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Cocaine<span itemscope itemtype="http://schema.org/Thing">
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<span itemprop="name">sedation</span>
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<span itemprop="name">breathing</span>
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<span itemprop="name">blood pressure</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Blood_pressure" />
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ATC code N06BA03
PubChem CID 1206
DrugBank DB01577
Synonyms N-methylamphetamine, desoxyephedrine
Formula C10H15N
Molecular<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">Molecular</span>
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</span> mass 149.2337 g/mol
Melting<span itemscope itemtype="http://schema.org/Thing">
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<span itemprop="name">alcohol dependence</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Ethanol" />
</span>, although there remains uncertainty about its efficacy<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">efficacy</span>
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</span> relative to other pharmacotherapies for alcohol dependence.The authors of a 2010 Cochrane<span itemscope itemtype="http://schema.org/Organization">
<span itemprop="name">Cochrane</span>
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<span itemprop="name">fibromyalgia</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Fibromyalgia" />
</span>.GHB is the active ingredient of the prescription medication sodium oxybate<span itemscope itemtype="http://schema.org/Thing">
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<span itemprop="name">cataplexy</span>
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GHB has been shown to reliably increase slow-wave sleep181920 and decrease the tendency for REM sleep<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">sleep</span>
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</span> in modified multiple sleep latency tests.
The FDA approved labeling for sodium oxybate suggests no evidence GHB has teratogenic, carcinogenic or hepatotoxic properties. Its favorable safety<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">safety</span>
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</span> profile relative to ethanol may explain why GHB continues to be investigated as a candidate for alcohol substitution.
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<span itemprop="name">cathinone</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Cathinone" />
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<span itemprop="name">dopamine</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Dopamine" />
</span> reuptake inhibitor (NDRI). It was first developed in the 1960s by a team at Boehringer Ingelheim<span itemscope itemtype="http://schema.org/Corporation">
<span itemprop="name">Boehringer Ingelheim</span>
<link itemprop="sameAs" href="https://en.wikipedia.org/wiki/Boehringer_Ingelheim" />
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Its activity at the dopamine transporter is six times stronger than at the norepinephrine<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">norepinephrine</span>
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Mephedrone<span itemscope itemtype="http://schema.org/Drug">
<span itemprop="name">Mephedrone</span>
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</span> is a stimulant drug<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">drug</span>
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<span itemprop="name">speed</span>
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Other names: ?-Pyrrolidinopentiophenone ?-PVP, O-2387, alpha-PVP, a-pvp ;
Purity and form: white crystalline form, the maximum purity 99.9%;
Effect: stimulation and euphoria<span itemscope itemtype="http://schema.org/Thing">
<span itemprop="name">euphoria</span>
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</span>, speed;
Formula: C15H21N?;
Molar mass: 231,33 g/mol
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