Indications
Treatment of malignant breast tumors in women during natural or artificially induced menopause after treatment with anti-estrogenic drugs.
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Add to wishlistTreatment of malignant breast tumors in women during natural or artificially induced menopause after treatment with anti-estrogenic drugs.
Endocrine status characteristic of the premenopausal period; pregnancy, lactation, hypersensitivity to letrozole.
1 tablet:
Active substance:
2.5 mg of letrozole. Â
Excipients:
magnesium aluminometasilicate 10 mg,
croscarmellose sodium 3 mg,
colloidal silicon dioxide 3 mg,
magnesium stearate 0.5 mg,
ludipress 81 mg.
Composition of the film shell:
Opadray II yellow 85F32733 (polyvinyl alcohol 35-49%, talc 9.8-25%, macrogol 3350 7.35-35.2%, titanium dioxide and iron oxide yellow 15.15-30%).
1 tablet:
Active ingredient:
2.5 mg of letrozole.
Auxiliary substances:
magnesium aluminometasilicate 10 mg,
croscarmellose sodium 3 mg,
colloidal silicon dioxide 3 mg,
magnesium stearate 0.5 mg,
ludipress 81 mg.
Composition of the film shell:
Opadray II yellow 85F32733 (polyvinyl alcohol 35-49%, talc 9.8-25%, macrogol 3350 7.35-35.2%, titanium dioxide and iron oxide yellow 15.15-30%).
Antitumor agent.
It is a non-steroidal aromatase inhibitor, an enzyme involved in the synthesis of estrogens in postmenopausal women.
Aromatase promotes the conversion of androgens synthesized in the adrenal glands (primarily androstenedione and testosterone) into estrone and estradiol.
Inhibition of aromatase activity is realized by competitive binding to the cytochrome P450 heme subunit of this enzyme, which leads to a decrease in estrogen biosynthesis in all tissues, including in the tissues of estrogen-dependent tumors.
Treatment of malignant breast tumors in women during natural or artificially induced menopause after treatment with anti-estrogenic drugs.
Endocrine status characteristic of the premenopausal period; pregnancy, lactation, hypersensitivity to letrozole.
Possible: Â headache, nausea, peripheral edema, general weakness, hot flashes, thinning hair, skin rash, vomiting, dyspepsia, weight gain, musculoskeletal pain, anorexia, vaginal bleeding, leukorrhea, constipation, dizziness, increased appetite, increased sweating.
Rarely: Â shortness of breath, thrombophlebitis, spotting from the vagina.
The dose is 2.5 mg 1 time / day daily.
Treatment continues during the period of disease progression.
In patients with creatinine clearance less than 10 ml/min, the safety of letrozole has not been studied, so if it is necessary to use it in such cases, the ratio between the expected therapeutic effect and the possible risk of treatment should be carefully weighed.
Under the influence of letrozole, the ability to concentrate and the speed of psychomotor reactions may decrease, so it is recommended to avoid driving vehicles and other potentially dangerous activities during treatment.
Pills.
Store in a dry place, protected from light, at a temperature not exceeding 25 °C. Keep out of reach of children.
life is 2 years.
Letrozole
By prescription
Tablets
For adults as directed by your doctor
Breast Cancer
Out of stock
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