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masteron 100mg-10 ml

PRODUCT NAME: Masteron 100
SUBSTANCE: Drostanolon Propionate
CONTENT: 10ml Vial / 100mg/1ml
MANUFACTURER: red dragon pharmaceuticals thailand


Masterone information Masteron(Masterolon 100) - dromostanolonum propionate 2000 mg Vials 20ml 10 mg/ml is a steroid highly valued as a part of a pre contest bodybuilders stack. Masteron(Masteron 100) doesn't aromatize - it can't be converted to estrogen. Drostanolonum is highly androgenic and a strong anti estrogen with minimal liver toxicity, it is usually used as a part of cutting stacks for the last few weeks of contest preparation, Masteron(Masteron 100) works best in stack with Primobolan, Anavar, Winstrol and Testosterone propinate (Testovis).
Masterone dosage The athlete can therefore use Masteron(Masteron 100) to about ten days before a drug test. The average dosage is 100 mg injected every other day. It is best to inject it every 2-3 days because it has a short duration of effect.
Masterone cycle and side effects Popular steroids stacked with Masteron(Masteron 100) (drostanolone propionate) include Parabolan (trenbolone hexahydrobencylcarbonate), Winstrol (stanozolol), and Anavar (oxandrolone). Athletes rarely experience any side effects. It is not hepatoxic, and gynecomastia should not be a concern since it does not convert into estrogen. Some possible side effects of Masteron(Masteron 100) include acne, accelerated hair loss, and increased aggression. The main disadvantage is a very poor availability on the black market and its high price.

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Masteron (Drostanolone Propionate)

Masteron is a European injectable preparation containing the steroid drostanolone propionate. Drostanolone is a derivative of dihydrotestosterone, most specifically 2alpha-methyldihydrotestosterone. As a result, the structure of this steroid is that of a moderate anabolic/potent androgen which does not aromatize to estrogen. Water retention and gynecomastia are therefore not a concern with this compound; as of course here estrogen is usually the culprit. Masteron may in fact exhibit antiestrogenic activity in the body, competing with other substrates for binding to aromatase. This would reduce the conversion rate of other steroids, Masteron acting in the same manner as the oral steroid Proviron®.


Bodybuilders have a strong appreciation for non-aromatizing androgens, and find Masteron very useful as a cutting agent. It is likewise generally used a number of weeks prior to a competition, in an effort to bring out an improved look of density and hardness to the muscles. For this purpose Masteron should work exceptionally well so long as the body fat percentage is low enough. Provided everything fits as if should, the user can achieve that "ripped" look so popular to professional bodybuilding. The androgenic effect can also be crucial during this period, a time when caloric intake is drastically lowered. The user is provided added "kick" or "drive" to push through the grueling training sessions leading up to the show. Drostanoione was once also popular with athletes subject to drug testing, as for a period of time this compound was not screened for during competition. The urinary metabolites of drostanoione were recognized by the early 90's however, and this drug now adjoins a long list of anabolic/androgenic steroids identifiable during urinalysis testing. Although some bodybuilders claim they can safely use Masteron if discontinued three to four weeks before a test, there are always uncertainties with the use of esterified injectable steroids. This perhaps makes the oral DHT Proviron® (1-ethyldihydrotestosterone) a slightly better choice, as orals offer much better control.


Recreational users might also be interested in Masteron. Although dihydrotestosterone is not highly active in muscle tissue, the 2 alkylation present on drostanoione considerably intensifies its anabolic effect. It can therefore be used somewhat effectively as bulking agent, providing a consistent gain of high quality muscle mass. It can also be successfully combined with other steroids for an enhanced effect. Mixing drostanoione with an injectable anabolic such as Deca-Durabolin® (nandroione decanoate) or Equipoise® (boldenone undecylenate) can prove quite useful for example, the two providing notably enhanced muscle gain without excessive water retention. For greater mass gains, one can alternately addition a stronger androgen such as Dianabol or an injectable testosterone. The result here can be an extreme muscle gain, with a lower level of water retention & other estrogenic side effects than if these steroids were used alone (usually in higher doses). Masteron could of course be used during cutting phases of training as well. A cycle of this drug combined with Winstrol®, Primobolan® or Cxandrolone should provide great muscle retention and fat loss, during a period which can be very catabolic without steroids. It is an added benefit that none of these steroids aromatize, and therefore there is no additional worry of unwanted water/fat retention.


