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Multiple people have mentioned not feeling anything from it and at least one person had blood tests indicating it wasn't legit. I'm not sure why you'd discourage someone from testing unless you're a shill for the company.For what reason?
Test base is the cheapest drug there is, even cheaper than most OTC supplements.
What would be their incentive to cheat you with this one?
I sent PPL's Masteron, Proviron and DHT for HPLC testing.
They all came back being what was advertised with 98% purity.
So if the most expensive compounds cleared the test, I would bet test does ...
His theory is sound and would afford someone the option to save money on testing compounds that might not be worth it ? but if people are reporting it to be bunk it might be worth testing or looking elsewhere.Multiple people have mentioned not feeling anything from it and at least one person had blood tests indicating it wasn't legit. I'm not sure why you'd discourage someone from testing unless you're a shill for the company.
The poster in question already bought the test. Why discourage them from using it? Just seems suspicious to me.His theory is sound and would afford someone the option to save money on testing compounds that might not be worth it ? but if people are reporting it to be bunk it might be worth testing or looking elsewhere.
Multiple people have mentioned not feeling anything from it and at least one person had blood tests indicating it wasn't legit. I'm not sure why you'd discourage someone from testing unless you're a shill for the company.
As the studies towards the end of the post demonstrate, not only is free/base T orally bioavailable, but even massive doses (400mg daily) have no negative side effects on the liver and in fact accelerates the activity of several liver detox enzymes. The latter effect is highly sought-after by Big Pharma and many drugs are currently being developed/tested with the hope that such a liver-metabolism-enhancing compound will be brought to market as it has tremendous potential for treating everything from obesity, to gyno, to side effects of toxic chemotherapy. Thus, as one of the studies below directly stated, artificial/synthetic T derivatives such as 17a-methylated varieties, 19-nortestosterone derivatives (and in general any other AAS with bizarre modifications to make them less metabolizable and longer acting) have no advantages over free/base T neither due to cost nor effectiveness. In fact, unlike the readily observed liver-toxicity (including liver cancer) from various synthetic AAS, using free/base T may actually cure 60%+ of even advanced cases of liver failure (cirrhosis), as confirmed by extensive human studies several decades ago.
[ON 2 CASES OF ASCITES DUE TO HEPATIC CIRRHOSIS IN SUBJECTS OPERATED ON BY SPLENECTOMY AND PRESENTING PORTA OBLITERATION--CLINICAL RECOVERY FOLLOWING TREATMENT WITH HIGH DOSES OF TESTOSTERONE AND VITAMIN B 1] - PubMed
[Possible clinical cure in a high percentage of cases of liver cirrhosis with a treatment based on high doses of testosterone and vitamin B 1] - PubMed
[THERAPY OF LIVER CIRRHOSIS WITH TESTOSTERONE AND VITAMIN B 1] - PubMed
https://www.tandfonline.com/doi/abs/10.1080/00325481.1964.11694984
So, what does that have to do with FDA’s recent T undecanoate approval? Well, according to one of the studies below, that specific T ester only works if it is dissolved in oil AND administered with a large meal containing significant amounts of fat. On the other hand, oral free/base T was absorbed without using any carriers or fatty meals. In addition, androgen esters often have unpredictable effects and in some cases may be even carcinogenic, while the free/base steroid is highly protective. It just so happens that the formulation FDA approved does NOT contain any oils as carrier/solvent and does not carry a recommendation to consume with a significant amount of fat. So, at best the formulation will be ineffective and at worst it may be carcinogenic.
2) it could just be that @haidut 's theory that test is orally bioavailable is wrong.
This is why I say 20mg is the lowest you can go doing it orally. For some reason alot on this forum thinks there's an additive effect. There's not. Whatever amount you take your body will adjust to. So you have to take the amount your body makes plus the extra that your trying to get to. As far as I see it 20mg a day is the absolute bare minimum one could take to actually feel a difference. This is where I felt the difference at. And now I'm slowly going up until I find the amount I'm going to stay atMaybe in some people they lower their own production of T as soon as they receive an external source, so no net effect, whereas with eunuchs their natural levels are already zero and cannot be lowered so they get a good effect from external T. But not all the studies @haidut lists are on eunuchs.
Also worth noting that the study posted was people taking 100mg orally 4x a day.People not feeling its effects could be because it's not bioavailable and that the theory is wrong.
Also worth noting that the study posted was people taking 100mg orally 4x a day.
So, taking 10mg orally and expecting to feel like HULK is quite a tall order...
Yes, that's what I'm saying.
His theory is that it works orally.
People not feeling its effects could be because it's not bioavailable and that the theory is wrong.
In the study linked it's not mentioned at all what levels were reached with oral delivery.
