(+) naloxone and epinephrine combination therapy
AssigneeUniversity of North Texas Health Science Center at Fort Worth
InventorJames L. Caffrey
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AssigneeUniversity of North Texas Health Science Center at Fort Worth
InventorJames L. Caffrey
Estimating the term…
A composition formulated for dose-wise delivery to a breathing passageway of a human, the composition comprising a carrier solution containing (+)naloxone and a pharmacologically effective amount of at least one adrenergic agonist, the (+)naloxone and agonist forming a mixture in the carrier. The at least one adrenergic agonist is selected from the group consisting of epinephrine, isoproterenol, albuterol, aminophylline, beclomethasone, dyphylline, flunisolide, isoetharine, metaproterenol, oxtriphylline, terbutaline, theophylline, pseudoephedrine, phenylephrine, ephedrine and norepinephrine. That composition is delivered by an atomizer means such as a liquid sprayer or inhaler to treat nasal congestion and asthmatic attacks. Further provided by the invention is a cardiovascular and respiratory stimulating composition for administration to a patient in doses, the composition comprising a pharmacologically effective concentration of (+)naloxone in a carrier solution. If necessary, the composition may also contain a pharmacologically effective amount of at least one adrenergic agonist.
A composition formulated for dose-wise delivery to a breathing passageway of a human, the composition comprising:
A cardiovascular and respiratory stimulating composition for administration to a patient in doses, the composition comprising:
A cardiovascular and respiratory stimulating composition for administration to a patient in doses, the composition comprising:
A method of alleviating breathing passageway compromise in humans, the method comprising:
A method of stimulating cardiovascular and respiratory output in a human during high-stress situations, the method comprising:
A method of enhancing local vasoconstriction and serve as an adjuvant administered with adrenergic agonists and other pharmaceuticals in order to contain those pharmaceuticals in a high therapeutically effective concentration at their site of administration, the method comprising:
Dependencies are inferred from the claim text.