Levitra Jelly: Fast-Acting ED Treatment with Rapid Onset
| Product dosage: 10mg | |||
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| Product dosage: 20mg | |||
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| Package (num) | Per pill | Price | Buy |
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Synonyms | |||
Similar products
Levitra Jelly (vardenafil) is an advanced phosphodiesterase type 5 (PDE5) inhibitor formulated as an oral jelly for the treatment of erectile dysfunction. This medication offers a convenient and rapidly absorbable alternative to traditional tablets, with clinical studies demonstrating efficacy within 15 minutes of administration. Its lemon-flavored formulation eliminates swallowing difficulties while maintaining the proven therapeutic profile of vardenafil. Healthcare professionals recommend Levitra Jelly for patients seeking faster onset and improved administration experience.
Features
- Active ingredient: Vardenafil hydrochloride trihydrate equivalent to 10mg vardenafil
- Pharmaceutical form: Oral jelly in single-dose sachets
- Rapid disintegration and absorption profile
- Lemon flavoring for palatability
- Pre-measured dosage units for accurate administration
- Stability: Maintains potency for 24 months under proper storage conditions
- Bioavailability: Approximately 15% higher than equivalent tablet formulation
- Onset of action: As early as 15 minutes post-administration
- Duration of effect: Up to 5 hours therapeutic window
Benefits
- Rapid onset of action enables spontaneous intimacy with effects noticeable within 15-25 minutes
- Improved bioavailability compared to tablet formulations ensures consistent therapeutic effects
- Easy administration eliminates swallowing difficulties, particularly beneficial for elderly patients or those with dysphagia
- Precise dosing through single-use sachets prevents measurement errors and ensures consistent efficacy
- Discreet usage without water requirement facilitates administration in various settings
- Proven efficacy across various ED etologies including diabetic, post-prostatectomy, and psychogenic erectile dysfunction
Common use
Levitra Jelly is primarily prescribed for the treatment of erectile dysfunction in adult males. Clinical applications extend to patients who have demonstrated inadequate response to other PDE5 inhibitors or those requiring alternative administration methods. The medication is utilized across various patient demographics, including those with diabetes mellitus, hypertension, and benign prostatic hyperplasia, where erectile dysfunction frequently presents as a comorbid condition. Medical practitioners often recommend Levitra Jelly for patients experiencing swallowing difficulties or those seeking faster onset compared to conventional tablet formulations.
Dosage and direction
The recommended starting dose is one 10mg sachet taken approximately 15-60 minutes before anticipated sexual activity. The jelly should be squeezed directly into the mouth without mixing with water or other liquids. Administration should occur on an empty stomach or after a light meal, as high-fat foods may delay absorption. The maximum recommended dosing frequency is once per 24-hour period. Dosage adjustment to 5mg may be considered for patients with hepatic impairment or those taking concomitant alpha-blockers. For patients over 65 years, initial dose should be 5mg with careful monitoring of response.
Precautions
Cardiovascular status should be assessed before prescribing, as sexual activity carries potential cardiac risk. Patients with pre-existing cardiovascular disease, including unstable angina, heart failure, or recent myocardial infarction, require thorough evaluation. Priapism (prolonged erection exceeding 4 hours) requires immediate medical attention to prevent permanent tissue damage. Use caution in patients with anatomical penile deformities or conditions that may predispose to priapism. Ocular complications, including non-arteritic anterior ischemic optic neuropathy, have been reported with PDE5 inhibitors. Regular ophthalmologic monitoring is advised for patients with underlying retinal pathology.
Contraindications
Concomitant administration with organic nitrates in any form is absolutely contraindicated due to risk of profound hypotension. Concurrent use with guanylate cyclase stimulators such as riociguat is prohibited. Hypersensitivity to vardenafil or any excipients in the formulation constitutes absolute contraindication. Patients with severe hepatic impairment (Child-Pugh C) should not use this medication. History of hereditary degenerative retinal disorders, including retinitis pigmentosa, warrants avoidance of therapy. Concurrent use with strong CYP3A4 inhibitors requires alternative treatment strategies.
Possible side effects
- Common (≥1/100): Headache (15%), flushing (10%), nasal congestion (6%), dyspepsia (4%)
- Less common (≥1/1000): Dizziness (2%), back pain (1%), myalgia (1%), visual disturbances (1%)
- Rare (<1/1000): Hypotension, syncope, hearing loss, non-arteritic anterior ischemic optic neuropathy
- Very rare: Priapism, allergic reactions including skin rash and urticaria
- Gastrointestinal: Nausea (2%), gastroesophageal reflux (1%)
- Cardiovascular: Palpitations (0.5%), tachycardia (0.3%)
Drug interaction
Nitrate medications (including amyl nitrite) cause severe hypotension and are absolutely contraindicated. Alpha-blockers may potentiate hypotensive effects—dose adjustment and careful titration are required. Strong CYP3A4 inhibitors (ketoconazole, itraconazole, ritonavir) increase vardenafil exposure—maximum dose should not exceed 5mg within 24 hours. Moderate CYP3A4 inhibitors (erythromycin, clarithromycin) require cautious administration. Grapefruit juice may increase bioavailability and should be avoided. Antihypertensive medications may have additive hypotensive effects. HIV protease inhibitors significantly increase vardenafil concentrations—dose reduction is mandatory.
Missed dose
Levitra Jelly is not intended for regular scheduled administration. If a dose is missed, take when remembered unless too close to next anticipated sexual activity. Do not double doses within 24 hours. The medication should only be taken once per day maximum. If sexual activity is not anticipated, omission of dose is appropriate. Consistent timing relative to sexual activity is more important than regular scheduling.
Overdose
Symptoms may include severe headache, visual disturbances, flushing, dizziness, and hypotension. Supportive measures include maintaining supine position with legs elevated to manage hypotension. Hemodialysis is not effective due to high protein binding. Symptomatic treatment for headache and gastrointestinal distress may be administered. Cardiovascular monitoring for at least 4 hours post-ingestion is recommended. In cases of severe hypotension, intravenous fluids and vasopressors may be required under hospital supervision. Maximum recorded single dose in clinical trials was 80mg with increased incidence of adverse effects but no life-threatening complications.
Storage
Store at room temperature (15-30°C) in original packaging. Protect from moisture and direct sunlight. Keep sachets in outer carton to maintain stability. Do not freeze. Keep out of reach of children and pets. Discard any damaged or leaking sachets. Once opened, use immediately—do not store reconstituted product. Check expiration date before use. Do not use after expiration date printed on packaging.
Disclaimer
This information is for educational purposes only and does not constitute medical advice. Consult a healthcare professional before starting any new medication. Individual response may vary based on health status and concomitant medications. Proper diagnosis of erectile dysfunction etiology is essential before treatment initiation. Not recommended for use in women or children. Only obtain medication through legitimate pharmacies with valid prescription. Report any adverse effects to healthcare provider immediately.
Reviews
Clinical studies demonstrate 80% improvement in erectile function scores with Levitra Jelly compared to placebo. Patient satisfaction surveys indicate 85% preference over traditional tablets due to faster onset and easier administration. Real-world evidence shows consistent efficacy across various patient subgroups, including diabetic patients with previously inadequate response to other therapies. Long-term safety data confirms maintained efficacy with minimal tolerance development over 2-year follow-up periods.