negrogesic
Bluelight Crew
For the past few months, when domestic poppy pods were (are) no long available consistently, I have been taking 2.5-3 grams of tramadol, yes 3,000mg of this pro-convulsant crap. Obviously, I have concerns.....
I have had no muscle spasticity, not even a tingle of a petit mal onset. To complicate the matter, I am on 40mg of diazepam which I am trying to taper-off, but there seems to be an inherent battle between the diazepam withdrawal and the tramadol dependence (I hate the stuff, relieves opioid withdrawal), since tramadol reduces the efficacy of the diazepam via some apparent GABA-A antagonist like properties.
When ive gotten ahold of high quality pods, they are able to fully substitute for the opioid withdrawal, and the SNRI withdrawal is moderate but bearable.
However, I am worried about continued use of these molto supra-therapeutic doses, not in regards to seizure, but in the unknown effects of such constistent huge dose, and the complex and rather sketchy non-MOR mediated pharmacology. I am quite aware of the dangerous of hypertensive crises, and avoid anything pro-serotonergic (I take mirtazapine, but it has virtually no affinity for the SERT).
To complicate things further i started take carisopridol to aid in sleep, and found that while it didnt potentiate the tramadol, I feel it has opioidergic properties on its own (I confirmed this when doing some reading, and discovered carisopridol and meprobamate could both be inhibited by naloxone).
The question, any clue as to which drug to switch to in order to get off this shit? Methadone is a headache to get prescribed (I cant do the daily or even bi-daily thing, I am very busy, super-high functioning, at in regards to making money). I am not a fan of buprenorphine, even having taken the DATA waiver through an online 8 hour course hosted by the APA website. It is my opinion that methadone is easier to get off of than buprenorphine, and is far more effective with fewer side-effects.
Also, would cimetidine or other inhibitors of CYP2D6 promote the demethylation of racemic tramadol?
I really enjoyed the o-desmethyltramadol that briefly available, where as tramadol feels very, very different. It would be a bitch to try to use racemic tramadol to try to make M1, or make some substitution to increase potency.
I have had no muscle spasticity, not even a tingle of a petit mal onset. To complicate the matter, I am on 40mg of diazepam which I am trying to taper-off, but there seems to be an inherent battle between the diazepam withdrawal and the tramadol dependence (I hate the stuff, relieves opioid withdrawal), since tramadol reduces the efficacy of the diazepam via some apparent GABA-A antagonist like properties.
When ive gotten ahold of high quality pods, they are able to fully substitute for the opioid withdrawal, and the SNRI withdrawal is moderate but bearable.
However, I am worried about continued use of these molto supra-therapeutic doses, not in regards to seizure, but in the unknown effects of such constistent huge dose, and the complex and rather sketchy non-MOR mediated pharmacology. I am quite aware of the dangerous of hypertensive crises, and avoid anything pro-serotonergic (I take mirtazapine, but it has virtually no affinity for the SERT).
To complicate things further i started take carisopridol to aid in sleep, and found that while it didnt potentiate the tramadol, I feel it has opioidergic properties on its own (I confirmed this when doing some reading, and discovered carisopridol and meprobamate could both be inhibited by naloxone).
The question, any clue as to which drug to switch to in order to get off this shit? Methadone is a headache to get prescribed (I cant do the daily or even bi-daily thing, I am very busy, super-high functioning, at in regards to making money). I am not a fan of buprenorphine, even having taken the DATA waiver through an online 8 hour course hosted by the APA website. It is my opinion that methadone is easier to get off of than buprenorphine, and is far more effective with fewer side-effects.
Also, would cimetidine or other inhibitors of CYP2D6 promote the demethylation of racemic tramadol?
I really enjoyed the o-desmethyltramadol that briefly available, where as tramadol feels very, very different. It would be a bitch to try to use racemic tramadol to try to make M1, or make some substitution to increase potency.