Works perfectly for me, not even need olive oil or anything else than a glass water to swallow it, 1st thing in the morning.
I posted the saliva test to give a proof, and anyone can also test for himself.
I can also say than 20mg is about the same (without any sides) as 120mg (0,5ml) of test enanthate/week, injected, as I used to take this for years a long time ago…
But it’s just me.
ps: current experiment is to stack test+preg+Melatonin+curcuma Longvida in home made suppositorie (with coco oil)…seems to work exactly the same, but much less powders to measure and to pop every day…
So, just like @ecstatichamster said - I simply posted a human study claiming it works. There are multiple studies with humans and oral T actually, not just this one. In addition, FDA already approved an oral form of T called Jatenzo.
JATENZO® (testosterone undecanoate) For Testosterone Replacement
JATENZO® is the #1 FDA approved oral softgel for Testosterone Replacement. JATENZO is made to fit in your day and your hand. See PI, including Boxed Warning.www.jatenzo.com
Furthermore, Peat has a patent on testosterone in vitamin E and olive oil, and has discussed oral usage of base T with people multiple times. Finally, there are several people in this thread saying oral T base in olive oil works quite well for them, to the point of anything more than 20mg per dose being too much.
So, in light of all this, not much about about oral T working is really "theory" anymore, let alone it being somehow "mine".
A bit of a side note, but still relevant. If it is widely accepted, and proven through studies, that oral pregnenolone (P5) and DHEA are well absorbed and active orally, it makes zero sense for other steroids like T, DHT, etc to somehow be magically ineffective orally. The same claims of first pass metabolism, excretion, etc apply to ALL oral steroids. So, again, if P5 and DHEA are known to work orally then so do T, DHT, etc.
In regards to blood tests - keep in mind that the clinical studies with Jatenzo (above) used the equivalent of 150mg base T twice daily in order to produce serum T levels in the 400s. So, pretty high doses are needed in order to see immediate changes in blood levels. The same peculiarity has been demonstrated with P5 and DHEA. Namely, if you take DHEA in doses below 100mg daily there won't be much change in blood DHEA/DHEA-S for the first 1-3 months, and only then those levels will start rising.
Effect of 1-year, low-dose DHEA therapy on climacteric symptoms and female sexuality - PubMed
Daily oral DHEA therapy at the dose of 10 mg, HRT and tibolone all provided a significant improvement in comparison with vitamin D in sexual function and in frequency of sexual intercourse in early postmenopausal women.pubmed.ncbi.nlm.nih.govLong-term low-dose dehydroepiandrosterone replacement therapy in aging males with partial androgen deficiency - PubMed
Dehydroepiandrosterone (DHEA) and dehydroepiandrosterone sulfate (DHEAS) age-related withdrawal is very likely to be involved in the aging process and the onset of age-related diseases, giving rise to the question of whether preventing or compensating the decline of these steroids may have...pubmed.ncbi.nlm.nih.gov
That does not mean DHEA is not being absorbed and does not work. If you measure its metabolites, then you see a massive increase and this confirms it is absorbed and works orally.
Physiological changes in dehydroepiandrosterone are not reflected by serum levels of active androgens and estrogens but of their metabolites: intracrinology - PubMed
This study analyzes in detail the serum concentration of the active androgens and estrogens, as well as a series of free and conjugated forms of their precursors and metabolites, after daily application for 2 weeks of 10 mL 20% dehydroepiandrosterone (DHEA) solution on the skin to avoid first...pubmed.ncbi.nlm.nih.gov
Same thing has been observed with P5. Individual doses of 200mg orally produce a very brief elevation in blood tests and then the levels rapidly go back to normal.
Oral pregnenolone as hormone replacement therapy (HRT) in humans
As many of my readers know, the first step in steroid synthesis is the so-called "side-chain cleavage", which converts cholesterol into pregnenolone (P5). That step is known as the rate-limiting step in the steroid cascade, and its function depends on the redox status and ATP levels. In other...raypeatforum.com
Only when supplementing with doses in the ~500mg range are robust changes seen in blood levels, and even then only after about 4-8 weeks.
Proof-of-Concept Trial with the Neurosteroid Pregnenolone Targeting Cognitive and Negative Symptoms in Schizophrenia (Table 6)
So, if somebody wants to verify that oral T is being absorbed and works even after a few days of usage should either test its metabolites or something like SHBG. The clinical trials with Jatenzo showed a massive and sustained drop in SHBG from even "low" doses oral T(U). Then, after using the lower doses of base T for several weeks, there should be a change in other results such as DHEA-S (drop), T (increase), DHT (increase), etc.
Damn ... Peat has Progest-T --- The secret sauce. The holy gravy. The freshly squeezed juice.Peat has a patent on testosterone in vitamin E and olive oil