• Psychedelic Drugs Welcome Guest
    View threads about
    Posting RulesBluelight Rules
    PD's Best Threads Index
    Social ThreadSupport Bluelight
    Psychedelic Beginner's FAQ
  • PD Moderators: Esperighanto | JackARoe | Cheshire_Kat

The Big & Dandy DXM Thread

Status
Not open for further replies.
i've tried DXM a few times and it seems every time the trip it so intense that i dont remember any of it. it also doesnt kick in until i vomit (which happens every time without fail 45min - 1hr after injesting). The 3 times ive taken it ive always done around 300 - 400mg (using coricidin) and since i cant really remember it i've just always thought of it as undesirable. It's been a long time since i've tried it and ive become alot more experienced using LSD and mushrooms and savia. i've thought alot about this and i figured i want to try it again. any suggestions? i want to be able to get the most out of it. i stay convinced i can learn something from this crazy chemical.
 
Of course you vomit. No body likes Suiciden {its slow suicide}. Buy some product with only DXM as the active ingredient. If you live anywhere near snivelization, finding a toxin-free DXM preparation should be trivial. I never vomited or even felt queasy and took many 500mg doses of syrup - free of nasty toxic additives. Read Erowid's Guide to DXM in Non-Prescription Drugs to find out the other nasties to avoid as well.

I have read many DXM reports with CPM included in the dose [Erowid is so concerned about this that they explicitly post CPM at the top of any DXM reports that include it]. Those who have used only a few times are usually positive, but virtually all the long-term users are either dead or survived by stopping their CPM ingestion. The correlation is just so tight that it's remarkable the product hasn't been pulled from the market decades ago. Or rather, its a remarkable testament to the power of corporate lobbying dollars over medical research and clinical reports.

The 'net is chock-full of evidence that this compound is leaving a trail of brain damage and death wherever it is used in overdosage, in particular among those taking Coriciden and other CPM-containing preparations for the DXM content.

One of Chlorpheniramine Maleate's classic characteristics is it causes nausea and vomiting in overdosage: "Symptoms Of Overdose In Children May Include Dizziness, Nausea/vomiting..."

A post on this very forum indicates what so many others have experienced:

Other Coriciden long-term effects noted by various forum users: stomach pain, permanent gastrointestinal damage, permanent vision damage (bright/black spots). The permanent nature of these physical damages even outside the brain is particularly concerning. Vision, for example, never recovers from permanent damage because the retina doesn't regenerate.

Furthermore, antihistamines including CPM cause drowsiness and loss of recall (amnesia) in overdosage. So don't expect to remember your trips. Your body will soon remember the taste though.

Chlorpheniramine Maleate in particular, especially combined with DXM and taken repeatedly, seems to cause a progressively worsening health condition and often results in death. Former users often report intense nausea at just the sight/smell/taste of their formerly-used CPM-containing preparation.

Overdosage of CPM can also cause Serotonin Syndrome: "chlorpheniramine has been shown to work as a Serotonin-norepinephrine reuptake inhibitor".

Serotonin syndrome in dextromethorphan ingestion responsive to propofol therapy:

"An 18-year-old male developed a severe serotonin syndrome after recreational ingestion of Coricidin HBP (chlorpheniramine 4 mg and dextromethorphan hydrobromide 30 mg). Propofol infusion rapidly normalized his agitation, neuromuscular hyperactivity, and autonomic instability. Confirmatory analysis demonstrated a dextromethorphan serum concentration of 930 ng/mL. Dextromethorphan can produce serotonin syndrome in the absence of another serotonergic drug."​

The abstract claims, contrary to the evidence it produces and showing no other, that 'Dextromethorphan can produce serotonin syndrome in the absence of another serotonergic drug.'

Having offered not a single case to support the statement, I'll do one better than the authors of the above case report and demonstrate the opposite: that such cases are nonexistent, or so exceedingly rare that careful searching does not turn them up. Not being able to find a single DXM-only case of Serotonin Syndrome after extensive Google searching, all that can be found are cases of combination with CPM or other serotonin agonists or reuptake inhibitors. If anyone can find a DXM-only Serotonin Syndrome report please post or PM.

This forum thread reports lots of nasty experiences combining DXM with serotonergic agents: DXM+Prozac=serotonin syndrome

The title of this thread on the Drugs and Booze forum speaks loudly: DXM + Diphenhydramine, IS NOT SAFE!

