Oral trenbolone. Does it work?

I'm planning on running metribolone, a little while after i come off the halo im taking now (yea i love my liver, but im taking precautions) I only plan on running the metribolone for a couple weeks max, just to see what it's about.
I'll have cheque drops too, but im saving that for later.
 
vados said:
Just make sure youre alive to tell us the results :).
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Agreed. Maybe do a log that you keep very to up date. If you stop updating, then we'll know what happened and use it as an example for others.
 
I'll definitely update with my results. Dont knock what you havent had personal experience with. Have you seen blood work of someone who has ran this compound? If not, you are basing everything on hearsay.
 
NYCEE said:
I'll definitely update with my results. Dont knock what you havent had personal experience with. Have you seen blood work of someone who has ran this compound? If not, you are basing everything on hearsay.
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That's why we are paying so much attention to you, even though I don't advocate you putting yourself at potential risk.
 
I just have a feeling that the toxicity is a bit overexaggerated. I'm going to be running a few liver protectants and running low dose for a short time. I will keep everyone in the loop as the days go by.
 
NYCEE said:
I just have a feeling that the toxicity is a bit overexaggerated. I'm going to be running a few liver protectants and running low dose for a short time. I will keep everyone in the loop as the days go by.
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just be careful bro.
 
NYCEE said:
I'm planning on running metribolone, a little while after i come off the halo im taking now (yea i love my liver, but im taking precautions) I only plan on running the metribolone for a couple weeks max, just to see what it's about.
I'll have cheque drops too, but im saving that for later.
Click to expand...

Your fucking nutts... There is a guy who knows his shit about this stuff and hes a mod from another board.. Cant remember his name but I remember a while back he got in a argument with a few of our mods... Havent seen him since... I wish I could remember his name as the guy new alot about the stuff....
 
@ OC (your PM box is full)


I haven't run any orals for over a year. Just not really a fan of liver damage. I would try cheque drops before I'd use oral tren though... I like parabolin so much, oral tren would be more negitives for the same positive I am already getting.
 
drk_diggler said:
Your fucking nutts... There is a guy who knows his shit about this stuff and hes a mod from another board.. Cant remember his name but I remember a while back he got in a argument with a few of our mods... Havent seen him since... I wish I could remember his name as the guy new alot about the stuff....
Click to expand...


Haha... If the name comes to mind let me know.
 
Golgo13 said:
@ OC (your PM box is full)


I haven't run any orals for over a year. Just not really a fan of liver damage. I would try cheque drops before I'd use oral tren though... I like parabolin so much, oral tren would be more negitives for the same positive I am already getting.
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empty
 
--------------------------------------------------------------------------------

Studies were done on 13 humans in Germany in 1966. GPT and GOT livervalues were measured. Now the max value of GPT (glutamaatpyruvaattransaminases) is 12.5 mu/ml. Some subjects got 0.1 (!) mg methyltrienolone per day and saw their GPT rise from
4.50 mu/ml to 224.0 mu/ml in only 2 weeks! That's fifty times higer than normal. Not two or three. Fifty! After a week off it was still at 68 mu/ml.
Some subjects who got the full 1.0mg/day saw their GPT rise to 299 mu/ml.
GOT (glutamaatoxalacetaatransaminases) testing: same explosive increase to highly pathologic values in two weeks.
Cholinesterase enzyme lowered in the 1.0 mg group. That damage was permanent.

Not only is methyltrienolone the most hepatoxic steroid, it is also the most androgenic with a 'displacing ability' of 165%. It is also the most prostate unfriendly.

All 13 test subjects suffered permanent liver damage. They all also exhibited poisoning symptoms during the 2 week cycle, even de 0.1mg group.



-Normal values for sgtp is 11-43 iu/l.A 224 result is not uncommon at all for a steroid user even after a 2 week use.I have seen results as high as 600 after a 6 week cycle of 50mg/ed of anavar,so this is probably another myth.
Also note that the 0,1mg and the 1mg (10 times the dosage) almost had the same results and that 224 is roughly 20 times the upper normal limit and not 50 ,so something's not right here.
Oh,and the problems were far from permanent.4 weeks on milk thistle/ala/nac got values to normal.
 
I'd think twice if I was you NYCEE... Health is more important... Do something a little less toxic and work a little harder and you'll get the same effect but will be healthy....
 
drk_diggler said:
I'd think twice if I was you NYCEE... Health is more important... Do something a little less toxic and work a little harder and you'll get the same effect but will be healthy....
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so you're saying that the patients who took 100MCG's a day for 2 weeks got PERMANENT liver damage? i call bs.
 
i'd also like to know what kinda "patients" were used in the studies......
age, health, prior drug use, current drug use

i think moderation is key here
 
"A study unearthed by Llewellyn shows that researchers at the University of Bonn (Germany) discerned the powerful effects of THG's molecular cousin, methyltrienolone, as early as 1966. What scared them was its side effect: the synthetic steroid lingers in the liver without breaking down. That led them to call it "the most hepatotoxic steroid" they'd seen. With visions of bodybuilders flooding hospital emergency rooms with damaged livers, they warned against it being commercially released." (reference)

PubMed reference of this study: http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=5955468&dopt=Abstract
 
Last edited:
Of a variety of triene analogs of testosterone that have been tested, only 17α-methyl-17β-hydroxyestra-4,9,11-trien-3-one (methyltrienolone, 53) showed significant activity in rats. Surprisingly, this compound had 300 times the anabolic and 60 times the androgenic potency of 17α-methyltestosterone when administered orally to castrated male rats. In this instance, however, the potent hormonal properties on rats did not correlate with later studies in humans. One study in patients with advanced breast cancer found methyltrienolone to have weak androgenicity and to produce severe hepatic dysfunction at very low doses.
(Reference)
 
bump incase some of you haven't seen the recent postings.

Why experiment on yourself when so many other hormones are available?
 
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