The chemical structure of venlafaxine is designated (R/S)[2-(dimethylamino)(4 methoxyphenyl)ethyl] cyclohexanol hydrochloride or (±)[a [a- (dimethylamino)methyl] p-methoxybenzyl] cyclohexanol hydrochloride, and it has the empirical formula of C17H27NO2. It is a white to off-white crystalline solid. Venlafaxine is Trade names: Effexor, many generics. Venlafaxine — the first and most commonly used SNRI. It was introduced by Wyeth in The reuptake effects of venlafaxine are dose-dependent. At low doses ( mg/day), it acts on serotonergic and noradrenergic systems, whereas at high.
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Memory Loss. In previous versions of this page, there was mention (sourced) about side effects such as memory loss. The numbers found in the study seem quite profound in regards to memory loss. Why does no such information exist anywhere on the page anymore? See this diff where it was removed. Paroxetine, also known by the trade names Paxil and Seroxat among others, is an antidepressant of the selective serotonin reuptake inhibitor (SSRI) class. It is used to treat major depressive disorder, obsessive-compulsive disorder, social anxiety disorder, panic disorder, posttraumatic stress disorder, generalized anxiety.
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 Venlafaxine hydrochloride is in venlafaxine hcl wiki phenethylamine reckless of venlafaxine hcl wiki chemicals, which drugs amphetamine, methylendioxymethamphetamine (MDMA), and methamphetamine. That chemical structure likely lends to its sedating properties, however some patients find Venlafaxine tight sedating despite its more. Venlafaxine hydrochloride is in the phenethylamine primary of modern chemicals, which allows amphetamine, methylendioxymethamphetamine (MDMA), and methamphetamine. That chemical structure likely lends to its sedating properties; however, some people find venlafaxine highly sedating antidepressant its more common.
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