Product image of Lafaval (Tadalafil) supplied by GNH India

Lafaval

Active Ingredient:
Tadalafil
Origin:
EU

Lafaval (Tadalafil)

Tadalafil, the active ingredient in Lafaval, is a phosphodiesterase type 5 (PDE5) inhibitor presented as a tablet for oral use. It is prescribed for erectile dysfunction, benign prostatic hyperplasia, and pulmonary arterial hypertension in adult males.

GNH India supplies Lafaval as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Genepharm S.A.

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Indications & Clinical Uses

Lafaval (tadalafil) acts on the phosphodiesterase type 5 pathway and is indicated for several vascular‑related conditions.

  • Erectile dysfunction: improves ability to achieve and maintain an erection when sexual stimulation occurs.
  • Benign prostatic hyperplasia: relieves urinary symptoms such as reduced flow and urgency.
  • Pulmonary arterial hypertension: enhances exercise capacity by lowering pulmonary vascular resistance.

How It Works

  • Tadalafil selectively inhibits the enzyme phosphodiesterase type 5, preventing the breakdown of cyclic guanosine monophosphate (cGMP). Elevated cGMP leads to smooth‑muscle relaxation in the corpus cavernosum, prostate, and pulmonary vasculature, facilitating increased blood flow to these tissues.

Side Effects

Adverse reactions may vary in frequency and severity.

Common Side Effects

  • Headache: mild to moderate pain in the head.
  • Dyspepsia: upset stomach or indigestion.
  • Back pain: muscular discomfort, often transient.
  • Nasal congestion: blocked or runny nose.
  • Flushing: warmth and redness of the face.
  • Vision changes: blurred or altered color perception.

Serious or Rare Side Effects

  • Sudden vision loss: may indicate non‑arteritic anterior ischemic optic neuropathy.
  • Sudden hearing loss: unexplained decrease in hearing ability.
  • Priapism: prolonged erection lasting more than 4 hours.
  • Cardiovascular events: chest pain, arrhythmia, or stroke in susceptible individuals.
  • Severe hypotension: marked drop in blood pressure, especially with nitrates.
  • Allergic reactions: rash, itching, or swelling of the face and throat.

Precautions & Warnings

Before prescribing Lafaval, clinicians should assess patient history and comorbidities.

  • Cardiovascular disease: evaluate risk of myocardial infarction or stroke.
  • Nitrate therapy: avoid concurrent use due to risk of severe hypotension.
  • Renal or hepatic impairment: consider dose adjustment or monitoring.
  • Concomitant alpha‑blockers: monitor blood pressure for additive effects.
  • Visual disorders: caution in patients with retinal disease.
  • Store at ambient temperature: keep below 25 °C, retain in original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Tadalafil may interact with several medication classes; awareness of interaction severity guides clinical decisions.

Major Interactions (Avoid)

  • Nitrates (e.g., nitroglycerin): can cause profound hypotension.
  • Guanylate cyclase stimulators (e.g., riociguat): risk of excessive blood pressure lowering.
  • Other PDE5 inhibitors: may lead to additive vasodilatory effects.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inhibitors (e.g., ketoconazole, erythromycin): increase tadalafil plasma levels.
  • Antihypertensives (e.g., alpha‑blockers): may enhance blood pressure reduction.
  • Alpha‑adrenergic antagonists (e.g., doxazosin): monitor for dizziness or fainting.

Frequently Asked Questions

Lafaval contains tadalafil and is prescribed for erectile dysfunction, benign prostatic hyperplasia, and pulmonary arterial hypertension. In each case the drug helps improve blood flow to the target tissue, supporting normal function.

Tadalafil blocks the phosphodiesterase type 5 enzyme, which normally degrades cyclic GMP. By preserving cyclic GMP levels, smooth‑muscle cells relax, allowing blood vessels to dilate and increase blood flow to the penis, prostate, or pulmonary arteries.

The specific dose of Lafaval is determined by the prescribing clinician based on the patient’s condition, response, and overall health. Dosage may differ for erectile dysfunction, BPH, or pulmonary hypertension, and should follow the prescriber’s instructions.

Lafaval is classified as Pregnancy Category B and is not indicated for use in women. Safety during breastfeeding has not been established, and the product should be avoided unless a healthcare professional determines that the benefits outweigh potential risks.

To request Lafaval, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Lafaval (tadalafil) has a longer half‑life than sildenafil or vardenafil, allowing a longer therapeutic window of up to 36 hours. This can provide more flexibility for timing of sexual activity, while efficacy and safety profiles remain comparable when used as directed.

Lafaval should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the tablets away from moisture, direct sunlight, and excessive heat to maintain product stability.

Lafaval is taken orally with water, with or without food, as directed by a healthcare professional. The tablet is swallowed whole and should not be split, crushed, or chewed unless specifically instructed.

Serious risks include sudden vision loss, sudden hearing loss, prolonged erection (priapism), and severe hypotension, especially when combined with nitrates or certain cardiovascular drugs. Patients should seek immediate medical attention if any of these events occur.

Lafaval is contraindicated in patients taking nitrates, those with a known hypersensitivity to tadalafil, or individuals with certain cardiovascular conditions where sexual activity is not advised. It should also be avoided in patients with severe liver impairment without specialist guidance.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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