The propionate ester used with this compound will extend its activity for only a few days. With such a short duration of effect, injections need to be repeated at least every 3 or 4 days in order to maintain a consistent level of hormone in the blood. Factoring this in with its low strength (50 mg/ml), men will generally inject a full 2 ml ampule of Masteron (100 mg) every two or three days. The weekly dosage therefore lands in the range of 200-350 mg, a level more than sufficient to receive good results. We also should mention that while some women do profess to using this item before a show, it is much too androgenic in nature to recommend. Virilization symptoms can result quickly with its use, making Masteron a very risky item to experiment with. If attempted, the dosage should be limited to no more than 25 to 50 mg each week. The female athlete would be further served by increasing the number of days between injections to prevent buildup of steroid in the body. In this case, Masteron can perhaps be administered once every 7 days.


Since estrogen offers us no trouble, side effects are generally mild with this steroid. As discussed earlier, gynecomastia and water retention go unseen. So are problems controlling blood pressure, again usually associated with estrogen. Masteron is also not liver toxic, so there is little concern stress will be placed on this organ, even during longer cycles. The only prominent side effects stem from the basic androgenic properties of dihydrotestosterone. This includes oily skin, acne, body/facial hair growth, aggression and accelerated hair loss. Since this compound is already a synthetic DHT, Proscar® would have no impact on the level of androgenic effects. Men with a receding hairline (or those with a known familial predisposition for baldness) may therefore wish to stay away from Masteron completely, as the potent androgenic effect of this steroid can easily exacerbate such a condition.

primobol 100mg-10 ml (methenolone enanthate)

Generic Name: methenolone enanthate
Primobolan depot is a registered trademark of Schering A/G avaiable in 50 mg/cc from Mexico and 100 mg/cc from Europe. It is is the \"Cleanest and Gentles\" anabolic steroid, will not aromatize, non-toxic, low in androgens.
Primobolan depot may be taken by both Men and Women. Dosages for men are 100-300 mg/week, Women 1/2 dosage. Primobolan depot is the only steroid that works well on a low calorie diet. Effective for bulking, but tends to harden and add muscle tone more that build big muscles.

Primobolan depot works great when added to a cycle (stacked) with other steroids, it tends to lessen water retention and harshness when stacked with more heavy duty testosterone injectables, like Omnadren / Sustanon, Cypoinate / Propionate, ect. It is an analog immune-stimulating steroid used by people with Aids and others with depressed immune systems to build up the immune system and add lean muscle mass. Primobolan is one of the finest steroids in the world today.

Effective Dose: 100 - 300 mg/week

sustabol 325mg

PRODUCT NAME: Sustabol 325
SUBSTANCE: 5Testosterones
CONTENT: 10 ml. Vial / 325mg/1ml
MANUFACTURER: red dragon- thailand
Dosages:Sustanon is usually injected at least once a week., which can be stretched up to 10 days. The dosage in bodybuilding and powerlifting ranges from 250 mg every 14 days up to 1000 mg or more per day. Since such high dosages are not recommended and fortunately are also not taken in most cases the rule is 250-1000 mg/week. A dosage of 500 mg/week is completely sufficient for most, and can often be reduced to 250 mg/week by combining with an oral steroid.

In order to gain mass fast Sustanon is often combined with Deca Durabolin, Dianabol (D-bol) or Anadrol while athletes who are more into quality prefer combining it with Parabolan, Winstrol, Anavar or Primobolan Depot.

