users and therefore the volume of ejaculate may well noticeably increase as well.
CLOMIL-50 is an post cycle steroid, this drug is also known as Clomid and is made by Global Anabolic.
Clomiphene Citrate is not an anabolic/androgenic steroid. Since it is a synthetic estrogen it belongs, however, to the group of sex hormones. In school medicine Clomiphene Citrate is normally used to trigger ovulation. Clomiphene Citrate also has a strong influence on the hypothalamohypophysial testicular axis. It stimulates the hypophysis to release more gonadotropin so that a faster and higher release of FSH (follicle stimulating hormone) and LH (luteinizing hormone) occurs. This results in an elevated endogenous (body's own) testosterone level. Clomiphene Citrate is especially effective when the body's own testosterone production, due to the intake of anabolic/androgenic steroids, is suppressed. In most cases Clomiphene Citrate can normalize the testosterone level and the spermatogenesis (sperm development) within 10- 14 days. For this reason Clomiphene Citrate is primarily taken after steroids are discontinued. At this time it is extremely important to bring the testosterone production to a normal level as quickly as possible so that the loss of strength and muscle mass is minimized. Even better results can be achieved if Clomiphene Citrate is combined with HCG or when Clomiphene citrate is used after the intake of HCG.
Paradoxically, although Clomiphene Citrate is a synthetic estrogen it also works as an anti-estrogen. The reason is that Clomiphene Citrate has only a very low estrogenic effect and thus the stronger estrogens which, for example, form during the aromatization of steroids, are blocked at the receptors. These would include those that develop during the aromatizing of steroids. This does not prevent the steroids from aromatizing but the increased estrogen is mostly deactivated since it cannot at-tach to the receptors. The increased water retention and the possible signs of feminization can thus be reduced or even completely avoided. Since the antiestrogenic effect of Clomiphene Citrate is lower than those found in Proviron, Nolvadex, and Teslac it is mainly taken as a testosterone stimulant. CLOMIL-50 is a medication that promotes the production of the body's own stimulating hormone, gonadotropin, which in turn increases the testosterone level. It is, for example, administered to women as a so-called anti-estrogen to trigger ovulation ("ovulation stimulator").
Originally developed as a female fertility aid, CLOMIL-50 has been popular among steroid users for quite some time now as a post-cycle therapy compound used to help recover natural testosterone production. The compound works by partially or completely blocking the effects of estrogen in the body. This is due to the fact that it is a synthetic estrogen with both agonist and antagonist properties. With a similar structure to that of tamoxifen citrate, CLOMIL-50 blocks the ability of estrogen to bind with receptors in certain tissues, these being located in the hypothalamus and being suprapituitary, although this is a somewhat contentious claim. Tamoxifen Citrate is selective to those receptors in the liver, breast, and bone. So in terms of use as a fertility drug in women, CLOMIL-50 helps to eliminate the negative feedback of estrogens on the hypothalamic-pituitary-ovarian axis and increases the production of luteinizing hormone and follicle stimulating hormone. This induces ovulation.
Therefore if these results can be translated to strength athletes and bodybuilders, this ability to raise the levels of luteinizing hormone and follicle stimulating hormone should be quite impressive. An increase in these hormones will result in an increase in testosterone production in users. This of course is something that is desperately desired when coming off of anabolic steroids. If testosterone levels can be raised quickly after a cycle a user is much more likely to maintain more of his gains than if he suffered through a crash in testosterone levels and his natural production came back slowly, all the while having to combat the increased levels of estrogen and cortisol.
While it is true that CLOMIL-50 has many "anti-estrogen" properties, there are a multitude of better options. It's is relatively weak in comparison to tamoxifen citrate and the anti-aromatase compounds that are available are much more potent in terms of controlling and/or eliminating estrogenic side effects that are likely to develop. The primary duty of clomiphine citrate should be left to post-cycle therapy.
