Methods and compositions for treating distress dysfunction and enhancing safety and efficacy of specific medications
The present invention relates to methods and compositions for reducing distress dysfunction, including emotional and physical distress. The invention entails co-administration of at least one Receptor Switcher and at least one Endorphin Enhancer. Additionally, at least one Synergistic Enhance and/or at least one Exogenous Opioid are also administered to enhance or prolong the therapeutic effects.
1. A method to safely and effectively treat Anxiety conditions, symptoms and/or disorders in a subject in need comprising:
(a) administering at least one Receptor Switcher to the subject, wherein the receptor switcher is N-acetyl cysteine; and
(b) administering at least one Endorphin Enhancer to the subject, wherein the endorphin enhancer is a compound comprising caffeine.
2. The method of claim 1 , wherein the Anxiety conditions, symptoms and/or disorders are selected from the group consisting of Panic Disorders, Agoraphobia, Specific Phobias, Social Phobias, Obsessive-Compulsive Disorder, Post-Traumatic Stress Disorder, Acute Stress Disorder, Generalized Anxiety Disorder, Substance-Induced Anxiety, Anxiety Related to Medical Disorders, Anxiety Disorder Not Otherwise Specified (NOS), as well as signs and symptoms of anxiety, stress, agitation, and worry that are not classified as an Anxiety Disorder.
3. The method of claim 1 , wherein the receptor switcher, when co-administered with the endorphin enhancer, reduces and/or resolves one or more anxiety symptoms.
4. The method of claim 1 , wherein the subject has previously taken:
(a) an endorphin enhancer, which is selected from the group consisting of ginkgo biloba, theophylline, roflumilast, ibudilast, caffeine, guarana, forskolin, glutamic acid, glutamine, mono-sodium glutamate (MSG) and N-methyl-D-asparate (NMDA),
(b) an exogenous opioid, which is selected from the group consisting of tramadol, morphine, oxycodone, hydrocodone, codeine, fentanyl, hydromorphone, buprenorphine and methadone,
(c) a synergistic enhancer, which is selected from the group consisting of non-opioid analgesics, non-steroidal anti-inflammatory drugs (NSAIDs), selective serotonin reuptake inhibitors (SSRI) and selective norepinephrine reuptake inhibitors (SNRIs), or
(d) any combination thereof.
5. The method of claim 1 , wherein:
(a) the mode of administration is selected from the group consisting of oral, pulmonary, nasal, sublingual, parenteral, and transdermal;
(b) the pharmaceutical formulation is delivered in a pharmaceutically-acceptable carrier that is rapid release, immediate-release, slow-release, delayed-released, controlled release, a combination of immediate release and controlled release, a nano-encapsulation formulations, and an abuse and/or tamper-resistant delivery system; or
(c) any combination thereof.
6. The method of claim 5 , wherein the mode of administration is oral.