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In one embodiment, the CNS active agent administered is in a time-dependent release form, preferably before the vagal neuromodulator's administration in order to ensure that the CNS active agent (already absorbed into the blood from the intestines) will be available for modulation of vagal afferent or efferent receptors while the neuromodulators are active in the stomach.
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As used herein, something could be reduced but not prevented, but something that is reduced could also be prevented.
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The subject was then given the active neuromodulators and told to start with them on the next day following ingestion of the regular alprazolam medication.
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In fact, many of the compounds disclosed herein as being suitable ions for the disclosed ionic liquids have already been proven to be effective alone or in some other preparation.
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Examples of those ionic liquid compositions include, but are not limited to, the mixture of at least two components of functionalized 5- and 6-membered, and bicyclic fused ring heterocyclic cations and anions containing 1, 2, 3, 4, or 5 atoms of nitrogen in the ring structure, where all carbon and nitrogen atoms in the ring structure can be functionalized with additional substituents such as alkyl, allyl, aryl, nitro, nitrile, azido, hydroxyl, carboxylic acid, ester, amide, amine, aldehyde, ketone, epoxy, or functionalized alkyl and aryl groups (with any functional mentioned above).
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The identifiers "first" and "second" are not intended to imply any particular order, amount, preference, or importance to the components or steps modified by these terms.
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Optional” or “optionally” means that the subsequently described event or circumstance can or cannot occur, and that the description includes instances where the event or circumstance occurs and instances where it does not.
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When Diphenhydramine Xepa-Soul Pattinson administered orally diphenhydramine has a sedative and hypnotic effects, has a moderate antiemetic effect and has a central holinoliticheskoy activity.
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The release of carbon dioxide from the ethylcellulose-coated sodium bicarbonate core causes particle buoyancy, thereby delaying the release of vagal neuromodulators from the particles.
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Yes, doses above 200mg result in D2 and D3 antagonism the atypical antipsychotic fashion while low doses seem to facilitate dopamine activity, now I don't really know if one can range between 50 and 200mg for antidepressant action, my pdoc states that amisulpride at 100mg dose already acts like antipsychotic but I'm not not sure.
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The letter, unusually for the Department of Health DH, was widely publicised, and I presume it was to hold the PSNC accountable and to make your points noted within the sector.
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In this embodiment the CNS agent maybe in an amount that is substantially the same as the conventionally accepted effective dosage, yet still have a reduction in at least one side-effect of the CNS.
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CNS active agents of the present invention also include “serotonin- and noradrenalin-reuptake inhibitors” (SNRIs).
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The Tmax of CNS agent will allow release of CNS agent once the vagal afferent neurons have already been stimulated and therefore, will prevent sedation-related effects associated with the CNS agent.
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Other delayed gastric-emptying approaches may be used in order to delay the release of vagal neuromodulators in the stomach.
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