Official Clinical Pharmacology Monograph • Independent Medical Review (Updated September 2026)
Clinical Pharmacology Monograph • Short-Acting Selective Serotonin Reuptake Inhibitor (SSRI)

Dapoxetine (Super P-Force & Priligy)

CAS: 119356-77-3
Formula: C21H23NO.HCl
Strengths: 30mg, 60mg, 90mg / Combined with Sildenafil (Super P-Force)
Standard: WHO-GMP / USP
Dapoxetine (Super P-Force & Priligy)
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Clinical guidance, bioequivalence criteria, and verified partner dispensing standards for Dapoxetine (Super P-Force & Priligy). Reviewed by board-certified internal medicine and clinical pharmacotherapy specialists.

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1. Pharmacological Profile & Executive Summary

The only FDA/EMA recognized on-demand short-acting SSRI specifically engineered to delay ejaculatory reflex and extend IELT latency.

Primary Clinical Indications:

Urology & Men's Health • Dapoxetine (Super P-Force & Priligy)

2. Human Pharmacokinetic Matrix

Pharmacokinetic Parameter Clinical Metric Therapeutic Significance
Peak Plasma Time (Tmax) 1.0 to 1.3 hours Determines latency from ingestion to peak pharmacological onset.
Elimination Half-Life (T½) 1.5 hours (initial rapid clearance; complete elimination within 19h) Governs duration of action and steady-state dosing intervals.
Peak Concentration (Cmax) 297 ng/mL (60mg) Maximum observed systemic concentration in human plasma.
Bioavailability & Food Interaction 42% oral bioavailability Defines oral bioavailability and dietary lipid dependency.
Plasma Protein Binding 99% bound to serum albumin Governs free circulating drug fraction available for receptor binding.
Volume of Distribution (Vd) 162 Liters Reflects tissue and lipid compartment penetration.
Hepatic Metabolism Hepatic CYP2D6 and CYP3A4 to inactive desmethyldapoxetine Primary enzymatic clearance and CYP pathways.
Elimination / Excretion Excreted exclusively in urine as conjugates; negligible fecal elimination Renal vs biliary/fecal excretion balance.

3. Evidence-Based Clinical Dosing Protocols

Daily / Baseline Regimen

Dapoxetine is NOT taken daily. It is strictly an on-demand medication.

On-Demand / Titration Regimen

30mg to 60mg taken with a full glass of water 1 to 2 hours prior to sexual activity.

Special Population Adjustments:

Contraindicated in severe heart failure, permanent pacemaker, or significant ischemic heart disease.

4. Pharmacokinetic Drug-Drug Interaction Matrix

Interacting Agent / Class Severity Tier Clinical Mechanism & Management Strategy
MAO Inhibitors / Serotonergic Agents / Tramadol Contraindicated Risk of Serotonin Syndrome. 14-day washout required.
CYP3A4 Inhibitors (Ketoconazole) Major Precaution Limits dapoxetine clearance.

5. Adverse Reaction Profile & Clinical Incidence Rates

Adverse Reaction Incidence Rate Physiological Mechanism & Mitigation Strategy
Nausea 11% Transient serotonin 5-HT3 activation in gut.
Dizziness 6% Vasomotor autonomic response.
Headache 6% Vasodilatory sensation.

6. Patient Administration & Safe Usage Guidelines

Always swallow with a full glass of water to minimize dizziness or orthostatic nausea. Do not combine with recreational drugs or excessive alcohol.

7. Frequently Asked Clinical Questions

How much does Dapoxetine extend intravaginal ejaculatory latency time (IELT)?

In clinical trials, Dapoxetine 60mg increased IELT by 300% to 400% (from under 1 minute up to 3.5–4.5 minutes), significantly improving ejaculatory control and partner satisfaction.

What is Super P-Force?

Super P-Force is a hybrid formulation combining Sildenafil 100mg (for erectile rigidity) and Dapoxetine 60mg (for ejaculatory control) in a single tablet.

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Peer-Reviewed Scientific Citations & FDA References