Примери за използване на Fluoxymesterone на Английски и техните преводи на Български
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Halotestin(Fluoxymesterone) 8 hours 8 weeks.
What Are the Possible Side Effects of Halotestin(Fluoxymesterone) raw powder?
The effects of fluoxymesterone administration on testicular function.
Halotestin is a relatively common anabolic androgenic steroid known as fluoxymesterone.
Normally Fluoxymesterone is taken for less than four weeks due to its hepatotoxicity.
Common anabolic steroid medicines may includes fluoxymesterone(such as Halotestin) and nandrolone(such as Durabolin).
As such, Fluoxymesterone should not be used with people predisposed to high cholesterol or blood pressure.
Halotestin, which is also referred as fluoxymesterone, is a very powerful androgenic compound.
Fluoxymesterone is a powerful anabolic steroid which is renowned for making its users feel powerful and aggressive.
This power is so great,some studies have suggested that Fluoxymesterone may actually promote phallic enlargement.
Human grade fluoxymesterone is very uncommon and is almost impossible to get, even on the black market.
Androgenic issues: Being strongly androgenic, one of the most obvious side effects of using Fluoxymesterone is virilization in women.
Preventive management with fluoxymesterone and oxymetholone in severely affected males and females.
In order to be sufficiently active when given by mouth, testosterone derivatives are alkylated at the 17 position,e.g. methyltestosterone and fluoxymesterone.
In medical scenarios, fluoxymesterone is commonly indicated as a treatment for low testosterone levels.
So as to be sufficiently Energetic when specified by mouth, testosterone derivatives are alkylated on the seventeenα position,e.g. methyltestosterone and fluoxymesterone.
Fluoxymesterone and trenbolone, the two drugs together have some serious differences from other types of anabolic steroids.
As a way to be adequately Lively when specified by mouth, testosterone derivatives are alkylated within the seventeenα position, e.g.,methyltestosterone and fluoxymesterone.
Fluoxymesterone is a testosterone derived anabolic androgenic steroid or more specifically a structurally altered form of Methyltestosterone.
One study comparing the effects of oxandrolone to other agents including as methyltestosterone,norethandrolone, fluoxymesterone and methAndriol clearly supports this notion.
Fluoxymesterone is an extremely powerful anabolic androgenic steroid that was first released in the late 1950's by Upjohn under the trade name Halotestin.
Popular anabolic/androgenic steroids that are associated with low visible water retention include fluoxymesterone, methenolone, nandrolone, oxandrolone, stanozolol, and trenbolone.
Structurally fluoxymesterone is a derivative of testosterone, differing from our base androgen by three structural alterations(specifically l7alpha-methyl, 11 beta-hydroxy and 9-fluoro group additions).
Those agents commonly associated with clinical hepatotoxicity include(but are not limited to) fluoxymesterone, methandrostenolone, methylandrostenediol, methyltestosterone, norethandrolone, oxymetholone, and stanozolol.
The anabolic steroids that have been most commonly used in the United States for this purpose are stanozolol and danocrine, although historically many other agents have also been prescribed including oxandrolone, methyltestosterone,oxymetholone, fluoxymesterone, and methandrostenolone.
Another study comparing the effects of oxandrolone to other alkylated agents including methyltestosterone,norethandrolone, fluoxymesterone, and methandriol demonstrated that oxandrolone causes the lowest sulfobromophthalein(BSP; a marker of liver stress) retention of the agents tested.
Oxandrolone is a steroid with low androgenic activity relative to its tissue-building actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone,methandrostenolone, or fluoxymesterone.
Oxandrolone is a steroid with low androgenic activity relative to its tissue-building actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone,methandrostenolone, or fluoxymesterone.
Oxandrolone is a steroid with low androgenic activity relative to its tissue-building actions, making the threshold for strong androgenic side effects comparably higher than with more androgenic agents such as testosterone,methandrostenolone, or fluoxymesterone.