narcomick
Bluelighter
- Joined
- Feb 14, 2017
- Messages
- 77
The drug:
If i open the capsule and swallow the white powder i find the effects to come on quicker, however the taste is unpleasant. I take zopiclone so have something of a tolerance to strange chemical tastes, and I find that pregabalin has a chemical, metallic taste very similar to zopiclone, but it doesn't linger in the mouth as long as the latter. Anyway, this is my experience of pregabalins effects, it's a little different to most people's but otherwise very similar. I personaly find the experience to have at least 4 or 5 stages, which i will now outline. This is with a moderate to heavy dose.
The effects:
T+00:00-30 nothing much other than some initial stimulation
T+00:30-1:30 come up. stimulation, apprehension building to euphoria and mild dissociation.
T+01:30- 04:00 peak. Euphoria and tactile sensations that may feel like anything from a mild satisfaction a full body orgasm. stimulation and sedation. Dry mouth. Empathogenic effects, aphrodisiac effects. Music enhancement. Colour enhancement. Mild but colourful 'mind movies' or CEV's/closed eye visuals. Change or expansion of conciousness. Appetite and taste enhancement. Effects come and go in waves.
04:00- 08:00 gradual come down. Effects slowly decrease. More sedating than previous stages. Feeling of well being.
08:00-15:00 afterglow. Mild mood lift, leftover dissociation slowly fade.
In my experience effects somewhat resemble marijuana minus the paranoia and anxiety, with some aspects more comparable to mdma or low dose ketamine/psychedelics.
Overall:
The effects of pregabalin on me are both stimulating and sedating, often with an intense mental and physical euphoria and a mild dissociative-psychedelic feel. I find it to be nothing like benzos.
I find it interesting that pregabalin does not apparently bind to seretonin receptors as many of its effects would be accounted for if such action was present. The dissociative effect i imagine is due to less glutamate being produced having an effect similar to antagonism of glutamate nmda receptors. A very interesting, mysterious compound that i think needs more research. Probably not advisable long term unless needed.
If i open the capsule and swallow the white powder i find the effects to come on quicker, however the taste is unpleasant. I take zopiclone so have something of a tolerance to strange chemical tastes, and I find that pregabalin has a chemical, metallic taste very similar to zopiclone, but it doesn't linger in the mouth as long as the latter. Anyway, this is my experience of pregabalins effects, it's a little different to most people's but otherwise very similar. I personaly find the experience to have at least 4 or 5 stages, which i will now outline. This is with a moderate to heavy dose.
The effects:
T+00:00-30 nothing much other than some initial stimulation
T+00:30-1:30 come up. stimulation, apprehension building to euphoria and mild dissociation.
T+01:30- 04:00 peak. Euphoria and tactile sensations that may feel like anything from a mild satisfaction a full body orgasm. stimulation and sedation. Dry mouth. Empathogenic effects, aphrodisiac effects. Music enhancement. Colour enhancement. Mild but colourful 'mind movies' or CEV's/closed eye visuals. Change or expansion of conciousness. Appetite and taste enhancement. Effects come and go in waves.
04:00- 08:00 gradual come down. Effects slowly decrease. More sedating than previous stages. Feeling of well being.
08:00-15:00 afterglow. Mild mood lift, leftover dissociation slowly fade.
In my experience effects somewhat resemble marijuana minus the paranoia and anxiety, with some aspects more comparable to mdma or low dose ketamine/psychedelics.
Overall:
The effects of pregabalin on me are both stimulating and sedating, often with an intense mental and physical euphoria and a mild dissociative-psychedelic feel. I find it to be nothing like benzos.
I find it interesting that pregabalin does not apparently bind to seretonin receptors as many of its effects would be accounted for if such action was present. The dissociative effect i imagine is due to less glutamate being produced having an effect similar to antagonism of glutamate nmda receptors. A very interesting, mysterious compound that i think needs more research. Probably not advisable long term unless needed.
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