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However, chlorpromazine quickly proved to reduce the effects of psychosis in a more effective and specific manner than the extreme lobotomy-like sedation it was known for.

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If an infection is present, the ear may appear red and swollen. There may also be a fluid discharge.

The term “bioactive property” is any local or systemic biological, physiological, or therapeutic effect in a biological system.

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Caution is advised when using Zoloft in children; they may be more sensitive to its effects, especially increased risk of suicidal thoughts or actions.

IR formulation of benzodiazepine followed by a combination of vagostimulators or other neuromodulator(s) in IR formulation (preferably as an effervescent formulation) with a delay of between administrating of benzodiazepine and neuromodulator cocktail at least 50% of a known Tmax of benzodiazepine in blood in order to obtain optimal synchronization between onset of neuromodulation and availability of benzodiazepine in circulation and CNS target site.

Unlike adrenaline and noradrenaline, PHE is not a catecholamine and is not influenced by the enzyme O-methyltransferase; therefore, it is more stable and has a prolonged effect.

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The term "cyclic group" is used herein to refer to either aryl groups, non-aryl groups (i.

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The participants declined to undergo rehabilitation but agreed to abstain from marijuana use for the entire period and were regularly tested for drug use, said study coauthor Dr.

In another embodiment of the present invention, the method for administering the pharmaceutical composition of the present invention (CNS active agent, plus mechanoreceptor stimulator and another vagal neuromodulator in amounts sufficient to reduce CNS active agent side-effect(s)) comprises co-administering the CNS active agent and the mechanoreceptor stimulator, and the vagal neuromodulator sequentially or in time-released form thereby ameliorating CNS active agent side-effects without reducing the conventionally accepted effective dosage of the CNS active agent.

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This test was done before doses of study drug and 2, 4 and 6 hours after doses of study drug (see FIG.

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Serotonin reuptake inhibitors” are compounds that inhibit reuptake of serotonin when systemically administered in mammals or that display receptor-binding properties or other mechanistic properties associated with serotonin-reuptake inhibitors when tested according to standard in vivo or in vitro assays such as are described in Wong, et al.

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TUESDAY, Aug. 19, 2014 HealthDay News Even though schizophrenia is one of the most severe forms of mental illness, nearly 40 percent of people with the disorder say theyre happy, new research contends.

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These conditions permit vagal afferent activation of the gastric milieu by the vagal neuromodulator concurrently with the achievement of a pharmacological "effective" CNS agent plasma concentration.

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