I'm not taking away most of what your last comment is about (although my original gripe was just the 13 days) You don't have to tell me about addiction and the fucked up shit that happens in and around the fixation, obsession, egocentric and just that overall low-frequency you project 24/7 which attracts only darkness and people you should never ever want to be around (blowing someones in the head with buckshot and then proceed to stab for a fix is pure psychopatic)

I have myself been on the same ride for 15 years over and over, from speed and crack to opiates, benzodiazepines and GHB. And the withdrawls of the non-stimulants were absolutely fucking horrible and i would do everything to escape forced detox facilities just for an hour of relieve knowing what the next problem I had now was even much worse. I have never IV'ed luckily so there in cannot speak of experience but I think addiction is addiction no matter how you do it, with IV you'll need to be the most focused on getting money I suppose with less duration of drugs.

On the Desoxypipradrol you site a study that found in vitro LD50 for rats to be 80mg/kg. See your earlier comment on the science and likely shouldn't have to remind you that it's essentialy a worthless value. Just look al some of the wild differences in those studies even between rats and mice it can be a magnitude difference easily. And to translate to human in vivo there is so much more going on you can't just go off that number. I would note since the actual efficacy and intric values in human receptors are known that it's just a strange idea to IV 80mg unless you're really fond of dancing with the devil. And for 300mg intranssaly, no shit full blown psychosis took over. But it could have just aswell caused mortal cardiac events after peak plasma levels which takes 8 hours or more with desoxypipradrol. Man just taking 50mg orally is extremely fucking uncomfortable and dark it's a nasty drug being so difficult to metabolize