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    Dapoxetine , marketed as Priligy , among others, is a medication used for the treatment of premature ejaculation PE in men 18—64 years old. However, unlike other SSRIs, dapoxetine is absorbed and eliminated rapidly in the body. Its fast-acting property makes it suitable for the treatment of PE, but not as an antidepressant. Randomized, double-blind, placebo-controlled trials have confirmed the efficacy of dapoxetine for the treatment of PE.

    Dapoxetine 60 mg significantly improves the mean intravaginal ejaculation latency time IELT compared to that of dapoxetine 30 mg in men with lifelong PE, but no difference is seen in men with acquired PE. Since PE is associated with personal distress and interrelationship difficulty, dapoxetine provides help for men with PE to overcome this condition.

    Waldinger's meta-analysis shows that the use of these conventional antidepressants increases IELT two- to nine-fold above baseline, compared to three- to eight-fold when dapoxetine is used. It is more rapidly absorbed and mostly eliminated from the body within a few hours. These pharmacokinetics are more favorable in that they might minimize drug accumulation in the body, habituation, and side effects.

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    Although it was initially thought of as unsuccessful in its intended use as an antidepressant, dapoxetine has been more recently investigated as a possible aid to one approach to depression treatment focused on stress reduction, based on an animal model of depression. Dapoxetine should not be used in men with moderate to severe hepatic impairment and in those receiving CYP3A4 inhibitors such as ketoconazole , ritonavir , and telithromycin.

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    Dapoxetine also cannot be used in patients with heart failure, permanent pacemaker, or other significant ischemic heart disease. Caution is advised in men receiving thioridazine , monoamine oxidase inhibitors , SSRIs, serotonin-norepinephrine reuptake inhibitors , or tricyclic antidepressants. If a patient stops taking one of these drugs, he should wait for 14 days before taking dapoxetine.

    If a patient stops taking dapoxetine, he should wait for 7 days before receiving these drugs. The most common effects when taking dapoxetine are nausea, dizziness, dry mouth, headache, diarrhea, and insomnia.

    Show references Partin AW, et al. Get the Mayo Clinic app. He lives in Madison, Wisconsin. Health Conditions Discover Plan Connect. It's best to check your chosen provider's website for more information.

    According to McMahon in recent study in Asia, the rate of discontinuation is 0. No case of drug overdose has been reported during clinical trials. Many men who have PE also suffer from erectile dysfunction ED. Treatment for these patients should consider the drug—drug interaction between dapoxetine and PDE5 inhibitors such as tadalafil Cialis or sildenafil Viagra. In Dresser study , plasma concentration of 24 subjects was obtained. Half of the sample pool were treated with dapoxetine 60 mg plus tadalafil 20 mg; the other half were treated with dapoxetine 60 mg plus sildenafil mg.

    These plasma samples were then analyzed using liquid chromatography-tandem mass spectrometry. The results showed that dapoxetine does not alter the pharmacokinetic of tadalafil or sildenafil.

    Ethanol does not affect the pharmacokinetics of dapoxetine when taking concurrently.

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    The mechanism through which dapoxetine affects premature ejaculation is still unclear, but dapoxetine is presumed to work by inhibiting serotonin transporter and subsequently increasing serotonin's action at pre- and postsynaptic receptors. These signals are passed on to the brain stem , which then is influenced by a number of nuclei in the brain such as medial preoptic and paraventricular nuclei.

    These effects cause an increase in pudendal motoneuron reflex discharge PMRD latency, though whether dapoxetine acts directly on LPGi or on the descending pathway in which LPGi located is unclear. Dapoxetine is a white, powdery, water-insoluble substance.

    Taken one to three hours before sexual activity, it is rapidly absorbed in the body. Its maximum plasma concentration C max is reached one to two hours after oral administration. The C max and AUC area under the plasma vs. A high-fat meal does reduce the C max slightly, but it is insignificant. In fact, food does not alter dapoxetine pharmacokinetics.

    It can be taken with or without food.

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    Erectile dysfunction. Thorough assessment process. Insurance: If you plan to use insurance, make sure the online provider accepts it. Like Cialis described aboveLevitra is also prescribed for similar uses as Viagra. In other cases, your doctor or a healthcare professional may adjust your medication dosage, which can help lower the possibility of drug interactions while using PDE5 inhibitors.

    Dapoxetine is absorbed and distributed rapidly in the body. The mean steady-state volume is L. Its initial half-life is 1.

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    The major product at the end of the metabolic pathway is circulating dapoxetine N-oxide, which is a weak SSRI and contributes no clinical effect. Desmethyldapoxetine is roughly equipotent to dapoxetine.

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    The metabolites of dapoxetine are eliminated rapidly in the urine with a terminal half-life of The cardiovascular safety profile of dapoxetine has been studied extensively during the drug development.

    Phase I trials showed that dapoxetine had neither clinically significant electrocardiographic effects nor delayed repolarization effects, with dosing up to four-fold greater than the maximum recommended dosage, which is 60 mg.

    Phase III studies in men with PE showed a safety and well tolerated profile of dapoxetine with dosing of 30 and 60 mg. No cardiovascular adverse had been found. Studies of SSRIs in patients with major psychiatric disorders prove that SSRIs are potentially associated with certain neurocognitive adverse effects such as anxiety , akathisia , hypomania , changes in mood, or suicidal thought.

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    McMahon's study in showed that dapoxetine has no effect on mood and is not associated with anxiety or suicidality.

    The incidence of antidepressant discontinuation syndrome symptoms in men using dapoxetine to treat PE has been described by reviewers as low or no different from the incidence of such symptoms in men withdrawn from placebo treatment. Currently, very few methods are used to synthesize S -dapoxetine.

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    This novel approach consists of only six steps in which three main steps are shown above. The initial reactant is trans -cinnamyl alcohol, which is commercially available.

    Sharpless asymmetric epoxidation and Mitsunobu reaction have been used to produce expected S -dapoxetine. This method is considered a good choice compared to the known methods due to high yield and easily obtainable reactants. Dapoxetine was created by Eli Lilly and in phase I clinical trial as an antidepressant.

    Some plans have tiered pricing that depend priligy 60mg where you have your 60jg filled. Poppers contain nitrate drugs such as amyl nitratealkyl nitrate, and butyl nitrate. Natural Medicines. Erectile dysfunction: Viagra and other oral medications. A class of drugs is a group of medications that act in a similar way. Alternatively, it may take place over the phone or via instant messaging.

    It never worked out well as a medication for the treatment of depression, though, and was shelved for a while before subsequently developed to treat PE. Eli Lilly may also receive royalties payment from PPD if the sale exceeds a certain amount.

    Research into the effectiveness of dapoxetine was revisited in Dapoxetine has been marketed and approved in more than 50 countries. Contents move to sidebar hide.

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    Retrieved 11 August International Journal of Impotence Research. PMID Therapeutic Advances in Urology.

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