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In yet another embodiment of the method for administering the pharmaceutical composition described immediately above, the method comprises co-administering the CNS active agent and the mechanoreceptor stimulator at a level sufficient to maintain the pharmacokinetic effectiveness of the CNS active agent while reducing associated side-effects.
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However, the combined CNS active agent comprising both chemoreceptor stimulator (PSE) and mechanoreceptor stimulator (GUA) was effective in reduction of the sedation outcome without disturbing anti-stress action of the drugs, In addition, delayed administration of GUA (at least for 10-30 minutes, preferably 15-20 minutes) was significant to synchronize between PK and PD of CNS active agent and neuromodulators.
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In another embodiment, at least two dosage form compartments may be present in a dosage form unit.
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The vagal neuromodulators are preferably in an amount sufficient to reduce a side-effect of the CNS active agent.
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Pimavanserin was generally well tolerated, although 10 pimavanserintreated patients discontinued treatment because of an adverse event four of which were due to psychosis versus two discontinuations for adverse events in the placebo group.
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The release of the (NM) contained in delayed-release (second) dosage form compartment initiated (meaning of "form compartment initiated" not clear) at least one hour after the first CNS active agent contained dosage form initiates release, with the initiation of the release generally occurring no more than six hours after initiation of release of CNS active agent from the first dosage form.
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Further, as is disclosed herein, this method can create a synergistic effect among the various ions present.
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Results were tabulated following a brief interview, consisting of a number of simple questions (See TABLES 9-14).
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The term "alkoxy" as used herein is an alkyl group bound through a single, terminal ether linkage; that is, an "alkoxy" group can be defined as -OAi where A' is alkyl as defined above.
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For example, the disclosed ionic liquid compositions can be used to allow fine tuning and control of the rate of dissolution, solubility, and bioavailability, to allow control over physical properties and mechanical strength, to improve homogenous dosing, and to allow easier formulations.
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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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