Of course due to the fact that there is little research to do with the use of CLOMIL-50 as it relates to steroid users, much of what we know about the dosing of it has been from anecdotal reports. For the most part users will maintain doses of the drug between 25 mgs to 150 mgs per day on a consistent basis. Often times users will "frontload" the compound using doses of between 200-300 mgs on the first day of their post-cycle therapy and then reduce the subsequent doses. However the side effects associated with large doses of the compound may hinder some individuals' abilities to do this.
Some users also advocate tapering the dose of CLOMIL-50 during the last few weeks of administration. However this is more a practice that is based upon theory rather than solid medical evidence of it's productivity.
In terms of dosing length it seems that at least 3 weeks of CLOMIL-50 therapy is recommended by users. Of course each has their own preferences along with individual recovery schedules. Also the types of compounds used and the duration of a cycle will of course influence the time it takes for a user to recover and the need for a lengthy post-cycle therapy. Due to the lack of serious side effects associated with the drug, as well as the fact that there is no risk of toxicity with the CLOMIL-50, users are able to use the compound for months on end with seemingly no significant negative consequences.
Male users generally find that a daily intake of 50-100 mg over a four to six weeks period will bring testosterone production back to an acceptable level. This raise in testosterone should occur slowly but evenly throughout the period of intake. Since an immediate boost in testosterone is often desirable, many prefer to combine Clomid with HCG for the first week or two after the steroids have been removed. The kick-start from HCG also helps to restore the normal ability for the testes to respond to endogenous LH, which may be hindered for some time after the cycle is ended due to a prolonged state of inactivity. Once the HCG is stopped, the user continues treatment with Clomid alone. HCG should not be used for longer than two or three weeks though, as the resulting increased testosterone and estrogen levels may again initiate negative feedback inhibition at the hypothalamus. When planning your ancillary drug program, it is also important to remember that injectable steroids can stay active for a long duration. Using ancillary drugs the first week after a long acting injectable like Sustanon has been stopped may prove to be wholly ineffective. Instead, the athlete should wait for two to three weeks, to a point where androgen levels will be diminishing. Here the body will be primed and ready to restore testosterone production.
Clomid and HCG are also occasionally used periodically during a steroid cycle, in an effort to prevent natural testosterone levels from diminishing. In many instances this practice can prove difficult however, especially when using strong androgens for longer periods of time. There is also no exact method for using the two drugs in this manner. Some have experimented by periodically administering small doses of HCG along with one or two tablets of Clomid, perhaps for a few days at a stretch followed by a longer break. An on/off schedule would be implemented; for fear that this combination may lose some effectiveness if used continuously for this purpose. This method of intake may prove to be effective, although it is really much more feasible to stimulate testosterone production after the cycle than to try and maintain it for the long duration during.
SIDE EFFECTS:
Despite these rather inconvenient side effects, for the most part CLOMIL-50 can be run for extended periods of time with no worries of serious negative consequences. Potentially things such as hot flashes, nausea, dizziness, and headaches may occur but anecdotally users report that these symptoms are quite rare. However emotional side effects along with vision problems are frequently reported with use of this drug. Visual tracers or blurry vision are often reported by users, even some who use extremely low doses of the compound. These are often reported to become more pronounced at night. However if this symptom becomes unbearable, it quickly dissipates after administration of the compound is ceased.
In terms of the emotional side effects associated with CLOMIL-50, some users complain that they become depressed, irritable or more emotional in general when using the drug. This can primarily be explained by way of CLOMIL-50 being a synthetic estrogen. By introducing a type of estrogen into a user's system some effects should be expected. Coupled with the fact that the natural testosterone production of the user is already suppressed this obviously could lead to some difficulties. Of course some users find these effects much more pronounced than others, with many finding CLOMIL-50 intolerable while others have little to no side effects.
Another possible effect of use of the compound is increased acne. This is a direct result in the shifting hormonal balance that a user would be experiencing while coming off of anabolic steroids and the introduction of CLOMIL-50 to their system. An increase in production of seminal fluid may also be experienced by some users and therefore the volume of ejaculate may well noticeably increase as well.
