Product image of Letrozol Ebrocite (Letrozole) supplied by GNH India

Letrozol Ebrocite

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Ebrocite (Letrozole)

Letrozole, the active ingredient in Letrozol Ebrocite, is an aromatase inhibitor presented as an oral tablet for oral use. By blocking the aromatase enzyme, it markedly reduces estrogen production, a key driver of hormone receptor‑positive breast cancer, and is therefore used in the endocrine treatment of this disease in postmenopausal women.

GNH India supplies Letrozol Ebrocite as a licensed, GDP‑compliant international pharmaceutical supplier, meeting EU quality standards and serving oncology centres, hospitals and pharmacies worldwide with reliable, on‑time delivery and comprehensive regulatory support.

Manufacturer / TM Owner

Laboratórios Azevedos - Indústria Farmacêutica, S.A.

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Indications & Clinical Uses

Letrozole is an aromatase inhibitor used in the management of hormone‑dependent breast cancer.

  • Adjuvant treatment of hormone receptor‑positive breast cancer: reduces risk of recurrence in postmenopausal women.
  • Metastatic hormone receptor‑positive breast cancer: slows disease progression in postmenopausal women.
  • Neoadjuvant therapy for breast cancer: may shrink tumors before surgery in postmenopausal women.

How It Works

  • Letrozole reversibly binds to the aromatase enzyme in peripheral tissues, acting as a non‑competitive inhibitor. This blocks the conversion of androgens to estrogens, leading to markedly lower circulating estrogen levels and consequently diminishing estrogen‑driven proliferation of hormone receptor‑positive breast cancer cells.

Side Effects

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

Common Side Effects

  • Hot flashes: sudden feeling of warmth, often with sweating.
  • Arthralgia: joint pain or stiffness.
  • Fatigue: persistent tiredness not relieved by rest.
  • Nausea: mild to moderate upset stomach.
  • Headache: intermittent or persistent head pain.
  • Dizziness: sensation of light‑headedness.

Serious or Rare Side Effects

  • Severe bone loss or osteoporosis: increased fracture risk.
  • Venous thromboembolism: deep‑vein thrombosis or pulmonary embolism.
  • Elevated liver enzymes: potential hepatic injury.
  • Anaphylaxis: rare severe allergic reaction requiring immediate medical attention.

Precautions & Warnings

When prescribing Letrozol Ebrocite, clinicians should observe several precautionary measures to ensure patient safety.

  • Assess bone health: obtain baseline DEXA scan and consider calcium/vitamin D supplementation.
  • Monitor liver function: periodic liver‑function tests are recommended.
  • Evaluate cardiovascular risk: avoid in patients with a history of thromboembolic events.
  • Contraindicated in pregnancy: do not use in women of childbearing potential without effective contraception.
  • Counsel patients on hot flashes and potential bone loss.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent estrogen replacement therapy: antagonizes letrozole’s effect.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce plasma concentrations.
  • Tamoxifen: opposing mechanisms may diminish therapeutic benefit.

Moderate Interactions (Monitor Closely)

  • Warfarin: letrozole may increase INR, requiring closer monitoring.
  • CYP2C19 inhibitors (e.g., fluconazole): can raise letrozole levels.
  • Statins: monitor for signs of myopathy when combined.

Frequently Asked Questions

Letrozol Ebrocite contains letrozole, an aromatase inhibitor indicated for the treatment of hormone receptor‑positive breast cancer in postmenopausal women. It is used in adjuvant, neoadjuvant and metastatic settings to reduce estrogen‑driven tumor growth.

Letrozole blocks the aromatase enzyme, which converts androgens into estrogen. By inhibiting this conversion, circulating estrogen levels fall dramatically, depriving estrogen‑dependent breast cancer cells of the growth signal they require.

The exact dose is determined by the prescribing physician based on clinical guidelines, patient characteristics and treatment goals. Healthcare professionals select the appropriate strength and dosing schedule for each individual patient.

Letrozole is contraindicated during pregnancy and is not recommended for breastfeeding women. It can cause fetal harm, and women of childbearing potential should use effective contraception throughout treatment and for a period after discontinuation.

To place an order, submit an enquiry on the Letrozol Ebrocite 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 required import documentation.

Letrozole, anastrozole and exemestane belong to the same class. Letrozole is often chosen for its potent and sustained estrogen suppression, while anastrozole has a similar efficacy profile with a slightly different safety spectrum. Choice depends on patient tolerance, prior therapy and physician preference.

Letrozol Ebrocite tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture, direct sunlight and extreme heat to maintain potency throughout the shelf‑life.

The medication is taken orally, usually as a tablet swallowed whole with water. It can be taken with or without food, but patients should follow the specific instructions provided by their healthcare provider.

Serious adverse events include severe bone loss leading to fractures, venous thromboembolism such as deep‑vein thrombosis or pulmonary embolism, significant liver enzyme elevations and rare anaphylactic reactions. Patients should be monitored regularly for these conditions.

Letrozole is not indicated for premenopausal women, pregnant or breastfeeding individuals, and anyone with a known hypersensitivity to letrozole or other aromatase inhibitors. Patients with uncontrolled cardiovascular disease or a history of severe thromboembolic events should also avoid its use.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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