M
Moon2023
Member
- Mar 13, 2023
- 10
Рвота и нитрит натрия. возможна ли рвота при приеме нитрита натрия, даже если вы принимали противорвотные средства?
what is meto?Firstly, from many other threads, it seems that most people vomit whether or not you take AEs. So taking multiple AEs would be a needless complication, risk interactions and side effects and possibly increase the chance of vomiting. In fact, I'm sure I've only read of one instance where the person didn't vomit. I think we can all count on vomiting, regardless of AE - what matters is how quickly that happens.
My understanding of it from others is that motion sickness med (the antihistamine) will not help.
And the purpose of using a dopamine blocker is to delay the vomit to allow the critical amount to be absorbed first. Also, there seems to be an added effect from meto of speeding absorption which is what's wanted- I think?
Also, from reading the protocols and several further threads here, taking too much SN is counter productive and again risks vomiting too soon.
For what it's worth, I feel that the right thing to do is stick to the 25g with a simple protocol of one antiemetic and not add unnecessary complications like extra SN or extra AE.
what is meto?
Where did you find this formula?I'm 225lbs. Using the half life method of 180 x 2 x 102kg ÷ 1000 equals the 36.7
Where did you find this formula?
I'm not so sure about the logic behind the ld100. Perhaps a mathematician can chip in, but wouldn't the graph be a curve rather than a straight line, and therefore ld100 isn't as simple as doubling the ld50?It's been floating around here, can't find the original post but its the ld50 formula I think little lady stated.
I'm not so sure about the logic behind the ld100. Perhaps a mathematician can chip in, but wouldn't the graph be a curve rather than a straight line, and therefore ld100 isn't as simple as doubling the ld50?
And it may vary depending on substance and test subject, and as there's never going to be an ld100 experiment on humans for obvious reasons, these figures are especially hard to come by.
Doubling the LD50 is the best estimate we can do. As you've said it's not like we can do LD100 experiments on humans, and it's not like the people here who succeeded to CTB off of the SN method can tell us how it went. >______>I'm not so sure about the logic behind the ld100. Perhaps a mathematician can chip in, but wouldn't the graph be a curve rather than a straight line, and therefore ld100 isn't as simple as doubling the ld50?
And it may vary depending on substance and test subject, and as there's never going to be an ld100 experiment on humans for obvious reasons, these figures are especially hard to come by.