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  • BDD Moderators: Keif’ Richards

Misc Ketamine - is it OK to do it every day?

yo ~ fair warning EGCG, when concentrated in pill form - can be awful for your liver. The amounts of ECGC found in Green Teas are the amounts your body finds beneficial. Higher concentrated doses have caused liver damage - like; acutely.
Yeah, it's toxic to the liver, but AFAIK it's toxic when taken more than 900mg I believe; my supplements were 700mg, and I take it about 1-1.5 hours prior to doing a line of K. But taking the 700mg supplement every day is toxic as well.

But honestly, I still felt a little pain during urination even with ECGC (same symptom when taking K without ECGC), so it didn't help much. But the benefits I was getting didn't supersede the side effect, so (at least for me) it wasn't worth damaging my bladder.
 
Just because no issues with your bladder yet doesn't mean you aren't doing damage. I'd chill if I was you.
If you feel like you haven't done too much drugs, it is only because you haven't made there yet.
There is often so narrow or non-existent window between warning signs and damage
Sometimes warning signs are direct result of damage done already
 
It's good to see others using PubChem and related databases. We CAN all have free access to the best scientific information. I tied to be subtle, I tried not to be obvious BUT BL now needs to host Sci-Hub or it will ALL be blocked.

I have a copy so anyone who can manage a tape-backup drive is welcome to a copy. As it is, I host the thing myself.
 
I can’t remember where I saw it but evidence suggests that even once a month use of ketamine damages the bladder but it can heal if you stop use.

So using daily you’re asking for trouble.

Also remember that if you’re using intramuscular the dose is twice as potent as intranasal, so it’s cheaper and lasts you longer and will do less damage as you’re not using as big of a dose.
Remember you must use pharma grade ketamine or micro-filters when injecting intramuscular. 👍
 
No data on MXE. I mean, it's x3 the potency of K and if resolved, x6 K....
So people wanting to use and keep bladder safe will use (S) MXE. I say this because MXE producers can CLEARLY do this. That we accept racemic K is on us,
 
No data on MXE. I mean, it's x3 the potency of K and if resolved, x6 K....
So people wanting to use and keep bladder safe will use (S) MXE. I say this because MXE producers can CLEARLY do this. That we accept racemic K is on us,

MXE was the shit but is no longer around after the US govt/Obama got China to ban it back around 2014/2015 or am I missing something?
 
Well someone who chased the patens did even better....`


The bottom one is x2 methoxetamine which is, in turn, x3 ketamine.

The name is merely expedient. I know over 130 patents were searched and for whatever reason, it got a patent all to itself. Generally it's because people panic that someone would like to patent it first.... but who knows.

So 10-15mg would work. 5-7.5 of the (S) isomer.
 
It's in a patent. I have published the patent and all the references a couple of times. The trick is - it's a GB patent, not a US patent. Their was a reason for that as well.
 
Yep, I used a needle to IV a few days ago and while I didn’t weigh my dose I’m guessing it was between 80 - 120mg. Was transported straight out of my body and into the most beautiful infinite landscape. Can’t describe what went on exactly but when I emerged, I burst into sobs of tears or job and just couldn’t stop for quite some time. Was truly incredible. I upped the dosage a few days later and that one, well, I believed I saw the universe and our place as life within it as it ‘truly’ is. Blown away doesn’t come close.

You know, I don't think their is ANY data to see if (S) ketamine (esketamine) is more/less or equally toxic to the bladder as (R) ketamine (arketamine). I think medically a lot of nations now use pure (S) ketamine which is the isomer that is an NMDA antagonist (the thing that makes you trip) whereas (R)ketamine is a weak NMDA antagonist but a DRI as potent as cocaine.

I'm almost 100% certain that all of the people who end up on crazy doses of ketamine are using the racemate (an equal mixture of both isomers).
 
Well S is more potent and that makes it less damaging. I never found it really better than racemic stuff but having to snort less was nice. When I used to get it back in the day I used to read how S is somewhat more psychedelic but I think that’s a wrong word, it’s more energetic I would say.
 
Well S is more potent and that makes it less damaging. I never found it really better than racemic stuff but having to snort less was nice. When I used to get it back in the day I used to read how S is somewhat more psychedelic but I think that’s a wrong word, it’s more energetic I would say.

Yes - I didn't take much because I was warned that it was a DRI but everyone else in the room was using it like cocaine i.e. ALL of it was used with people redosing every 20-30 minutes.

Have you noted that benocyclidine, a close relative of PCP is a pure DRI? It has been detected in fake MDMA tablets. I briefly talked to the French guy who had the unenviable job of finding the appropriate dose. He mentioned that had an extremely steep dose/response curve and displayed (subjective) toxic symptoms only slightly above an active dose.

He remarked that he had tried 60mg and 'was glad I didn't go any higher or I would never have tested anything EVER AGAIN' (my capitalizations) by which I infer that 60mg almost killed him.

I don't consider a TI of less than 6 to make it a reasonable product to market. To misrepresent it as another drug on top of that strongly suggests that the makers were callous and/or unable or unwilling to simply market the product truthfully OR throw it away.

The latter seems rare but a good friend of mine in The Netherlands (the guy who made the MDMA tablets with the Audi TT logo on it was sold 5Kg of 4-MTA and he did indeed destroy it (and possibly whoever sold it to him) rather than put the lives of customers at risk. He has 2 kids of his own and recognized that THEY could have become victims.
 