Diphenhydramine (as too Dimenhydrinate) are both, like Chlorpheniramine Maleate, antihistamines and quite toxic in overdosage. In addition, and unlike CPM, Diphen and Dimen are also potent anticholinergics, which raises another danger of toxicity. Anticholinergic toxicity produces a psychosis of its own, often long-lasting as a perusal of Erowid reports indicates.

It can be expected that overdosing on both DXM and either Dimen or Diphen would produce two distinct toxic effects: Anticholinergic toxicity and Serotonin Syndrome. Indeed, a quick Google and there we have it folks:

SEROTONIN REUPTAKE INHIBITION BY DIPHENHYDRAMINE AND CONCOMITANT LINEZOLID USE CAN RESULT IN SEROTONIN SYNDROME

In the case concommitant Linezolid enhanced the serotonin syndrome by inhibition of both MAO functional variants. Though the case does not involve DXM, it demonstrates the potency of both Dimen and Diphen as serotonin-syndrome co-inducers when combined with a secondary agent.

Together, the case report with previously linked forum threads which contain substantial use reports on DXM with serotonin reuptake inhibitors or agonists paints a clear picture of an unwise, and sometimes deadly combination.

Beyond all this, one might indulge in a little speculation. Why does it seem Coriciden is somewhat more addictive than DXM-only preparations? It doesn't seem that the acquisition demographic is sufficiently different to account for the observation.

A suspicious thread of addictivity runs through the many hundreds of Coriciden reports thus far reviewed. Something more than DXM alone. It seems another actor, or perhaps a pair of them, is playing a tune behind the mainline. Or was it a masquerade?

DXM itself has a mild SSRI effect when taken alone. When taken with an overdose of CPM, serotonin receptor activation can easily surpass damaging levels. Regardless of serotonin syndrome damage, one or both of reception and production within the serotonin system is adaptively re-regulated. ie. receptor downregulation/destruction, and ligand production decrease.

Thus the unique combination of DXM with CPM can produce a single or double effect on the serotonin system, depending on dose. Re-regulation at low doses, receptor/cell death at higher doses. As two agents acting simultaneously via differing molecular mechanisms, they can together achieve more than either apart. That is called synergy.

A second synergy amplifies the first - both DXM and CPM share a single breakdown enzyme, and together saturate it leading to multiplicative potentiation:


Because CPM is far more toxic on a weight basis than DXM, the effect in a combined formulation is that DXM enhances CPM's effects and toxicity by inhibiting its breakdown metabolism via the shared isoenzyme.

Either or both of these paths leads to a chronically depressed state post-trip. One that worsens with each trip {somewhat like the post-MDMA binge depression}, yet is only relieved while intoxicated with the unique, and uniquely destructive, combination of high-dose DXM and high-dose Chlorpheniramine Maleate.

In short, Coriciden is uniquely pleasureable - often addictively so - because of the way that both DXM and CPM mutualistically multiply by co-potentiation their individual effects to increase serotonin receptor activation. That happy, almost MDMA-like song of joy quickly leads to a drain of sorrow for the repeat user. For that unfortunate individual, both the pleasure and pain are together sinking in an ocean of tolerance:

... and with repeated use the water level rises, often leading to dose elevation and enhanced serotonergic destruction in a futile, repetitive spiral. As the dose is raised, psychosis from CPM and DXM becomes ever stronger.

With repeated dosing, it leads to ever-worsening chronic depression due to one or both of downregulation and toxicity in the serotonergic system, often followed by psychosis, hospitalization, and death, as so many reports testify.

At first the glad master, the frequent user becomes a damaged slave to this toxic combination. Often continued knowing the nausea and vomiting to come, the evils of dosing show by their weight the counterweight of pleasure hanging like fruit from this miserable concoction.

Luckily, it is a simple matter to avoid such dangerous combinations: the careful shopper can have his cake and eat it too, with a little ingredients label reading.
 
Last edited:
As a sidenote, if the hypothesis is true then a firstline treatment for Coriciden addiction would be replacement of the serotonergic effect with a non-toxic SSRI, which would usually require discontinuation of DXM concurrency to avoid a continuation of or risk of serotonin syndrome.

It would be vital to avoid CPM, DXM and particularly combinations of the two (relapse) during SSRI treatment due to doubly enhanced serotonin syndrome.

