Description
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 vial is 10 ml, the dosage is 250 mg.
Due to the long duration of action of enanthate, this is 2 – To 3 weeks, the need for frequent injections is minimized. Thus, the athlete’s hormonal background remains at a stable level without the risk of local allergic reactions (bumps, hyperemia, itching).
The indicators of the anabolic and androgenic activity of the Depot Test 250 Yunigen coincide with those of testosterone. The ability to convert to estrogen is high, the probability of suppression of the hypothalamus-pituitary-testicular axis is pronounced. But due to the low liver toxicity, the possibility of a negative effect on the liver is less. The duration of the drug is 15 days.
Test And Unigen Effects
- accelerated muscle building;
- general strengthening of the body, strengthening the immune system;
- activation of regenerative processes;
- reduction of body fat;
- strengthening of the joints and ligaments.
- Among the negative reactions resulting from taking a steroid, signs of excessive sexual stimulation (priapism and others), a high frequency of erections, hypertrophy of the male genital tract, disorders in the maturation of sperm, gynecomastia, acne, depression can be distinguished , aggression.
Pharmacodynamic properties:
Testosterone Enanthate is an ester of testosterone. Testosterone is the main male sex hormone synthesized and secreted by the testes. Stimulates the growth and development of male sex organs and secondary sex characteristics (maturation of the prostate, seminal vesicles, penis and scrotum, distribution of male pattern hair on the face, pubic bone, chest), development of the larynx, body muscles and fat distribution. It 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 and growth arrested. It stimulates the production of erythropoietin and erythrocytes. Through the mechanism of negative feedback (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 are normalized.
In women, it inhibits the gonadotropic function of the pituitary gland, the function of the ovaries, mammary glands and causes atrophy of the endometrium. The antagonistic action of estrogen is used in the treatment of uterine fibroids, endometriosis, breast cancer. It shows a beneficial effect on ailments of the climacteric period.
Pharmacokinetic properties:
Testosterone enanthate is absorbed slowly. The maximum concentration in the blood is observed 72 hours after administration. The promotion lasts 2-4 weeks. In the blood, nearly 98% of testosterone binds to a specific globulin fraction that binds testosterone and estradiol. Biotransformation occurs in the liver into various 17-keto steroids, which are excreted in the urine after conjugation with glucuronic or sulfuric acid (approximately 90%). About 6% of the absorbed drug is excreted unbound in the faeces.
Instructions
In men: androgenic insufficiency after castration, eunucoidism, 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 radiation therapy for breast and ovarian cancer (usually in women under 60 years of age); 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, enlarged penis and premature closure of the epiphyses; damage to spermatogenesis and decreased sperm maturation, oligospermia and decreased ejaculate volume; abnormalities of the prostate gland; 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, edema; symptoms of hypercalcemia; thrombophlebitis; nausea, cholestatic jaundice, increased levels of hepatic aminotransferases (when you stop taking, they normalize); headache, depression, aggression, anxiety, sleep disturbance, paraesthesia.