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

The side effects of Sustanon are similar to those of Testosterone enanthate (see also Testosterone enanthate) only that they are usually less frequent and less severe

decabol 200mg

Decabol 200mg 10 ml

Deca-Durabolin; 19-Nortestoterone decanoate
Molecular Formula : C28H44O3
Molecular Weight : 428.65
CAS Registry Number : 360-70-3
EINECS : 206-639-3
Melting point : 33-37 ºC
alpha : 32 º

Possibly the most popular steroid compound of the last few decades, Deca-Durabolin earns its reputation by producing large muscle gains, aiding with joint pain and improving the immune system. These benefits come from a substance that has a relatively low rate of side effects because it doesn’t convert to estrogen as much as many of its counterparts. Not that Deca is without its problems. First, Deca needs to be taken over long periods of time (cycles of 12 weeks minimum) for it to be effective. Also, Deca must be taken with testosterone because the body's natural levels will drop. Testosterone should also be a part of a Deca cycle's post-cycle-therapy. Deca can also cause a good deal of water retention and acne.
Deca-Durabolin® is the Organon brand name for the injectable steroid nandrolone decanoate. This compound came around early in the wave of commercial steroid development, first being made available as a prescription medication in 1962. World wide "Deca" is one of the most widely used anabolic steroids. Its popularity is due to the simple fact that it exhibits many very favorable properties. Structurally nandrolone is very similar to testosterone, although it lacks a carbon atom at the 19th position (hence its other name 19-nortestosterone). The resulting structure is a steroid that exhibits much weaker androgenic properties than testosterone. Of primary interest is the fact that nandrolone will not break down to a more potent metabolite in androgen target tissues. You may remember this is a significant problem with testosterone. Although nandrolone does undergo reduction via the same (5-alpha reductase) enzyme that produces DHT from testosterone, the result in this case is dihydronandrolone. This metabolite is weaker than the parent nandroloness, and is far less likely to cause unwanted androgenic side effects. Strong occurrences of oily skin, acne, body/facial hair growth and hair loss occur very rarely. It is however possible for androgenic activity to become apparent with this as any steroid, but with nandrolone higher than normal doses are usually responsible.
Nandrolone also show an extremely lower tendency for estrogen conversion. For comparison, the rate has been estimated to be only about 20% of that seen with testosterones. This is because while the liver can convert nandrolone to estradiol, in other more active sites of steroid aromatization such as adipose tissue nandrolone is far less open to this process'. Consequently estrogen related side effects are a much lower concern with this drug. An anti-estrogen is likewise rarely needed with Deca, gynecomastia only a worry among sensitive individuals. At the same time water retention is not a usual concern. This effect can occur however, but is most often related to higher dosages. The addition of Proviron and/or Nolvadex should prove sufficient enough to significantly reduce any occurrence. Clearly Deca is a very safe choice among steroids. Actually, many consider it to be the best overall steroid for a man to use when weighing the side effects and results. It should also be noted that in HIV studies, Deca has been shown not only to be effective at safely bringing up the lean body weight of patient, but also to be beneficial to the immune system.
It is of note however that nandrolone is believed to have some activity as a progestin in the body. Although progesterone is a c-19 steroid, removal of this group as in 19-norprogesterone creates a hormone with greater binding affinity for its corresponding receptor. Sharing this trait, many 19-nor anabolic steroids are shown to have some affinity for the progesterone receptor as well. This can lead to some progestin-like activity in the body, and may intensify related side effects. The side effects associated with progesterone are actually quite similar to those of estrogen, including negative feedback inhibition of testosterone production, enhanced rate of fat storage and possibly gynecomastia. Many believe the progestin activity of Deca notably contributes to suppression of testosterone synthesis, which can be marked despite a low tendency for estrogen conversion.
