While I have read through the history of posts and know that this can be a substance that can cause harm, the pharmacology and interaction is something I want to clarify. I have read that it has serotonin agonism, a serotonin releaser, as well as MAOI 
How strong is the 2c-t-7 MAOI for A as well as B in comparison to Harmala ?
To counter nausea potential , can a 5HT3 antagonist (lemon oil) be used safely?
If there were concerns and the trip needed to be ended, what could be used? I would think SSRI would be cause for SS, but atypicals like risperdone might work as well as benzo.
Oral ROA , reports of various doses even up to 50mg by some. I won't get near that without tolerance, but what have been your limits with T7 alone and combo'd?
If combo's with tryptamines occur, it looks like a low dose for the tryptamine would be all that is needed. If the above is true about receptor activity and MAOI, probably not a good idea to take NBOMe with T7.
How strong is the 2c-t-7 MAOI for A as well as B in comparison to Harmala ?
To counter nausea potential , can a 5HT3 antagonist (lemon oil) be used safely?
If there were concerns and the trip needed to be ended, what could be used? I would think SSRI would be cause for SS, but atypicals like risperdone might work as well as benzo.
Oral ROA , reports of various doses even up to 50mg by some. I won't get near that without tolerance, but what have been your limits with T7 alone and combo'd?
If combo's with tryptamines occur, it looks like a low dose for the tryptamine would be all that is needed. If the above is true about receptor activity and MAOI, probably not a good idea to take NBOMe with T7.
