Product image of Letrozolo Almus (Letrozole) supplied by GNH India

Letrozolo Almus

Active Ingredient:
Letrozole
Origin:
EU

Letrozolo Almus (Letrozole)

Letrozole, the active ingredient in Letrozolo Almus, is an aromatase inhibitor presented as an oral tablet for oral use. It is employed in the treatment of hormone receptor‑positive breast cancer in postmenopausal women, where it lowers estrogen production to help control tumor growth. The medication is administered once daily and is part of standard endocrine therapy protocols.

GNH India supplies Letrozolo Almus as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company ensures quality assurance, regulatory compliance, and reliable logistics for global healthcare partners.

Manufacturer / TM Owner

Almus S.R.L.

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Indications & Clinical Uses

  • Letrozole acts as an aromatase inhibitor and is indicated for conditions driven by estrogen signaling in breast cancer.
  • Hormone receptor‑positive breast cancer (postmenopausal): reduces tumor growth by decreasing circulating estrogen levels.
  • Adjuvant therapy for early‑stage hormone receptor‑positive breast cancer (postmenopausal): helps prevent disease recurrence after surgery.
  • Advanced or metastatic breast cancer (postmenopausal): delays progression when used alone or with other endocrine agents.

How It Works

  • Letrozole selectively and non‑competitively inhibits the aromatase enzyme, a cytochrome P450 isoform responsible for converting adrenal and ovarian androgens into estrogens in peripheral tissues. By binding to the enzyme’s active site, it blocks the final step of estrogen biosynthesis, leading to markedly reduced plasma estradiol concentrations. The resulting hypo‑estrogenic state diminishes estrogen‑driven proliferation of breast cancer cells in postmenopausal patients.

Side Effects

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

Common Side Effects

  • Hot flashes: transient increase in body temperature sensation.
  • Joint and muscle pain: arthralgia or myalgia.
  • Nausea: mild gastrointestinal upset.
  • Fatigue: reduced energy levels.

Serious or Rare Side Effects

  • Severe liver injury: elevated transaminases or hepatitis.
  • Bone fractures: decreased bone mineral density leading to fracture risk.
  • Pulmonary embolism: formation of blood clots in the lungs.

Precautions & Warnings

When prescribing Letrozolo Almus, clinicians should observe several precautionary measures to ensure patient safety.

  • Liver function monitoring: assess baseline enzymes and repeat periodically.
  • Bone health assessment: evaluate bone mineral density and consider calcium/vitamin D supplementation.
  • Cardiovascular risk evaluation: screen for thromboembolic history and manage risk factors.
  • Pregnancy avoidance: contraindicated in pregnancy; ensure effective contraception in women of childbearing potential.
  • Drug interaction review: check concomitant medications for potential CYP interactions.
  • Store at ambient temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

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

Major Interactions (Avoid)

  • Strong CYP2C19 inhibitors (e.g., fluconazole): may increase letrozole plasma levels.
  • Estrogen‑containing hormone therapy: antagonizes letrozole’s estrogen‑lowering effect.
  • Tamoxifen: concurrent use reduces therapeutic benefit of both agents.

Moderate Interactions (Monitor Closely)

  • Anticoagulants (e.g., warfarin): letrozole may enhance anticoagulant effect, requiring INR monitoring.
  • Statins: potential for altered lipid metabolism; monitor lipid profile.
  • CYP3A4 inducers (e.g., rifampin): may lower letrozole concentrations, reducing efficacy.

Frequently Asked Questions

Letrozolo Almus 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 lower estrogen levels and help control tumor growth.

Letrozole works by selectively binding to the aromatase enzyme, which converts androgens to estrogens in peripheral tissues. By blocking this conversion, the drug markedly reduces circulating estrogen, depriving estrogen‑dependent breast cancer cells of a growth stimulus.

The specific dose of Letrozolo Almus 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.

Letrozole is contraindicated in pregnancy because it can interfere with fetal development. Women of childbearing potential should use effective contraception while taking the medication. Safety during breastfeeding has not been established, and breastfeeding is generally not recommended.

To order Letrozolo Almus, 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.

Letrozolo Almus (letrozole) is a non‑steroidal aromatase inhibitor with a long half‑life, offering once‑daily dosing. Compared with anastrozole, it may provide slightly greater estrogen suppression, while exemestane is a steroidal inhibitor with a different safety profile. Choice of agent depends on clinical judgment, tolerability, and patient factors.

Letrozolo Almus should be stored at ambient temperature, below 25 °C, in its original packaging. Protect the product from moisture, direct sunlight, and extreme temperature fluctuations to maintain potency throughout its shelf life.

Letrozolo Almus is taken orally, usually as a tablet swallowed whole with water. It is typically administered once daily, with or without food, as directed by the prescribing clinician.

Serious risks include severe liver injury, significant bone loss leading to fractures, and rare thromboembolic events such as pulmonary embolism. Patients should be monitored regularly for liver function, bone mineral density, and any signs of clotting disorders.

Letrozolo Almus should not be used by pregnant women, individuals with known hypersensitivity to letrozole or other aromatase inhibitors, and patients with severe liver impairment without close monitoring. It is also contraindicated in premenopausal women unless ovarian suppression is medically indicated.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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