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Clinical data
Trade namesPriligy, others (see below)
AHFS/Drugs.comInternational Drug Names
Routes of administrationOral (tablets)
ATC codeG04BX14 ( WHO )
Legal status
Legal statusIn general: ℞ (Prescription only)
Pharmacokinetic data
Bioavailability15–76% (mean 42%), T max = 1–1.3 hours
Protein binding>99%
MetabolismLiver (CYP2D6, CYP3A4), kidney (FMO1)
MetabolitesDapoxetine- N -oxide, desmethyldapoxetine, didesmethyldapoxetine
Elimination half-life1.5–1.6 h
ExcretionKidneys [1]

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Time Frame: 4-weeks The evaluation of premature ejaculation symptom scores compared to baseline. Time Frame: 4-weeks The evaluation of Premature Ejaculation priligy dapoxetine dosage measured by Premature Ejaculation Profile PEP Time Frame: 4-weeks The Rate of Premature Ejaculation Profile PEP priligy dapoxetine dosage Time Frame: 4-weeks The evaluation of safety of study drug Number of Participants with Abnormal Laboratory Values and/or Adverse Events That Are Related to Treatment Time Frame: 4-weeks Choosing to participate in a priligy dapoxetine dosage is an important personal decision.Multiple doses of dapoxetine 60 mg/day for 6 days followed by a single 50 mg dose of desipramine increased the mean Cmax and AUCinf of desipramine by approximately 11% and 19% respectively, compared to desipramine administered alone.

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