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[Mega] Opioids (codeine, hydrocodone, oxycodone, heroin, etc.) and Ecstasy

most of u make me laugh honestly.. im not trying to sound like a prick, but come on now... u pop 2,3,4 or more illicit ecstasy tabs, but god forbid you want to combine tylenol with it. does this seem somewhat ridiculous to only me? and opiates with mdma... wow, take some morphine/methadone/oxy with mdma and your body will be buzzing like never before... its an amazing combination and has never reduced my roll, only made it better, even on as little as 2 tabs and 10mg methadone with mild tolerance..
 
mattn said:
most of u make me laugh honestly.. im not trying to sound like a prick, but come on now... u pop 2,3,4 or more illicit ecstasy tabs, but god forbid you want to combine tylenol with it. does this seem somewhat ridiculous to only me? and opiates with mdma... wow, take some morphine/methadone/oxy with mdma and your body will be buzzing like never before... its an amazing combination and has never reduced my roll, only made it better, even on as little as 2 tabs and 10mg methadone with mild tolerance..

How much do you actually know about the pharmacology of acetaminophin?

What amazes me is the fact that people bitch about the DEA and emergency scheduling of MDMA and how illogical (not to mention potentially unconstitutional) it was and yet these same people think that just because you can buy Tylenol over the counter it is safe as hard candy, as if suddenly the scheduling whims of the agency are rational in this case.

Depending on the individual, toxicity begins at around 4g. That's just 8 Extra Strength Tylenol. Not much of a margin for people who pop three at a time.

Toxicity is definately developed even in adults around 7g.

These figures are substantially reduced for alcholoics, malnourished or anorexics, or if you've been drinking prior to taking the stuff.

Describing the toxicity itself:

"In acute overdose or when maximum daily dose is exceeded over a prolonged period, the normal pathways of metabolism become saturated. Excess APAP is then metabolized in the liver via the mixed function oxidase P450 system to a toxic metabolite, N-acetyl-p-benzoquinone-imine (NAPQI). NAPQI has an extremely short half-life and is rapidly conjugated with glutathione, a sulfhydryl donor, and removed from the system. Under conditions of excessive NAPQI formation or reduced glutathione stores, NAPQI is free to covalently bind to vital proteins and the lipid bilayer of hepatocytes; this results in hepatocellular death and subsequent centrilobular liver necrosis." (Susan E. Farrell, MD "Toxicity, Acetaminophen.")

Acetaminophen is among the most common causes of overdose reporting to American Poison Control Centers. It is the number one cause of hepatic failure related liver transplants in both the U.S. and the U.K.

Wonder why no one has bothered to schedule it?

It's not a pleasent overdose either. Again from Farrell:

Phase 1 (0-24 h)
Asymptomatic
Anorexia
Nausea and vomiting
Diaphoresis
Malaise

Phase 2 (18-72 h)
Decreasing symptoms of phase 1
Right upper quadrant abdominal pain and rising liver enzymes (alanine aminotransferase [ALT], aspartate aminotransferase [AST])

Phase 3 (72-96 h)
Centrilobular hepatic necrosis with accompanying abdominal pain
Jaundice
Coagulopathy
Hepatic encephalopathy
Recurrence of nausea and vomiting
Renal failure
Fatality

Phase 4 (4 d to 3 wk)
Complete resolution of symptoms
Complete resolution of organ failure

Yum! Pass the Tylenol!
 
Yeah, I don't think you're gonna find anyone over the age of about 5, who is going to get clinically relavent liver damage from 4000mg of acetaminophen.

There's also limited evidence that in reality, alcoholics are that much more susceptable to acetaminophen damage.
 
Herron makes aspirin, acetaminophen (called paracetamol in Australia) and ibuprofen painkillers. Don't rely on brand names, read what's on the box FFS.

I agree that the risk from taking 1000mg acetaminophen is pretty low. However of the three I've mentioned, which is the safest? I've always suggested and taken ibuprofen, as I thought it was the least likely to contraindicate. Am I wrong?
 
As a few people have said, if I have a headache before I roll, the Mdxa always makes it feel allll better. :)

The only experience I've had with E and painkillers was when I came home from a party and had an awful headache. My mom gave me one of her Vics... it was either 7.5 or 10, dun remember. But this was a good 12-15 hours after I had dropped the E... So, I took the vic, sprawled out in a chair... and proceeded to talk my mom's ear off. XD It was a really nice, suble E feeling.. I'm assuming the normal vic affects coupled with the recent E use made it feel more like the happy E feeling. Didn't have any adverse symptoms though. *shrugs*
 
"I'll also be tempted to take opiates during the comedown"

Agreed, and I have given in the last few comedowns...I just make sure not to take too many as I'd rather not too ingest too much of the APAP mixed with them...
 
i wouldnt take a painkiller before dropping because the head ache usually goes away any how. Im talking about afterwards.. A few days after ive taken an e i have a head ache, which feels as if its coming from eye strain, which is likely because of the size my pupils reach....

Interested in knowing how long to wait till i take a painkiller and wats best to take.
 
tramadol and mdma

I know that being on an SSRI inhibits your ability to roll until several weeks after you come off. I have been taking tramadol about twice a week for a month. I know it's a mild SNRI or SSRI so is it possible to roll a week after last tramadol use?
 
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The half-life of tramadol is about 5 hours, and it's metabolite about 9 hours. After a week you'll be fine, though you may experience slightly muted effects.

Here's a graph of the amount remaining in your system, t axis plotted in days
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Actually another source I found says the half life is 6-7 hours. Eh, it's close enough anyway.
 
It's got SSRI effects. Tramadol is nasty stuff... the amount of seizures it induces in people is quite unreal.

Anyway, it is unlikely that it will effect your roll....
 
I have read reports of both in the archives. Very few though. It would be nice for a definitive answer or someone that has tried it.

I believe tramadol has more of an SNRI effect. Is this true? If it does affect the serotinin levels significantly should 2 weeks of waiting be enough without a doubt?

thanks for the half-life info!
 
BilZ0r said:
It's got SSRI effects. Tramadol is nasty stuff... the amount of seizures it induces in people is quite unreal.

Anyway, it is unlikely that it will effect your roll....
are the seizures the only thing i have to worry about? i never will exceed 150mg so i dont think i need to worry about seizures. is it "nasty stuff" for any other reason?
 
Be very carefull, according to the MIMS, basically the drug information book for docs/nurses/pharms, tramadol is actually an MAOI, MAOI+MDxx=dangerous, and MAOI's can be dangerous even after their halflife has expired
 
I didn't think tramadol was an MAOI.

Hennies HH, Friderichs E, Wilsmann K, Floh e L.
Effect of the opioid analgesic tramadol on inactivation of norepinephrine and serotonin.
Biochem Pharmacol. 1982 Apr 15;31(8):1654-5.

Looks like that paper would have the answer, but I can't find access to its abstract
 
so selective seretonin reputake inhibitor means that seretonin can't be released while on an SSRI?

I guess I'll wait a while to roll. :(

It's been over 3 years.
 
selective serotonin reuptake inhibitors (SSRIs) block serotonin reuptake transporters. MDMA works by being brought into a brain cell and causing the transporter to work in reverse. Becuase SSRIs block the transporter, MDMA can't get into the cell, and hence it can't work.
 
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