Thanks man! I have a question: is there a source on that 8:1 ratio between Br0m0n0re and Diaz? Just curious cause I know i need to properly read my shit when it gets below 15pg on my .000 weighter... you know.
So unfortunately the 6 pages is equal to 10 of d1@z3p@m claim is solely anecdotal as far as I can tell. For now I would stick to around 8mg per ml. Dissolves great in PG with a little heat and mag stirrer. And we don't know what other medications these subjects were on, but then again they could feel the anxiety leave their mind and body without any lethargy or hypnosis:
I really think even though it's so similar to d1@z3p@m or nordi@z3p@m, it acts quite different. Pubmed has one focused pretty much on gid@z3p@m, and then there's one more in English I'm reading and they hit on its main metabolite, br0m0n0rd1@z3p@m. And that's what we're all interested in.
It's a metabolite of gid@zep@m.(G1d@z3p@m is 2:1 weaker than v@l1um; 20 pages of gid@z3p@m is approximately 10 pages of Valium, but they act differently,.despite being so chemically similar. It does not hit nearly the amount of the bzd sites that most and almost all potent ones do. It hits the normal ones like
From scientific literature:
"Gid@zepam has prominent anxiolytic properties without producing the sedative and muscle relaxant effects that are associated with other benzodiazepines, such as diaz3p@m."
These research chemical websites are quoting a dose of 6–9 mg for desalkygidazepam (for ethical reasons, no information for specific sites are given), and this dosage is supported by the various trip reports. The user comments from “trip reports” also confirm the lack of sedative effects, the long half-life and the anxiolytic effects, but also that gidazepam and desalkylgidazepam use may not become widespread. Some comments are as follows: “It’s a quite functional benzo, very little hypnotic effects but eliminates anxiety very well [.] I’ve got up to 30 mg with it and no ill effects from that dosage […] I feel like it would be a good tapering benzo due to the long half-life and not much recreational potential”
It seems the vendors just settled on a little more than gid@z3p@m's conversion to v@l1um. Which does make sense as it is more potent by weight and but is really only an anxiolytic. But isn't this the kind of ch3ms a lot of people wanted. This is one of the safer ones we've had in awhile, especially because it's common to combine depressants (op10d$, a1c0h0l, g@b@p3ntoids, and geehbhhbeeee.
This suggests a wide separation between the anxiolytic and sedative dosages of gidazepam, when compared with diazepam, an example of a typical benzodiazepine. In human studies, the lack of sedative effects of gidazepam is confirmed, for example, in a controlled study where subjects were given either 100 mg of gidazepam or a placebo for 14 days and then asked to perform psychological testing investigating alertness, reaction time, attention and memory, there was no significant difference between the placebo and gidazepam (
30,
31).
Br0m0n0r is an amazing taper drug, and i think the medical community should look at it as a potential future medication since it literally solely alleviates anxiety, unless you REALLY push the dose like I said. And that's not worth it and expensive.and I think primarily that's how it should be used. Otherwise you're wasting money taking a not very potent benzo.(effects wise, still not sure about the dose since that was all anecdotal).
That's why the withdrawal depends on the compound used and not just time on,.etc. Ive found through personal experience and medical journals that some ch3m1c4ls really just shouldn't be out on the street. Some have a higher binding affinity to the receptors than others.
Anyways, I believe that br0m0 acts more like it's parent compound gidzepam, just more potent by weight and it hits g@b@ A harder than gid@z3p@m. Gidazepam is one of the more gentle b3mz0s out there, like pyr@zol@m with a really long half life . Therefore, since it's not hammering almost every BZD site in your brain, this should result in an easier, well not as harsh, taper and withdrawal compared to br0m@z0l@m, flu@lpr@zol@m, c1onaz0l4m, and regular old @lpr@z0l@m, theoretically. List goes on. Tri@zolam is a good one for a procedure, pretty potent. This is theory that has some roots to it.
I know we're talking br0m0m0r..But because there's another much better scientific study done on gid@z3pam and it delves semi-deeply into its main active metabolite, br0m0m0rdi@zep@m.
From the study (this was done on rats, not humans):
From scientific literature:
"Gid@zepam has prominent anxiolytic properties without producing the sedative and muscle relaxant effects that are associated with other benzodiazepines, such as diaz3p@m."
Anecdotal notes:
These research chemical websites are quoting a dose of 6–9 mg for desalkygidazepam (for ethical reasons, no information for specific sites are given), and this dosage is supported by the various trip reports. The user comments from “trip reports” also confirm the lack of sedative effects, the long half-life and the anxiolytic effects, but also that gidazepam and desalkylgidazepam use may not become widespread. Some comments are as follows: “It’s a quite functional benzo, very little hypnotic effects but eliminates anxiety very well [.] I’ve got up to 30 mg with it and no ill effects from that dosage […] I feel like it would be a good tapering benzo due to the long half-life and not much recreational potential”
^^^^Those statements above are all anecdotal. People like you and me taking it and recording their experiences which is great, but we don't know what else they have taken,.etc., and there's several ways for errors to occur this way. But their statements seem to add up to my experience.
Theres one control study done with humans, at least that I could get in English. Here it is:
"This suggests a wide separation between the anxiolytic and sedative dosages of gid@z3pam, when compared with di@zepam as an example of a typical b3nzodiazepine. In human studies, the lack of sedative effects of gidazepam is confirmed, for example, in a controlled study where subjects were given either 100 mg of gidazepam or a placebo for 14 days and then asked to perform psychological testing investigating alertness, reaction time, attention and memory, there was no significant difference between the placebo and gidazepam (
30,
31)."
Quick comment: that's pretty wild. 100 pagea and there was no significant difference in physical and mental performance. Wow.
Br0m0n0r is an amazing taper drug, and I think primarily that's how it should be used. Otherwise you're wasting money taking a not very potent b3nzo.(effects wise, still not sure about the dose since that was all anecdotal). But it's a safer one. And I'm all about harm reduction.
That's why the withdrawal depends on the compound used and not just time on, amount etc. Ive found through personal experience and medical journals that some ch3m1c4ls really just shouldn't be available, or for those that really do their research lol. Some have a higher binding affinity to the receptors than others.
Anyways, I believe that br0m0 is decently potent as far as anxiety alleviation goes and getting off of these chems ultimately, but this won't fuck you up and make you forget your problems unless you take 80 pages. Gid@zepam is one of the more gentle b3nz0s out there, and this is its main metabolite. It did show in the studies that it's absolutely more potent by weight, but that doesn't necessarily mess with the effects of the compound. I think of br0m0n0r like pyr@zol@m with a really long half life . Therefore, since it's not hammering almost every BZD site in your brain, this should result in an easier, well not as harsh, taper and withdrawal compared to br0m@z0l@m, flu@lpr@zol@m, c1onaz0l4m, and regular old @lpr@z0l@m. List goes on.
Maybe a chemist can chime in, but it's not a full agonist at the G@B@ A receptor, so to me that could mean not as intense withdrawals, length would still be the same. At least that's how it works for some other variety of ch3ms.
Anyways, sorry if this a bit unorganized. I didn't use any AI and that took me over 2 hours using a phone to type. I love researching. I love learning. This is all interesting to me. But i didn't want to use my work computer to look at any of this lol. Don't worry I finished my workload by 12 and had to hang around till 3 so this passed the time fast!