yoyo50
Bluelighter
20/30mg in the sun is perfect
Oddly I actually prefer insnuffulation. I only need tiny amounts (there's no feeling that I've even put something up my nose) and I feel it within minutes. The anti-depressant component is the first thing to hit me. My outlook changes drastically, especially if I'm having a rocky day. The other effects are pretty subtle in this range and it's definitely sub-psychedelic and only gives a hint of dissociation. I can't even comment on what my dosage is because my scale won't even register it. I got 2g over two months ago, use the stuff frequently, have given a bunch away and shared about the same amount, and there is easily a gram+ remaining that will last for months to come at my current levels of intake.
I advocate snorting a tiny, tiny line sometime. Less than you think will even have any effect. Go into it with a sober head. You might be surprised by how nice it is. Do another after 40 minutes if you don't register it. You can function in any normal capacity like this. I'm enamored with the substance in dosage range. Sounds like I'm an outlier though.
I prefer snorting tiny amounts if I need to interact with other people, its kind of just there as a background high, elevating my mood..... but this drug has such +'s where ever used..... you can do a tiny bit and just enjoy the mood and the high or you can go fully into outer space, or inner space sorry lol... immerse yourself fully into the experience...... It offers everything this drug. Will go down as a classic
mxe and heroin dont mix
i od'ed on a smallish shot andhad to narcaned.
Modification of Drug Tolerance and Dependence
PCP, or other PCP-like NMDA antagonists such as dizocilpine, given repeatedly in combination with other drugs of abuse, can block or reduce development of tolerance and dependence [e.g., to opioids (74)] and sensitization [e.g., to effects of amphetamines, cocaine, and nicotine (32, 63)]. Competitive as well as noncompetitive NMDA antagonists are able to block tolerance development (72). Although the neural basis by which NMDA antagonists modify tolerance and dependence development is not known, it is possible that their interference with NMDA-receptor-mediated neuroadaptive processes is involved.
http://www.acnp.org/g4/gn401000171/ch167.html
thanks for that.Regarding oral dosing -- N-ethyl groups have a tendency to prevent MAO degradation of amines; see also DMT vs. MET, the latter being orally active. It is not therefore surprising that this is orally active.
Regarding oral dosing -- N-ethyl groups have a tendency to prevent MAO degradation of amines; see also DMT vs. MET, the latter being orally active. It is not therefore surprising that this is orally active.
OK. Please call me dumb if you must but I am on Methadone Maintenance. I will not take drugs thats make me get sick or overwhelmed with uncomfortable. I have a bit of this stuff. Should I avoid mixing this stuff? Would it be cool to drink half of my dose which is 99mgs, and do some then my other dose when it wears off or will I still get sick. I am afraid of an OD which is why I left it alone but my tolerance for shit is wild most time.^I think this might have something to do with the negative combos being reported.
I'd avoid stims and opiates with MXE.
I used to have a mild kratom habit (eliminated by MXE), and I puked after having some last night which would normally only happen on much larger doses.
I'd say any tolerance I had has been reset, which oddly makes me less hesitant to use kratom when I feel it would be useful (for focus/energy etc) since I know MXE could take care of any withdrawals/desire to use.
I may be mistaken but N-demethylation is likely occuring with CYP3A4, as has been demonstrated with ketamine
OK. Please call me dumb if you must but I am on Methadone Maintenance. I will not take drugs thats make me get sick or overwhelmed with uncomfortable. I have a bit of this stuff. Should I avoid mixing this stuff? Would it be cool to drink half of my dose which is 99mgs, and do some then my other dose when it wears off or will I still get sick. I am afraid of an OD which is why I left it alone but my tolerance for shit is wild most time.If it matters I have been using opiates for about 2 years STRAIGHT 5 or six on and off. Have also been on Methadone for a year and a half almost. If that helps with anything.
I wouldn't take them at the same time and would definitely proceed with caution.
I'd take the MXE when the opiate withdrawals are starting to see if it helps (which I suspect it could), then go on the assumption that the MXE has affected your existing tolerance and take a much lower dose of methadone if needed well after the MXE has worn off.
50mg of MXE would be very high for a first time dose ('hard head' or not). After an allergy test I'd start with 25mg oral, but that's assuming no other substances are involved and no risk of interaction, so less might be appropriate in your case.
Remember what the poster above said. He OD'd on a SMALL dose...
-----------------
Btw, I tried oral for the first time last night. 25mg then watched Inception for the first time. I was feeling the effects within 20 minutes so it seemed just as quick as intranasal and I'd say at least as potent. I think oral is the way to go because then people are less likely to equate it with ketamine and start going overboard with big lines..
Really good for chronic pain. I had a great sleep and woke up pain free which is a weird, but nice feeling.![]()
Oral metabolism of methoxetamineAny info if MXE is also broken by the CYP3A4 enzyme like K and DXM? If so, I guess MXE wouldn't work properly after a week long daily usage of Modafinil that is supposed to upregulate CYP3A4 ( http://www.erowid.org/smarts/modafinil/modafinil_interactions.shtml ). Might test this soon.
Has anyone tested the grapefruit thing?
What does this basically mean or how would the process change if CYP3A4 is down- or upregulated?