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

Letrozol Orifarm

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Orifarm (Letrozole)

Letrozole, the active ingredient in Letrozol Orifarm, is an aromatase inhibitor presented as a tablet for oral use. It reduces estrogen production and is used in the treatment of postmenopausal estrogen receptor‑positive breast cancer.
GNH India supplies Letrozol Orifarm as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Orifarm Generics A/S

1
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Indications & Clinical Uses

Letrozole acts on the estrogen‑dependent pathway of breast cancer, providing endocrine therapy for hormone‑responsive disease.

  • Postmenopausal estrogen receptor‑positive breast cancer: lowers recurrence risk and slows disease progression.
  • Adjuvant treatment of hormone‑responsive breast cancer: improves disease‑free survival after surgery.
  • Metastatic breast cancer in postmenopausal women: delays tumor growth and extends survival.

How It Works

  • Letrozole is a reversible, non‑steroidal inhibitor of the aromatase enzyme. By binding to the enzyme's active site, it blocks the conversion of androgens to estrogens in peripheral tissues, leading to markedly reduced circulating estrogen levels. The resulting hypo‑estrogenic state deprives estrogen‑dependent tumor cells of growth stimulation, thereby inhibiting tumor proliferation.

Side Effects

Letrozole may cause a range of adverse reactions, from mild to severe. Patients should be monitored for both common and serious events.

Common Side Effects

  • Hot flashes: transient episodes of intense warmth.
  • Joint and muscle pain: arthralgia and myalgia.
  • Fatigue: persistent tiredness.
  • Nausea: mild to moderate upset stomach.
  • Headache: occasional throbbing pain.
  • Dizziness: light‑headed sensation.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, elevated enzymes.
  • Pulmonary embolism: sudden shortness of breath.
  • Bone fracture: increased risk due to reduced bone density.
  • Allergic reaction: rash, swelling, or anaphylaxis.
  • Elevated cholesterol: hyperlipidaemia.
  • Cardiac arrhythmia: QT prolongation.

Precautions & Warnings

Before initiating Letrozol Orifarm, clinicians should assess patient-specific risk factors and monitor therapy closely.

  • Bone health monitoring: perform baseline and periodic DEXA scans.
  • Liver function assessment: check transaminases prior to and during treatment.
  • Cardiovascular risk evaluation: monitor blood pressure and lipid profile.
  • Pregnancy avoidance: contraindicated in pregnancy (Category X).
  • Elderly caution: start at lowest effective dose and monitor for toxicity.
  • Store below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Letrozole can interact with several medicines, altering its efficacy or safety profile.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce letrozole plasma levels.
  • Estrogen‑containing hormonal therapy: antagonizes letrozole's anti‑estrogen effect.
  • Live hormonal vaccines: potential reduced vaccine efficacy.

Moderate Interactions (Monitor Closely)

  • Warfarin: may increase INR, requiring closer coagulation monitoring.
  • Cholesterol‑lowering agents (statins): possible additive effect on liver enzymes.
  • Antidepressants (SSRIs): may influence hormone metabolism.
  • Antifungal azoles (ketoconazole): can increase letrozole exposure.
  • Herbal supplements (St. John’s wort): may induce metabolism and lower efficacy.

Frequently Asked Questions

Letrozol Orifarm contains letrozole, an aromatase inhibitor indicated for the treatment of postmenopausal women with estrogen receptor‑positive breast cancer. It is used both as adjuvant therapy after surgery and for managing metastatic disease, helping to reduce tumor growth by lowering estrogen levels.

Letrozole blocks the aromatase enzyme, which converts androgens into estrogens in peripheral tissues. By inhibiting this conversion, circulating estrogen concentrations fall dramatically, depriving estrogen‑dependent cancer cells of a key growth signal and thereby slowing or halting tumor progression.

The specific dose of Letrozol Orifarm is determined by the prescribing clinician based on the patient’s condition, treatment stage, and overall health. Physicians typically follow established guidelines for letrozole, but the exact regimen should always be confirmed with the treating oncologist.

Letrozol Orifarm 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 letrozole can be excreted in breast milk and may affect the infant.

To place an order, visit the product page on gnhindia.com, submit an enquiry with the required quantity, and provide your institutional or trade credentials. GNH India’s team will verify eligibility, then respond with pricing, availability, shipping details, and any necessary import documentation.

Letrozole is a non‑steroidal aromatase inhibitor, offering more potent estrogen suppression than older agents like anastrozole. Compared with selective estrogen receptor modulators such as tamoxifen, letrozole does not have partial agonist activity, which can result in a different side‑effect profile and may be preferred in certain postmenopausal patients.

Letrozol Orifarm tablets should be stored at temperatures below 25 °C (77 °F). Keep them in the original container, protect from moisture and direct sunlight, and ensure the packaging remains tightly closed to maintain product stability.

Letrozol Orifarm is taken orally, usually once daily with or without food, as directed by the prescribing physician. Patients should swallow the tablet whole with water and follow any specific instructions regarding timing relative to meals.

Serious risks include severe liver injury, pulmonary embolism, bone fractures due to decreased bone mineral density, and rare allergic reactions such as anaphylaxis. Patients should be monitored regularly for signs of these conditions, and any concerning symptoms should prompt immediate medical evaluation.

Letrozol Orifarm should not be used by pregnant or breastfeeding women, premenopausal patients, or individuals with known hypersensitivity to letrozole or any component of the tablet. It is also contraindicated in patients with severe liver impairment or uncontrolled cardiovascular disease without careful risk assessment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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