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

Letrozol Sun

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Sun (Letrozole)

Letrozole, the active ingredient in Letrozol Sun, is a aromatase inhibitor presented as an oral tablet for oral use. It reduces estrogen production and is used in the treatment of hormone receptor‑positive breast cancer in postmenopausal women. It is indicated for postmenopausal women whose tumors express estrogen receptors, helping to slow disease progression.

GNH India supplies Letrozol Sun as a licensed, GDP‑compliant international pharmaceutical supplier, adhering to EU quality standards and providing the product to oncology centres, hospitals and pharmacies worldwide.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

Letrozole is an aromatase inhibitor used in hormone‑dependent breast cancer therapy.

  • Hormone receptor‑positive breast cancer in postmenopausal women: reduces estrogen‑driven tumor growth and delays disease progression.
  • Adjuvant treatment of early‑stage disease: improves disease‑free survival after surgery.
  • Metastatic breast cancer: helps control tumor spread and prolongs overall survival.

How It Works

  • Letrozole selectively and non‑competitively inhibits the aromatase enzyme, which converts androgens to estrogens in peripheral tissues. By blocking this conversion, systemic estrogen levels fall, depriving estrogen‑dependent tumor cells of a growth stimulus and thereby slowing or halting cancer progression.

Side Effects

Adverse reactions may occur with Letrozol Sun and are categorized by frequency.

Common Side Effects

  • Hot flashes: sudden feeling of warmth and sweating.
  • Joint and muscle pain: aching in limbs and back.
  • Nausea: mild to moderate upset stomach.
  • Fatigue: persistent tiredness.
  • Headache: mild to moderate intensity.
  • Increased sweating: excessive perspiration.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, elevated enzymes.
  • Bone fracture: increased risk of osteoporosis‑related breaks.
  • Pulmonary embolism: sudden shortness of breath and chest pain.
  • Allergic reaction: rash, itching, swelling, or anaphylaxis.
  • Elevated cholesterol: significant rise in blood lipid levels.

Precautions & Warnings

Patients should be counseled on safety measures before starting Letrozol Sun.

  • Monitor bone mineral density: assess risk of osteoporosis and consider supplementation.
  • Check liver enzymes: perform baseline and periodic hepatic function tests.
  • Assess cardiovascular health: evaluate for thrombosis risk factors.
  • Contraindicated in pregnancy: avoid use in pregnant women due to teratogenicity.
  • Counsel on menopausal symptoms: provide strategies for managing hot flashes and sweating.
  • Store at ambient temperature: keep in the original pack, protect from moisture and direct sunlight.

Avoid Interactions

Letrozol Sun may interact with other medicines; interactions are grouped by clinical significance.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may markedly reduce letrozole exposure.
  • Tamoxifen: antagonistic hormonal effects can diminish therapeutic benefit.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): may increase bleeding tendency.
  • Statins (e.g., simvastatin): potential rise in plasma concentrations.
  • Selective serotonin reuptake inhibitors (e.g., fluoxetine): may affect metabolism and plasma levels.

Frequently Asked Questions

Letrozol Sun contains letrozole, an aromatase inhibitor prescribed to treat hormone receptor‑positive breast cancer in postmenopausal women. It works by lowering estrogen levels, which helps slow tumor growth and can be used in early‑stage, adjuvant, or metastatic settings.

Letrozole blocks the aromatase enzyme, preventing the conversion of androgens into estrogen in peripheral tissues. The resulting drop in circulating estrogen deprives estrogen‑dependent cancer cells of a key growth signal, thereby inhibiting tumor proliferation.

The specific dose of Letrozol Sun is determined by the prescribing physician based on the patient’s clinical condition, disease stage, and other individual factors. Only a qualified healthcare professional should set the dosing regimen.

Letrozol Sun is classified as pregnancy category X, meaning it is contraindicated in pregnancy because it can cause fetal harm. It is also not recommended while breastfeeding, as it may pass into breast milk and affect the infant.

To request Letrozol Sun, 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.

Letrozol Sun (letrozole) is a non‑steroidal aromatase inhibitor similar to anastrozole and exemestane. Compared with anastrozole, letrozole often shows slightly higher potency in estrogen suppression, while exemestane is a steroidal inhibitor with a different binding profile. Choice depends on physician judgment, patient tolerance and specific clinical guidelines.

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

Letrozol Sun is taken orally, usually as a whole tablet swallowed with water. It is generally taken once daily, at the same time each day, with or without food, as directed by the prescribing clinician.

Serious risks include severe liver injury, bone fractures due to decreased bone mineral density, and rare events such as pulmonary embolism or severe allergic reactions. Patients should be monitored regularly for liver function, bone health and any signs of thromboembolic events.

Letrozol Sun should not be used by pregnant women, individuals with known hypersensitivity to letrozole or any component of the formulation, and patients with severe liver impairment without careful monitoring. It is also contraindicated in premenopausal women unless ovarian function suppression is confirmed.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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