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The amount of NMDA-receptor antagonist in compositions of the invention will vary according to the type and identity of the NMDA-receptor antagonist, the concentration and identity of the antidepressant, and the painful indiction treated.

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CNS) active agent; at least two vagal neuromodulators; and a pharmaceutically-acceptable vehicle, carrier or diluent, wherein the vagal neuromodulators are in an amount sufficient to reduce a side-effect of the CNS active agent and at least one of the vagal neuromodulators is a mechanoreceptor stimulator.

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When a compound as disclosed herein is used contemporaneously with one or more other drugs, a pharmaceutical composition containing such other drugs in addition to the compound disclosed herein may be utilized, but is not required.

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Certain derivatives, such as 5-ethyl-5-phenyl barbituric acid (Phenobarbital), for example, have an anticonvulsive effect and are therefore employed in the treatment of epilepsy.

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The composition of claim 31, wherein the pharmaceutical active comprises aspirin, chlordiazepoxide HCl, isoniazid, penicillin, sulfamidochrysoidine, cisplatin, 6-mercaptopurine, chimeric anti-CD20 antibody, paclitaxel, phenobarbital, fluoxetine, fexofenadine, rofecoxib, quinine, ivermectin, L-dopa, 10-(3-dimethylaminoproply)-2-chlorphenothiazine, salvarsan, cimetidine, zidovudine, indinavir sulfate, salbutamol, digoxin, fluride, zidovudine, erythropoietin, hydrocortisone, insulin, oral contraceptive, oxytocin, mifepristone, thyroxine, thalidomide, cyclosporine, fentanyl, methadone, morphine, botox, vitamins, methylphenidate, sildenafil, pantoprazole, rabeprazole, risedronate, alendronate, losartan, fosinopril, atorvastatin, pravastatin, montelukast, or an ionic derivative thereof.

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The kit preferably comprises a central nervous system (CNS) active agent; and at least two vagal neuromodulators, wherein the vagal neuromodulators are in an amount sufficient to reduce a side-effect of the CNS active agent and at least one of the vagal neuromodulators is a mechanoreceptor stimulator.

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In one embodiment deuterium enrichment is no less than about 1%, in another no less than about 5%, in another no less than about 10%, in another no less than about 20%, in another no less than about 50%, in another no less than about 70%, in another no less than about 80%, in another no less than about 90%, or in another no less than about 98% of deuterium at the specified position.

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In another embodiment (a) CNS active agent(s) are selected from the following groups: benzodiazepines, atypical neuroleptics, barbiturates, sodium oxybate, opiates, or combinations thereof; (b) hypertensive agent is a selective alpha ADR receptor agonist Phenylephrine (vagal afferent neuromodulator); © and instructions for delay of about 15-30 minutes between administration of (a) and (b).

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