Methods of treating and preventing pain, anxiety, and incontinence using derivatives of (−)-venlafaxine
Methods of preparing, and compositions comprising, derivatives of (−)-venlafaxine are disclosed. Also disclosed are methods of treating and preventing diseases and disorders including, but not limited to, affective disorders such as depression, bipolar and manic disorders, attention deficit disorder, attention deficit disorder with hyperactivity, Parkinson's disease, epilepsy, cerebral function disorders, obesity and weight gain, incontinence, dementia and related disorders.
1. A method of treating or preventing pain, which comprises administering to a human in need of such treatment or prevention a therapeutically or prophylactically effective amount of a (−)-venlafaxine derivative, of pharmaceutically acceptable salt thereof, substantially free of its (+) stereoisomer.
2. The method of claim 1 wherein the amount of (−)-venlafaxine derivative, or pharmaceutically acceptable salt thereof, is insufficient to cause adverse effects associated with the administration of racemic venlafaxine.
3. The method of claim 2 wherein the pain is chronic pain.
4. A method of treating or preventing anxiety, which comprises administering to a human in need of such treatment or prevention a therapeutically or prophylactically effective amount of a (−)-venlafaxine derivative, or a pharmaceutically acceptable salt thereof, substantially free of its (+) stereoisomer.
5. The method of claim 4 wherein the amount of (−)-venlafaxine derivative, or pharmaceutically acceptable salt thereof, is insufficient to cause adverse effects associated with the administration of racemic venlafaxine.
6. The method of claim 4 wherein the anxiety is obsessive compulsive disorder.
7. A method of treating or preventing incontinence, which comprises administering to a human in need of such treatment or prevention a therapeutically
or prophylactically effective amount of a (−)-venlafaxine derivative, or a pharmaceutically acceptable salt thereof, substantially free of its (+) stereoisomer.
8. The method of claim 7 wherein the amount of (−)-venlafaxine derivative, or pharmaceutically acceptable salt thereof, is insufficient to cause adverse effects associated with the administration of racemic venlafaxine.
9. The method of claim 7 wherein the incontinence is fecal incontinence, overflow incontinence, passive incontinence, reflex incontinence, stress urinary incontinence, urge incontinence, urinary exertional incontinence of the urine.
10. The method of claim 1 , 4 , or 7 wherein the (−)-venlafaxine derivative is (−)-O-desmethylvenlafaxine, (−)-N-didesmethylvenlafaxine, (−)-N,O-didesmethylvenlafaxine, or (−)-N,N-didesmethylvenlafaxine.
11. The method of claim 10 wherein the (−)-venlafaxine derivative is (−)-O-desmethylvenlafaxine or (−)-N,O-desmethylvenlafaxine.
12. The method of claim 10 wherein (−)-venlafaxine derivative is administered by intravenous infusion, transdermal delivery, or orally as a tablet of a capsule.
13. The method of claim 10 wherein the amount administered is from about 10 mg to about 100 mg per day.
14. The method of claim 13 wherein the amount administered is from about 50 mg to about 500 mg per day.
15. The method of claim 14 wherein the amount administered is from about 75 mg to about 350 mg per day.