Hi all. I'm from Ukraine and my English level is poor, I used a translator for this thread, so don't blame me for the grammar.
I have been using amphetamine for more than a year now, mostly by oral route. Recently I decided to try potentiation and bought calcium carbonate + magnesium carbonate (if I'm not mistaken, the composition of tums is similar). The effect was not quite like the typical amphetamine effect I imagined. The main change in effect was felt mainly as a potentiation of l-amphetamine/norepinephrine effects - strong tunnel vision, hyperfocus, "zombie" sensation. At the same time, euphoria did not intensify, but rather weakened and became much shorter in time, quickly turning into dysphoria. It reminded me of my experience with a-pvp, which I didn't like at all. And this experience is consistent with the experience of some other users who only felt the negative effects increase without any benefit.
The duration of the overall effect did not change significantly. I've taken fairly high doses of amphetamine without antacids in my time and it felt much more euphoric, more natural and the pleasurable sensations lasted longer, even with the higher dosage it didn't feel crappy.
So what is the pharmacological mechanism that makes amphetamines feel this way when taking antacids? Is levoamphetamine more bioavailable and more slowly eliminated than dexamphetamine at a higher pH? I also read a claim that vitamin C blocks the action of levoamphetamine, making the racemate feel cleaner, similar to dexamphetamine. So, is it safe to assume that the left-sided isomer is more sensitive to pH changes than dexamphetamine?
I took 500mg of vitamin C about 1-2 hours ago after the comedown started to speed up the amphetamine elimination and go to sleep, but I'm still focused, just got rid of the nervous and manic feeling...
Would like to see some research on this.
I have been using amphetamine for more than a year now, mostly by oral route. Recently I decided to try potentiation and bought calcium carbonate + magnesium carbonate (if I'm not mistaken, the composition of tums is similar). The effect was not quite like the typical amphetamine effect I imagined. The main change in effect was felt mainly as a potentiation of l-amphetamine/norepinephrine effects - strong tunnel vision, hyperfocus, "zombie" sensation. At the same time, euphoria did not intensify, but rather weakened and became much shorter in time, quickly turning into dysphoria. It reminded me of my experience with a-pvp, which I didn't like at all. And this experience is consistent with the experience of some other users who only felt the negative effects increase without any benefit.
The duration of the overall effect did not change significantly. I've taken fairly high doses of amphetamine without antacids in my time and it felt much more euphoric, more natural and the pleasurable sensations lasted longer, even with the higher dosage it didn't feel crappy.
So what is the pharmacological mechanism that makes amphetamines feel this way when taking antacids? Is levoamphetamine more bioavailable and more slowly eliminated than dexamphetamine at a higher pH? I also read a claim that vitamin C blocks the action of levoamphetamine, making the racemate feel cleaner, similar to dexamphetamine. So, is it safe to assume that the left-sided isomer is more sensitive to pH changes than dexamphetamine?
I took 500mg of vitamin C about 1-2 hours ago after the comedown started to speed up the amphetamine elimination and go to sleep, but I'm still focused, just got rid of the nervous and manic feeling...
Would like to see some research on this.