Product image of Letrofam (Letrozole) supplied by GNH India

Letrofam

Active Ingredient:
Letrozole
Origin:
EU

Letrofam (Letrozole)

Letrozole, the active ingredient in Letrofam, is a aromatase inhibitor presented as a 2.5 mg tablet for oral use. It treats postmenopausal estrogen receptor‑positive breast cancer, including adjuvant and metastatic disease.

GNH India supplies Letrofam as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

Manufacturer / TM Owner

G.L. Pharma Gmbh

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Indications & Clinical Uses

Letrofam, an aromatase inhibitor, is employed in the management of estrogen‑driven breast cancer.

  • Postmenopausal estrogen receptor‑positive breast cancer: Reduces tumor growth by lowering circulating estrogen levels.
  • Adjuvant treatment of breast cancer: Decreases risk of disease recurrence after surgery.
  • Metastatic breast cancer: Provides disease control in advanced hormone‑sensitive tumors.

How It Works

  • Letrozole reversibly binds to the aromatase enzyme, blocking the conversion of androgens to estrogens in peripheral tissues. This inhibition markedly lowers systemic estrogen concentrations, depriving estrogen‑dependent tumor cells of a growth stimulus and thereby slowing or halting disease progression.

Side Effects

Letrofam may cause a range of adverse reactions.

Common Side Effects

  • Hot flashes: Sudden feeling of warmth, often with sweating.
  • Joint and muscle pain: Aching discomfort in limbs or back.
  • Fatigue: Persistent tiredness not relieved by rest.
  • Nausea: Mild to moderate upset stomach.
  • Headache: Pressure or throbbing pain in the head.
  • Increased cholesterol: Elevated blood lipid levels.

Serious or Rare Side Effects

  • Severe liver injury: Jaundice, dark urine, abdominal pain.
  • Allergic reactions: Rash, itching, swelling, or difficulty breathing.
  • Pulmonary embolism: Sudden shortness of breath, chest pain.
  • Osteoporotic fractures: Bone weakening leading to breaks.
  • Severe hypertension: Markedly high blood pressure.
  • Deep vein thrombosis: Swelling and pain in a limb.

Precautions & Warnings

Patients should be monitored for safety considerations before and during therapy.

  • Bone health monitoring: Assess bone mineral density regularly because estrogen depletion can accelerate bone loss.
  • Lipid profile assessment: Check cholesterol levels periodically as they may rise.
  • Liver function tests: Perform baseline and periodic liver enzyme measurements.
  • Cardiovascular risk evaluation: Review blood pressure and cardiovascular history.
  • Pregnancy avoidance: Do not use in women who are pregnant or may become pregnant.
  • Store at ambient temperature: Keep below 25°C in the original container, protected from moisture and direct sunlight.

Avoid Interactions

Letrofam can interact with other medicines, requiring attention to avoid reduced efficacy or increased toxicity.

Major Interactions (Avoid)

  • Estrogen replacement therapy: Counteracts aromatase inhibition and may diminish therapeutic benefit.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): Can raise letrozole plasma levels, increasing risk of adverse effects.

Moderate Interactions (Monitor Closely)

  • CYP2C19 inhibitors (e.g., fluconazole): May modestly increase letrozole exposure.
  • Warfarin: Potential for altered anticoagulant effect; monitor INR.
  • Statins: Possible additive impact on liver enzymes; check hepatic function.
  • Antidepressants (SSRIs): May affect hormone metabolism; observe clinical response.

Frequently Asked Questions

Letrofam contains letrozole, an aromatase inhibitor indicated for the treatment of postmenopausal estrogen receptor‑positive breast cancer. It is used as adjuvant therapy after surgery and as a systemic option for metastatic disease to reduce estrogen‑driven tumor growth.

Letrozole blocks the aromatase enzyme, which normally converts adrenal androgens into estrogens in peripheral tissues. By inhibiting this conversion, circulating estrogen levels fall, depriving hormone‑sensitive breast cancer cells of the estrogen signal they need to proliferate.

The prescribed dose of Letrofam is determined by the treating physician based on the individual’s clinical situation. In most settings, the standard tablet strength is 2.5 mg taken once daily, but the exact regimen should follow the prescriber’s instructions.

Letrozole’s safety in pregnancy and lactation has not been established. It is classified as contraindicated for women who are pregnant or may become pregnant, and breastfeeding is generally discouraged because the drug may pass into milk and affect the infant.

To request Letrofam, 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.

Letrofam (letrozole) belongs to the non‑steroidal aromatase inhibitor class, similar to anastrozole. Compared with steroidal inhibitors like exemestane, letrozole generally offers a more potent and reversible inhibition of aromatase, which may translate into slightly greater estrogen suppression, though clinical choice depends on patient tolerance and physician preference.

Letrofam tablets should be stored at ambient temperature, preferably below 25 °C. Keep the medication in its original blister pack, protect it from moisture and direct sunlight, and keep out of reach of children.

Letrofam is taken orally as a whole tablet with a glass of water. It is usually taken once daily, at the same time each day, and can be taken with or without food according to the prescriber’s guidance.

Serious risks include severe liver injury, allergic reactions such as rash or swelling, pulmonary embolism, deep‑vein thrombosis, and significant bone loss leading to fractures. Patients should promptly report symptoms like jaundice, sudden shortness of breath, severe pain, or unexplained bruising to their healthcare provider.

Letrofam should not be used by premenopausal women, pregnant or nursing mothers, or individuals with known hypersensitivity to letrozole or any tablet excipients. Caution is also advised for patients with severe liver disease or uncontrolled cardiovascular conditions.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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