Anabolic androgenic steroids have several varieties of forms, there are oral steroids (in tablets). Anabolics in tablets are most often taken by people who do not want to take injections, or who have a first course, then such people will be well suited for stavors in tablets or methandrostenolone. The same active substance of steroids can be contained in tablets and injections, the only difference is that in injections, more of the drug is absorbed by the body because it does not break down in the liver, here is an example of such anabolics that can be in both oral and injectable forms ( course Primobolan, Methandrostenolone, Stanozolol). There are also oral steroids that are available only in tablets for example (Turinabol, Oxymetholone, Oxandrolone).
Similarly, anabolic tablets are good because they have a short half-life, getting quickly into the blood and starting their action within an hour after taking, which can also be quickly excreted from the body before the competition, or simply begin sooner after the course therapy. The most often courses with steroids in tablets do not take more than 8 weeks, because oral steroids have a negative effect on the liver and the effectiveness of the course after 8 weeks may decrease, do not be afraid if you take oral steroids in dosages as indicated below, and no more 8 weeks, then nothing bad will happen to your liver.
The best choice is to combine anabolics in tablets and injectable steroids because the injections are roughly speaking background, and this pill has already been adjusted, due to this one drug strengthens the effect of the other and you get a more pronounced anabolic effect in the set of muscle mass and strength indicators. Never mix more than one drug on tablets with oral steroids, as this can have a negative effect on the liver.
In fact, the harm of tablets is greatly exaggerated, it is enough to follow a few simple rules to avoid a negative effect on your body, for this you should not drink alcohol on a course of steroids, you need to take enough food that anabolic helps you build muscles, you need to take enough fluids for your body, go to bed early, balance the diet and exclude sweet, fried, fatty, take vitamins taking into account the needs of your body.
STEROID TEST – CT FLETCHER
Reception of oral steroids
Consider the approximate dosages of steroids in tablets, the first dosage for beginners and the last for advanced chemists (the amount of substance indicated per day): Solo courses
Stanozolol 30-50 mg
Methandrostenolone – 20-50mg
Turinabol – 30-50mg
Oxandrolone – 30-100 mg
Oxymetholone – 50-150 mg
Courses of oral aas with injections
.Stanozolol 50 mg per day + testosterone propionate 100 mg every other day (good course for drying)
Methandrostenolone 30mg per day + Testosterone enanthate 250-500mg per week (excellent course for weight)
Oxandrolone 50mg per day + testosterone propionate 100mg a day + nandrolone phenylpropionate 100mg every other day (excellent course for dry weight)
Oxymetholone 100mg per day + Sustanon 500mg per week + Nandrolone decanoate 200mg per week (explosive course for weight).
Effect and effect of oral steroids
Steroids in tablets have positive effects:
Strengthen bone tissue
Help restore after hard training
Accelerate the synthesis of protein in the body
Increase the reserves of creatine phosphate
Improve the filling of muscles with blood
Deliver useful substances to the muscle
On steroids, your muscles grow 10 times faster than naturally.
Anabolics in tablets are not desirable for people who have heart problems, liver problems, low immunity, which have a breast tumor, people with diabetes, as well as liver-kidney failure.
As with any other drug, steroids have side effects, but if you follow these dosages and take breaks between courses, as well as taking aromatase inhibitors or anti-estrogens, most of you will be able to avoid them.
Increase in blood pressure.
Coarsening of the voice.
Negative effects on the liver.
Reviews about taking steroids
I took methane 30 mg every day, I gained 6 kg for 4 weeks, I was satisfied.
For the first course took a tourist, ate 40mg per day for 6 weeks, scored 5kg of quality muscles and after the course all remained.
He drank on stanovere with propionate, perfectly prepared for the summer.
Took Oksandrolon for his girlfriend from the guys, everything is fine, the original oxana.
Oral steroids of all time.
I think it will be useful for general development.
