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I don’t trust that guy nor do I have the patience to listen to that knucklehead for 32 minutes repeating the same thing 30 different ways. He may have some good points but he can sum it all up in under 2 minutes. I know on YouTube the longer the vid the more money you can make.I'm about to try this. I'll be deploying 5mg sublingual anavar daily additional to TRT+200mg Deca.
Unfortunately i don't have access to raw Oxandrolone so got to do it with the junk fillers which i reckon won't be pleasant tasting.
the difference with sublingual adm. should be lower liver enzymes compared to normal oral administration if you are one that anavar raises said enzymes...I've tried sublingual and oral and personally I couldn't tell a damn bit of difference. Maybe a troche or some other form designed specifically for sublingual use might change things. I was putting a crushed tablet under my tongue for 15 minutes. I went back to just swallowing them.
Probably easier and cheaper making a tablet or capsule. Plus a lot of people are stupid and won’t even know what sublingual means…My question is this. If sublingual anavar is superior then why didn't big pharmaceutical companies make it in this form? Am I missing something?
Yeah it is currently sitting up above in lala land purgatory. Did somebody flag it? Weird.If you got some good info can you cut and paste for us? I'm really kinda interested in this.
Aha, I will correct myself. If you can get drug into systemic circulation (while avoiding first pass) where it presents at reduced systemic serum concentration (vs concentration upon introduction into portal vein) and metabolic clearance typically first order function of serum concentration, I can see where this concept has legs although effect may be quite minimal with highly bioavailable oxandrolone. Especially if most of the metabolic clearance is done in kidneys anyway. In short, dilution may be the solution.But, just because the drug doesn’t get delivered to liver/circulation via portal system doesn’t mean it can’t come back to the liver/kidney via serum for additional metabolism. Seems to me a troche’s strength is to get molecules (which have low oral bioavailability) into circulation by increasing bioavailability (avoid digestive system) and not to minimize end-organ metabolism damage. I can’t find an example of the latter in the literature.
Nice.Physiological and Pharmaceutical Considerations for Rectal Drug Formulations - PMC
Although the oral route is the most convenient route for drug administration, there are a number of circumstances where this is not possible from either a clinical or pharmaceutical perspective. In these cases, the rectal route may represent a ...www.ncbi.nlm.nih.gov
Make a log too... it'll be interesting. Ha log.
Maybe I missed it but if someone is going to try the sublingual route does it need to be in a specifically prepared sublingual formula or would crushed tablets,capsules or raws be sufficient?