Deca is not known as a very "fast" builder. The muscle building effect of this drug is quite noticeable, but not dramatic. The slow onset and mild properties of this steroid therefore make it more suited for cycles with a longer duration. In general one can expect to gain muscle weight at about half the rate of that with an equal amount of testosterone. A cycle lasting eight to twelve weeks seems to make the most sense, expecting to elicit a slow, even gain of quality mass. Although active in the body for much longer, Deca is usually injected once or twice per week. The dosage for men is usually in the range of 300-600mg/week. If looking to be specific, it is believed that Deca will exhibit its optimal effect (best gain/side effect ratio) at around 2mg per pound of lean bodyweight/weekly. Deca is also a popular steroid among female bodybuilders. They take a much lower dosage on average than men of course, usually around 50mg weekly. Although only slightly androgenic, women are occasionally confronted with virilization symptoms when taking this compound. Should this become a concern, the shorter acting nandrolone Durabolin would be a safer option. This drug stays active for only a few days, greatly reducing the impact of androgenic buildup if withdrawal were indicated.
Endogenous testosterone levels can be a concern with Deca-Durabolin, especially after long cycles. It is therefore mandatory to incorporate ancillary drugs at the conclusion of therapy. An estrogen antagonist such as Clomid or Nolvadex is therefore commonly used for a few weeks. These both provide a good level of testosterone stimulation, although they may take a couple of weeks to show the best effect. HCG injections could be added for extra reassurance, acting to rapidly restore the normal ability of the testes to respond to the resumed release of gonadotropins. For this purpose one could administer three injections of 2500-50001.U., spaced five days apart. After which point the antagonist is continued alone for a few more weeks in an effort to stabilize the production of testosterone. Remember not to begin post cycle therapy (PCT) until after Deca has been withdrawn for around three weeks. Deca stays active for quite some time so the ancillary drugs will not be able to exhibit their optimal effect when the steroid is still being released into the bloodstream. The major drawback for competitive purposes is that in many cases nandrolone metabolites will be detectable in a drug screen for up to a year (or more) after use. This is clearly due to the form of administration. Esterified compounds have a high affinity to stay stored in fatty tissues. While we can accurately estimate the time frame it will take for a given dose to enter circulation from an injection site, we cannot know for sure that 100% of the steroid will have been metabolized at any given point. Small amounts may indeed be stubborn in leaving fatty tissue, particularly after heavy, longer-term use. Some quantity of nandrolone decanoate may therefore be left to sporadically enter into the blood stream many months after use. This process may be further aggravated when dieting for a show, a time when body fat stores are being actively depleted (possibly freeing more steroid). This has no doubt been the cause for many unexpected positives on a drug screen. The fact that nandrolone has been isolated as the "hands-off" injectable for the drug tested athlete is most likely due to its popularity (and therefore common appearance on drug screens). The same risk would of course hold true for other long chain esterified injectables such as Equipoise, and Primobolan.
Those not worried about drug screens are likely to find the low water retention and good effect of this drug favorable for use in pre-contest cutting stacks. A combination of Deca and Winstrol during the weeks/months leading up to a show for example, is noted to greatly enhance to look of muscularity and definition. A strong non-aromatizing androgen like Halotestin or trenbolone could be further added, providing an enhanced level of hardness and density to the muscles. Being an acceptable anabolic, Deca can also be incorporated into bulk cycles with good results. The classic Deca and Dianabol cycle has been a basic for decades, and always seems to provide excellent muscle growth. A stronger androgen such as Anadrol or testosterone could also be substituted, producing greater results. When mixed with Deca, the androgen dosage can be kept lower than if used alone, hopefully making the cycle more comfortable. Additionally one may choose to continue Deca for a number of few weeks after the androgen has been stopped. This will hopefully harden up some of the bloat produced by the androgen, giving a more quality appearance. Remember that endogenous testosterone production will not resume during Deca therapy, and ancillaries are likewise still needed.