Such interventions would be more successful early in the decay cycle for obvious reasons.
 
i've tried DXM a few times and it seems every time the trip it so intense that i dont remember any of it. it also doesnt kick in until i vomit (which happens every time without fail 45min - 1hr after injesting). The 3 times ive taken it ive always done around 300 - 400mg (using coricidin) and since i cant really remember it i've just always thought of it as undesirable. It's been a long time since i've tried it and ive become alot more experienced using LSD and mushrooms and savia. i've thought alot about this and i figured i want to try it again. any suggestions? i want to be able to get the most out of it. i stay convinced i can learn something from this crazy chemical.
If you're getting amnesia from such a low dose, it is possible that you have the CYP2D6 enzyme deficiency (this enzyme is a major metabolic catalyst for breaking down DXM). Because a significant portion of the population has this deficiency, it is always recommended to start low with this substance, like 100 mg, and in case of an unusually strong reaction to such a low dosage steer clear of this this substance altogether.
 
Tolerance/diminishing effects of DXM after very little use?

My rabbit has been using dex for about 3 months now, normally leaving 1 to 2/2+half weeks in between trips. She weighs about 126lbs. The stomach content was always little on all occasions, consuming food about 4 hours beforehand and always using syrup, i.e Benalyn Dry Cough Non-Drowsy, Vicks Cough Syrup with honey (this is a relatively new dextrometorphan only syrup available in the UK) of course Robitussin Dry Cough and Rhinathiol Adult. She has tripped 7 times in those past months, first time dose being 150mg, second 350mg, third 390mg, fourth 230mg, fifth 210mg, sixth 410mg, and yesterday 265mg. Apart from the first 3 occasions, she has used grapefruit juice to potentiate. When taking that 230 and and 210 dose she took it the day after the other. That 210 mg did hardly anything for her, apart from the full body buzz, cognitive impairment and double vision. Apart form that very fisrt time taking DXM they were all 2nd plateau experiences, maybe that 410mg being the transitional phase between 2nd and 3rd. After that 210mg dose she didn't get hardly any CEV's and barely any 'mental' effects. It felt like she maybe hit a wall or something. Over 350mg she gets extremely confused, and has black-out moments, where she does not remember anything that happens over a course of time, and the same time feeling very agitated sometimes even anxious, even though my rabbit finds the experience mostly pleasant and enjoyable. That 390mg experience left my rabbit heavily dissociated, and she was sure that she was suffering from hypomania for a week after the trip. It was getting to the point that she thought she may have to take a visit to the doctors since she felt she may have had some screws loose. Eventually it stopped gradually over a course of another 3-4 days. She heard that piracetam might help with dxm hangovers, -which my rabbit gets the worst of unfortunately- so she took some for two days following the 410mg trip. It seemed to work, so she stopped, but a day after the dysphoric and lethargic afterglow came on, probably twice as bad as on previous occasions.

Yesterday when she took that 260mg she barely felt anything. My rabbit had a decent buzz and some weird trail of thought, then after 3 hours it all seemed to stop very suddenly, resulting in a very unpleasant comedown, which left her extremely annoyed. Knowing that she couldn’t have went to sleep just like that (my rabbit becomes insomnic on dex) she took two benzos, (xanax) altogether 1mg. After what seemed like an eternity she fell asleep, but does not remember what happened after she took the xanax. Around 5 o’clock in the morning she woke up feeling extremely disorientated, sick and nauseos, and she has never previously thrown up before, or even had an upset stomach because of dxm. She was sure she was going to puke, so she lay in her bed motionless, waiting for it to happen. But then she fell asleep again, waking up in the morning still feeling the bodyload from dex, but generally feeling relaxed and content, probabaly because of the xanax. My rabbit got up this afternoon and feels like crap, and finds it hard to complete just about any task that involves the slightest bit of effort. The question is, has my poor rabbit hit some kind of a wall with dex or is her tolerance very rapidly growing? Any insightful suggestions would be well appreciated.
 
Anyone, any ideas what might have happened? My rabbit doesn't wan to give up dxm and she doesn't think she could.
 
Ketamine is not easy to find in my rabbit's area. In fact, it's virtually impossible most of the time.
 
DXM tolerance can build rapidly and last for quite a while. Also if bunny is dosing much she should avoid benylin like the plague, the inactive ingredients in the syrup can make life unpleasant if you take much. Best to find another product.
 
Hmm, as far as the rabbit is concerned, Benylin and Robitussin are the only DXM product available without perscription in the UK. Robitussin comes only in 100ml bottles and it's just not worth the money. Along with that Vicks syrup which doesn't contain much of the stuff. Tesco's used to have something but they took it off the shelves and the nice sales lady person looks at my bunny suspicious when she asked if they have any.
 
the triple Cs are much harder on your memory than dxm-only preparations. the triple Cs make it feel like your tripping dramamine and dxm at the same time. you shouldn't have much memory problems in that dose range with a dxm-only preparation. try bringing a notebook and jotting down "key phrases." you can keep track of pretty much every thought-train you had with diligent note-taking.

i think coricidin experiences are mostly insanity and weirdness. pure dxm is preferable in pretty much every way. way healthier, too. don't doubt the damage that coricidin does.
 
