GNH USA

Europe — EMA

Letrolan

GNH USA supplies Letrolan (Letrozole), a aromatase inhibitor for postmenopausal estrogen receptor‑positive breast cancer. Request a quote for global supply.

Letrozole

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What is Letrozole?

Letrozole, the active ingredient in Letrolan, is a aromatase inhibitor presented as an oral tablet for oral use. It is used to treat postmenopausal estrogen receptor‑positive breast cancer, helping to slow tumor growth and improve survival outcomes.

GNH USA supplies Letrolan as a licensed, GDP‑compliant international pharmaceutical supplier serving oncology centres worldwide.

What is Letrozole used for?

Letrozole belongs to the aromatase inhibitor class and is employed in the management of hormone‑dependent breast cancer.

- Postmenopausal estrogen receptor‑positive breast cancer: reduces tumor progression and disease recurrence. - Adjuvant therapy for early‑stage hormone‑receptor‑positive breast cancer: lowers risk of cancer returning after surgery. - Metastatic hormone‑receptor‑positive breast cancer: improves overall survival and delays disease spread.

What are the side effects of Letrozole?

Letrozole may cause a range of adverse reactions, from mild to serious.

Common Side Effects: - Hot flashes: sudden feeling of warmth and sweating. - Joint and muscle pain: aching in limbs and joints. - Fatigue: persistent tiredness. - Nausea: upset stomach and possible vomiting. - Headache: mild to moderate cranial pain. - Dizziness: sensation of light‑headedness.

Serious or Rare Side Effects: - Severe liver injury: jaundice, elevated enzymes. - Bone fracture: increased risk due to bone density loss. - Pulmonary embolism: sudden shortness of breath, chest pain. - Allergic reaction: rash, swelling, anaphylaxis. - QT interval prolongation: cardiac rhythm disturbance. - Hypercholesterolemia: significant rise in cholesterol levels.

What precautions apply to Letrozole?

Before initiating Letrozole therapy, several safety considerations are essential.

- Pregnancy contraindication: avoid use in pregnant women; teratogenic risk. - Breastfeeding prohibition: do not use while nursing; drug passes into milk. - Bone health monitoring: assess bone mineral density periodically. - Liver function assessment: check hepatic enzymes before and during treatment. - Lipid profile surveillance: monitor cholesterol levels regularly. - Avoid use in premenopausal women: efficacy not established. - Store at ambient temperature: keep in original packaging, protect from moisture.

What does Letrozole interact with?

Letrozole can interact with other medicines, altering its effectiveness or safety.

Major Interactions (Avoid): - Tamoxifen: antagonistic effect reduces therapeutic benefit. - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): markedly lower letrozole plasma levels. - Strong CYP2A6 inhibitors (e.g., methoxsalen): increase letrozole exposure and toxicity. - Estrogen replacement therapy: diminishes aromatase inhibition.

Moderate Interactions (Monitor Closely): - Warfarin: possible increase in INR, requiring closer coagulation monitoring. - Statins (especially simvastatin): heightened risk of myopathy. - SSRIs (e.g., fluoxetine): may modestly affect QT interval. - Anticonvulsants (e.g., phenytoin): may alter hormone metabolism. - Proton pump inhibitors: occasional effect on absorption, monitor clinical response.

Frequently asked questions

What is Letrolan used for?+
Letrolan contains letrozole, an aromatase inhibitor prescribed for postmenopausal women with estrogen receptor‑positive breast cancer. It helps to lower estrogen levels, slowing tumor growth and reducing the chance of disease recurrence.
How does letrozole work in the body?+
Letrozole blocks the aromatase enzyme, which converts androgens into estrogen. By inhibiting this conversion, systemic estrogen concentrations drop, depriving hormone‑dependent cancer cells of a key growth signal and limiting tumor proliferation.
What is the usual dose of Letrolan?+
The specific dose of Letrolan is determined by the prescribing physician based on the patient’s clinical condition, treatment stage, and individual health factors. Patients should follow the dosage instructions provided by their healthcare professional.
Is Letrolan safe during pregnancy or breastfeeding?+
Letrolan is classified as pregnancy category X, meaning it is contraindicated in pregnancy due to known fetal risk. It is also not recommended for breastfeeding women because the drug can be excreted in breast milk and may harm the infant.
How do I order Letrolan from GNH USA?+
To request Letrolan, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA works with hospitals, pharmacies, and procurement teams worldwide, confirming trade or institutional credentials before providing pricing, availability, shipping details, and necessary import documentation.
How does Letrolan compare with other aromatase inhibitors?+
Letrolan (letrozole) is a third‑generation aromatase inhibitor with a high potency and a longer half‑life compared with earlier agents such as anastrozole. Clinically, it often shows greater estrogen suppression, which can translate into improved disease control in certain breast‑cancer subtypes.
What are the storage requirements for Letrolan?+
Letrolan should be stored at ambient temperature, below 25 °C, in its original packaging. Keep the tablets away from moisture, direct sunlight, and excessive heat to maintain product stability.
How is Letrolan administered?+
Letrolan is taken orally, usually as a tablet swallowed with water. The exact timing (e.g., with or without food) should follow the prescribing physician’s guidance, and the tablet should be taken consistently each day to maintain steady drug levels.
What are the most serious risks associated with Letrolan?+
Serious risks include severe liver injury, bone fractures due to decreased bone density, pulmonary embolism, allergic reactions such as anaphylaxis, and cardiac QT‑interval prolongation. Patients should be monitored regularly for these events, especially if they have pre‑existing risk factors.
Who should not use Letrolan?+
Letrolan is contraindicated in pregnant women, breastfeeding mothers, premenopausal women, and patients with known hypersensitivity to letrozole or any tablet excipients. It should also be avoided in individuals with severe liver impairment unless specifically directed by a specialist.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Letrozole
Route
Oral Use
Manufacturer
Avansor Pharma Oy
Origin
EU

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