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Template:DangerousInteractions/Amphetamines: Difference between revisions
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>BronzeManul m Corrected GHB/GBL warning language to refer to GHB/GBL in place of it previously mistakenly referring to an 'opiate'. |
>Cardboardbox92 Explained the pharmacodynamics of cocaine and amphetamine, and described how the displacement of monoamines due to a pH mediated effect of amphetamine due to Na+/K+ ATPase removes the rewarding effects of cocaine. In simple form, if you've dosed amphetamine before cocaine, then the cocaine will not cause any rewarding mechanisms by a DA mediated mechanism. |
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*'''[[UncertainInteraction::GHB]]'''/'''[[UncertainInteraction::GBL]]''' - Stimulants increase respiration rate allowing a higher dose of sedatives. If the stimulant wears off first then the depressant effects of the GHB/GBL may overcome the user and cause respiratory arrest. | *'''[[UncertainInteraction::GHB]]'''/'''[[UncertainInteraction::GBL]]''' - Stimulants increase respiration rate allowing a higher dose of sedatives. If the stimulant wears off first then the depressant effects of the GHB/GBL may overcome the user and cause respiratory arrest. | ||
*'''[[UncertainInteraction::Opioids]]''' - Stimulants increase respiration rate allowing a higher dose of opiates. If the stimulant wears off first then the opiate may overcome the patient and cause respiratory arrest. | *'''[[UncertainInteraction::Opioids]]''' - Stimulants increase respiration rate allowing a higher dose of opiates. If the stimulant wears off first then the opiate may overcome the patient and cause respiratory arrest. | ||
*'''[[UncertainInteraction::Cocaine]]''' - | *'''[[UncertainInteraction::Cocaine]]''' - The rewarding effects of cocaine are mediated by DAT inhibition, and an increase of exocytosis of dopamine through the cell membrane. Amphetamine reverses the direction of DAT and the direction vesicular transports within the cell by a pH mediated mechanism of displacement, thus excludes the regular mechanism of dopamine release through means of exocytosis because the effects Na+/K+ ATPase are inhibited. You will find cardiac effects with the combination of cocaine and amphetamine due to a SERT mediated mechanism from the subsequent activation of 5-HT2B, which is related to serotonin-related valvulopathy. Amphetamines generally cause hypertension in models of abuse, and this combination can increase the chances of syncope due to turbulence blood flow during valve operation. The rewarding mechanisms of cocaine are reversed by administration of amphetamine. {{#l:Sustained Release d-Amphetamine Reduces Cocaine but not Speedball-Seeking in Buprenorphine-Maintained Volunteers.pdf}} | ||
*'''[[UncertainInteraction::Caffeine]]''' - This combination of stimulants is generally considered unnecessary and may increase strain on the heart, as well as potentially causing anxiety and physical discomfort. | *'''[[UncertainInteraction::Caffeine]]''' - This combination of stimulants is generally considered unnecessary and may increase strain on the heart, as well as potentially causing anxiety and physical discomfort. | ||
*'''[[DangerousInteraction::Tramadol]]''' - Tramadol and stimulants both increase the risk of seizures. | *'''[[DangerousInteraction::Tramadol]]''' - Tramadol and stimulants both increase the risk of seizures. |
Revision as of 19:49, 24 June 2021
- Alcohol - Drinking alcohol on stimulants is considered risky because it reduces the sedative effects of the alcohol that the body uses to gauge drunkenness. This often leads to excessive drinking with greatly reduced inhibitions, increasing the risk of liver damage and increased dehydration. The effects of stimulants will also allow one to drink past a point where they might normally pass out, increasing the risk. If you do decide to do this then you should set a limit of how much you will drink each hour and stick to it, bearing in mind that you will feel the alcohol and the stimulant less.
- GHB/GBL - Stimulants increase respiration rate allowing a higher dose of sedatives. If the stimulant wears off first then the depressant effects of the GHB/GBL may overcome the user and cause respiratory arrest.
- Opioids - Stimulants increase respiration rate allowing a higher dose of opiates. If the stimulant wears off first then the opiate may overcome the patient and cause respiratory arrest.
- Cocaine - The rewarding effects of cocaine are mediated by DAT inhibition, and an increase of exocytosis of dopamine through the cell membrane. Amphetamine reverses the direction of DAT and the direction vesicular transports within the cell by a pH mediated mechanism of displacement, thus excludes the regular mechanism of dopamine release through means of exocytosis because the effects Na+/K+ ATPase are inhibited. You will find cardiac effects with the combination of cocaine and amphetamine due to a SERT mediated mechanism from the subsequent activation of 5-HT2B, which is related to serotonin-related valvulopathy. Amphetamines generally cause hypertension in models of abuse, and this combination can increase the chances of syncope due to turbulence blood flow during valve operation. The rewarding mechanisms of cocaine are reversed by administration of amphetamine. {{#l:Sustained Release d-Amphetamine Reduces Cocaine but not Speedball-Seeking in Buprenorphine-Maintained Volunteers.pdf}}
- Caffeine - This combination of stimulants is generally considered unnecessary and may increase strain on the heart, as well as potentially causing anxiety and physical discomfort.
- Tramadol - Tramadol and stimulants both increase the risk of seizures.
- DXM - Both substances raise heart rate, in extreme cases, panic attacks caused by these substances have led to more serious heart issues.
- Ketamine - No unexpected interactions. Likely to increase blood pressure but not an issue with sensible doses. Moving around on high doses of this combination may be ill advised due to risk of physical injury.
- PCP - Increases risk of tachycardia, hypertension, and manic states.
- Methoxetamine - Increases risk of tachycardia, hypertension, and manic states.
- Psychedelics - Increases risk of anxiety, paranoia, and thought loops.
- 25x-NBOMe - Amphetamines and NBOMes both provide considerable stimulation that when combined they can result in tachycardia, hypertension, vasoconstriction and, in extreme cases, heart failure. The anxiogenic and focusing effects of stimulants are also not good in combination with psychedelics as they can lead to unpleasant thought loops. NBOMes are known to cause seizures and stimulants can increase this risk.
- 2C-x
- 2C-T-x
- 5-MeO-xxT
- aMT
- Cannabis - Stimulants increase anxiety levels and the risk of thought loops and paranoia which can lead to negative experiences.
- DMT
- DOx
- LSD
- Mescaline
- Psilocybin mushrooms
- MAOIs - MAO-B inhibitors can increase the potency and duration of phenethylamines unpredictably. MAO-A inhibitors with amphetamine can lead to hypertensive crises.