rachel_s_n
Bluelighter
center said:Delete it then.
I think this is a good topic. I like seeing how diffrent people think.
center said:Delete it then.
Dextromoramide (Palfium®, Palphium®, Jetrium®, Dimorlin®) is the right-handed isomer of the moramide molecule. The left handed molecule is called levomoramide, and a mixture of the two is called racemoramide. Its full chemical name is (+)-1-(3-Methyl-4-morpholino-2,2-diphenylbutyryl)pyrrolidine, and its molecular formula: C25H32N2O2, with an atomic weight of ~392.5. It is one of a group of molecules known as substituted α,α-Diphenyl-γ-Amino-Butyramides.
It is a powerful opioid analgesic, and as such is subject to drug prohibition regimes, both internationally through UN treaties, and by the criminal law of individual states.
It was discovered and patented in 1956 by Dr Paul Janssen at Janssen Pharmaceutica, who also discovered fentanyl, another important synthetic opioid, widely used to treat pain and in combination with other drugs as an anaesthetic. It has the proprietary name Palfium, though as of mid 2004 the drug was dicontinued in the UK due to limited supplies of precursor chemicals.
As is the case with so many drug discoveries, dextromoramide was discovered by accident during research into almost identical compounds, namely α,α-Diphenyl-γ-Dialkyamino-Butyramides, which show no analgesic activity, but are extremely active physiologically as inhibitors of gastric secretions in man.
In many countries dextromoramide is unused, for example the USA, where it is considered a Schedule 1 drug, alongside cannabis and LSD, as having no medicinal uses. It is still rarely used in Australia, but prescription is avoided due to its abuse potential and so use of Palfium is now mainly limited to terminal care.
The typical dose is 5mg four hourly for cancer pain - the drug has a short half life comparable with pethidine. Dextromoramide is also used as a short-acting analgesic for minor surgical procedures. In this case it is administered sublingually and reaches a therapeutic concentration after around 12 minutes.
Dextromoramide was much favoured by drug abusers in Australia in the 1970s. A single case report and a review of the subject appears in the Australian Journal of Pharmacy 1980;61:641-644
phrozen said:Out of what you listed, I'd pick intranasal oxycodone.
I've never tried oxymorphone though.
center said:I've come to the conclusion that I'm going to step away from the crowd and scream at the top of my lungs that ALL OPIATES ARE NEGATIVE FOR RECREATIONAL USE.
There, I said it. What good has come out of recreational use of opiates? Yeah. Justification time. Excuse me while I go figure something out.

rachel_s_n said:I think this is a good topic. I like seeing how diffrent people think.

Ungoliath said:I auctually prefer the mylan/gel-less ovre gelled, one reason is the generic non gels, a 100mcg/h patch has 16.9mg of fent in it, compared to 10mg in a duragesic.
Its better because of fents short duration, pure fents kinda harsh on the body, extended release is hella better. I live my life with a chunk of patch in my mouth.
%)delta_9 said:Are you looking to prove which opiate is the best? Or are you trying to just get opinions from people about which opiate they like best? Because the last thing we need at Bl is another opinionated thread![]()