Product image of Letrozol Jgl 2,5 Mg (Letrozole) supplied by GNH India

Letrozol Jgl 2,5 Mg

Active Ingredient:
Letrozole
Origin:
EU

Letrozol Jgl 2,5 Mg (Letrozole)

Letrozole, the active ingredient in Letrozol Jgl 2,5 Mg, is an aromatase inhibitor presented as a 2.5 mg tablet for oral use. It treats hormone receptor‑positive breast cancer in postmenopausal women.

GNH India supplies Letrozol Jgl 2,5 Mg as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres and pharmacies worldwide.

Manufacturer / TM Owner

Jadran-Galenski Laboratorij D.D.

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Indications & Clinical Uses

Letrozole is an aromatase inhibitor used in the management of hormone‑dependent breast cancer.

  • Hormone receptor‑positive breast cancer: reduces tumor growth in postmenopausal women.
  • Adjuvant therapy for early‑stage disease: lowers risk of recurrence after surgery.
  • Metastatic breast cancer: prolongs progression‑free survival in advanced disease.

How It Works

  • Letrozole selectively binds to the aromatase enzyme, blocking the conversion of androstenedione and testosterone into estrone and estradiol. By inhibiting estrogen synthesis, systemic estrogen levels fall, depriving estrogen‑dependent tumor cells of a growth stimulus and thereby slowing or halting cancer progression.

Side Effects

Letrozole may cause a range of adverse reactions.

Common Side Effects

  • Hot flashes: sudden feeling of warmth and sweating.
  • Joint and muscle pain: aching in limbs or back.
  • Fatigue: persistent tiredness not relieved by rest.
  • Nausea: mild to moderate upset stomach.
  • Headache: pressure or throbbing pain.
  • Increased sweating: excessive perspiration.

Serious or Rare Side Effects

  • Osteoporosis or bone loss: increased fracture risk.
  • Cardiovascular events: hypertension, thromboembolism.
  • Liver function abnormalities: elevated enzymes or hepatitis.
  • Severe allergic reactions: rash, swelling, anaphylaxis.
  • Pulmonary embolism: sudden shortness of breath.
  • Severe skin reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.

Precautions & Warnings

Before initiating therapy, clinicians should evaluate patient‑specific risk factors and monitor for adverse events.

  • Bone health assessment: perform baseline densitometry and consider calcium/vitamin D supplementation.
  • Liver function monitoring: check transaminases periodically.
  • Cardiovascular risk review: assess blood pressure and lipid profile.
  • Pregnancy avoidance: letrozole is contraindicated in pregnancy (Category X).
  • Hepatic impairment caution: dose adjustment may be required in severe liver disease.
  • Storage at ambient temperature: keep in the original container, protect from moisture and direct sunlight.

Avoid Interactions

Letrozole can interact with other medicines that affect its metabolism or hormonal pathways.

Major Interactions (Avoid)

  • Strong CYP3A4 inhibitors (e.g., ketoconazole, itraconazole): may increase letrozole exposure.
  • Estrogen‑containing hormone therapy: antagonizes letrozole’s effect.
  • Certain antiepileptic enzyme inducers (e.g., carbamazepine, phenytoin): may reduce efficacy.

Moderate Interactions (Monitor Closely)

  • Warfarin: may alter anticoagulant control.
  • Statins: potential for increased muscle toxicity.
  • SSRIs and SNRIs: possible additive effects on mood or fatigue.
  • Glucocorticoids: may affect bone health when combined.
  • NSAIDs: monitor for gastrointestinal irritation.

Frequently Asked Questions

Letrozol Jgl 2,5 Mg 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 metastatic settings to reduce estrogen‑driven tumor growth.

Letrozole blocks the aromatase enzyme, which converts androgens into estrogen. By inhibiting this conversion, systemic estrogen levels fall, depriving estrogen‑dependent breast cancer cells of a key growth signal and thereby slowing disease progression.

The prescribed dose of letrozole is determined by the treating physician based on the patient’s clinical condition and guidelines. Typically, a single 2.5 mg tablet is taken once daily, but the exact regimen should follow the prescriber’s instructions.

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

To place an order, 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.

Letrozole, as a third‑generation aromatase inhibitor, offers more potent estrogen suppression than earlier agents like anastrozole. Compared with selective estrogen receptor modulators such as tamoxifen, letrozole does not have partial agonist activity and generally provides superior disease‑free survival in postmenopausal patients.

Letrozol Jgl tablets should be stored at ambient temperature, below 25 °C, in the original packaging. Protect them from moisture, heat and direct sunlight to maintain potency throughout the shelf life.

The medication is taken orally, usually as a single 2.5 mg tablet taken once daily with or without food. Patients should swallow the tablet whole and follow the dosing schedule prescribed by their healthcare provider.

Serious risks include severe bone loss leading to osteoporosis and fractures, cardiovascular events such as hypertension or thromboembolism, and rare but potentially life‑threatening reactions like severe allergic responses or liver injury. Regular monitoring can help mitigate these risks.

Letrozole should not be used by pregnant or breastfeeding women, patients with known hypersensitivity to letrozole or any component of the tablet, and individuals with severe hepatic impairment without appropriate dose adjustment. It is also contraindicated in patients receiving estrogen‑containing therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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