I sympathise with bunny in this respect, buying dxm from the shops in this country is not as easy as across the pond. I even thought our robitussin was different and non-dxm
 
I believe this is the one. Only 7.5mg/5ml mind. Same as Benylin.
*snip*
 
Last edited by a moderator:
As this is specific to the UK the DXM in the UK thread in EADD may be of some help to you too. Please leave the bunny behind though - "I" will do just fine or "a friend" if you are especially paranoid about "I" :)

Tolerance to DXM is covered extensively in the DXM thread so I'll pop this one one over there for you to have a read through :)

Also, as you're in the UK it's probably easier to get hold of ketamine as suggested above than it is DXM - cheaper and way more fun too =D
 
Anyone else got any recommendations of what to mix with the syrup? Dosing tonight & I cant stand the taste of the syrup. It takes me about 15 minutes to keep taking shot after shot til i get to 600mgs. I've tried mixing it with Coke but it still tastes shit
 
Also, how come the Robitussin DX syrup takes so long to kick in? At about an hour i start to feel something then another half hour i start to peak and dont worry bout my last post i already drank the feral tasting shit 5 mins ago hahaha
 
My rabbit has been using dex for about 3 months now, normally leaving 1 to 2/2+half weeks in between trips. She weighs about 126lbs. The stomach content was always little on all occasions, consuming food about 4 hours beforehand and always using syrup, i.e Benalyn Dry Cough Non-Drowsy, Vicks Cough Syrup with honey (this is a relatively new dextrometorphan only syrup available in the UK) of course Robitussin Dry Cough and Rhinathiol Adult. She has tripped 7 times in those past months, first time dose being 150mg, second 350mg, third 390mg, fourth 230mg, fifth 210mg, sixth 410mg, and yesterday 265mg. Apart from the first 3 occasions, she has used grapefruit juice to potentiate. When taking that 230 and and 210 dose she took it the day after the other. That 210 mg did hardly anything for her, apart from the full body buzz, cognitive impairment and double vision. Apart form that very fisrt time taking DXM they were all 2nd plateau experiences, maybe that 410mg being the transitional phase between 2nd and 3rd. After that 210mg dose she didn't get hardly any CEV's and barely any 'mental' effects. It felt like she maybe hit a wall or something. Over 350mg she gets extremely confused, and has black-out moments, where she does not remember anything that happens over a course of time, and the same time feeling very agitated sometimes even anxious, even though my rabbit finds the experience mostly pleasant and enjoyable. That 390mg experience left my rabbit heavily dissociated, and she was sure that she was suffering from hypomania for a week after the trip. It was getting to the point that she thought she may have to take a visit to the doctors since she felt she may have had some screws loose. Eventually it stopped gradually over a course of another 3-4 days. She heard that piracetam might help with dxm hangovers, -which my rabbit gets the worst of unfortunately- so she took some for two days following the 410mg trip. It seemed to work, so she stopped, but a day after the dysphoric and lethargic afterglow came on, probably twice as bad as on previous occasions.

Yesterday when she took that 260mg she barely felt anything. My rabbit had a decent buzz and some weird trail of thought, then after 3 hours it all seemed to stop very suddenly, resulting in a very unpleasant comedown, which left her extremely annoyed. Knowing that she couldn’t have went to sleep just like that (my rabbit becomes insomnic on dex) she took two benzos, (xanax) altogether 1mg. After what seemed like an eternity she fell asleep, but does not remember what happened after she took the xanax. Around 5 o’clock in the morning she woke up feeling extremely disorientated, sick and nauseos, and she has never previously thrown up before, or even had an upset stomach because of dxm. She was sure she was going to puke, so she lay in her bed motionless, waiting for it to happen. But then she fell asleep again, waking up in the morning still feeling the bodyload from dex, but generally feeling relaxed and content, probabaly because of the xanax. My rabbit got up this afternoon and feels like crap, and finds it hard to complete just about any task that involves the slightest bit of effort. The question is, has my poor rabbit hit some kind of a wall with dex or is her tolerance very rapidly growing? Any insightful suggestions would be well appreciated.

Are you eating well during periods of use?
 
Status
Not open for further replies.
Top