Super P Force: Dual-Action Solution for Erectile Dysfunction and Premature Ejaculation
| Product dosage: 160mg | |||
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Super P Force is a combination medication designed to address two of the most common male sexual health concerns: erectile dysfunction and premature ejaculation. It contains two active pharmaceutical ingredients—sildenafil citrate and dapoxetine—that work synergistically to improve both the ability to achieve and maintain an erection and to prolong intravaginal ejaculatory latency time. This dual-mechanism approach offers a comprehensive treatment option for men experiencing these concurrent conditions, under appropriate medical supervision. It is intended for use in adult males and requires a thorough clinical evaluation prior to prescription to ensure suitability and safety.
Features
- Contains 100mg sildenafil citrate and 60mg dapoxetine hydrochloride per tablet
- Oral film-coated tablet formulation for ease of administration
- Rapid onset of action, typically within 30–60 minutes post-administration
- Effects may last up to 4–6 hours for the erectile component
- Requires sexual stimulation for efficacy
- Manufactured under strict pharmaceutical quality control standards
Benefits
- Simultaneously addresses both erectile dysfunction and premature ejaculation in a single tablet
- Enhances confidence and sexual performance by supporting firmer, longer-lasting erections
- Significantly extends time to ejaculation, improving sexual satisfaction for both partners
- Reduces performance-related anxiety through reliable pharmacological support
- Offers a discreet and convenient treatment option compared to multiple separate medications
- Clinically proven efficacy in improving sexual function parameters
Common use
Super P Force is prescribed for the treatment of erectile dysfunction (ED) concomitant with premature ejaculation (PE) in adult men. It is typically used on an as-needed basis prior to anticipated sexual activity. The medication is not intended for daily use or as a continuous therapy unless specifically directed by a healthcare provider. Patients should have a confirmed diagnosis of both conditions through proper medical evaluation before initiation of treatment.
Dosage and direction
The recommended dosage is one tablet taken orally with a full glass of water approximately 1–3 hours before anticipated sexual activity. The tablet should be swallowed whole and not crushed, chewed, or broken. Administration with a high-fat meal may delay the onset of action. The maximum recommended dosing frequency is once per 24-hour period. Dosage adjustments may be necessary based on individual tolerance, efficacy, and hepatic function, particularly in elderly patients or those with comorbidities.
Precautions
Patients should undergo cardiovascular assessment before initiation, as sexual activity carries potential cardiac risk. Those with anatomical penile deformities or conditions predisposing to priapism should use with extreme caution. Avoid alcohol consumption during treatment due to increased risk of adverse effects including orthostatic hypotension. Not recommended for patients with severe hepatic impairment (Child-Pugh class C). Caution advised when operating machinery or driving until individual response is established.
Contraindications
Concomitant use with nitrates or nitric oxide donors in any form. History of hypersensitivity to sildenafil, dapoxetine, or any excipients. Patients with severe cardiovascular disorders, unstable angina, or recent myocardial infarction. Hereditary degenerative retinal disorders. Significant hepatic impairment. Concomitant strong CYP3A4 inhibitors. Patients with a history of mania or severe depression.
Possible side effects
Common adverse reactions include headache, flushing, dizziness, nasal congestion, dyspepsia, and nausea. Visual disturbances including blurred vision and altered color perception may occur. Orthostatic hypotension has been reported. Less frequently, palpitations, tachycardia, and dry mouth may present. Rare but serious side effects include priapism, syncope, and serotonin syndrome symptoms. Most side effects are mild to moderate and transient in nature.
Drug interaction
Contraindicated with nitrates and recreational drugs containing nitrites. Potent CYP3A4 inhibitors (e.g., ketoconazole, ritonavir) may significantly increase plasma concentrations. Concurrent use with alpha-blockers may potentiate hypotensive effects. Serotonergic drugs including SSRIs, SNRIs, and triptans increase risk of serotonin syndrome. Moderate interactions possible with erythromycin, saquinavir, and other CYP3A4 substrates.
Missed dose
As Super P Force is taken on an as-needed basis rather than regularly scheduled dosing, the concept of a “missed dose” does not apply. Patients should not take an additional tablet to make up for a missed dose. If a dose is not taken within the appropriate timeframe before sexual activity, patients should wait until the next anticipated sexual encounter to administer the medication.
Overdose
Symptoms may include severe hypotension, syncope, prolonged erection, and serotonin syndrome manifestations. In case of suspected overdose, immediate medical attention is required. Supportive measures should be implemented including cardiovascular monitoring. Priapism lasting more than 4 hours requires urgent urological intervention to prevent permanent tissue damage. There is no specific antidote; treatment should be symptomatic and supportive.
Storage
Store at room temperature (15–30°C) in original packaging protected from light and moisture. Keep out of reach of children and pets. Do not use after the expiration date printed on the packaging. Tablets should be kept in their blister packs until immediately before use to maintain stability and prevent degradation.
Disclaimer
This medication requires a prescription and should only be used under medical supervision. This information is for educational purposes only and does not replace professional medical advice. Individual results may vary. Patients should disclose full medical history and current medications to their healthcare provider before use. Not approved for use in women or individuals under 18 years of age.
Reviews
Clinical studies demonstrate significant improvement in International Index of Erectile Function (IIEF) scores and intravaginal ejaculatory latency time compared to placebo. Patient-reported outcomes indicate high satisfaction rates with both the erectile and ejaculatory control aspects of therapy. Real-world evidence supports the efficacy and tolerability profile when used appropriately in indicated populations. Long-term safety data continue to be collected through post-marketing surveillance programs.