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The purpose of this investigation was to demonstrate the continuing efficacy of neuromodulated alprazolam and the reduction of sedation-related effects associated with alprazolam with the concomitant administration of pseudoephedrine and guaifenesin in GAD or PD patients.
Oxaprozin is a nonsteroidal anti-inflammatory drug (NSAID) with analgesic and antipyretic properties.
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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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In certain embodiments, the compounds disclosed herein can be combined with one or more anti-psychotics known in the art, including, but not limited to, chlorpromazine, levomepromazine, promazine, acepromazine, triflupromazine, cyamemazine, chlorproethazine, dixyrazine, fluphenazine, perphenazine, prochlorperazine, thiopropazate, trifluoperazine, acetophenazine, thioproperazine, butaperazine, perazine, periciazine, thioridazine, mesoridazine, pipotiazine, haloperidol, trifluperidol, melperone, moperone, pipamperone, bromperidol, benperidol, droperidol, fluanisone, oxypertine, molindone, sertindole, ziprasidone, flupentixol, clopenthixol, chlorprothixene, thiothixene, zuclopenthixol, fluspirilene, pimozide, penfluridol, loxapine, clozapine, olanzapine, quetiapine, tetrabenazine, sulpiride, sultopride, tiapride, remoxipride, amisulpride, veralipride, levosulpiride, lithium, prothipendyl, risperidone, clotiapine, mosapramine, zotepine, pripiprazole, and paliperidone.
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This medication does not affect the transmission of impulses in the nerve-muscle synapses; reduces skeletal muscle tone; has a moderate analgesic effect.
At no time during the experiment did he feel somnolent or any desire to sleep.
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The pharmaceutical composition of the invention does not require a high CNS active agent (benzodiazepine) concentration that may lead to dose-dependent side-effects.
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For example, wherein delay in the release of the NM is within 30 minutes, more preferably within about 20 minutes, and most preferably within about 10 minutes of the difference of the TmaxCNS and TmaxNM.
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Depending upon the groups that are selected, a first group can be incorporated within second group or, alternatively, the first group can be pendant (i.
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The results of the studies performed in examples 10 and 11 suggest that concomitant administration of pseudoephedrine and guaifenesin with alprazolam reduce sedation-related effects associated with alprazolam without affecting the therapeutic efficacy of the drug in GAD patients.
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Significantly, when taking lmg Lorazepam together with Pseudoephedrine followed by Guaifenesin after 15 minutes, Volunteer A did not feel sedated and reported feeling at ease and anxiety free.
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The method of any of the preceding claims, wherein the cation precursor comprises a zwitterion with at least one carboxylate group and the anion precursor comprises a neutral acid or salt, and wherein combining the cation precursor and anion precursor results in a decarboxylation reaction.
Department of Health and Human Services, FDA, 2004).
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In one embodiment, CNS active agent particles, and particles from at least two vagal neuromodulators are formulated in a single solid dosage form, such as multi-layered tablets, suspension tablets, effervescent tablets, powder, pellets, granules or capsules comprising multiple beads.
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