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For example, the first CNS agent, a benzodiazepine for example, may be combined with neuromodulators as an adjunctive to reduce the sedation-related effects associated with benzodiazepine usage.

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The present invention reduces or prevents the side-effects of depression, dizziness, drowsiness, lethargy, weakness in the extremities, difficulty in being mobile, and orthostatic hypotension and other blood pressure effects associated with therapeutic CNS acting agents without compromising the positive clinical effects of those same therapeutic agents.

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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 purpose of this example was to determine if the co-administration of pseudoephedrine and guaifenesin with alprazolam has effective in reducing the sedation commonly seen with the administration of alprazolam alone.

Materials and Compositions Certain materials, compounds, compositions, and components disclosed herein can be obtained commercially or readily synthesized using techniques generally known to those of skill in the art.

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This may not be a complete list of all interactions that may occur.

The term “sulfone” as used herein is represented by the formula A 1S(O) 2A 2, where A 1 and A 2 can be, independently, an alkyl, halogenated alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocycloalkyl, or heterocycloalkenyl group described above.

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The study was carried out in two sessions with one week in between.

In addition to nurturing weakened cells, glucose reacts with the cell components to enhance movement into the cells of excessive potassium ions already present in the blood, thus alleviating the hyperkalemic condition and replacing the potassium lost from the cells during diarrhea.

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Sequential release would be used if it is required to synchronize the release of the CNS agent with the action of the neuromodulators by delaying the release of neuromodulator in the stomach (ex.

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Other medicines with similar action are fluoxetine (Prozac) and paroxetine (Paxil).

The brain isn't neatly split up into compartments, it is a neuronal network of interdependent pathways which rely on these connections to function as a whole.

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The study was carry out by two sessions with interval for one week between.

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In this embodiment, the delay in the administration or release of mechanoreceptor stimulator is typically equal to the Tmax of the CNS active agent minus the Tmax of the mechanoreceptor stimulator plus about 5 to about 30 minutes.

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In another embodiment, the first dosage form initiates release of NM agent(s) at a time later as compared to when the CNS active agents would be released from an immediate release dosage form.

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The term "alkenyl" as used herein is a hydrocarbon group of from 2 to 24 carbon atoms with a structural formula containing at least one carbon-carbon double bond.

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In accordance with the purposes of the disclosed materials, compounds, compositions, devices, and methods, as embodied and broadly described herein, the disclosed subject matter, in one aspect, relates to compounds and compositions and methods for preparing and using such compounds and compositions.

By the term “effective amount” of a compound as provided herein is meant a nontoxic but sufficient amount to provide the desired result.

Thus, the existence and control of polymorphism and pseudo-polymorphism can be the biggest challenge to obtaining a drug product of constant quality.

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Barbiturates in high concentrations may also prove neuroprotective; however, the dosages necessary to confer neuroprotection are toxic and cause lethargy, stupor, coma, or are lethal, making accepted dosages of barbiturates unsuitable for treatment of ischemia and other neurodegenerative diseases.

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The compositions and methods disclosed herein meet these and other needs including the introduction of enhanced or new functionality.

The following examples are set forth below to illustrate the methods' and results according to the disclosed subject matter.

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HF, HCl, HBr, or HI) or by treating a halogenated compound with a nucleophile such as an amine.

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The term "sulfo-oxo" as used herein is represented by the formulas -S(O)Al, -S(O)2A1, -OS(O)2Al, or -OS(O)20A1, where Al can be hydrogen, an alkyl, halogenated alkyl, alkenyl, alkynyl, aryl, heteroaryl, cycloalkyl, cycloalkenyl, heterocycloalkyl, or heterocycloalkenyl group described above.

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Pharmaceutical actives that exist as ions or can be converted to ions, and which are suitable for use in preparing the disclosed ionic liquid compositions, include the following categories and specific examples.

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From Martindale, The Extra Pharmacopoeia, 30th ed, p1206) Indication: For use as an adjunct to rest, physical therapy, and other measures for the relief of discomforts associated with acute, painful musculoskeletal conditions.

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The product is then cooled and may be sieved or granulated and compressed using a suitable tablet press, such as a rotary tablet press.

Quinine is also a mild antipyretic and analgesic and has been used in common cold preparations for that purpose.

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In one embodiment, the pharmaceutical composition of the present invention is formulated as a single dosage form comprising multiple beads contained in hard or soft gelatin capsules.

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For all of the foregoing reasons, a medicine with a longer half-life may result in greater efficacy and cost savings.

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In either case, the treatment regimen will provide beneficial effects of the drug combination in treating the disorders described herein.

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While the atypical, second-generation medications were marketed as offering greater efficacy in reducing psychotic symptoms while reducting side effects (and extra-pyramidal symptoms in particular) than typical medications, these results showing these effects often lack robustness.

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Indication: For use in the treatment of the following infections when.

One or more types of aliphatic benzylalkyl ammonium cation can be used in the ionic liquid compositions disclosed herein.

In one embodiment, the sequence of the CNS active agent and Phenylephrine, or other Neuromodulator(s) is delayed at least 15-30 minutes so that Phenylephrine is administered after the CNS active agent to address hypertension while reducing the conventionally accepted effective dose of the CNS active agent by at least twice.

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