Bromocriptin 2.5mg 30 tablets Bromocriptine is a dopamine agonist drug (meaning it acts like dopamine in the brain), primarily activating the dopamine D2 receptors. It"s main use is for the treatment of high prolactin, Parkinson"s disease, and acromegaly; it was also used by bodybuilders for treatment of deca gyno or trenbolone gyno. However, it"s metabolic effects are far greater than that. Lately however, bromocriptine has gained prominence particularly on the World Wide Web as a weight loss agent. In genetically obese rats, bromocriptine normalizes metabolism and there are many good reasons to think it will do the same in humans. Bromocriptine has use during dieting (to minimize the negative adaptations), muscle gain when very lean, and may be beneficial post-steroid cycle. It may also be useful for diabetes treatment and may have pro-sexual effects.
CLEN-40 is an weight loss drug, its active substance is Clenbuterol. This drug is manufactured by Global Anabolic.
Clenbuterol belongs to the class of drugs classified as sympathomimetics. Sympathomimetic drugs are compounds that mimic or imitate the effects of the hormone epinephrine (adrenaline) and the hormone/neurotransmitter norepinephrine (noradrenaline).
Clenbuterol is a popular drug prescribed as a decongestant and bronchodilator and commonly used by sufferers of asthma. However, it is now becoming popular as a dietary supplement endorsed as an effective slimming pill.
CLEN-40 is on of the most popular and potent cutting agents available. CLEN-40 is known to burn fat with thermogenic properties and also build lean muscle mass. Clenbuterol is a potent, long-lasting bronchodilator that is used in some European countries to treat asthma and related lung disorders. However, the drug is also a potent thermogenic agent and can selectively decrease fat and increase lean muscle mass. This property of CLEN-40 has made it a widely abused drug among many individuals. Because of this selective partitioning effect, the drug is widely abused by both amateur and professional athletes around the world.
Many bodybuilders, as well as other athletes, find CLEN-40 beneficial because of its thermogenic abilities. As a thermogenic it increases blood pressure, stimulating the heart muscles. This stimulation, in turn, leads to an increase in body temperature. In addition, CLEN-40 boosts glycogenolysis, or the breakdown of glycogen. This process results to release of glycogen into the bloodstream (in the form of glucose) and renders the body incapable of storing or using more glycogen. This hikes the rate at which fat and protein are used up in the body for these three essential purposes – energy production, for recycling of their molecular components, or for their excretion. This is how CLEN-40 users lose adipose (fat) tissues.
CLEN-40 is also particularly appealing to bodybuilders and other athletes because it heightens aerobic capacity. Aerobic means "with oxygen", and refers to the use of oxygen in the body's metabolic or energy-generating process. In simple terms, CLEN-40 improves oxygen transportation via increased blood pressure. This makes Clenbuterol a staple of many endurance athletes’ drug protocol.
This drug is also used as an anabolic agent although its anabolism effect remains a contentious issue. In several animal studies, it has exhibited anabolism resulting to muscle gains. However, this has not been observed on human subjects.
The recommended regimen with this drug is to gradually ramp up its dosage. Slowly build up the intake each day until an effective and comfortable range is established. This way, most of the drug’s effects can be avoided, specifically its negative effect on blood pressure. Males typically take 2-8 tablets a day while females take 2 - 4 tablets a day.
The length of time this drug is to be cycled is dependent on the goal of the user. If your objective is to lose fat, CLEN-40 highest efficacy is observed when taken in a period of 4 - 6 weeks. During this phase, it is important to monitor temperature increase or decrease.
Remember that as a thermogenic this drug works by elevating the temperature, and thus a decrease or a drop in temperature means its losing its potency. This also signals that you need to break for at least several weeks. Increasing the dosage or prolonging the intake will prove to be ineffective and a total waste of money since the decreased efficacy may mean that the body is growing immune or resistant to its effects.
To heighten its fat-burning ability, many stack CLEN-40 with other drugs such as the thyroid hormone Cytomel. This stack is great during contest preparation or cutting cycle when bodybuilders need to get rid of undesirable fat without sacrificing caloric intake.
CLEN-40 is also typically stacked with non-aromatizing anabolic steroids, those that do not cause water retention. This stack regimen induces the so-called synergistic effect of drugs.
