Why to not take consecutive doses of LSD analogues

[rippedzipper]

A little back story on my experience with psychedelics in general. Under my belt; morning glory extract (LSA), cubies, salvia, ketamine, DXM, 4-ACO-DMT, 2C-E, 2C-C.

It has been months since I ate a mushroom, and had always entertained the idea of doing LSD though, never could obtain it. So I found myself some analogues known as 1-P LSD, ETH-LAD, and AL-LAD.
100ug of each compound on 15 pieces of blotter, except the AL-LAD which was 150ug.

I started slow, taking a hit of ETH-LAD. The experience was extremely pleasurable and left me bewildered as well as anxious to re-dose, but good logic kept that from happening. Within the next week I started dosing more Etizolam, sub-sequently changing my thoughts on taking more analogues so soon. I started taking blotter after blotter of ETH-LAD, and only 2 days later I noticed a rapid tolerance had built. I dosed all 5 blotters of 1-P within 5 hours as well as 4 blotters of AL-LAD. I'm thinking 500ug 1-P and 600ug AL-LAD, why the heck aren't I tripping. By morning i had thrown up once and still felt little to no effects. I came to the conclusion that it was a rapid tolerance that had built over a few days. Another possibility is that the blotters were poorly stored for that weeks time and lost most all potency.

 

[CrypticArc]

well duh, this is common knowledge psychedelic tolerance builds notoriously fast. you have to wait at least a week or two between doses or you're wasting your drugs.

 

[Clocktower]

Well, at least this anecdote suggests that other lysergamides have a safety profile similar to LSD's. That's good news.

Of course, advising others against binging on psychedelics is good HR. That LSD analogs build tolerance rapidly and are cross-tolerant with each other should be no surprise to anyone. It's also possible that your Etizolam regimen was a factor.

 

[Solipsis]

They are probably around as safe, but this anecdote hardly even suggests it. You can't prove the risks of NBOMe compounds either the same way, because if you get high tolerance and drop a lot of an NBOMe with hardly any effects, that also means it is also hardly the same risk from overactivity at those serotonergic receptors that would normally cause you to trip. Those are still the main suspect of toxicity.

Taking high doses with tolerance or without tolerance aren't the same thing, not in terms of effect and potentially not for toxicity. So no conclusions I'm afraid.

Here is the LSD and shrooms (etc) tolerance thread:
http://www.bluelight.ru/vb/showthread.php?t=479297

or faq, poll, graph