Turanabol 100 tab. (10 mg/1 tab.)


Turanabol from TN Pharma can be characterized as methandrostenolone without the effect of fluid retention in the body. This is a delayed-acting steroid. During the turinabol course, weight, strength indicators and relief progress very slowly, however, according to athletes, these results are of better quality.

Turanabol (Turanabol) from Balkan Pharmaceuticals is produced on the basis of the active substance (chlorodehydromethyltestosterone, which in its essence is very similar to methandrostenolone. The difference of this oral steroid is an additional chlorine atom at the fourth carbon atom. The drug was patented in 1961 by a German pharmaceutical company. It is also sold turanabol from British Dispensary and British Dragon companies.

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One of the distinctive features of the drug is the absence of estrogenic effects (since it is not aromatized due to the addition of a chlorine atom to the molecule), that is, side effects such as fluid retention, gynecomastia, etc. practically do not meet. Although there are reviews that report the development of gynecomastia, the mechanism of its development remains unclear. The most likely reason is the presence of methyltestosterone in the composition, which is connected with the peculiarities of synthesis.

Turanabol steroid profile

  • Anabolic activity 180%
  • Androgenic activity 50%
  • Aromatization (conversion to estrogens) is absent
  • Suppression of the hypothalamus-pituitary-testis axis is moderate-high
  • Liver toxicity is moderate
  • Method of oral administration (in tablets)
  • The half-life is 16 hours
  • Detection time up to 250 days (long-lived fat-soluble metabolites)

The maximum concentration in the plasma after 3 hours after reception.

Turanabol can be classified as a derivative of Dianabol (methandienone), but the modified molecular structure leads to a positive balance of its characteristics and action. Turanabol has significantly lower androgenic activity than Dianabol, and a significantly better balance of anabolic and androgenic effects.

Turanabol gives strength and endurance, reduces fat and builds individual muscles.According to its action, it can be characterized as a combination of the best actions of Anavar and Dianabol (metandienone).

Also, it was determined that the concentration of SHBG decreases, therefore the level of free testosterone in the blood increases. There are data that turinabol reduces the risk of blood clots in blood vessels and the heart.

The course of taking Turanabol

The drug can be used both for gaining muscle mass and for drying. The course of turinabol does not require the inclusion of gonadotropin (if it does not exceed 6-8 weeks), however PCT is carried out with estrogen receptor blockers (tamoxifen). The turinabol monocourse is considered one of the simplest and safest in bodybuilding, so it is often recommended for beginners. For the first course, the optimal dosage is considered to be 40 mg/day for 6 weeks. This allows you to get impressive results, both in terms of the increase in quality muscle mass, and in the progress of speed and strength results.

To gain muscle mass, a combination course of Turinabol (20 mg per day) + testosterone enanthate 250 mg per week (or + sustanon) is best suited. The average duration is 6 weeks. Enanthate is canceled first, and turinabol after a week.

Side effects

Turinabol is a 17-alkylated anabolic steroid, which makes it possible to take it orally, but it creates a toxic effect on the liver, comparable to methandrostenolone. In general, side effects occur quite rarely and are most often associated with exceeding the duration of the course and high doses. This drug strongly suppresses the secretion of own testosterone. Possible erectile dysfunction after withdrawal, there were cases of development of premature ejaculation.

Liver disorders: cholestatic jaundice, necrosis of hepatocytes with liver failure, liver cancer.In terms of biochemical parameters, an increase in the level of bilirubin, alkaline phosphatase and transaminases is determined. Cholestatic jaundice may develop after 6 months or more (it is of toxic origin) and is manifested by stasis in bile capillaries with hyperbilirubinemia and increased alkaline phosphatase activity. When used for several years, the frequency of liver cancer may increase.


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