CLEN-40 dosage is dependent on body weight and can be optimized by measuring the body temperature. Athletes usually take 5 - 7 tablets, 100 - 140 mcg per day. For women 80 - 100 mcg/day is usually sufficient. It is advisable to begin CLEN-40 by taking only one tablet on the first day and then increasing the dosage by one tablet each of the following days until the desired maximum dosage is reached. The compound is usually taken over a period of 8 - 10 weeks.
SIDE EFFECTS:
Possible side effects of CLEN-40 include restlessness, palpitations, tremor (involuntary trembling of fingers), headache, increased perspiration, insomnia, muscle spasms, increased blood pressure, and nausea. Individuals who have been diagnosed of cardio-vascular problems should not take CLEN-40.
Cytomel is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodide-thyronine. The thyroid of a healthy person usually produces two hormones, the better known L-thyroxine and the aforementioned L-triiodine-thyronine. Since Cytomel is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-Cytomel is clearly the stronger and more effective of these two hormones. This makes Cytomel more effective than the commercially available L-T4 compounds such as L-thyroxine or Synthroid. Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking Cytomel, which causes a faster conversion of carbohydrates, proteins and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means increased fat burning. Competing bodybuilders, in particular, use Cytomel during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of Cytomel report that by the simultaneous intake of steroids, the steroids become more effective, most likely as the result of the faster conversion of protein.
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 Cytomel 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.
Until recently, Cytomel was used by bodybuilders and female bodybuilders, in particular on a daily basis over several months to remain "hard" and in good shape all year round. Believe us when we tell you that to a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and defined look in photos, eat fast food and iron this out by taking Cytomel. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of Cytomel, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat.
Cytomel is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given todays standards. A drastic reduction of food and calories below the 1000 calorie/day mark can often be avoided by taking Cytomel. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of Cytomel in a reasonable dosage is certainly "healthier" than an extreme hunger diet. As for the dosage, one should be very careful since Cytomel is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25 mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100 mcg/day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also important that Cytomel not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and not be ended abruptly.
25mg - 100mg per day
T3-Cytomel is an weight loss drug, it is also known as Cytomel. This drug is manufactured by LA Pharma.
T3-Cytomel is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodide-thyronine. The thyroid of a healthy person usually produces two hormones, the better known L-thyroxine and the aforementioned L-triiodine-thyronine. Since T3-Cytomel is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-T3-Cytomel is clearly the stronger and more effective of these two hormones. This makes T3-Cytomel more effective than the commercially available L-T4 compounds such as L-thyroxine or Synthroid.
Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking T3-Cytomel, which causes a faster conversion of carbohydrates, proteins and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means increased fat burning. Competing bodybuilders, in particular, use T3-Cytomel during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of T3-Cytomel report that by the simultaneous intake of steroids, the steroids become more effective, most likely as the result of the faster conversion of protein.
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 T3-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 T3-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 T3-Cytomel 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 T3-Cytomel. An in-between point is Synthroid (synthetic T-4), still weaker in action than T3-Cytomel. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.
Until recently, T3-Cytomel was used by bodybuilders and female bodybuilders, in particular on a daily basis over several months to remain "hard" and in good shape all year round. Believe us when we tell you that to a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and defined look in photos, eat fast food and iron this out by taking T3-Cytomel. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of T3-Cytomel, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat.
T3-Cytomel is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given todays standards. A drastic reduction of food and calories below the 1000 calorie/day mark can often be avoided by taking T3-Cytomel. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of T3-Cytomel in a reasonable dosage is certainly "healthier" than an extreme hunger diet.
As for the dosage, one should be very careful since T3-Cytomel is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25 mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100 mcg/day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also important that T3-Cytomel not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and not be ended abruptly.
SIDE EFFECTS:
One should take caution if considering using this drug. T3-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 administering T3-Cytomel, one must remember to increase the dosage slowly. Generally one 25 mcg 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 100 mcg. This will help the body adjust to the increased thyroid hormone, hopefully avoiding any sudden "shock" to the system. The daily dose is also to be split evenly throughout the day, in an effort to keep blood levels steadier. Women are more sensitive to the side effects of T3-Cytomel than men, and usually opt to take no more than 50 mcg daily.
