Probably the second. The main danger is dehydration, and as a fact - it is difficult to control the behavior.Did you have any negative effects at all, or was it just a normal empathogen + dissociative combo?
I like ketamine. but it just feels obvious for me that you shouldn't mix speed and K. intuition kinda thing...
10min later I was floored, breathing heavily, mentally fuckin high in a good way. physically it felt like meltdown is imminent (feelings of fainting; slight deja vu feeling of this n2o-cracking-noise-in-your-ears (some will know, I'm sure) was there too, now that I think of it). VERY high temperature and heart rate and bloodpressure. having laid down a friend took care of me, gave me some water, sprinkled me with some water, light massage. with the k-peak subsiding it slowly got better and turned out to be quite a nice experience (even took 2 small(!) bumbs later
)...
but anyway: this combo did definitely feel dangerous. I would not do it again and I would not advise anyone else to do it. (both doses were relatively high though)
Mixing opioids with acid is perfectly fine, mixing any stimulant (including coffee) or opiate with any NMDA antagonist such as PCP, DXM, or K is extremely dangerous so you should make a couple changes.
Wow that sucks that Mdma and Mxe will never mix =_(
And I love having a six pack with K why is this that detrimental?
Can someone please make an antipsychotics section? I feel like that is a very important class of drugs and this post should be updated accordingly. I'm schizophrenic and I'm on olanzapine
kingme said:would it be possible to add a list for each type of substance, that is more specific than the examples given in the ()? such as a long list of serotonin releasers, one for maois etc? or is this too risky as it oversimplyfies things?
Anyone able to link any studies about how potent aMT is as an MAOI? We all know that it is one, but I've seen a constant back and forth between people arguing that it's only as strong an MAOI as something like amphetamine, and others saying it's as strong as harmine etc.
I would imagine the first piece of evidence for it being weak would be the fact that it too releases serotonin and doesn't seem to exhibit PMA/PMMA type effects. That said though, that's not a definitive answer.
Maybe someone could shed some light, because I seem to remember someone explaining in detail why aMT was only a weak MAOI inhibitor and its MAOI action was negligible at best - but I've lately been going ahead and repeating that without even remembering the reasoning for it, and I don't wish to continue doing that!
Jesusgreen said:Anyone able to link any studies about how potent aMT is as an MAOI? We all know that it is one, but I've seen a constant back and forth between people arguing that it's only as strong an MAOI as something like amphetamine, and others saying it's as strong as harmine etc.
The increase after iproniazid was antagonized to the same extent by all the tryptamine derivatives and by harmaline, whereas dexamphetamine showed less effect.
In the other experiments with brain, the tryptamine derivatives were less potent than harmaline, but somewhat more active than dexamphetamine.
In rats, three alpha-alkylated tryptamine derivatives (alpha-methyl, alpha-ethyl, and alphaalpha-dimethyltryptamine) caused alterations of 5-hydroxytryptamine metabolism typical of monoamine-oxidase inhibitors with short duration of action, viz., an increase of endogenous 5-hydroxytryptamine in brain, enhancement of the increase of 5-hydroxytryptamine in brain and heart after 5-hydroxytryptophan administration