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 an aromatase inhibitor presented as an oral tablet for oral use. It selectively reduces estrogen production and is employed in the treatment of hormone receptor‑positive breast cancer in postmenopausal women. By inhibiting the aromatase enzyme, it lowers circulating estrogen levels, helping to control tumor growth.

GNH India supplies Letrozol Sun as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide. The company adheres to EU quality standards and provides reliable global distribution.

Manufacturer / TM Owner

Sun Pharmaceutical Industries Europe B.V.

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Indications & Clinical Uses

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

  • Early‑stage hormone receptor‑positive breast cancer: reduces risk of recurrence when given as adjuvant therapy.
  • Metastatic hormone receptor‑positive breast cancer: slows disease progression in postmenopausal patients.
  • Postmenopausal estrogen suppression: supports endocrine therapy by lowering systemic estrogen levels.

How It Works

  • Letrozole is a selective, non‑steroidal inhibitor of the aromatase enzyme, which converts androstenedione and testosterone to estrone and estradiol. By binding to the aromatase active site, it blocks estrogen synthesis, leading to markedly reduced circulating estrogen concentrations and thereby limiting estrogen‑driven tumor proliferation in hormone‑sensitive breast cancer.

Side Effects

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

Common Side Effects

  • Hot flashes: sudden feeling of warmth, often with sweating.
  • Joint and muscle pain: arthralgia or myalgia.
  • Fatigue: persistent tiredness.
  • Nausea: mild to moderate upset stomach.
  • Headache: occasional throbbing pain.
  • Increased sweating: excessive perspiration.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, elevated enzymes.
  • Bone fracture: increased risk due to reduced estrogen.
  • Deep vein thrombosis or pulmonary embolism: signs of clot formation.
  • Allergic reaction: rash, itching, swelling.
  • Elevated cholesterol: dyslipidemia.
  • Severe hypertension: markedly high blood pressure.

Precautions & Warnings

Before initiating Letrozol Sun, clinicians should consider several safety measures.

  • Monitor bone mineral density: assess risk of osteoporosis and consider supplementation.
  • Assess liver function: obtain baseline tests and repeat periodically.
  • Evaluate cardiovascular risk: review history of thromboembolic events.
  • Avoid use in pregnancy: drug is contraindicated in pregnant women.
  • Store at ambient temperature below 25°C: keep in the original pack, protect from moisture.

Avoid Interactions

Letrozol Sun may interact with other medicines; awareness of interaction severity is essential.

Major Interactions (Avoid)

  • Tamoxifen: concurrent use reduces the efficacy of both agents.
  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may lower letrozole plasma concentrations.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase letrozole exposure and toxicity.

Moderate Interactions (Monitor Closely)

  • Anticoagulants such as warfarin: may enhance anticoagulant effect and raise INR.
  • CYP2C19 inhibitors (e.g., fluoxetine, fluvoxamine): may affect letrozole metabolism.
  • Hormone replacement therapy: may alter estrogen levels and affect therapeutic outcomes.

Frequently Asked Questions

Letrozol Sun contains letrozole, an aromatase inhibitor indicated for the treatment of hormone receptor‑positive breast cancer in postmenopausal women, including both early‑stage adjuvant therapy and metastatic disease management.

Letrozole blocks the aromatase enzyme, preventing the conversion of androgens to estrogen. This reduction in estrogen levels limits the growth stimulus for estrogen‑dependent breast cancer cells, thereby inhibiting tumor progression.

The specific dose of Letrozol Sun is determined by the prescribing physician based on the patient’s clinical condition, treatment setting, and individual factors. Patients should follow the dosage instructions provided by their healthcare professional.

Letrozol Sun is contraindicated in pregnancy because it can affect fetal development. Its safety during breastfeeding has not been established, and breastfeeding mothers should consult their physician before using the product.

To request Letrozol Sun, submit an enquiry on the product page at gnhindia.com with 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 with a high potency and longer half‑life compared with anastrozole, another commonly used agent. Clinical studies suggest comparable efficacy, while side‑effect profiles may differ slightly, making individual patient factors important in selection.

Letrozol Sun should be stored at ambient temperature below 25 °C, in its original packaging, and protected from moisture and direct sunlight. Keep the product out of reach of children and do not use if the packaging is damaged.

Letrozol Sun is taken orally, usually as a tablet swallowed whole with water. It is typically administered once daily, preferably at the same time each day, but patients should follow the exact instructions given by their prescriber.

Serious risks include severe liver injury, bone fractures due to decreased estrogen, and rare thromboembolic events such as deep‑vein thrombosis or pulmonary embolism. Patients should be monitored regularly for signs of these conditions and report any concerning symptoms promptly.

Letrozol Sun should not be used by pregnant women, individuals with known hypersensitivity to letrozole or any excipients, and patients with severe liver impairment without careful monitoring. Clinicians should also exercise caution in patients with a history of osteoporosis or thromboembolic disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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