51 results about "Sertraline" patented technology

Provided are hydrogenation processes of sertraline imine intermediates with catalysts in various reactors.

A controlled release dosage form for sertraline has a core comprising a sertraline-containing composition and a water-swellable composition wherein the water-swellable composition is in a separate region within the core. A coating around the core is water-permeable, water-insoluble, and has at least one delivery port therethrough. In one embodiment, the dosage form releases sertraline to the use environment at an average rate of 6 to 10 wt % per hour from the second to the twenth hour after introduction to a use environment and less than about 25 wt % for the first two hours and at least 70 wt % by the twelfth hour, where the percentages correspond to the mass of drug released from the tablet divided by the total mass of drug originally present in the tablet. In another embodiment, the dosage form releases less than about 25 wt % of sertraline to the use environment by the second hour after introduction of the dosage form to the use environment, and delivers at least 25 wt % from the eighth to the twenty-fourth hour.

The invention relates to sertraline oral solution for treating depression. The invention provides the sertraline aqueous solution for oral administration and a preparation method thereof. The sertraline oral aqueous solution comprises sertraline, pharmacologically acceptable salt thereof, and a or more pharmacologically acceptable excipients. The invention adopts a method of adding the surfactant to prepare the sertraline oral aqueous solution, and overcomes the defects that the nonaqueous solution has no good taste and the patient compliance is not good. Moreover, the invention adopts unit dose package so as to have accurate dosage and convenient administration.

The present invention provides methods of treating, reducing, preventing, or inhibiting symptoms of diabetes and / or lowering plasma levels of HbA1c by co-administration of therapeutic or subtherapeutic doses of telenzepine and sertraline to a subject in need thereof.

Provided are hydrogenation processes of sertraline imine intermediates with catalysts in various reactors.

Provided is a recycling process for preparing sertraline, which may be carried out on an industrial scale.

The present invention relates to a method for curing and preventing neurosism or somatic formal disturbance and its medicine composition. Said invention belongs to the field of pharmacy. Said invention provides a medicine composition containing norepinephrine reuptake inhibitor with medicinal dose or its medicinal salt and selective 5-hydroxytryptamine reuptake inhibitor with medicinal dose or its medicinal salt for preventing and curing neurosism or somatic formal disturbance. The norepinephrine reuptake inhibitor is selected from reboxetine, tomoxetine, amfebutamone, nortriptyline, norimipramine, maprotiline and protiline, and the selective 5-hydroxytryptamine reuptake inhibitor is selected from sertraline, citalopram, s-citalopram, fluoroxeline, paroxetine and fluvoxamine.

The pharmaceutical composition of the present invention comprises (1) a carbostyril derivative and (2) a serotonin reuptake inhibitor in a pharmaceutically acceptable carrier. The carbostyril derivative may be aripiprazole or a metabolite thereof, which is a dopamine-serotonin system stabilizer. The serotonin reuptake inhibitor may be fluoxetine, duloxetine, venlafaxine, milnacipran, citalopram, fluvoxamine, paroxetine, sertraline or escitalopram. The pharmaceutical composition of the present invention is useful for treating patients with mood disorders, particularly depression or major depressive disorder.

The present application relates to compositions for use in a method of treating and / or preventing mental and behavioral disorders and / or improving mental health and cognitive functions in a subject, comprising:a) Docosahexaenoic acid (DHA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof;b) Eicosapentaenoic acid (EPA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof;c) γ-linolenic acid (GLA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof; andat least a psychostimulant compound selected among methylphenidate HCl, atomoxetine, amphetamine, gamma-hydroxybutyrate, dextroamphetamine, sibutramine, methylenedioxymethamphetamine, and / or an anxiolytic compound selected among fluoxatine, sertraline, paroxetine, fluoroxamine, citralopram, venlafaxine, bupropion, nefazodone, and mirtazapine.The present application also relates to the method of treating and / or preventing mental and behavioral disorders and / or improving mental health and cognitive functions in a subject, comprising administering an effective amount of a composition comprising:a) Docosahexaenoic acid (DHA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof;b) Eicosapentaenoic acid (EPA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof;c) γ-linolenic acid (GLA) and / or the pharmaceutically acceptable derivatives and / or precursors thereof; andat least a psychostimulant compound selected among methylphenidate HCl, atomoxetine, amphetamine, gamma-hydroxybutyrate, dextroamphetamine, sibutramine, methylenedioxymethamphetamine, and / or an anxiolytic compound selected among fluoxatine, sertraline, paroxetine, fluoroxamine, citralopram, venlafaxine, bupropion, nefazodone, and mirtazapine.

The present invention provides methods of treating, reducing, preventing, or inhibiting symptoms of diabetes and / or lowering plasma levels of HbA1c by co-administration of therapeutic or subtherapeutic doses of telenzepine and sertraline to a subject in need thereof.

The pharmaceutical composition of the present invention comprises (1) a carbostyril derivative and (2) a serotonin reuptake inhibitor in a pharmaceutically acceptable carrier. The carbostyril derivative may be aripiprazole or a metabolite thereof, which is a dopamine-serotonin system stabilizer. The serotonin reuptake inhibitor may be fluoxetine, duloxetine, venlafaxine, milnacipran, citalopram, fluvoxamine, paroxetine, sertraline or escitalopram. The pharmaceutical composition of the present invention is useful for treating patients with mood disorders, particularly depression or major depressive disorder.