Fluoxymesterone (halotestin) Description: Fluoxymesterone is an oral anabolic steroid derived from testosterone. More precisely, it is a methyltestosterone derivative, which is distinguished by the addition of 11b-hydroxy and 9-a-fluor groups. As a result, we have a potent orally active, non-aromatizing steroid with strong androgenic activity. Fluoxymesterone is much more androgenic than testosterone, at the same time, anabolic properties are more moderate. This makes fluoxymesterone a drug for increasing strength, but not the most ideal and best oral steroid anabolic. Fluoxymesterone significantly increases strength, increases muscle density, improves drawing, but weakly adds muscle volume. Ethyl estrinol (orabolin)
Description: Ethylestrenol is an anabolic steroid, very similar in structure to nandrolone. He has mild-moderate anabolicity, accompanied by mild estrogenicity and high progestogenicity. Structurally, this drug is similar to norethandrolone and differs from it in the absence of oxygen in position 3. Although ethylestrenol is more anabolic than androgen, this steroid is very weak. Its effect is much weaker than that of norethandrolone or nandrolone, and it is even less effective than stanozolol or oxandrolone. Prior to the title, the best oral steroid is still far away 🙂
Testosterone undecanoate (andriol)
Description: Andriol is an oral testosterone preparation that contains 40 mg of undecanoate testosterone in a gelatin capsule. This drug is different from most oral AAS, which are usually 17-alpha-alkylated, to prevent primary metabolism in the liver. Esterification and dissolution in oil help testosterone undecanoate in andriol to be absorbed through the lymphatic system, like food fats. This allows you to bypass the liver, the first physiological barrier. The actual level of bioavailability of andriol is approximately 7%. Essentially, this is a non-toxic, orally active testosterone, which is an alternative to other AAS. This drug is not included in the rating of the best oral steroids.
Description: Norethandrolone is an anabolic steroid, very similar in structure to nandrolone. He has mild-moderate anabolicity, accompanied by a certain share of androgenic and estrogenic actions. Although this preparation is an alkylated nandrolone, it can not be presented as an oral replacement for nandrolone. The high estrogenicity of norethandrolone may be problematic when recruiting mass. When taken in the amount necessary for muscle growth, the user gets his share of estrogenic side effects. Muscles on the course of oral steroid norethandrolone gain a lot of water and fat, which is not the best way to affect the appearance. Oxymetalone (anadrol-50)
Oxymetholone is a potent oral anabolic steroid derived from dihydrotestosterone. More specifically, he is a relative of mesanolone, and differs from him by the addition of a hydroxymethylene group in position 2. One of the most popular drugs on the course of oral steroids. This change makes the steroid activity completely different. Oxymetholone is a powerful anabolic steroid. Dihydrotestosterone and melanolone are very weak, because they are very easily exposed to 3-alpha hydroxysteroid dehydrogenase. Oxymetholone, however, remains active. In standard animal tests, it shows significantly greater anabolicity than testosterone or methyltestosterone. The same tests show that its androgenicity is more than 4 times less than its anabolicity, although in humans it is not so. Oxymetholone, as many believe, one of the most powerful selling oral anabolic steroids. Beginner for 6 weeks, he can grow by 9-15kg. He delays the water, and most of the increase will be water. This may not really appeal to the athlete, although he may feel larger and stronger under oxymetholone. Oxymetalon increases the volume and strength of muscles. Muscles contract better, a large amount of water provides better protection of connective tissues. Increases elasticity, reduces the risk of injury under weight. It should be noted that too much weight gain can increase the burden on connective tissues. Traumas of the thoracic and biceps are usually associated with the limiting weight, and here oxymetholone can have to do with it. and most of the increase will be water. This may not really appeal to the athlete, although he may feel larger and stronger under oxymetholone. Oxymetalon increases the volume and strength of muscles. Muscles contract better, a large amount of water provides better protection of connective tissues. Increases elasticity, reduces the risk of injury under weight. It should be noted that too much weight gain can increase the burden on connective tissues. Traumas of the thoracic and biceps are usually associated with the limiting weight, and here oxymetholone can have to do with it. and most of the increase will be water. This may not really appeal to the athlete, although he may feel larger and stronger under oxymetholone. Oxymetalon increases the volume and strength of muscles. Muscles contract better, a large amount of water provides better protection of connective tissues. Increases elasticity, reduces the risk of injury under weight. It should be noted that too much weight gain can increase the burden on connective tissues. Traumas of the thoracic and biceps are usually associated with the limiting weight, and here oxymetholone can have to do with it. Increases elasticity, reduces the risk of injury under weight. It should be noted that too much weight gain can increase the burden on connective tissues. Traumas of the thoracic and biceps are usually associated with the limiting weight, and here oxymetholone can have to do with it. Increases elasticity, reduces the risk of injury under weight. It should be noted that too much weight gain can increase the burden on connective tissues. Traumas of the thoracic and biceps are usually associated with the limiting weight, and here oxymetholone can have to do with it.
