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

Letrozole Stada

Active Ingredient:
Letrozole
Origin:
EU

Letrozole Stada (Letrozole)

Letrozole, the active ingredient in Letrozole Stada, is an aromatase inhibitor presented as an oral tablet for oral use. It is employed to treat hormone receptor‑positive breast cancer in postmenopausal women by lowering estrogen levels that can stimulate tumor growth and is approved for use in the European Union market.

GNH India supplies Letrozole Stada as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide. The company adheres to stringent quality standards and provides reliable logistics for bulk and individual orders across global markets.

Manufacturer / TM Owner

Stada Arzneimittel Ag

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Indications & Clinical Uses

Letrozole acts on estrogen‑dependent pathways and is indicated for the following conditions:

  • Hormone receptor‑positive breast cancer (postmenopausal): Reduces tumor progression by decreasing estrogen production.
  • Ovulation induction in anovulatory women: Facilitates follicular development by lowering estrogen feedback.
  • Endometriosis‑related pain (off‑label): Alleviates symptoms through suppression of estrogen‑driven tissue growth.

How It Works

  • Letrozole selectively and reversibly binds to the aromatase enzyme, inhibiting the conversion of androstenedione and testosterone to estrone and estradiol. By blocking peripheral estrogen synthesis, systemic estrogen concentrations decline, depriving estrogen‑dependent tumor cells of a growth stimulus while preserving other hormonal pathways. The inhibition is dose‑dependent and results in a marked reduction of circulating estradiol levels, which is the primary driver of hormone‑sensitive breast cancer growth.

Side Effects

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

Common Side Effects

  • Hot flashes: Sudden feeling of warmth, often with sweating.
  • Joint and muscle pain: Arthralgia or myalgia affecting daily activities.
  • Fatigue: Persistent tiredness not relieved by rest.
  • Nausea: Mild to moderate upset stomach.

Serious or Rare Side Effects

  • Severe liver injury: Elevated enzymes or hepatitis.
  • Bone fractures: Increased risk due to lowered estrogen.
  • Deep vein thrombosis or pulmonary embolism: Blood clots in veins or lungs.
  • Allergic reactions: Rash, swelling, or anaphylaxis.

Precautions & Warnings

When prescribing Letrozole, clinicians should observe the following precautions to ensure patient safety.

  • Bone health monitoring: Assess bone mineral density regularly due to risk of osteoporosis.
  • Liver function assessment: Check hepatic enzymes before initiation and periodically.
  • Cardiovascular risk evaluation: Review history of thromboembolic events.
  • Pregnancy avoidance: Contraindicated in pregnancy; ensure effective contraception.
  • Drug interaction review: Avoid concurrent use with estrogen‑containing therapies.
  • Store at ambient temperature: Keep below 25 °C in original packaging, protect from moisture.

Avoid Interactions

Letrozole interacts with several medicines; awareness of the interaction level guides clinical management.

Major Interactions (Avoid)

  • Estrogen‑containing hormone therapy: Counters Letrozole’s effect.
  • Tamoxifen: May reduce therapeutic benefit when combined.
  • Strong CYP3A4 inhibitors (e.g., ketoconazole): Increase Letrozole plasma levels.

Moderate Interactions (Monitor Closely)

  • CYP3A4 inducers (e.g., rifampin, carbamazepine): May lower effectiveness.
  • Anticoagulants (e.g., warfarin): Potential alteration of INR.
  • SSRIs and SNRIs: May affect hot‑flash management.

Frequently Asked Questions

Letrozole Stada contains the aromatase inhibitor letrozole and is used primarily to treat hormone receptor‑positive breast cancer in postmenopausal women by lowering estrogen levels that can promote tumor growth.

Letrozole selectively and reversibly inhibits the aromatase enzyme, which converts androgens into estrogens. This blockade reduces peripheral estrogen synthesis, leading to lower circulating estrogen and depriving estrogen‑dependent cancer cells of a growth stimulus.

The prescribed dose of Letrozole Stada is determined by the treating physician based on the patient’s clinical condition, renal and hepatic function, and treatment guidelines. Patients should follow the exact dosing instructions provided by their healthcare professional.

Letrozole is classified as pregnancy category X, meaning it is contraindicated during pregnancy because it can cause fetal harm. It is also not recommended while breastfeeding, as it may pass into breast milk and affect the infant.

To request Letrozole Stada, submit an enquiry on the product page at gnhindia.com indicating 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.

Letrozole is a third‑generation aromatase inhibitor with a high potency and a long half‑life, offering consistent estrogen suppression. Compared with anastrozole or exemestane, letrozole often provides slightly greater estrogen reduction, which may translate into marginally improved disease control in certain patients, though individual response varies.

Letrozole Stada tablets should be stored at ambient temperature, preferably below 25 °C, in the original blister pack or container. Protect the tablets from moisture, direct sunlight, and excessive heat to maintain product stability.

Letrozole Stada is taken orally, usually once daily, with or without food. The tablet should be swallowed whole with a glass of water and not chewed or crushed, unless otherwise directed by a healthcare professional.

Serious risks include severe liver injury, bone fractures due to decreased estrogen, and thromboembolic events such as deep‑vein thrombosis or pulmonary embolism. Patients should be monitored for signs of liver dysfunction, bone health deterioration, and any symptoms of clot formation.

Letrozole Stada should not be used by pregnant or breastfeeding women, patients with known hypersensitivity to letrozole or any tablet excipients, and individuals receiving estrogen‑containing hormone therapy. Caution is also advised for patients with severe liver impairment or uncontrolled cardiovascular disease.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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