finaplix acetate trembolone 100mg -10 ml

Trenbolone Enanthate vs acetate trembolone

For bulking up, there may be no better steroid than trenbolone and with enanthate ester, users will only need one injection per week. Its anabolic effect is five times that of testosterone and it doesn’t convert to estrogen, which makes it free from side effects like gynocomastia, water-retention, etc.

Trenbolone is not without its fair share of side effects, however. Testicular atrophy, hair loss, enlarged prostate and acne have been reported from using this drug. Trenbolone will also shut down the body’s natural testosterone production, which can lead to sexual dysfunction.
Trenbolone Enanthate is only available from underground labs and was not designed for human consumption, although it is considered to be an ideal drug for bodybuilders who want to burn fat and gain muscle, although its long ester makes unwise for professional athletes who undergo testing to use.
Trenbolone is a very potent androgen with strong anabolic activity. It is well suited for the rapid buildup of strength and muscle mass, usually providing the user exceptional results in a relatively short time period. The anabolic effect of this drug is often compared to popular bulking agents such as testosterone or Dianabol, with one very important difference. Trenbolone does not convert to estrogen. This is indeed a very unique compound since mass drugs, almost as a rule, will aromatize (or cause other estrogen related troubles) heavily. When we think of taking milder (regarding estrogen) steroids we usually expect much weaker muscle growth, but not so with Trenbolone. Here we do not have to worry about estrogen related side effects, yet still have an extremely potent mass/strength drug. There is no noticeable water retention, so the mass gained during a cycle of Trenbolone will be very hard and defined (providing fat levels are low enough). Gynecomastia is also not much of a concern, so there shouldn't be any need to addition an anti-estrogen if trenbolone is the only steroid administered.
The high androgen level resulting from this steroid, in the absence is excess estrogen, can also accelerate the burning of body fat. The result should be a much tighter physique, hopefully without the need for extreme dieting. Trenbolone can therefore help bring about an incredibly hard, ripped physique and is an ideal product for competitive bodybuilders. Trenbolone is notably more potent than testosterone, and has an effect that is as much as three times as strong on a milligram for milligram basis. Likewise we can expect to see some level of androgenic side effects with use of this compound. Oily skin, aggressive behavior, acne and hair loss are therefore not uncommon during a cycle with this steroid. The androgenic nature of this drug of course makes it a very risky item for women to use, the chance for virilization symptoms extremely high with such a potent androgen.
Trenbolone is also much more potent than testosterone at suppressing endogenous androgen production. This makes clear the fact that estrogen is not the only culprit with negative feedback inhibition, as here there is no buildup of this hormone to report here. There is however some activity as a progestin inherent in this compound, as trenbolone is a 19-nortestosterone (nandrolone) derivative (a trait characteristic of these compounds). However it seems likely that much of its suppressive nature still stems from its powerful androgen action. With the strong impact trenbolone has on endogenous testosterone, of course the use of a stimulating drug such as HCG and/or Clomid/Nolvadex is recommended when concluding steroid therapy (a combination is preferred). Without their use it may take a prolonged period of time for the hormonal balance to resume, as the testes may at first not be able to normally respond to the resumed output of endogenous gonadotropins due to an atrophied state. Those who have used Trenbolone regularly would often claim it to be indispensable. A daily dosage of 37.5-75 mg is the most popular range when running a cycle. While Trenbolone is quite potent when used alone, it was generally combined with other steroids for an even greater effect. During a cutting phase one could add a non-aromatizing anabolic such as Winstrol or Primobolan. Such combinations will elicit a greater level density and hardness to the muscle. One could also bulk with this drug, with the addition of stronger compounds like Dianabol or Testosterone. While the mass gain would be quite formidable with such a stack, some level of water retention would probably also accompany it. Moderately effective anabolics such Deca-Durabolin or Equipoise would be somewhat of a halfway point, providing extra strength and mass but without the same level of water bloat we see with more readily aromatized steroids.

hcg

HCG (human chorionic gonadotropin)

HCG is one of the most important substances used in post-cycle-therapy. It stimulates the body to make natural testosterone, which is suspended during cycles of anabolic steroid use. As medicine, HCG is used to treat hypogodadism and as a fertility treatment in men. In a steroid cycle, it is important to not use too much HCG as it will cause the testes to shut down via negative feedback.