Description: Oxandrolone is an oral anabolic steroid derived from dihydrotestosterone. It was developed for a pure anabolic effect, without significant estrogenic and progestin activity. Oxandrolone is known for being a fairly mild steroid with no side effects. This oral anabolic steroid is 6 times more anabolic than testosterone, but significantly less androgenic. This drug is loved by athletes preparing for competitions, in speed-strength sports where pure muscles without water and fat are needed.
Mmboleron (check dropps)
Description: Mobilonone is a potent oral steroid derived from nandrolone. This preparation is 7.17 dimethylated nandrolone, which shows more activity than nandrolone. Myboleron has maintained a reputation as one of the most powerful steroids in the world. During standard animal tests, mibolerone showed a 41-fold higher anabolic activity than methyltestosterone. Androgenic activity was 18 times higher. Estrogenic and progestogenic side effects are also evident. Usually it was used by athletes in mass-gathering courses and to stimulate aggression before training or competitions.
Description: Methyltestosterone is an orally active form of testosterone. It is similar in its structure to testosterone and differs only in the addition of a methyl group in the position of c17-alpha, to enhance bioavailability when taken orally. The resulting steroid is the world’s first oral steroid. Further studies gained momentum and methyltestosterone became only the first of many other drugs. The effect of this steroid is moderately anabolic and androgenic, with high estrogenic activity due to aromatization in 17-alpha methyl estradiol. This makes methyltestosterone very problematic for use in bodybuilding.
Methenolone acetate (primabolan)
Description: Primobolan is a trademark of the anabolic steroid methenolone acetate. This drug is very similar in effect to primobolan depot, but is available in the form of tablets. Methenolone acetate is a non-alkylated oral steroid, one of the drugs that does not give a serious load on the liver. He is successful for his moderate anabolic properties, low androgenicity, and the lack of estrogenicity. It is used on drying, when it is necessary to add a little muscle and increase the dryness. Methandrostenal (dianabol)
Dianabol is the most popular brand for methandrostenolone, produced in many countries. Methandrostenolone is a derivative of testosterone, modified so that the androgenic properties of the hormone are reduced, and the anabolic properties are preserved. With a lower level of androgenicity than testosterone, methandrostenolone is classified as an anabolic steroid, although androgenicity is present. This drug is sold mainly in the form of tablets, but there are also injectable veterinary drugs. Methandrostenolone is historically the most used steroid for improving physique. Mesterolone (proviron)
Proviron is a trademark of Schering for oral androgen, placeolone (1-methyl-dihydrotestosterone). Like dihydrotestosterone, placerolone is a strong androgen with mild anabolicity. This is a consequence of the fact that, like dihydrotestosterone, placerolone is rapidly metabolized into inactive metabolites in muscle tissue where the concentration of 3-hydroxysteroid dehydrogenase is high. One can not take seriously the statement that proviron blocks androgen receptors in muscle tissue and thus prevents other powerful steroids from working. In fact, because of the high degree of binding by the blood globulins, the placerolon allows you to work better with other steroids, increasing their percentage in a free state. Among the athletes, the traveler is used primarily to increase the level of androgens, during drying or preparing for competitions,
Chlordehydromethyltestosterone is a potent derivative of methandrostenolone. This oral steroid is a structural mixture of methandrostenolone and clostebol, the basic structure of methandrostenolone, and 4-chlorine from clostebol. This change makes chlordehydromethyltestosterone more moderate, compared with methandrostenolone, without estrogenic activity and with much less androgenic activity. The anabolic effect of chlordehydromethyltestosterone is somewhat lower than that of methandrostenolone, but the balance of anabolic effects to androgenic is better. This means that at any level, chlordehydromethyltestosterone produces fewer androgenic side effects. Chloromethylandrostene diol (promagnon)
Chloromethylandrostenediol is an oral anabolic steroid derived from testosterone. It is very similar in structure to chloromethyltestosterone, which is a non-aromatizing and milder analogue of methyltestosterone. In animal studies, chloromethyltestosterone showed approximately 30-50% anabolicity from methyltestosterone and 10% androgenicity from methyltestosterone. Chloromethylandrostenediol differs only by replacing the 3-keto group by 3-hydroxyl. This steroid is not aromatized and has sufficient potential in terms of anabolic effect.
