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  1. #1
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    Methyltrienolone???

    has anyone here used Methyltrienolone ? Isnt it oral tren ? if so does it work the same as injectable tren? thanks for the feedback

  2. #2
    juiceinthehood's Avatar
    juiceinthehood is offline Anabolic Member
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    fina pellets is oral tren
    tren is oral that was made into an inject
    tren is trenbolone acetate

  3. #3
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    Yes, MethylTrienolone is oral Tren ....it's a 17aa version of Trenbolone .

    About 750mcgs/day orally is equal, results-wise, to 150-225mgs/day of Trenbolone Acetate.

  4. #4
    juiceinthehood's Avatar
    juiceinthehood is offline Anabolic Member
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    Quote Originally Posted by hooker
    Yes, MethylTrienolone is oral Tren ....it's a 17aa version of Trenbolone .

    About 750mcgs/day orally is equal, results-wise, to 150-225mgs/day of Trenbolone Acetate.
    okay shut me up
    is it as good as the inject
    and is it as bad for your liver as drol or dbol

  5. #5
    G-1000's Avatar
    G-1000 is offline Cycle King/AR-Hall of Famer/RETIRED
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    hooker is b.d the only one making oral tren

  6. #6
    swoll4589's Avatar
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    Isnt it spost to be really bad on your liver. Like as bad as drol or close to as bad.

  7. #7
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    TF is the only person I know of who has MethylTrienolone . People who used it at 2mg/day experienced extreme liver complications (Jaundice, highly elevated liver values, etc...).

    BD doesn't make MethylTrienolone...they make Tren tabs (regular tren, in tab form, not 17aa like MethylTrienolone)...the BD stuff would be exactly like eating the pellets you make fina out of.

  8. #8
    G-1000's Avatar
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    Quote Originally Posted by hooker
    TF is the only person I know of who has MethylTrienolone . People who used it at 2mg/day experienced extreme liver complications (Jaundice, highly elevated liver values, etc...).

    BD doesn't make MethylTrienolone...they make Tren tabs (regular tren, in tab form, not 17aa like MethylTrienolone)...the BD stuff would be exactly like eating the pellets you make fina out of.
    thank you

  9. #9
    swoll4589's Avatar
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    would fina tabs be effective at all if you just let them dissolve under your tounge.

  10. #10
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    Quote Originally Posted by swoll4589
    would fina tabs be effective at all if you just let them dissolve under your tounge.
    Not really. Since it isn't 17-AA it will get almost comlpetely destroyed after the first pass through the liver.

  11. #11
    Bryan2's Avatar
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    methyl trienolone is THE MOST toxic oral available!!!

  12. #12
    Two4the$$ is offline Senior Member
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    Sublingual, literally 'under the tongue', from Latin, refers to a pharmacological route of administration in which certain drugs are entered directly into the bloodstream via absorption under the tongue. Many pharmaceuticals are prepared for sublingual administration. These commonly include cardiovascular drugs, steroids , barbiturates, some enzymes and increasingly frequently, certain vitamins and minerals.
    The principle behind sublingual administration is fairly simple. When a chemical comes in contact with the mucous membrane, or buccal mucosa, it diffuses into the epithelium beneath the tongue. This region contains a high density of blood vessels, and as a result, via diffusion, the substance quickly enters the venous circulation, which returns to the heart and then travels to the systemic arterial circulation. In contrast, substances absorbed by the bowel are subject to "first pass metabolism" in the liver before they are distributed to the rest of the body.

    In theory, sublingual routes of administration have certain advantages over simple oral administration. This route is often faster, and entering a drug into one's body sublingually ensures that the substance will only come in contact with the enzymes in saliva prior to entry into the bloodstream. Drugs otherwise orally administered must instead survive the incredibly hostile environment of the gastrointestinal tract. This may mean a much greater percentage of the original substance is degraded either by the myriad of enzymes in the GI tract, such as monoamine oxidase, or the strong acids it contains. Additionally, after GI absorption, the drug is sent to the liver where the drug may be extensively metabolized; this is known as the first pass effect of drug metabolism. Due to the degradative qualities of the stomach and intestine, or the solubility of the GI tract, certain substances, such as salvinorin A may only be administered orally via the sublingual route.

  13. #13
    shrpskn is offline Anabolic Member
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    ^^Why did you bump a thread that is almost 2 years old.

  14. #14
    Two4the$$ is offline Senior Member
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    because I never look at the date ... because the date is irrelevant if the subject is worth discussing.

    For instance ... people still discuss Lyle Alzedo, which is to say the least a VERY OLD issue - yet people DO still discuss it, because of the propaganda that has ensued. That lie was the funding for intentions contrary to the interest of everyone on this board, making it not only "old news" ... but a current affair as well.

    Any time there is a subject I'm interested in ... I will do a search first - and if those search results are inconclussive, I will bump it to restart the flow of information, which could VERY well have changed over the years.

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