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The term “cycloalkyl” as used herein is a non-aromatic carbon-based ring composed of at least three carbon atoms.

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For example, the disclosed ionic liquid compositions can contain an ion from a drug known to have an undesirable side effect along with a counterion that is a drug known to alleviate or counteract that side effect.

As used herein, “opioid” means all agonists and antagonists of opioid receptors, such as mu (which can be denoted by mu or μ), kappa (which can be denoted by kappa or K), and delta (which can be denoted by delta or Δ) opioid receptors and subtypes thereof.

Significantly, when taking 1 mg 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 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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Users typically take smaller doses during the day for the neuroleptic properties and larger dose at bedtime for the sedative effects, or divided in two equal high doses every 12 hours (75 - 400 mg bid).

To introduce deuterium at one or more positions of R 13-R 14, bis(2-methoxyethoxy)aluminum deuteride can be used.

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This medication belongs to a class of so called tricyclic antidepressants.

It helps to restore the balance of certain natural substances (serotonin, among others) in the brain.

Additional secretagouges comprise etyron (S- ethylisothiouronium bromide), S-alkylisothiouronium derivatives, and S- ethylisothiouronium diethylphosphate, variously for treatment of high blood pressure, hyperoxia and acute hypotension, (e.

For example, to introduce deuterium at one or more positions of R 1-R 14, compound 6 with the corresponding deuterium substitutions can be used.

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Around two-thirds of people in controlled drug trials discontinue antipsychotics, partly due to adverse effects.

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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.

Methyl-1-ethylpyrrolidine-2-carboxylate: In a sealed tube at ambient temperature and over a period of about 15 minutes, bromoethane (2.

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Lorazepam (BDR) by his family doctor for anxiety and anxiety related insomnia.

Evidence from comparison studies indicates that at least some individuals recover from psychosis without taking antipsychotics, and may do better than those that do take antipsychotics.

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The composition of claim 31, wherein the at least one kind of anion comprises the anion of 2-hexyldecanoic acid, 6-azauridine, 6-mercaptopurine, 9-aminocamptothecin, acadesine, acetarsone, acetosulfone, acetylcysteine, acetylsalicylsalicylic acid, acifran, acitretin, acrivastine, adrenalone, aldioxa, alibendol, allopurinol, aminitrozole, amlexanox, antimony thioglycolate, arsanilate, azidamfenicol, balsalazide, benfunolol, benzoylpas, beraprost, brequinar, bromo-salicylchloranilide, bucillamine, bufexamac, bufuralol, bumadizon, bunitrolol, buthalital, cannabinol, captopril, carbarsone, carbazochrome, carbidopa, carboprost, carnitine, carprofen, cephaeline, cetapril, cetraxate, chenodiol, chloramphenicol, chromocarb, clanobutin, clometocillin, cortivazol, cromolyn, cyclazocine, dermatol, diacerein, dibunate, diphetarsone, dobesilate, docusate, eflomithine, enfenamic acid, enoxolone, etodroxizine, flufenamic acid, folinic acid, foscarnet, hydroxystilbamidine, isoetharine, isotretinoin, lodoxamide, mercaptomerin, mercumatilin, mesalamine, methionine, metyrosine, nadoxolol, niclosamide, omapatrilat, orotic acid, oxaceprol, ozagrel, pamidronic acid, p-aminobenzoate, p-aminobenzoic acid, penicillamine, phenol, phentolamine, picosolfate, pidotimod, prostaglandin E 2, prostaglandin f2 a, ramatroban, retinoic acid, risedronate, ritodrine, salicylate, solisobenzone, succinimide, sulfapyridine, sulprostone, tenuazonic acid, terbutaline, tetradecyl sulfate, thiamphenicol, thioctic acid, thiopental, ticrynafen, timonacid, tiopronin, triglycollamate, tropicamide, ursodiol, valproic acid, or zanamivir, or an anionic derivative thereof.

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The term "in conjunction with" means that when the CNS and the neuromodulators are administered in separate dosage forms, there is at least some chronological overlap in their physiological activity.

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Cholinergic: aceclidine, bethanechol chloride, carbachol, demecarium bromide, dexpanthenol, echothiophate iodide, isoflurophate, methacholine chloride, neostigmine bromide, neostigmine methylsulfate, physostigmine, physostigmine salicylate, physostigmine sulfate, pilocarpine, pilocarpine hydrochloride, pilocarpine nitrate, pyridostigmine bromide.

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NMDA-receptor antagonist suitable for use in the invention can be identified by testing NMDA-receptor antagonist for local-anesthetic and peripheral antinociceptive properties according to standard pain models.

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In one aspect, disclosed herein are uses of a delivery device to deliver an ionic liquid composition as disclosed herein to a subject.

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Norepinephrine-reuptake inhibitors comprise amitriptyline, desmethylamitriptyline, clomipramine, doxepin, imipramine, imipramine-oxide, trimipramine, adinazolam, amiltriptylinoxide, amoxapine, desipramine, maprotiline, nortriptyline, protriptyline, amineptine, butriptyline, demexiptiline, dibenzepin, dimetacrine, dothiepin, fluacizine, iprindole, lofepramine, melitracen, metapramine, norclolipramine, noxiptilin, opipramol, perlapine, pizotyline, propizepine, quinupramine, reboxetine, and tianeptine.

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The method comprises: administering to a patient between about 5 to about 80 percent, more preferably less than about 60%, and most preferably less than about 50% of the conventionally accepted effective dosage of the addictive CNS active agent for the desired treatment.

Anti-cancer supplementary potentiating agents: tricyclic anti-depressant drugs (e.

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Pharmacological action Alprazolam is an anxiolytic drug (tranquilizer), a derivative of triazolo-benzodiazepine.

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Abilify) - Dosing 1 mg up to maximum of 30 mg has been used.

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In another embodiment, the vagal neuromodulators in the separate dosage form are formulated as suspension tablet, effervescent tablet, chewable tablet or powder for suspension for compliance of neuropsychotic or addicted patients.

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Artificial red blood cells, as described herein, are further delivery devices that can be used to deliver the compositions disclosed herein.

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In routine clinical practice, antipsychotics may be used as part of risk management, and to control difficult patients since the patient becomes deenergized or deenervated, will or volition is crushed, and passivity and docility are induced therefore the patient complains less and becomes more manageable, although this is controversial.

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