Description
Excipients
Lactose monohydrate – 50 mg, sodium carboxymethyl starch – 2.5 mg, colloidal silicon dioxide – 0.5 mg, microcrystalline cellulose – 28 mg, crospovidone – 4 mg, pregelatinised maize starch – 11.5 mg, magnesium stearate – 1 mg.
Composition of the coating
opadray Y 1-7000 (hypromellose, titanium dioxide, macrogol (polyethylene glycol)) – 3.73 mg, yellow iron oxide – 0.27 mg.
Indications
- Early stages of invasive breast cancer whose cells have hormone receptors, in postmenopausal women, as adjuvant therapy.
- Early stage invasive breast cancer in postmenopausal women after completion of standard adjuvant therapy with tamoxifen for 5 years as prolonged adjuvant therapy.
- Disseminated hormone-dependent breast cancer in postmenopausal women (first-line therapy).
- Disseminated breast cancer with disease recurrence or progression in postmenopausal women (natural or artificially induced) who have received prior anti-estrogen therapy.
- Hormone-dependent HER-2 negative breast cancer in postmenopausal women as neoadjuvant therapy when chemotherapy is contraindicated and emergency surgery is not required.
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