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

Letrozol Teva

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Teva (Letrozole)

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

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

Manufacturer / TM Owner

Teva B.V

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Indications & Clinical Uses

Letrozol Teva is an aromatase inhibitor used in the treatment of hormone‑dependent breast cancer.

  • Hormone receptor‑positive breast cancer (postmenopausal): reduces estrogen production to slow tumor growth.
  • Adjuvant therapy for early‑stage hormone receptor‑positive breast cancer (postmenopausal): helps prevent disease recurrence.
  • Advanced or metastatic hormone receptor‑positive breast cancer (postmenopausal): provides disease control when other endocrine therapies are unsuitable.

How It Works

  • Letrozole selectively and non‑steroidally inhibits the aromatase enzyme, which converts androgens to estrogens in peripheral tissues. By blocking this conversion, systemic estrogen levels decline, depriving estrogen‑dependent tumor cells of a growth stimulus and thereby limiting proliferation of hormone receptor‑positive breast cancer cells.

Side Effects

Adverse reactions may occur with letrozole therapy and are categorized by frequency and severity.

Common Side Effects

  • Hot flashes: sudden feeling of warmth, often with sweating.
  • Joint and muscle pain: aches affecting mobility.
  • Fatigue: persistent tiredness not relieved by rest.
  • Nausea: mild to moderate upset stomach.
  • Headache: tension‑type or throbbing pain.
  • Increased sweating: excessive perspiration.

Serious or Rare Side Effects

  • Severe liver injury: jaundice, elevated enzymes, hepatic failure.
  • Bone fractures: increased risk due to reduced estrogen.
  • Pulmonary embolism: sudden shortness of breath, chest pain.
  • Severe allergic reactions: rash, swelling, anaphylaxis.
  • Elevated cholesterol: significant rise in LDL levels.

Precautions & Warnings

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

  • Bone health monitoring: assess bone mineral density regularly.
  • Liver function assessment: perform baseline and periodic liver enzyme tests.
  • Cardiovascular risk evaluation: check lipid profile and blood pressure.
  • Drug interaction review: verify concomitant medications for potential interactions.
  • Pregnancy and lactation warning: avoid use in pregnant or breastfeeding women.
  • Store at room temperature: keep in original container, protect from moisture and direct sunlight.

Avoid Interactions

Letrozole may interact with other medicines, influencing its efficacy or safety.

Major Interactions (Avoid)

  • Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce letrozole plasma levels.
  • Estrogen‑containing hormone therapy: antagonizes letrozole’s estrogen‑lowering effect.
  • Tamoxifen: concurrent use can diminish therapeutic benefit.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (SSRIs): may increase risk of bone loss.
  • Warfarin: potential alteration of anticoagulant effect, requiring INR monitoring.
  • Glucocorticoids: may enhance risk of osteoporosis when combined with letrozole.

Frequently Asked Questions

Letrozol Teva contains letrozole, an aromatase inhibitor indicated for the treatment of hormone receptor‑positive breast cancer in postmenopausal women. It is used in both early‑stage (adjuvant) and advanced disease to lower estrogen levels and help control tumor growth.

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

The prescribed dose of Letrozol Teva is determined by the treating physician based on the patient’s clinical condition, renal and hepatic function, and other individual factors. Patients should follow the dosing instructions provided by their healthcare professional.

Letrozol Teva is contraindicated in pregnancy because it can harm a developing fetus. It is also not recommended for breastfeeding women, as it may pass into breast milk and affect the infant. Women of child‑bearing potential should use effective contraception while on therapy.

To order Letrozol Teva, 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 Teva (letrozole) is a third‑generation, non‑steroidal aromatase inhibitor with a long half‑life, offering once‑daily dosing. Compared with earlier agents such as anastrozole, letrozole generally provides a slightly greater reduction in estrogen levels, which may translate into modestly improved disease control in certain patient populations.

Letrozol Teva should be stored at room temperature, below 25 °C, in its original packaging. Protect the product from moisture, excessive heat, and direct sunlight to maintain its stability and potency throughout its shelf life.

Letrozol Teva 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, bone fractures due to decreased estrogen, and rare events such as pulmonary embolism or severe allergic reactions. Patients should be monitored regularly for liver function, bone health, and any signs of thromboembolic events.

Letrozol Teva should not be used by premenopausal women, pregnant or breastfeeding individuals, and patients with known hypersensitivity to letrozole or any of its excipients. Caution is also advised in patients with severe hepatic impairment.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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