Test E


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Unigen Test E is a Testosterone Enanthate based steroid in the form of a liquid for injection. The main active ingredient has the ability to maintain long-term activity. The volume of one bottle is 10 ml, the dose is 250 mg.

Due to the long duration of action of enanthate, which is 2 to 3 weeks, the need for frequent injections is minimized. Thus, the athlete's hormonal background is maintained at a stable level without the risk of local allergic reactions (bumps, hyperemia, itching).

The indicators of the anabolic and androgenic activity of Depot Test 250 Yunigen coincide with those of testosterone. The ability to convert into estrogen is high, the probability of suppression of the hypothalamic-pituitary-testicular axis is pronounced. But due to the low hepatic toxicity, the possibility of a negative effect on the liver is less. The duration of the drug is 15 days.

Unigen test and effects

  • accelerated muscle building,
  • general strengthening of the body, strengthening of the immune system,
  • activation of regenerative processes,
  • body fat reduction,
  • strengthening of joints and ligaments.
  • Among the negative reactions resulting from taking a steroid, one can distinguish signs of excessive sexual stimulation (priapism and others), high frequency of erections, hypertrophy
  • of the male genital apparatus, sperm maturation disorders, gynecomastia, acne, depression, aggression.

Pharmacodynamic properties:

Testosterone enanthate is an ester of testosterone. Testosterone is the main male sex hormone synthesized and secreted by the testicles.Stimulates the growth and development of the male sexual organs and secondary sexual characteristics (maturation of the prostate, seminal vesicles, penis and scrotum, male pattern hair distribution on the face, pubic bone, chest), development of the larynx, body muscles and fat distribution. Maintains nitrogen, sodium, potassium and phosphorus, improves anabolism and reduces protein catabolism. A premature increase in the concentration of testosterone in the blood plasma in the period before puberty causes the pineal gland to close down and growth to stop. It stimulates the production of erythropoietin and erythrocytes. Through the negative feedback mechanism (feedback), it inhibits the secretion of luteinizing and follicle-stimulating hormones from the pituitary gland and inhibits spermatogenesis. In men with primary hypergonadotropic hypogonadism, gonadotropin levels normalize.

In women, it inhibits the gonadotropic function of the pituitary gland, the function of the ovaries, the mammary glands, and causes atrophy of the endometrium. The antagonistic action of estrogens is used in the treatment of uterine fibroids, endometriosis, breast cancer. It shows a beneficial effect on the ailments of the climacteric period.

Pharmacokinetic properties:

Testosterone Enanthate is slowly absorbed. The maximum concentration in the blood is observed 72 hours after administration. The promotion lasts from 2 to 4 weeks. In the blood, nearly 98% of testosterone is bound to a specific globulin moiety that binds testosterone and estradiol. Biotransformation occurs in the liver to various 17-ketosteroids, which are excreted in the urine after conjugation with glucuronic or sulfuric acid (approximately 90%). About 6% of the absorbed drug is excreted free in the feces.


In men: androgen insufficiency after castration, eunuchoidism, impotence of hormonal origin, symptoms of male menopause (decreased libido, mental and physical activity), acromegaly, with prostatic hypertrophy, osteoporosis caused by androgen deficiency, with angioneurotic forms of angina pectoris.

In women: with climacteric vascular and nervous disorders in cases where estrogenic drugs are contraindicated (for tumors of the genital organs and mammary glands, uterine bleeding), simultaneously with radiotherapy for breast and ovarian cancer (usually in women under 60 years), with dysfunctional uterine bleeding in older women.

Side effects

Priapism and other signs of excessive sexual stimulation (frequent erections) in boys in the prepubertal period: accelerated sexual development, increased frequency of erections, enlargement of the penis and premature closure of the epiphyses, damage to spermatogenesis and decreased maturation of sperm , oligospermia and decreased ejaculate volume, prostate abnormalities, in women: bleeding from the birth canal, increased libido, with prolonged use of the drug, virilization symptoms are possible, hirsutism, gynecomastia, seborrhea, acne , oily skin, accelerated hair loss, sodium and water retention, oedema, symptoms of hypercalcaemia, thrombophlebitis, nausea, cholestatic jaundice, increased levels of hepatic aminotransferases (when stopped, they normalize), headache, depression, aggression, anxiety, sleep disorders, paresthesia.


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