Chorionic gonadotropin is a hormone found in the female body during the early months of pregnancy (it is produced in the placenta). It is in fact the pregnancy indicator looked at by the over the counter pregnancy test kits, as due to its origin it is not found in the body at any other time. Blood levels of this hormone will become noticeable as early as seven days after ovulation. The level will rise evenly, reaching a peak at approximately two to three months into gestation. After this point, the hormone level will drop gradually until the point of birth. As a prescription drug, HCG offers us some interesting benefits. In the United States, we have the two popular brands, Pregnyl, made by Organon, and Profasi, made by Serono. These are FDA approved for the treatment of undescended testicles in young boys, hypogonadism (underproduction of testosterone) and as a fertility drug used to aid in inducing ovulation in women. When prepared as a medical item, this hormone comes from a human origin. Although there is often a fear of biological origin products, there is little research to be found regarding pathogen or sterility problems with HCG. The problems seen with human origin growth hormone are certainly not to be repeated with HCG, as this compound is obtained in a much different way.
While HCG offers the female no performance enhancing ability, it does prove very useful to the male steroid user. The obvious use of course being to stimulate the production of endogenous testosterone. The activity of HCG in the male body is due to its ability to mimic LH (luteinizing hormone), a pituitary hormone that stimulates the Leydig's cells in the testes to manufacture testosterone. Restoring endogenous testosterone production is a special concern at the end of each steroid cycle, a time when a subnormal androgen level (due to steroid induced suppression) could be very costly. The main concern is the action of cortisol, which in many ways is balanced out by the effect of androgens. Cortisol sends the opposite message to the muscles than testosterone, or to breakdown protein in the cell. Left unchecked (by an extremely low testosterone level) in the body, cortisol can quickly strip much of your new muscle mass away.
The main focus with HCG is to restore the normal ability of the testes to respond to endogenous luteinizing hormone. After a long period of inactivity, this ability may have been seriously reduced. In such a state testosterone levels may not reach a normal point, even though the release of endogenous LH has been resumed. Many who have suffered severe testicular shrinkage may be able to relate, as it is often some time before normal testicle size and feelings of virility are restored if ancillary drugs had not been used. The excessive stimulation brought forth by administration of HCG can likewise cause the testicles to rapidly return to their normal size and level of activity. We are not simply looking for it to fix the problem however, as the resulting high testosterone level can itself trigger negative feedback inhibition at the hypothalamus. Estrogen production is also heightened with the use of HCG, due to its ability to increase aromatase activity in the Leydig's cells. This is due to the main action of HCG, namely the increase of cycIicAMP (a secondary messenger that regulates cellular activity). When stimulated by HCG, the ability of the testes to aromatize androgens could potentially be heightened several times greater than normal. This also may inhibit testosterone production, so we therefore use HCG only as a quick shock to the testes.
The usual protocol is to inject 1500-3000 I.U. every 4th or 5th day, for a duration usually no longer than 2 or 3 weeks. If used for too long or at too high a dose, the drug may actually function to desensitize the Leydig's cells to luteinizing hormone, further hindering a return to homeostasis. Timing the initial dose is also very crucial. If your were coming off a cycle of Sustanon for example, testosterone levels in your blood will likely stay elevated for at least 3 to 4 weeks after your last injection. Taking HCG on the day of your last shot would therefore be useless. Instead one would want to calculate the last week in which androgen levels are likely to be above normal, and begin ancillary drug therapy at this point. In this case HCG would be started around the third or fourth week. Likewise, after ending a cycle of Dianabol (an oral) your blood levels will be sub normal after the third day. Here you may want to begin HCG therapy a few days before your last intake of tablets, giving it a few days to take effect. One would also want to give some thought to the level of suppression that the cycle might have brought about. After an 8 week cycle of Equipoise for example, 1500-2500 I.U. would likely be a sufficient initial dosage. The lower amount of hormonal suppression one associates with this drug would probably not require much more. On the other hand, 750-1000mg of Sustanon per week might incline the user to inject a much larger HCG dose, perhaps as much as 5000 I.U. for the opening application. It may thereafter also be a good idea to reduce the dosage on subsequent shots, so as to step down the intake of HCG during the two or three weeks of intake.
As discussed above, HCG acts only to mimic the action of LH. It is likewise not the perfect hormone to combat testosterone suppression, and for this reason it is used most often in conjunction with estrogen antagonists such as Clomid, Nolvadex or cyclofenil. These drugs have a different effect on the regulating system, namely inhibiting estrogen-induced suppression at the hypothalamus. This of course also helps to restore the release of testosterone, although through a much different mechanism than HCG. A combination of both drugs appears to be very synergistic, HCG providing an immediate effect on the testes (shocking them out of inactivity) while the anti-estrogen helps later to block inhibition on the hypothalamus and resume the normal release of gonadotropins from the pituitary. The typical procedure involves giving the Clomid/Nolvadex dose from the start with HCG, but continuing it alone for a few weeks once HCG has been discontinued. This practice should effectively raise testosterone levels, which will hopefully remain stable once Clomid/Nolvadex have been discontinued. While unfortunately there is no way to retain all of the muscle gains produced by anabolic steroids, using ancillaries to restore a balanced hormonal state is the best way to minimize the loss felt with ending a cycle.