A friendly rules reminder:
5) Suggesting or encouraging any illegal activity is cause for immediate deletion and suspension of posting privileges. You can share information on what is legal, and what is not legal, but our forums are not a place to seek, or offer help, on how to break the law.
7) Don't spam, PM, or post promotional material. No soliciting of any kind.
16. At DrugBuyers.com we do not ask what are the medical needs of visitors and we do not want to know. Our sites is about buying prescription drugs. We assume a legitimate need. Any post that indicates the poster is a drug abuser or recreational drug user will result in that user being banned.
Pharmacy List: US List · International List · Canadian List · Black List | Drug List · Compare Prices
Recent Posts: Past 24 Hours · Past 48 Hours · Past Week
my best guess is that proglumide would be a safer and less dependance increasing enhancer than inhibiting CYP metabolism, since its just a CCK Peptide inhibitor. it wouldn't increase blood levels of the opioid, but rather hinder ONE mechanism of tolerance, the build up of CCK peptide, which is the body's anti-opioid. but there is no study i know of comparing the safty of the two.
Quote:
Also, any chance it would potentiate tramadol? I'm guessing "no", but can't hurt to ask.
Im guessing yes, it would, because part of tramadol's mechanism is the same as any other painmed, Mu Opioid Agonist. For me tramadol is very much an opioid but i think i have extensive 2D6 metabolism and metabolize a lot into M1. Tramadol's M1 metabolite is 200 times more of an opioid than tramadol it's self. the other metabolites, generated by 3A4, are almost inactive in comparison according to my research.