Andro 50

Epiandrosterone was first introduced as a prohormone to the market by LG Sciences in 2006. At that time people were skeptical, however once they started using this amazing prohormone to DHT, the market for it took off! DHT (dihydrotestosterone) is often considered the “bad” hormone for men, but in fact science is starting to realize that perhaps we have gotten DHT all wrong! Epiandrosterone is a naturally occurring steroid synthesized in the adrenal cortex, gonads, brain and gastrointestinal tract. It is less active than androsterone and excreted in small amounts in normal human urine. Epiandrosterone is a metabolite of the most abundant adrenal androgenic steroid dehydroepiandrosterone (DHEA) in young adult humans and is a precursor of dihydro-testosterone which has hypolipidemic and anabolic properties.

”Both my husband and I take Andro 400 on a regular basis. I have found that  I feel better, have more energy and I easily dropped weight even when I was not dieting , and I felt like it was  particularly in the tummy region.  I will continue to take it just for the energy benefits, I think it's much better than any energy drink. My husband is a Fitness trainer and he recommends it to his clients because he himself enjoys the energy and muscle tone that he gets from using this supplement. I would definitely say that Andro 400 can do everything that it claims to do. It's an excellent product!”
--Emma Daley, Mesa, AZ

There has been increasing interest in the development of effective agents that can be safely used to promote anabolism in the clinical setting for patients with chronic wasting conditions as well as in the prevention and treatment of frailty associated with loss of muscle tissue in aging (sarcopenia). One such agent is the anabolic androgenic steroid (AAS) oxandrolone, which has been used in such clinical situations as HIV-related muscle wasting, severe burn injury, trauma following major surgery, neuromuscular disorders and alcoholic hepatitis for over 30 years. In the US, oxandrolone is the only AAS that is US FDA-approved for restitution of weight loss after severe trauma, major surgery or infections, malnutrition due to alcoholic cirrhosis, and Duchenne's or Becker's muscular dystrophy. Our review of the use of oxandrolone in the treatment of catabolic disorders, HIV and AIDS-related wasting, neuromuscular and other disorders provides strong evidence of its clinical efficacy. Improvements in body composition, muscle strength and function, status of underlying disease or recovery from acute catabolic injury and nutritional status are significant in the vast majority of well designed trials. However, oxandrolone has not yet been studied in other orally administered C17alpha-alkylated AASs, the novel chemical configuration of oxandrolone confers a resistance to liver metabolism as well as marked anabolic activity. In addition, oxandrolone appears not to exhibit the serious hepatotoxic effects (jaundice, cholestatic hepatitis, peliosis hepatis, hyperplasias and neoplasms) attributed to the C17alpha-alkylated AASs. Oxandrolone is reported to be generally well tolerated and the most commonly documented adverse effects are transient elevations in transaminase levels and reductions in high density lipoprotein cholesterol , optimal risk:benefit ratios for oxandrolone and other agents in its class will need to be refined before widespread clinical acceptance of AASs as a therapeutic option in sarcopenia and other chronic wasting conditions.

Andro 50

andro 50

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