Hell no, it fucks up your bladder and urinary tract. Plus, ketamine builds up a ridiculous tolerance super fast. Idk what do ppl find cool about ket, it's not even euphoric at all. It's just a weird anesthetic, you lose coordination, feel dizzy but 4 me it doesn't feel good at all. I'll never understand k-heads.
I dont stand by the "I don't get how people like x substance so much" claim. I love ket and salvia, I dont see why people like cocaine so much.

But yes. Say thst again. It can destroy your bladder
 
I dont stand by the "I don't get how people like x substance so much" claim. I love ket and salvia, I dont see why people like cocaine so much.

But yes. Say thst again. It can destroy your bladder
Haha.
Time changes ppl. I went through a K phase during late 2024 and all this year. Ive been IMing pure ketamine vials 500mg/10ml ketanir brand.
Jesus Christ I miss the kholes-trips-revelations I had months ago, I have a permatolerance now and no matter how much I stay clean for I don't get those cool FX no more.
I wanna slap myself from the past for saying that ket isn't euphoric, it's one of the best drugs out there to trip.
But yeah the side effects deter me from using it again too.
Cheers man
 
The latter seems rare but a good friend of mine in The Netherlands (the guy who made the MDMA tablets with the Audi TT logo on it was sold 5Kg of 4-MTA and he did indeed destroy it (and possibly whoever sold it to him) rather than put the lives of customers at risk. He has 2 kids of his own and recognized that THEY could have become victims.
Audi TT, these were very good MDMA. Att their 2 dominating pill s.
This one with around 80 mg MDMA, and Marlboro s with average 118 mg MDMA.
Everyone went for the high dose, i for the TT s. [both tested] pure.
Good Chemist vs bad chemist, MDMA should be MDMA.

Well obvious it isn t. Even in equivalent doses TT way better.
Then Marlboro shit, once i had real weird HQ MDMA powder.
Came up like say Psilocybine/ psychedelic.
Real slow never developed into a psychedelic, only the come up.
The 'Roll' was characterised by real evident long slow waves sinus,
from lucid to out of my mind, no over pronounced empathy or euphoria.
No comedown, day after blues.

So you had MDMA like that, TT the hybrid, these were emphatic and euphoric.
Kicked in as MDMA. And MehDMA 'the Marlboro'. The other side of the spectrum.

The difference between em remarkable, the TT were warmer, softer.
a more pleasant overall experience, slow waves, not high speed like the Marlboro.
That didn t feel any stronger, just less pleasant/ bad made MDMA ?

throwing away that 54 kg. was a gift to humanity. My friend a speedfreak too.
They took 4-MTA [still legal then] with MDMA. As then you got totally mashed.
Maybe their tolerance to drugs saved em, i read no deaths.

But the leftover that were sold to the UK, 'Flatliner s' they were called.
Did a killer round Brittain. If my meory s serves me correct.
I never bought that one, i read Bluelight and Erowid.
 
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Haha.
Time changes ppl. I went through a K phase during late 2024 and all this year. Ive been IMing pure ketamine vials 500mg/10ml ketanir brand.
Jesus Christ I miss the kholes-trips-revelations I had months ago, I have a permatolerance now and no matter how much I stay clean for I don't get those cool FX no more.
I wanna slap myself from the past for saying that ket isn't euphoric, it's one of the best drugs out there to trip.
But yeah the side effects deter me from using it again too.
Cheers man
I didnt realize it had a magic to be lost like molly. I abused grams a night. My friend said that molly can keep its magic, you just need to do more each time. Thst thought terrifies me so I only do molly less than once every two years. Ket however, I just did more and more and more. 500 mg lines all night. Leaking and frosting my mustache. It seems to fuck with memory somewhat similar to cocaine. I guess the only drug that is good with no side affects is moderate caffiene. Probably moderate ket/mushrooms too but i threw moderation out the windows like 5 years ago... besides with molly, thst shit scares me, I feel like it skins your brain of its serotonin receptors.
 
I didnt realize it had a magic to be lost like molly. I abused grams a night. My friend said that molly can keep its magic, you just need to do more each time. Thst thought terrifies me so I only do molly less than once every two years. Ket however, I just did more and more and more. 500 mg lines all night. Leaking and frosting my mustache. It seems to fuck with memory somewhat similar to cocaine. I guess the only drug that is good with no side affects is moderate caffiene. Probably moderate ket/mushrooms too but i threw moderation out the windows like 5 years ago... besides with molly, thst shit scares me, I feel like it skins your brain of its serotonin receptors.
Omg, you never experienced k cramps before? Even with a few shots of ket, I have some discomfort while peeing
 
Never severe enough for me to care.
U haven't done enough them or u get fked up easily on k.
For us long term users(abuser in my case), ketamina give me so many problems for peeing, bladder pain an shit so I don't indulge anymore
IN kay-tamine. Anyway cheers man, enjoy it while u can. I fucked up my tolerance forever, don't be as stupid as me, kids. Safe tripping.
 
U haven't done enough them or u get fked up easily on k.
For us long term users(abuser in my case), ketamina give me so many problems for peeing, bladder pain an shit so I don't indulge anymore
IN kay-tamine. Anyway cheers man, enjoy it while u can. I fucked up my tolerance forever, don't be as stupid as me, kids. Safe tripping.
5 grams will last me 3 days max if i try to save it. Its been this way for over 2 years. I do it pretty much more days than I don't. I wouldn't say it gets me fucked up easily, I'm just on my way to tearing up my system though im not there yet. And if I do, that's okay, I'll just do more to make me numb. (In all seriousness I dont want to downplay the damage it does. I just personally dont feel pain from it)
 
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