25 - 100 mcg per day
T3-50 is an weight loss drug, it is also known as Cytomel. This drug is manufactured by Platinum Biotech.
T3-50 is not an anabolic/androgenic steroid but a thyroid hormone. As a substance it contains synthetically manufactured liothyronine sodium which resembles the natural thyroid hormone tricodide-thyronine. The thyroid of a healthy person usually produces two hormones, the better known L-thyroxine and the aforementioned L-triiodine-thyronine. Since T3-50 is the synthetic equivalent of the latter hormone, it causes the same processes in the body as if the thyroid were to produce more of the hormone. It is interesting to note that L-T3-50 is clearly the stronger and more effective of these two hormones. This makes T3-50 more effective than the commercially available L-T4 compounds such as L-thyroxine or Synthroid.
Bodybuilders take advantage of these characteristics and stimulate their metabolism by taking T3-50, which causes a faster conversion of carbohydrates, proteins and fats. Bodybuilders, of course, are especially interested in an increased lipolysis, which means increased fat burning. Competing bodybuilders, in particular, use T3-50 during the weeks before a championship since it helps to maintain an extremely low fat content, without necessitating a hunger diet. Athletes who use low dosages of T3-50 report that by the simultaneous intake of steroids, the steroids become more effective, most likely as the result of the faster conversion of protein.
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 T3-50 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 T3-50 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 T3-50 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 T3-50. An in-between point is Synthroid (synthetic T-4), still weaker in action than T3-50. Once the user is ready however, the fat burning effect of this hormone can be extremely dramatic.
Until recently, T3-50 was used by bodybuilders and female bodybuilders, in particular on a daily basis over several months to remain "hard" and in good shape all year round. Believe us when we tell you that to a great extent several bodybuilders who are pictured in "muscle magazines" and display a hard and defined look in photos, eat fast food and iron this out by taking T3-50. The over stimulated thyroid burns calories like a blast furnace. Nowadays, instead of T3-50, athletes use Clenbuterol which is becoming more and more popular. Those who combine these two compounds will burn an enormous amount of fat.
T3-50 is also popular among female bodybuilders. Since women generally have slower metabolisms than men, it is extremely difficult for them to obtain the right form for a competition given todays standards. A drastic reduction of food and calories below the 1000 calorie/day mark can often be avoided by taking T3-50. Women, no doubt, are more prone to side effects than men but usually get along well with 50 mcg/day. A short-term intake of T3-50 in a reasonable dosage is certainly "healthier" than an extreme hunger diet.
As for the dosage, one should be very careful since T3-50 is a very strong and highly effective thyroid hormone. It is extremely important that one begins with a low dosage, increasing it slowly and evenly over the course of several days. Most athletes begin by taking one 25 mcg tablet per day and increasing this dosage every three to four days by one additional tablet. A dose higher than 100 mcg/day is not necessary and not advisable. It is not recommended that the daily dose be taken all at once but broken down into three smaller individual doses so that they become more effective. It is also important that T3-50 not be taken for more than six weeks. At least two months of abstinence from the drug needs to follow. It is also important that the dosage is reduced slowly and evenly by taking fewer tablets and not be ended abruptly.
SIDE EFFECTS:
One should take caution if considering using this drug. T3-50 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 administering T3-50, one must remember to increase the dosage slowly. Generally one 25 mcg 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 100 mcg. This will help the body adjust to the increased thyroid hormone, hopefully avoiding any sudden "shock" to the system. The daily dose is also to be split evenly throughout the day, in an effort to keep blood levels steadier. Women are more sensitive to the side effects of T3-50 than men, and usually opt to take no more than 50 mcg daily.
Clenbuterol 40 is an weight loss drug, its active substance is Clenbuterol. This drug is manufactured by LA Pharma.
Clenbuterol belongs to the class of drugs classified as sympathomimetics. Sympathomimetic drugs are compounds that mimic or imitate the effects of the hormone epinephrine (adrenaline) and the hormone/neurotransmitter norepinephrine (noradrenaline).
