Levitra Jelly: Fast-Acting Erectile Dysfunction Relief

Levitra

Levitra

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Product dosage: 10mg
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Product dosage: 20mg
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Synonyms

Similar products

Levitra Jelly (vardenafil) is an advanced oral treatment for erectile dysfunction (ED), formulated as a strawberry-flavored gel for rapid absorption and reliable performance. This phosphodiesterase type 5 (PDE5) inhibitor offers a convenient, discreet alternative to traditional tablets, with a clinically proven onset of action often within 15 minutes. Its unique formulation is designed for patients who may experience difficulty swallowing pills or desire quicker dissolution and predictable results, making it a preferred option for spontaneous intimacy.

Features

  • Active ingredient: Vardenafil hydrochloride trihydrate
  • Form: Oral jelly (strawberry-flavored)
  • Available strengths: 10 mg per sachet
  • Rapid disintegration and absorption profile
  • Pre-measured, single-use sachets for accurate dosing
  • No water required for administration
  • Manufactured under strict pharmaceutical quality standards

Benefits

  • Rapid onset: Clinical studies indicate effects may be noticeable in as little as 15 minutes post-administration.
  • High efficacy rates: Demonstrated success in achieving and maintaining erections sufficient for sexual activity across various ED severities.
  • Convenient administration: Gel formulation eliminates swallowing difficulties and allows discreet use without water.
  • Predictable duration: Provides a therapeutic window of up to 4-5 hours for spontaneous intimacy.
  • Improved bioavailability: Enhanced absorption compared to some traditional tablet formulations.
  • Patient preference: Pleasant flavor and easy administration improve treatment adherence.

Common use

Levitra Jelly is primarily prescribed for the treatment of erectile dysfunction in adult males. It is suitable for patients with various underlying causes of ED, including vascular, neurological, and psychological factors. The medication may be used by patients who have demonstrated inadequate response to other PDE5 inhibitors or who prefer a rapid-dissolving formulation. It is particularly beneficial for those with dysphagia or who seek more spontaneous intimate opportunities without planning around tablet ingestion timing.

Dosage and direction

The recommended starting dose is one 10 mg sachet taken approximately 15-60 minutes before anticipated sexual activity. The jelly should be squeezed directly into the mouth from the sachet and swallowed without water. Do not exceed one dose per 24-hour period. Dosage adjustment to 5 mg may be considered for patients taking certain concomitant medications or with hepatic impairment. The maximum recommended frequency is once daily. Sexual stimulation is required for the medication to be effective.

Precautions

Patients should undergo thorough cardiovascular assessment before initiating treatment. Use with caution in patients with anatomical penile deformity, bleeding disorders, or active peptic ulceration. Avoid concomitant use with other ED treatments. Patients should seek immediate medical attention if an erection persists beyond 4 hours. Those with cardiovascular risk factors should avoid sexual activity if not deemed medically appropriate. Visual disturbances have been reported and may affect ability to drive or operate machinery.

Contraindications

Concomitant administration with nitrates in any form (including amyl nitrite) is absolutely contraindicated. Additional contraindications include hypersensitivity to vardenafil or any excipients, severe hepatic impairment (Child-Pugh C), end-stage renal disease requiring dialysis, hypotension (BP <90/50 mmHg), recent stroke or myocardial infarction, unstable angina, and hereditary degenerative retinal disorders.

Possible side effects

Common adverse reactions (≥2%) include headache, flushing, dyspepsia, nasal congestion, and dizziness. Less frequently reported effects include visual disturbances (abnormal vision, photophobia), palpitations, and back pain. Rare but serious side effects include priapism, sudden hearing loss, non-arteritic anterior ischemic optic neuropathy, and cardiovascular events. Most side effects are dose-dependent and transient in nature.

Drug interaction

Concomitant use with nitrates may cause profound hypotension. Potent CYP3A4 inhibitors (ketoconazole, ritonavir) increase vardenafil exposure—dose reduction to 5 mg is recommended. Alpha-blockers may enhance hypotensive effects. Grapefruit juice may increase bioavailability. Moderate interaction with other antihypertensives. Caution with drugs prolonging QT interval.

Missed dose

Levitra Jelly is taken on an as-needed basis rather than scheduled dosing. No missed dose protocol applies. Do not take extra medication to make up for a missed dose. The next dose may be taken when needed, maintaining the 24-hour minimum interval between administrations.

Overdose

Symptoms may include severe headache, visual disturbances, hypotension, syncope, and prolonged erection. Standard supportive measures should be implemented, including cardiovascular monitoring. Priapism requires immediate urological intervention. Dialysis is unlikely to be beneficial due to high protein binding. Contact poison control center for latest management guidelines.

Storage

Store at room temperature (15-30°C) in original packaging. Protect from moisture and direct sunlight. Keep out of reach of children and pets. Do not use after expiration date printed on sachet. Do not freeze or expose to excessive heat.

Disclaimer

This information is for educational purposes only and does not replace professional medical advice. Levitra Jelly is a prescription medication requiring proper medical evaluation and supervision. Individual results may vary. Only a qualified healthcare provider can determine appropriate treatment based on comprehensive medical assessment.

Reviews

Clinical trials demonstrate 80% improvement in erectile function scores versus placebo. Real-world evidence supports high patient satisfaction rates particularly regarding speed of onset and convenience of administration. 72% of patients reported successful intercourse attempts within 30 minutes of dosing in phase III studies. Long-term users report consistent efficacy with proper dosing guidance.