CPC A61K 31/496 (2013.01) [A61K 9/0053 (2013.01); A61K 31/05 (2013.01); A61K 31/13 (2013.01); A61K 31/198 (2013.01); A61K 31/4545 (2013.01); A61K 31/495 (2013.01); A61K 31/55 (2013.01); A61K 45/06 (2013.01); A61P 25/16 (2018.01)] | 16 Claims |
1. A pharmaceutically-acceptable oral unit dose, for treating or reducing risk of L-DOPA induced dyskinesia in a human patient having Parkinson's Disease, comprising:
at least one of agent selected from the group consisting of vilazodone and vortioxetine, in a sufficient amount to treat the L-DOPA induced dyskinesia of the human patient; and
at least one second agent selected from the group consisting of:
DOPA decarboxylase inhibitor in an effective amount to reduce peripheral decarboxylation of L-DOPA,
a catechol-O-methyl transferase inhibitor,
a monoamine oxidase type B inhibitor,
a dopamine receptor agonist,
an anticholinergic agent,
an antimuscarinic agent, and
a cannabinoid.
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