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TESTOSTERONE CYPIONATE INJECTIONS

"Low Testosterone or LOW T affects about two in ten men between the ages of 40 and 60 - and more than three in ten over the age of 60." Boost sex drive, build muscle, burn fat, look better & feel great. - Testosterone Cypionate Injections Boost Low T Levels! - Testosterone Cypionate: Get Low Testosterone Treatment Information @ www.TestosteroneTherapy.orgGet Low T Info

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Testosterone Cypionate Injections - Testosterone Therapy

Testosterone Cypionate Injections are used to Increase Low Testosterone Levels in Men with Andropause (Hypogonadism)

With over 18,000 patients our Hormone Therapy Center can offer the best pricing on Testosterone Cypionate

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About Testosterone Cypionate Injection, USP

By Prescription Only

Testosterone Cypionate Description

Testosterone Cypionate Injection, USP for intramuscular injection contains Testosterone Cypionate, USP which is the oil-soluble 17 (beta)- cyclopentylpropionate ester of the androgenic hormone testosterone. Testosterone Cypionate, USP is a white or creamy white crystalline powder, odorless or nearly so and stable in air. It is insoluble in water, freely soluble in alcohol, chloroform, dioxane, ether, and soluble in vegetable oils.

The chemical name for Testosterone Cypionate, USP is androst-4-en-3-one,17-(3-cyclopentyl-1-oxopropoxy)-, (17β)-. Its molecular formula is C27H40O3, and the molecular weight 412.61.

Testosterone Cypionate Manufacturers

  • Paddock
  • Watson
  • Pfizer (Depo-Testosterone)
  • West-Ward Pharmaceutical
  • Hikma Pharmaceutical
  • Sun Pharmaceutical
  • Caraco Pharmaceautical
  • Pharmacia and Upjohn Co.
  • A-S Medication Solutions
  • Physicians Total Care

Testosterone Cypionate Injection, USP is available in one strength, 200 mg/mL Testosterone Cypionate, USP.

Each mL of the 200 mg/mL solution contains:

Testosterone Cypionate, USP 200 mg
Benzyl Benzoate, USP 0.2 mL
Cottonseed Oil, USP 560 mg
Benzyl Alcohol, USP (as preservative) 9.45 mg

Testosterone Cypionate - Clinical Pharmacology

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Endogenous androgens are responsible for normal growth and development of the male sex organs and for maintenance of secondary sex characteristics. These effects include growth and maturation of the prostate, seminal vesicles, penis, and scrotum; development of male hair distribution, such as beard, pubic, chest, and axillary hair; laryngeal enlargement, vocal cord thickening, and alterations in body musculature and fat distribution. Drugs in this class also cause retention of nitrogen, sodium, potassium, and phosphorous, and decreased urinary excretion of calcium. Androgens have been reported to increase protein anabolism and decrease protein catabolism. Nitrogen balance is improved only when there is sufficient intake of calories and protein. Androgens are responsible for the growth spurt of adolescence and for eventual termination of linear growth, brought about by fusion of the epiphyseal growth centers. In children, exogenous androgens accelerate linear growth rates, but may cause disproportionate advancement in bone maturation. Use over long periods may result in fusion of the epiphyseal growth centers and termination of the growth process. Androgens have been reported to stimulate production of red blood cells by enhancing production of erythropoietic stimulation factor. During exogenous administration of androgens, endogenous testosterone release is inhibited through feedback inhibition of pituitary luteinizing hormone (LH). At large doses of exogenous androgens, spermatogenesis may also be suppressed through feedback inhibition of pituitary follicle stimulating hormone (FSH).

Cypionate Pharmacokinetics

Testosterone esters are less polar than free testosterone. Testosterone esters in oil injected intramuscularly are absorbed slowly from the lipid phase; thus, Testosterone Cypionate can be given at intervals of two to four weeks. Testosterone in plasma is 98 percent bound to a specific testosterone-estradiol binding globulin, and about 2 percent is free. Generally, the amount of this sex-hormone binding globulin in the plasma will determine the distribution of testosterone between free and bound forms, and the free testosterone concentration will determine its half-life. About 90 percent of a dose of testosterone is excreted in the urine as glucuronic and sulfuric acid conjugates of testosterone and its metabolites; about 6 percent of a dose is excreted in the feces, mostly in the unconjugated form. Inactivation of testosterone occurs primarily in the liver. Testosterone is metabolized to various 17-keto steroids through two different pathways. The half-life of Testosterone Cypionate when injected intramuscularly is approximately eight days.

In many tissues the activity of testosterone appears to depend on reduction to dihydrotestosterone, which binds to cytosol receptor proteins. The steroid-receptor complex is transported to the nucleus where it initiates transcription events and cellular changes related to androgen action.

Indications and Usage for Testosterone Cypionate

Testosterone Cypionate Injection, USP is indicated for replacement therapy in the male in conditions associated with symptoms of deficiency or absence of endogenous testosterone.

  • Primary hypogonadism (congenital or acquired)-testicular failure due to cryptorchidism, bilateral torsion, orchitis, vanishing testis syndrome; or orchidectomy.
  • Hypogonadotropic hypogonadism (congenital or acquired)-idiopathic gonadotropin or LHRH deficiency, or pituitary-hypothalamic injury from tumors, trauma, or radiation.

Cypionate Contraindications

  • What causes testosterone deficiency?
  • What are the symptoms of testosterone deficiency or LOW T?
  • What changes occur in the body due to testosterone deficiency?
  • How do I find out if I have a testosterone deficiency?
  • How is testosterone deficiency treated?
  • What is the cost of testosterone cypionate?
  • Where can I buy testosterone injections online?
  • Who shouldn't take testosterone replacement therapy?
  • What are the side effects of testosterone replacement therapy?
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