Anadrol is known as one of the most powerful oral anabolic steroids on the market. It constantly competes with Dianabol (Methandrostenolone) and there is a constant debate in the bodybuilding community using steroids about which drug is stronger.

Anadrol is both a brand and trade name for an anabolic steroid, better known as Oxymetholone. But, it should not be confused with Oxandrolone, which is otherwise called Anavar. Oxymetholone is Anadrol. The Anadrol formula was first developed and introduced in 1959. Almost immediately, Syntex began to sell Oxymetholone under the brand name Anadrol-50. At the same time, Parke Davis & Co also produced the drug, but sold it under the name Anadroyd. Soon after entering the pharmaceutical market, Anadrol began to be used to treat a variety of diseases, ranging from geriatric atrophy to the fight against infections.

Anadrol (Oxymetholone)

However, Anadrol gained fame and popularity precisely as a drug for the treatment of anemia. Patients with anemia were prescribed Anadrol to increase the number of red blood cells and increase the level of hemoglobin in the blood. With the development of pharmaceuticals, less dangerous drugs began to be used in therapy, and the release of Anadrol was significantly reduced.

Anadrol has the ability to quickly stimulate erythropoiesis (hematopoiesis). Despite the fact that all anabolic steroids are endowed with similar properties, it is Anadrol that demonstrates hematopoiesis indicators that are superior to other drugs. For a more accurate characterization, it should be noted that Anadrol increases the production of red blood cells by 5 times.

Studies have shown that Anadrol has an obvious anabolic effect on patients with muscular dystrophy and a diagnosis of AIDS. Patients taking Anadrol gained up to 8 kg in weight, while the placebo groups not only lost weight, but also showed an increase in mortality rates. Thanks to the discovery of new properties of the drug, production was resumed and Anadrol is currently prescribed as a priority for patients with malnutrition caused by the immunodeficiency virus.

Chemical characteristics of Anadrol

Anadrol is an oral anabolic steroid. This means that the substance must pass through the liver before it enters the bloodstream. The C17-alpha-alkyd group, which maintains the integrity and penetrating abilities of the drug, helps Anadrol not break down under the influence of metabolic processes. Severe hepatoxicity is a well-known characteristic of Anadrol. The chemical structure and modification of the drug (including the presence of a C17-alpha-alkyd group) makes it exceptionally resistant to liver metabolism. Simply put, Anadrol is not broken down as it passes through the liver. However, the higher the resistance of a substance to destruction under the action of biochemical processes, the stronger the load that it exerts on the body. This is indicative of the extreme toxicity of Anadrol, which is known to be one of the most damaging oral anabolic steroids ever available.

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Courses and application

Courses with Oxymetholone, as a rule, are aimed at increasing the mass and overall volume of muscles, but do not provide relief and the effect of dried muscles. For this reason, it is useless to use it during the preparation for the competition, for the purposes of drying and reducing adipose tissue. The drug can be used to speed up fat burning processes, but the estrogenic manifestations of Anadrol, in combination with water retention and swelling, make it a poor alternative. A similar side effect makes the body plump and smooth, blurring the outlines, thereby making it difficult to visually assess the level of reduction in adipose tissue. All this is exacerbated by the fact that Anadrol does not convert into estrogen, and this imposes on the user a number of hitherto unexplored side effects. Aromatase inhibitors also do not reduce puffiness, as they do not work in the case of Anadrol.

Courses and application

Anadrol courses usually consist of a 4-6 week intake. The steroid is used as the main (kickstart) compound, in combination with other injectable base drugs of a similar spectrum of action: Testosterone Enanthate, Deca-Durabolin (Nandrolone Decanoate), Trenbolone Enanthate, etc. Anadrol can also be administered in the middle of the cycle to move off the ground and push the processes of muscle growth during training. In addition, some users bring it to the end of the course to speed up the final phase, and also as a connection to complete the cycle. This allows you to achieve an impressive increase in strength and muscle size during the transition to the stage of PCT (post cycle therapy).

Due to the hepatoxicity of Anadrol, the course of administration should not exceed 4-6 weeks. Injectables used simultaneously with Anadrol can continue to be used after the course is completed.

Side effects

Being a strong oral C-17-alpha-alkylated anabolic steroid, Anadrol exhibits high hepatoxicity and adverse effects on the liver. In terms of toxic effects, the drug really shows itself as the most dangerous among all anabolic steroids available for sale. This characterization of the drug is common among bodybuilders and, most likely, exaggerated, but nevertheless, such information should be taken very seriously. Interestingly, Anadrol has a chemical structure that should actually reduce hepatoxicity. In fact, the use of Anadrol increases the level of liver enzymes.

Side effects

When you study the other side effects of Anadrol, things become even more confusing. It is well known that Anadrol is a derivative of DHT and does not convert to estrogen. However, Anadrol is characterized by side effects that occur when taking estrogens: water retention in the body (often appears to an extreme degree) with a concomitant increase in blood pressure and the development of gynecomastia. The use of selective estrogen receptor modulators (or Nolvadex) reduces the manifestations of gynecomastia, but does not solve problems with edema and high blood pressure. Aromatase inhibitors will also not work with Anadrol as it does not interact with this enzyme in the first place. Anadrol can presumably act like a progestin, causing similar side effects. It is most likely (although not certain) that Anadrol can interact with the estrogen receptor directly, or perhaps Anadrol’s metabolite has a similar property.