Product image of Lerana (Letrozole) supplied by GNH India

Lerana

Active Ingredient:
Letrozole
Origin:
EU

Lerana (Letrozole)

Letrozole, the active ingredient in Lerana, is an aromatase inhibitor presented as a tablet for oral use. It is employed in the treatment of hormone‑receptor positive breast cancer in postmenopausal women, both as adjuvant therapy and for metastatic disease.

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

Manufacturer / TM Owner

Heaton K.S.

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Indications & Clinical Uses

Letrozole acts on estrogen‑dependent breast cancer pathways and is indicated for the following conditions:

  • Adjuvant treatment of hormone‑receptor positive breast cancer in postmenopausal women: reduces risk of disease recurrence after surgery.
  • Metastatic breast cancer in postmenopausal women: helps control tumor progression and prolongs survival.
  • Hormone‑sensitive breast cancer in postmenopausal patients: lowers circulating estrogen levels to inhibit tumor growth.

How It Works

  • Letrozole selectively inhibits the aromatase enzyme, which converts adrenal and peripheral androgens into estrogens. By blocking this conversion, systemic estrogen concentrations decline, depriving estrogen‑dependent tumor cells of a growth stimulus and thereby slowing or halting cancer progression.

Side Effects

Letrozole may cause a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Hot flashes: transient episodes of intense warmth.
  • Joint and muscle pain: aching or stiffness in limbs.
  • Fatigue: persistent tiredness not relieved by rest.
  • Nausea: mild to moderate upset stomach.
  • Headache: pressure or throbbing pain.
  • Dizziness: sensation of light‑headedness.

Serious or Rare Side Effects

  • Osteoporotic fractures: increased risk due to bone density loss.
  • Deep vein thrombosis: formation of blood clots in deep veins.
  • Elevated liver enzymes: signs of hepatic stress.
  • Severe allergic reaction: rash, swelling, or difficulty breathing.
  • Pulmonary embolism: blockage of lung arteries.
  • Cardiovascular events: rare heart‑related complications.

Precautions & Warnings

Before initiating Letrozole therapy, several safety considerations should be observed.

  • Monitor bone health: assess bone mineral density periodically due to estrogen depletion.
  • Evaluate liver function: check hepatic enzymes before and during treatment.
  • Assess cardiovascular risk: consider history of thromboembolic disease.
  • Review concomitant medications: avoid drugs that may interfere with aromatase inhibition.
  • Store at ambient temperature below 25°C: keep in the original container, protect from moisture.

Avoid Interactions

Letrozole can interact with other medicines, affecting efficacy or safety.

Major Interactions (Avoid)

  • Estrogen replacement therapy: antagonizes Letrozole’s intended effect.
  • Strong CYP2C19 inhibitors (e.g., fluconazole): may raise Letrozole plasma levels.
  • Tamoxifen: concurrent use reduces therapeutic benefit of both agents.

Moderate Interactions (Monitor Closely)

  • Warfarin: Letrozole may potentiate anticoagulant effect, increasing INR.
  • CYP3A4 inducers (e.g., rifampin): may lower Letrozole concentrations.
  • SSRIs (e.g., fluoxetine): may increase incidence of hot flashes.
  • Antihypertensives: monitor blood pressure as Letrozole can affect vascular tone.

Frequently Asked Questions

Lerana contains letrozole, an aromatase inhibitor indicated for the treatment of hormone‑receptor positive breast cancer in postmenopausal women. It is used both as adjuvant therapy after surgery and for managing metastatic disease, helping to lower estrogen levels that can fuel tumor growth.

Letrozole works by selectively blocking the aromatase enzyme, which converts androgens into estrogens in peripheral tissues. By inhibiting this conversion, systemic estrogen concentrations fall, depriving estrogen‑dependent breast cancer cells of a key growth signal and thereby slowing tumor progression.

The dose of Lerana is determined by the prescribing clinician based on the patient’s clinical condition, treatment goals, and tolerability. Physicians typically start with a standard oral dose and may adjust it according to response and safety monitoring.

Lerana is classified as Pregnancy Category X, indicating it is contraindicated in pregnancy because it can cause fetal harm. It is also not recommended for breastfeeding women, as letrozole may be excreted in milk and affect the infant.

To order Lerana, 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 necessary import documentation.

Lerana (letrozole) is a third‑generation aromatase inhibitor with high potency and a longer half‑life compared with earlier agents such as anastrozole. It often provides more consistent estrogen suppression, which can translate into improved disease control in many postmenopausal breast‑cancer patients.

Lerana tablets should be stored at ambient temperature below 25 °C. Keep the product in its original packaging, protect it from moisture and direct sunlight, and ensure the container is tightly closed to maintain stability.

Lerana is taken orally, usually once daily, with or without food. Patients should swallow the tablet whole with a glass of water and follow the dosing schedule prescribed by their healthcare provider.

The most serious risks include osteoporotic fractures due to bone density loss, deep‑vein thrombosis or pulmonary embolism, and severe liver enzyme elevations. Patients should be monitored regularly for signs of these complications and report any concerning symptoms promptly.

Lerana should not be used by pregnant or breastfeeding women, premenopausal patients, or individuals with known hypersensitivity to letrozole or any excipients in the tablet. It is also contraindicated in patients with severe liver impairment or uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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