Clenbuterol is a popular drug prescribed as a decongestant and bronchodilator and commonly used by sufferers of asthma. However, it is now becoming popular as a dietary supplement endorsed as an effective slimming pill.
Clenbuterol 40 is on of the most popular and potent cutting agents available. Clenbuterol 40 is known to burn fat with thermogenic properties and also build lean muscle mass. Clenbuterol is a potent, long-lasting bronchodilator that is used in some European countries to treat asthma and related lung disorders. However, the drug is also a potent thermogenic agent and can selectively decrease fat and increase lean muscle mass. This property of Clenbuterol 40 has made it a widely abused drug among many individuals. Because of this selective partitioning effect, the drug is widely abused by both amateur and professional athletes around the world.
Many bodybuilders, as well as other athletes, find Clenbuterol 40 beneficial because of its thermogenic abilities. As a thermogenic it increases blood pressure, stimulating the heart muscles. This stimulation, in turn, leads to an increase in body temperature. In addition, Clenbuterol 40 boosts glycogenolysis, or the breakdown of glycogen. This process results to release of glycogen into the bloodstream (in the form of glucose) and renders the body incapable of storing or using more glycogen. This hikes the rate at which fat and protein are used up in the body for these three essential purposes – energy production, for recycling of their molecular components, or for their excretion. This is how Clenbuterol 40 users lose adipose (fat) tissues.
Clenbuterol 40 is also particularly appealing to bodybuilders and other athletes because it heightens aerobic capacity. Aerobic means "with oxygen", and refers to the use of oxygen in the body's metabolic or energy-generating process. In simple terms, Clenbuterol 40 improves oxygen transportation via increased blood pressure. This makes Clenbuterol a staple of many endurance athletes’ drug protocol.
This drug is also used as an anabolic agent although its anabolism effect remains a contentious issue. In several animal studies, it has exhibited anabolism resulting to muscle gains. However, this has not been observed on human subjects.
The recommended regimen with this drug is to gradually ramp up its dosage. Slowly build up the intake each day until an effective and comfortable range is established. This way, most of the drug’s effects can be avoided, specifically its negative effect on blood pressure. Males typically take 2-8 tablets a day while females take 2 - 4 tablets a day.
The length of time this drug is to be cycled is dependent on the goal of the user. If your objective is to lose fat, Clenbuterol 40 highest efficacy is observed when taken in a period of 4 - 6 weeks. During this phase, it is important to monitor temperature increase or decrease.
Remember that as a thermogenic this drug works by elevating the temperature, and thus a decrease or a drop in temperature means its losing its potency. This also signals that you need to break for at least several weeks. Increasing the dosage or prolonging the intake will prove to be ineffective and a total waste of money since the decreased efficacy may mean that the body is growing immune or resistant to its effects.
To heighten its fat-burning ability, many stack Clenbuterol 40 with other drugs such as the thyroid hormone Cytomel. This stack is great during contest preparation or cutting cycle when bodybuilders need to get rid of undesirable fat without sacrificing caloric intake.
Clenbuterol 40 is also typically stacked with non-aromatizing anabolic steroids, those that do not cause water retention. This stack regimen induces the so-called synergistic effect of drugs.
Clenbuterol 40 dosage is dependent on body weight and can be optimized by measuring the body temperature. Athletes usually take 5 - 7 tablets, 100 - 140 mcg per day. For women 80 - 100 mcg/day is usually sufficient. It is advisable to begin Clenbuterol 40 by taking only one tablet on the first day and then increasing the dosage by one tablet each of the following days until the desired maximum dosage is reached. The compound is usually taken over a period of 8 - 10 weeks.
SIDE EFFECTS:
Possible side effects of Clenbuterol 40 include restlessness, palpitations, tremor (involuntary trembling of fingers), headache, increased perspiration, insomnia, muscle spasms, increased blood pressure, and nausea. Individuals who have been diagnosed of cardio-vascular problems should not take Clenbuterol 40.
20mcg - 120mcg perday using a pyramid approach.