
Letrozole Fempro Tablets USP 2.5 Mg
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What is Letrozole (Fempro) Used For?
- Letrozole (Fempro) is used for:
- Hormone Receptor-Positive Breast Cancer β First-line treatment in postmenopausal women
- Adjuvant Treatment β After surgery to reduce recurrence risk
- Extended Adjuvant Therapy β Following 5 years of tamoxifen treatment
- Advanced Breast Cancer β Disease progression after anti-estrogen therapy
How Does Letrozole Work?
- Letrozole is a third-generation aromatase inhibitor, which:
- Selectively and potently inhibits the aromatase enzyme
- Reduces estrogen synthesis in peripheral tissues by 98%
- Deprives hormone-dependent cancer cells of estrogen required for growth
How to Use Letrozole
Dosage: 2.5mg once daily
Administration: Take orally with or without food; no dose adjustment needed for time of day
Precaution: For postmenopausal women only; monitor bone mineral density; assess lipid profiles; oncologist supervision required
Side Effects of Letrozole
Common Side Effects: Hot flashes, arthralgia, fatigue, increased sweating, nausea, edema
Serious Side Effects (seek medical help): Bone fractures, cardiovascular events, severe allergic reactions, hepatotoxicity
Benefits
- Third-generation aromatase inhibitor achieving ~98% estrogen suppression β highest among aromatase inhibitors
- Inhibits CYP19A1 (aromatase) selectively β no interference with adrenal steroid synthesis
- Demonstrated non-inferiority vs. anastrozole (BIG 1-98 trial) and superior efficacy in advanced disease vs. tamoxifen
- Once-daily oral tablet β simple outpatient adherence without food restrictions
- Medionix Pharma also carries other hormone therapy options including Anastrozole (Anaridex, Arimidex, Armotraz) and Tamoxifen (Cytotam) for premenopausal or DCIS patients
Warnings and Precautions
- For postmenopausal women only β premenopausal use requires confirmed ovarian suppression (GnRH agonist)
- Bone loss: DXA scan at baseline and every 1β2 years; calcium, vitamin D, and bisphosphonate therapy as needed
- Arthralgia: joint pain and stiffness affects up to 30β40% of patients β usually manageable; rarely requires discontinuation
- Cardiovascular risk: assess lipid levels at baseline; monitor for hypercholesterolaemia during long-term use
- Contraindicated in pregnancy β potential fetal harm
- Liver function monitoring if pre-existing hepatic disease is present
Drug Interactions
- Estrogen-containing medications (HRT, oral contraceptives): directly antagonize Letrozole β contraindicated
- Tamoxifen concurrent use: not recommended β reduces effectiveness of both agents
- Strong CYP3A4 inducers (rifampicin): may reduce Letrozole plasma levels β monitor treatment response
- CYP2A6 inhibitors (some antifungals): may increase Letrozole levels β monitor for enhanced effects
Storage Information
- Store at room temperature 20Β°Cβ25Β°C; protect from light and moisture
- Keep in original blister packaging, out of reach of children
- Do not use after expiry date
Frequently Asked Questions
Q1: What is Letrozole (Fempro) used for?
Letrozole is a third-generation aromatase inhibitor used to treat hormone receptor-positive (HR+) breast cancer in postmenopausal women β as first-line advanced disease treatment, adjuvant therapy post-surgery, and extended adjuvant therapy following 5 years of tamoxifen.
Q2: How does Letrozole work against breast cancer?
Letrozole potently and selectively inhibits the aromatase enzyme (CYP19A1), which converts androgens to estrogens in peripheral tissues. This reduces plasma estrogen by up to 98%, depriving HR+ cancer cells of the estrogen needed for growth.
Q3: How does Letrozole compare to Anastrozole and Exemestane?
All three are third-generation aromatase inhibitors with similar efficacy. Letrozole achieves the greatest estrogen suppression (~98%). Clinical trials (BIG 1-98) have shown letrozole to be equivalent to anastrozole in adjuvant settings.
Q4: How is Fempro 2.5mg taken?
Take one 2.5mg tablet once daily, with or without food, at a consistent time each day. Treatment is continuous without scheduled breaks unless directed by your oncologist.
Q5: How long is Letrozole treatment continued?
Adjuvant treatment is typically 5 years. Extended adjuvant treatment (following tamoxifen) may continue for an additional 5 years. For advanced disease, treatment continues until progression or unacceptable toxicity.
Q6: What are the most common side effects?
Hot flashes, arthralgia (joint pain), fatigue, increased sweating, nausea, and mild peripheral edema are most common. Joint symptoms are experienced by a significant proportion of patients.
Q7: What serious side effects require monitoring?
Bone fractures (due to osteoporosis), cardiovascular events, severe allergic reactions, and liver problems (jaundice, dark urine) require prompt medical attention.
Q8: How does Letrozole affect bone density?
Letrozole reduces bone mineral density by suppressing estrogen. DXA bone scans are recommended at baseline and every 1β2 years. Calcium, vitamin D, and bisphosphonate therapy may be needed to protect bones.
Q9: Can Letrozole be taken by premenopausal women?
Letrozole is only approved for postmenopausal women. Premenopausal women can use it only in combination with confirmed ovarian suppression (via GnRH agonist). Standalone use in premenopausal women is not approved.
Q10: What drugs interact with Letrozole?
Estrogen-containing medications (HRT, oral contraceptives) counteract Letrozole and are contraindicated. Strong CYP3A4 inducers (rifampicin) may reduce Letrozole plasma levels. Tamoxifen should not be used concurrently.
Q11: Is Letrozole safe during pregnancy?
No. Letrozole is contraindicated during pregnancy and is only indicated for postmenopausal women. It may cause fetal harm and should not be used by women of childbearing potential without confirmed postmenopausal status.
Q12: Is a prescription required for Fempro?
Yes. Letrozole is a prescription-only oncology medication. It requires oncologist prescribing and periodic monitoring of bone density, lipid levels, and cardiovascular risk.
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Dr. Priya Nair
India Β· 2 months ago
βSourced Nivolumab for a clinical case. Vials arrived cold-packed and within specification. Documentation was thorough.β
Dr. Charles Monroe
USA Β· 4 months ago
βSourced Enzalutamide for prostate cancer patients. Medionix handled the order professionally with full documentation.β
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The information provided on Medionix Pharma is intended for general informational purposes only. It should not be considered as medical advice, diagnosis, or treatment. Always consult a qualified healthcare professional before using any medication or starting any treatment.
Medionix Pharma does not encourage self-medication. Customers are responsible for ensuring that purchases comply with local laws and prescription requirements in their country. If you have any questions or concerns regarding the content on our website, please contact us at sales@medionixpharma.com.