Description: Oxymesterone is an oral anabolic steroid derived from testosterone. It is very similar in structure to 4-hydroxytetosterone, and differs only in the addition of a methyl group in position 17-alpha. Like its unmethylated analogue, oxymesterone is considered an effective steroid for increasing the dry mass. This steroid does not have estrogenic and progestin activity. Oxymesterone – “pure” drug: a powerful, non-aromatizing and also almost full anabolic. According to studies, oxymesterone is three times more anabolic than methyltestosterone, but it is half less androgenic. Oxymeters are also good for athletics.
Description: Methyltrienolone is the most potent oral steroid ever obtained. This drug is a close relative of trenbolone and differs only in 17-alpha alkylation. This modification makes it significantly more powerful than the trenbolone. It is 120-300 times more potent than methyltestosterone. This is the most powerful steroid available on the market, a dose of 0.5-1mg is already sufficient for a powerful anabolic effect. Its activity is accompanied by strong toxicity, and this is what limits its use to laboratory conditions.
Description: Meteopithiosten is an oral anabolic steroid derived from dihydrotestosterone. This preparation with a 17-alpha alkylated analogue of epithiostane, and like it, shows a good balance between anabolic and androgenic effects. In this case, the difference is greater, and the anabolic effect of the drug is 12 times higher than the androgenic effect. This was confirmed by experiments on animals. This drug has never been tested in humans, and all data are based on animal experiments. Meteopothiosten is an anabolic steroid, which shows a significant anabolic effect for the growth of dry mass and strength. It also has some anti-estrogenic properties, and is used for the period of diet, drying, and a set of dry mass.
Description: Mestanolone is an oral analogue of dihydrotestosterone. This steroid is the methylated form of this potent endogenous androgen, and is the same for dihydrotestosterone as methyltestosterone for testosterone. Mestanolone, above all, an androgenic drug. Mestanolone has no estrogenic activity and has anti-estrogenic properties, competes with flavoring substances for binding to aromatase. This drug is valued by athletes for its ability to give strength and aggression with minimal body weight gain.
Description: Mepithiostan is an esterified derivative of epithiostane. Ether is necessary for oral administration, so the drug is absorbed through the lymphatic system, like quinbolone. Epiostione is an active steroid, and in fact is an unmethylated derivative of dihydrotestosterone. Mepithiosten is a mild anabolic steroid that shows an anabolic effect analogous to methyltestosterone, but it has moderate androgenicity. It is not aromatized and has anti-estrogenic properties. This steroid is not used widely, but it gives a good result in terms of muscle growth, fat loss and better drawing.
chlordehydromethylandrostene diol (halodrol)
Description: Chlordehydromethylandrostenediol is an oral anabolic steroid derived from testosterone. It is very similar in structure to oral-turbinebol and differs only by replacing the 3-keto group with 3-hydroxyl. This is a “diol” form of oral-turinabol, which allows it to be called a prohormone. This steroid is not aromatized and has a great potential in terms of anabolic effect.
Description: Normethandrolone is an orally active relative of nandrolone. It is also called methylnandrolone or methylnortestosterone. It differs from the parent hormone only by the addition of a methyl group in position c17-alpha. Studies in animals have shown that it is 3-6 times more anabolic than methyltestosterone, but only 10-25% of androgenic methyltestosterone. Its ratio ranges from 3 to 1 to 5.5 to 1. This is not an ideal steroid for bodybuilders and athletes whose sport means dry weight. The weight gain on this preparation is accompanied by water retention and fat gain.
