Tieeurrrop
Bluelighter
- Joined
- Nov 19, 2018
- Messages
- 87
I am a very health conscious person and always look up the long term possible toxic effects and get scared off taking something if the studies show it to be carcinogenic or genotoxic and that stuff.
But as I looked up downers nearly ALL of them I found studies saying they have some horrible toxicity. I think every benzo I found studies that any one is either carcinogenic or genotoxic or both and if I found a study which says a benzo isn't either of these I would find another study that says it is.
Also things like gabapentin/pregabalin, which seemed like ones I would have otherwise liked to try, I read cause tumors in rats. So that worried me.
I don't get why downers seem to be so toxic. But the question is, how much is the risk of cancer and tumors and such increased from taking a given downer a couple of times a week?
I read a study about the carcinogenicity of benzoes lately and it said the risk increase from long term use of the sample group studied was something like 15-20% increase risk of cancer. That is a very high figure! although the study said they had been using some form of benzo daily for several years.
Oh ye and what of the z drugs like zopiclone which I read are the most carcinogenic of the lot. I found these the best for me in the past in terms their direct utility at inducing sleep without annoying side effects (the oft maligned metallic taste didn't bother me) while not making you too groggy the next day but I haven't taken them again since I found out they were so carcinogenic.
And etizolam would fall into the same camp? toxicity wise? there have been no 'official' toxicity tests I could find and the medical literature just said they haven't been done but I suppose since it has been used for a long time in india and such we can infer it has the same sort of toxicity profile as the better known classical benzos.
So how much does it increase from the couple times a week sporadic use? How much more would the risk be compared to baseline at this kind of use?
Also 2m2b is it still in the risky research chemical kind of zone in terms of speculated toxicity? I know they say it is proven to be less toxic than alcohol in terms of its metabolism because it doesn't produce that same toxic byproduct normal alcohol does but what about carcinogenicity and genotoxicity? we just don't know eh? is it a 'safer bet' to take these benzoes that are indeed proven to have some of either of the aforementioned toxicities as the risk is minimal in moderation?
2m2b sounded very interesting to me as I read it as a mix between a barb feeling and alcohol with much heavier sedation than alcohol with no hangover. That sounds great minus the camphor smell it is said to make your body give off but the question mark about its toxicity is what really put me off trying it.
I know we know well that alcohol causes cancer and many people drink in moderation their whole lives. So is it the same with benzoes and the gabapentoids with tumors and whatever else that is used commonly in medical practice but has some proven toxicity? and would 2m2b be out on its own in more risky territory again?
I am just trying to get an idea of the general relative increase of risk above baseline with the couple of times a week/now and then kind of sporadic use I mentioned.
GHB or opiods seem the only safe bets in terms of lack of toxicity however I don't get on well with the gaba b drugs as my previous posts attests so I have still been searching for a good depressant to induce sedation and sleep (on occasion if required) but as I said all the others seemed to have these proven toxicities.
But as I looked up downers nearly ALL of them I found studies saying they have some horrible toxicity. I think every benzo I found studies that any one is either carcinogenic or genotoxic or both and if I found a study which says a benzo isn't either of these I would find another study that says it is.
Also things like gabapentin/pregabalin, which seemed like ones I would have otherwise liked to try, I read cause tumors in rats. So that worried me.
I don't get why downers seem to be so toxic. But the question is, how much is the risk of cancer and tumors and such increased from taking a given downer a couple of times a week?
I read a study about the carcinogenicity of benzoes lately and it said the risk increase from long term use of the sample group studied was something like 15-20% increase risk of cancer. That is a very high figure! although the study said they had been using some form of benzo daily for several years.
Oh ye and what of the z drugs like zopiclone which I read are the most carcinogenic of the lot. I found these the best for me in the past in terms their direct utility at inducing sleep without annoying side effects (the oft maligned metallic taste didn't bother me) while not making you too groggy the next day but I haven't taken them again since I found out they were so carcinogenic.
And etizolam would fall into the same camp? toxicity wise? there have been no 'official' toxicity tests I could find and the medical literature just said they haven't been done but I suppose since it has been used for a long time in india and such we can infer it has the same sort of toxicity profile as the better known classical benzos.
So how much does it increase from the couple times a week sporadic use? How much more would the risk be compared to baseline at this kind of use?
Also 2m2b is it still in the risky research chemical kind of zone in terms of speculated toxicity? I know they say it is proven to be less toxic than alcohol in terms of its metabolism because it doesn't produce that same toxic byproduct normal alcohol does but what about carcinogenicity and genotoxicity? we just don't know eh? is it a 'safer bet' to take these benzoes that are indeed proven to have some of either of the aforementioned toxicities as the risk is minimal in moderation?
2m2b sounded very interesting to me as I read it as a mix between a barb feeling and alcohol with much heavier sedation than alcohol with no hangover. That sounds great minus the camphor smell it is said to make your body give off but the question mark about its toxicity is what really put me off trying it.
I know we know well that alcohol causes cancer and many people drink in moderation their whole lives. So is it the same with benzoes and the gabapentoids with tumors and whatever else that is used commonly in medical practice but has some proven toxicity? and would 2m2b be out on its own in more risky territory again?
I am just trying to get an idea of the general relative increase of risk above baseline with the couple of times a week/now and then kind of sporadic use I mentioned.
GHB or opiods seem the only safe bets in terms of lack of toxicity however I don't get on well with the gaba b drugs as my previous posts attests so I have still been searching for a good depressant to induce sedation and sleep (on occasion if required) but as I said all the others seemed to have these proven toxicities.
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