Letrozolexin (Letrozole) – 2.5mg/tab – 50 tab/bag USA Euro-Pharmacies
€132.00
General introduction and principle of operation (Letrozolexin (Letrozole) – 2.5mg/tab – 50 tab/bag USA Euro-Pharmacies)
Letrozolexin (Letrozole) is a potent aromatase inhibitor primarily indicated for the treatment of hormone-receptor-positive breast cancer in postmenopausal women. It works by obstructing the aromatase enzyme, which is responsible for converting androgens into estrogens in the body. By reducing estrogen levels, Letrozolexin helps to deprive certain cancer cells of the hormones they require to grow and proliferate, thus enhancing the efficacy of breast cancer treatment. Its daily dosage of 2.5 mg allows for optimal absorption and utilization by the body, making it a preferred choice in oncology settings.
Main components and active substances
The pharmaceutical formulation of Letrozolexin contains Letrozole as its active component. This key ingredient is essential for its therapeutic effects. Below are key attributes and features of the main components:
- Letrozole: A highly effective synthetic non-steroidal aromatase inhibitor that plays a crucial role in managing estrogen-dependent cancers.
- Inactive Ingredients: Other components that assist in the stabilization and delivery of the active substance may include excipients that support the formulation without altering its efficacy.
- Chemical Structure: Letrozole is chemically recognized as 4,4′-(1H-1,2,4-Triazol-1-ylmethylene)dibenzonitrile, with a molecular formula of C17H11N5, contributing to its pharmacological action.
Mechanisms of action and expected results
Letrozolexin functions by specifically inhibiting the aromatase enzyme, leading to a significant decrease in circulating estrogen levels. This mechanistic action can result in various positive outcomes, particularly in hormone-sensitive conditions. Some expected results include:
- Estrogen Level Reduction: Significant decreases in serum estrogen levels, essential for targeted cancer therapy.
- Hormonal Balance: Increased levels of luteinizing hormone (LH) and follicle-stimulating hormone (FSH), which may support reproductive functions in certain patients.
- Tumor Growth Inhibition: Myriad clinical studies have shown inhibition of tumor growth and improved survival rates in patients with estrogen receptor-positive breast cancer.
Recommendations for use
For optimal results, specific guidelines should be followed when using Letrozolexin. These include dosing schedules, medical supervision, and monitoring. The recommendations for use include:
- Dosage: The standard dosing is 2.5 mg daily, but some scenarios may necessitate a reduced dosage depending on individual medical assessments.
- Regular Monitoring: It is advisable to conduct liver function tests, lipid profiles, and bone density assessments periodically to ensure patient safety and drug efficacy.
- Consultation: Patients should always consult healthcare providers for personalized advice and adjustments in treatment as required.
Possible risks and contraindications (Letrozolexin (Letrozole) – 2.5mg/tab – 50 tab/bag USA Euro-Pharmacies)
While Letrozolexin is generally well-tolerated, there are potential risks and contraindications that patients should be aware of. Common concerns include:
- Side Effects: These may encompass hot flashes, joint pain, fatigue, and an increased risk of osteoporosis.
- Contraindications: Individuals with a known hypersensitivity to Letrozole or any inactive ingredients should avoid using this medication.
- Blood Pressure Changes: Letrozolexin may cause a decrease in blood pressure, necessitating monitoring in patients with existing hypertension.
| Active substance | Letrozole |
|---|---|
| Water Retention | Reduces water retention |
| Hepatotoxicity | Low hepatotoxicity |
| Lab Test | Monitoring of liver function tests, lipid profiles, and bone density |
| Also known as | Letrozol |
| Blood pressure | Can cause a decrease in blood pressure |
| Trade name | Femara |
| Storage conditions | Store at room temperature away from moisture and heat |
| Chemical name | 4,4'-(1H-1,2,4-Triazol-1-ylmethylene)dibenzonitrile |
| Formula | C17H11N5 |
| Substance class | Aromatase inhibitor |
| Main action | Inhibits the enzyme aromatase, preventing the synthesis of estrogen |
| Half-life | 2 days |
| Dosage (medical) | 2.5 mg daily |
| Dosage (sports) | Typically 0.5 mg to 2.5 mg daily depending on purpose and cycling needs |
| Effects | Reduces estrogen levels, increases luteinizing hormone and follicle-stimulating hormone levels |
| Side effects | Hot flashes, joint pain, fatigue, increased risk of osteoporosis, nausea |
| Use in sports | Used by bodybuilders and athletes to reduce estrogen levels and increase testosterone levels |
| Manufacturer | Euro-Pharmacies |
| Packing | 50 tabs (2.5mg / tab) |
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