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

Letrozol Stada

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Stada (Letrozole)

Letrozole, the active ingredient in Letrozol Stada, is an aromatase inhibitor presented as an oral tablet for oral use. It treats hormone receptor‑positive breast cancer in postmenopausal women.

GNH India supplies Letrozol Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

Manufacturer / TM Owner

Laboratorio Stada, S.L.

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Indications & Clinical Uses

Letrozol Stada is an aromatase inhibitor indicated for conditions driven by estrogen production.

  • Hormone receptor‑positive breast cancer in postmenopausal women: reduces estrogen synthesis to inhibit tumor growth.
  • Adjuvant therapy for early‑stage breast cancer: helps prevent disease recurrence after surgery.
  • Metastatic breast cancer: provides disease control when used with other systemic agents.

How It Works

  • Letrozole reversibly binds to the aromatase enzyme, blocking the conversion of androgens to estrogens in peripheral tissues. By lowering circulating estrogen levels, it deprives estrogen‑dependent tumor cells of a growth stimulus, thereby slowing or halting disease progression in hormone‑sensitive breast cancer.

Side Effects

Letrozol Stada may cause a range of adverse reactions. Patients should be informed of both common and serious possibilities.

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: pressure or throbbing pain.
  • Dizziness: light‑headed sensation.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, elevated enzymes.
  • Bone fracture: increased risk due to lowered estrogen.
  • Pulmonary embolism: sudden shortness of breath, chest pain.
  • Allergic reaction (anaphylaxis): hives, swelling, airway compromise.
  • QT interval prolongation: cardiac rhythm disturbance.

Precautions & Warnings

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

  • Assess bone health: monitor for osteoporosis and consider calcium/vitamin D supplementation.
  • Monitor liver function: check transaminases periodically.
  • Evaluate cardiovascular risk: watch for signs of thromboembolic events.
  • Avoid use in premenopausal women: drug is ineffective without postmenopausal estrogen levels.
  • Pregnancy warning: contraindicated in pregnancy; effective contraception required.
  • Store at ambient temperature: keep in the original container, protect from moisture and light.

Avoid Interactions

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

Major Interactions (Avoid)

  • Concurrent tamoxifen: antagonistic effect on estrogen blockade.
  • Strong CYP2C19 inhibitors (e.g., fluconazole): may raise letrozole plasma levels.
  • Hormone replacement therapy: diminishes letrozole’s therapeutic effect.

Moderate Interactions (Monitor Closely)

  • Warfarin: potential alteration of anticoagulant effect; monitor INR.
  • CYP3A4 inducers (e.g., rifampin): may lower letrozole concentrations.
  • Selective serotonin reuptake inhibitors: monitor for additive central nervous system effects.

Frequently Asked Questions

Letrozol Stada contains letrozole, an aromatase inhibitor used to treat hormone receptor‑positive breast cancer in postmenopausal women. It works by lowering estrogen levels, which helps slow or stop the growth of estrogen‑dependent tumors.

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

The prescribed dose of Letrozol Stada is determined by the treating physician based on the patient’s clinical condition, renal and hepatic function, and other individual factors. The prescriber will set the exact regimen.

Letrozol Stada is contraindicated during pregnancy because it can harm the developing fetus. Its safety in breastfeeding has not been established, and women are advised not to breastfeed while receiving the medication.

To order Letrozol Stada, 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 Stada (letrozole) is a third‑generation aromatase inhibitor with a long half‑life, allowing once‑daily dosing. Compared with anastrozole or exemestane, letrozole often achieves slightly greater estrogen suppression, but individual response and side‑effect profiles guide the choice of agent.

Store Letrozol Stada at ambient temperature, below 25 °C, in its original blister pack or container. Protect the tablets from moisture, direct sunlight, and excessive heat to maintain potency.

Letrozol Stada is taken orally, usually as a whole tablet with water. It is generally administered once daily, preferably at the same time each day, and can be taken with or without food.

Serious risks include severe liver injury, bone fractures due to decreased estrogen, pulmonary embolism, allergic reactions such as anaphylaxis, and cardiac QT‑interval prolongation. Patients should report any sudden chest pain, shortness of breath, jaundice, severe bone pain, or signs of an allergic reaction immediately.

Letrozol Stada should not be used by premenopausal women, pregnant or nursing individuals, patients with known hypersensitivity to letrozole, or those with severe liver impairment without careful monitoring. Clinicians must evaluate each patient’s medical history before prescribing.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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