Them Witches
Bluelighter
- Joined
- Apr 21, 2025
- Messages
- 797
My concurred proxy my friend... What is the reason why "international big pharma" has dropped the ball on Kratom, 7-OH, and hybrid 7-OH+PI...? That's what I would like to know upfront. There should be a long list of medical interventions with 7-OH with too many to choose from patient studies, the "pros & cons" of 7-OH, we know everything about everything else to the fullest extent. My other upfront question is how come Germany was not adding 7-OH+PI to it's home run hits in the early 1900's? Germany made Methadone because they didn't want to have to struggle to obtain raw opium during a war. Germany made about everything know to man and no Kratom or 7-OH.@Them Witches - I would certainly like to see a proper instrumental analysis of products being sold AS -OHM because from what I hear, preparative chromatorgrpahy is the only way to obtain a pure product but if a side-product is active and can be isolated, would you throw it away or added to the wholesale material? I've heard someone HAS found a much safer route than the two offered by the original Japanese (?) researchers which makes use of KH2SO5 (Oxone)... but even with that, yield is around 65% at best.
What do we know about mitragynine pseudoindoxyl other than it having an extremely high (low) affinity for the MOR? Is there research that may be able to spot it in product?
Is 7-OH something that was supposed to be not mentioned on the world's fronts for all to hear..? We do not have to grow a ton of poppy only. We can grow a ton of Kratom too.
As far as purity I am all game here. I like Pseudoindoxyl mixed with 7-OH. It is the whole package as far as the subject goes.
I am offended that the 3rd opium war is happening in the United States. These wonderful people are "drawing the short straw using nasty RC hybrid fentanyl with Xylazine, and unknown Benzo/barb everywhere so...
why not prescribe 7-OH in a variety of ways -- 7-OH IR, 7-OH ER, 7-OH hybrid IR outer shell & ER inner core, 7-OH+PI all versions again, sublingual, buccal, etc.
If I was MAT, I would change up the Methadone and Suboxone ritual. Offer 7-OH at the beginning because they typically start at 30mg of Methadone. Stop 7-OH and get a reasonable Methadone MME daily dose. After that is done, offer 7-OH for urges to use relating to the case per patient.
Same with pain management. Offer 7-OH for bad breakthru days to help the patient get through without having to increase the narcotic MME. A perfect register for tapering and opioid rotation. It would add another opioid (opioid type) to the narcotics list. There are not a lot of options in the pain medicine stock for out-patient long-term treatment use.
I would like to see a "proper and accurate" medical trials performed with 7-OH for opioid prescribed patients :
>> opioid naive, honeymoon opioid tolerance, long-term opioid tolerant, pain management, and pain management rotation. Adding in the medical trials, acute post-op pain.
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