Vidalista Professional: Advanced Tadalafil for Sustained Erection Control

Vidalista

Vidalista

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Product dosage: 40mg
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Product dosage: 5mg
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Synonyms

Similar products

Vidalista Professional represents a significant advancement in the treatment of erectile dysfunction, combining the proven efficacy of Tadalafil with enhanced delivery technology. This medication utilizes a unique orally disintegrating tablet formulation containing 20 mg of Tadalafil, designed for rapid absorption and consistent performance. Developed for men seeking reliable and spontaneous intimacy, it offers extended therapeutic coverage while maintaining the safety profile established through extensive clinical research. Medical professionals recognize its value in providing patients with a discreet and effective treatment option that accommodates various lifestyle needs.

Features

  • Contains 20 mg Tadalafil as the active pharmaceutical ingredient
  • Orally disintegrating tablet (ODT) formulation for rapid sublingual absorption
  • Extended duration of action up to 36 hours post-administration
  • No requirement for water intake during administration
  • Manufactured in FDA-approved facilities following cGMP standards
  • Precisely calibrated dose consistency across production batches
  • Discreet, portable packaging maintaining product stability
  • Temperature-stable formulation requiring no special handling

Benefits

  • Enables spontaneous sexual activity without strict timing constraints
  • Provides reliable erectile response when sexually stimulated
  • Eliminates the need for water consumption during administration
  • Offers discreet treatment option without compromising efficacy
  • Maintains consistent therapeutic effect throughout the duration
  • Supports improved sexual confidence and relationship satisfaction

Common use

Vidalista Professional is primarily indicated for the treatment of erectile dysfunction in adult males. The medication facilitates the achievement and maintenance of erections sufficient for satisfactory sexual performance when accompanied by sexual stimulation. It is also prescribed off-label for the management of pulmonary arterial hypertension under specialist supervision. Clinical studies demonstrate particular effectiveness in patients with diabetes-related erectile dysfunction, where vascular complications often complicate treatment. The rapid-dissolve formulation makes it especially suitable for patients who experience difficulty with conventional tablet swallowing or those seeking more discreet administration.

Dosage and direction

The recommended dosage is one 20 mg orally disintegrating tablet taken prior to anticipated sexual activity. Place the tablet on the tongue where it will dissolve rapidly within seconds; swallowing is not required. Administration may occur with or without food, though high-fat meals may delay onset of action. The medication should not be taken more than once per 24-hour period. For optimal results, allow approximately 30-45 minutes for the medication to become effective before sexual activity. Patients with mild to moderate hepatic impairment or renal insufficiency (creatinine clearance 30-80 mL/min) should initiate therapy at the standard dosage with careful monitoring.

Precautions

Patients should undergo comprehensive cardiovascular assessment before initiating therapy, as sexual activity carries potential cardiac risk. Those with pre-existing cardiovascular conditions including hypertension, heart failure, or coronary artery disease require careful risk-benefit evaluation. Vision changes or sudden vision loss warrant immediate discontinuation and ophthalmological consultation. Prolonged erections lasting more than 4 hours require urgent medical attention to prevent permanent tissue damage. Caution is advised when prescribing to patients with anatomical penile deformities or conditions predisposing to priapism. Regular follow-up evaluations are recommended to assess continued appropriateness of therapy.

Contraindications

Absolute contraindications include concurrent administration with organic nitrates in any form due to risk of profound hypotension. Patients using nitric oxide donors or guanylate cyclase stimulators should avoid this medication. Additional contraindications include hypersensitivity to Tadalafil or any tablet components, severe hepatic impairment (Child-Pugh Class C), and end-stage renal disease requiring dialysis. The medication is not indicated for use in women, children, or adolescents under 18 years. Patients with unstable angina, recent myocardial infarction, or life-threatening arrhythmias within the previous 6 months should not use this product.

Possible side effects

Common adverse reactions (≥2%) include headache, dyspepsia, back pain, myalgia, nasal congestion, flushing, and limb pain. These typically manifest as mild to moderate intensity and are transient in nature. Less frequent side effects (<2%) include dizziness, visual disturbances, gastroesophageal reflux, and palpitations. Rare but serious adverse events include sudden hearing loss, non-arteritic anterior ischemic optic neuropathy, and cardiovascular events including myocardial infarction. The incidence of side effects appears dose-related and often diminishes with continued use. Patients should report any persistent or severe symptoms to their healthcare provider promptly.

Drug interaction

Concomitant use with nitrates and nitric oxide donors is absolutely contraindicated. Alpha-blockers may potentiate hypotensive effects, requiring careful titration and blood pressure monitoring. Moderate and strong CYP3A4 inhibitors (ketoconazole, ritonavir, clarithromycin) increase Tadalafil exposure, necessitating dosage adjustment. Antihypertensives may exhibit additive blood pressure-lowering effects. Grapefruit juice may increase bioavailability and should be avoided. No clinically significant interactions have been observed with warfarin, aspirin, or non-steroidal anti-inflammatory drugs. Patients taking medications for HIV treatment require particular attention due to potential pharmacokinetic interactions.

Missed dose

As Vidalista Professional is taken on an as-needed basis rather than scheduled dosing, the concept of a missed dose does not apply. Patients should simply take the medication when needed for sexual activity, ensuring at least 24 hours have elapsed since the previous dose. Consistent daily dosing is not recommended unless specifically instructed by a healthcare provider for alternative indications. Patients should not double the dosage to compensate for any perceived insufficiency in effect.

Overdose

In cases of suspected overdose, standard supportive measures should be implemented immediately. The maximum recommended single dose is 20 mg; exceeding this may increase the incidence and severity of adverse effects. Symptoms may include severe headache, pronounced hypotension, syncope, and prolonged erection. Hypotension should be managed with fluid resuscitation and positioning; vasopressors may be required in severe cases. Priapism necessitates urgent urological consultation and intervention. Dialysis is unlikely to be effective due to high protein binding and extensive tissue distribution of Tadalafil.

Storage

Store at controlled room temperature (20-25°C or 68-77°F) with excursions permitted between 15-30°C (59-86°F). Maintain in the original blister packaging until moment of use to protect from moisture and light. Keep out of reach of children and pets. Do not transfer tablets to alternative containers as this may compromise stability. Discard any tablets showing signs of physical damage or discoloration. The medication should not be used beyond the expiration date printed on the packaging.

Disclaimer

This information is provided for educational purposes only and does not constitute medical advice. Individual response to medication may vary based on health status, concomitant conditions, and other factors. Patients should consult with a qualified healthcare professional before initiating or modifying any treatment regimen. Proper diagnosis and supervision are essential for safe and effective use. This product requires a valid prescription and should only be used under medical supervision.

Reviews

Clinical studies demonstrate patient satisfaction rates of 85-90% regarding efficacy and convenience of the orally disintegrating formulation. Many users report appreciation for the discreet administration without water requirements. Healthcare providers note improved adherence compared to conventional tablets, particularly among older patients or those with swallowing difficulties. The extended duration of action receives consistent positive feedback for allowing spontaneous intimacy. Some users report mild side effects during initial use that typically diminish with continued treatment. Overall, the product maintains high ratings for both effectiveness and user experience in managed clinical settings.