Description: Methyl-1-testosterone (methyldihydroboldenone) is an oral anabolic steroid derived from dihydrotestosterone. It is similar in its structure to 1-testosterone and differs only in the addition of a methyl radical in the position of c-17-alpha. Methyl-1-testosterone can be considered as a kind of association of primobolan, stanozolol and trenbolone. It has 1-en structure primobolan, bioavailability of stanozolol and high activity of trenbolone. According to standard studies, methyl-1-testosterone exceeds the activity of any actively sold steroid. It is popular with bodybuilders as a drug to increase muscle volume with a rapid increase in size and strength, with some level of water retention and fat growth.
Quinbolon (anabolicum wister)
Description: Quinbolone is a modified form of boldenone. This preparation is chemically identical to equipose, but contains cyclopentenyl ether instead of the undesilinate ester. It is used in this case to increase oral bioavailability. This steroid is similar in form to andriol. The bioavailability of andriol is 7%, which indicates that such an administration route is not the most effective, but it allows keeping a stable level of hormones in the blood. With a sufficient dose, the effect of quinbolone will be similar to boldenone undsilinate, that is, it will be a muscle gain with mild estrogenic and androgenic actions.
Description: Bolaterone is an oral anabolic steroid structurally associated with methyltestosterone. It is distinguished by the addition of a methyl group at position c7, which is why the chemical name is 7,17-dimethyltestosterone. The addition of the methyl group changed the actininity of this drug compared with methyltestosterone. For starters, bolasterone is a fairly powerful steroid, about 2 times more anabolic than methandrostenolone, unlike methyltestosterone, which is much weaker. Despite the fact that bolasterone is a derivative of testosterone, it is much more anabolic compared to androgenicity. At the therapeutic level, the occurrence of androgenic and virilizing side effects is unlikely. It has one similarity with methyltestosterone – it has estrogenic activity. Therefore, both of these drugs are used most often during the mass-gathering period.
Description: Striant is a form of testosterone absorbed in the mouth. This is a small tablet containing 30 mg of free testosterone. The tablet is not swallowed, but put on the cheek. This method is not new, it has been used before, especially in the case of testosterone propionate and methyltestosterone. The adhesive base of the striatite one is more perfect, since it sticks to 12 hours and then is removed. This is a longer and more effective method of supplying the hormone to the body. Two tablets per day is enough to maintain testosterone levels within 24 hours.
Description: Methylhydroxynandrolone is a potent derivative of nandrolone. It is an active drug when taken orally, does not aromatize and is an anabolic steroid without estrogenic activity. According to early research results, methylhydroxynadrolone is 13 times more anabolic and 3 times more androgenic than methyltestosterone. It is more like an androgenic effect on trenbolone than on nandrolone. Its 4-hydroxy group prevents its transformation into active metabolites in the skin and in the prostate.
Description: Methyl drostanolone, also known as metastron, is a potent oral anabolic steroid derived from dihydrotestosterone. In structure, he is a relative of drostanolone. The only difference is the addition of a methyl radical in position 17-alpha, to increase bioactivity in oral administration. These two drugs are very similar. Both drostanolone and metidrostanolone are not aromatized, have no estrogenic activity and have the same ratio of anabolic to androgenic action. Laboratory studies have shown that methyl-drostanolone is 4 times more anabolic than methyltestosterone and still has only 20% of the androgenicity of methyltestosterone. He was in demand among athletes, because of his ability to increase the dry weight without delaying water or fat growth. Dimethazine (roxylon)
Description: Dimethazine, also known as mebolazine, is a potent oral anabolic steroid derived from dihydrotestosterone. The dimetazine molecule is unique in structure and consists of two molecules of methyl-drostanolone, connected by an azine bridge. In the human body, the connection is broken and the free methyl-drostanolone enters the bloodstream. Dimetazin is a strong anabolic steroid, with moderate androgenicity, but without noticeable estrogenicity or progestagenicity. Now this drug is unavailable, but once it was in demand among athletes, because of its ability to increase the dry weight without delaying water or fat growth. The drug behaves like drostanolone (master), but because of the 17-alpha alkylation is a great danger to the liver.
Not included in this list is only stanozolol oral. There is also a story for each of the drugs, did not insert it, since too much is written about each separately.