Estonija - estonski - Ravimiamet

actavis italy s.p.a. - doksorubitsiin - süstelahuse pulber - 50mg 1tk

Europska Unija - estonski - EMA (European Medicines Agency)

accord healthcare s.l.u. - doxorubicin hydrochloride, liposomal - ovarian neoplasms; sarcoma, kaposi; multiple myeloma - doxorubicin - zolsketil pegylated liposomal is a medicine used to treat the following types of cancer in adults:• breast cancer that has spread to other parts of the body in patients at risk of heart problems. zolsketil pegylated liposomal is used on its own for this disease;• advanced ovarian cancer in women whose previous treatment including a platinum-based cancer medicine has stopped working;• multiple myeloma (a cancer of the white blood cells in the bone marrow), in patients with progressive disease who have received at least one other treatment in the past and have already had, or are unsuitable for, a bone marrow transplantation. zolsketil pegylated liposomal is used in combination with bortezomib (another cancer medicine);• kaposi’s sarcoma in patients with aids who have a very damaged immune system. kaposi’s sarcoma is a cancer that causes abnormal tissue to grow under the skin, on moist body surfaces or on internal organs. zolsketil pegylated liposomal contains the active substance doxorubicin and is a ‘hybrid medicine’. this means that it is similar to a ‘reference medicine’ containing the same active substance called adriamycin. however, in zolsketil pegylated liposomal the active substance is enclosed in tiny fatty spheres called liposomes, whereas this is not the case for adriamycin.

Estonija - estonski - Ravimiamet

medac gesellschaft für klinische spezialpräparate mbh - mitomütsiin - intravesikaal-/süstelahuse pulber - 1mg 1ml 10mg 1tk; 1mg 1ml 2mg 1tk; 1mg 1ml 40mg 5tk; 1mg 1ml 10mg 5tk; 1mg 1ml 2mg 10tk; 1mg 1ml 40mg 1tk; 1mg 1ml 20mg 5tk; 1mg 1ml 40mg 10tk; 1mg 1ml 20mg 1tk; 1mg 1ml 10mg 10tk

Europska Unija - estonski - EMA (European Medicines Agency)

plusultra pharma gmbh - sirolimus - angiofibroma; tuberous sclerosis - hyftor is indicated for the treatment of facial angiofibroma associated with tuberous sclerosis complex in adults and paediatric patients aged 6 years and older.

Europska Unija - estonski - EMA (European Medicines Agency)

yes pharmaceutical development services gmbh - doksorubitsiini vesinikkloriid - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - antineoplastilised ained - celdoxome pegylated liposomal is indicated in adults:as monotherapy for patients with metastatic breast cancer, where there is an increased cardiac risk. or treatment of advanced ovarian cancer in women who have failed a first-line platinum-based chemotherapy regimen. in combination with bortezomib for the treatment of progressive multiple myeloma in patients who have received at least one prior therapy and who have already undergone or are unsuitable for bone marrow transplant. for treatment of aids-related kaposi’s sarcoma (ks) in patients with low cd4 counts (< 200 cd4 lymphocytes/mm3) and extensive mucocutaneous or visceral disease. celdoxome pegylated liposomal may be used as first-line systemic chemotherapy, or as second line chemotherapy in aids-ks patients with disease that has progressed with, or in patients intolerant to, prior combination systemic chemotherapy comprising at least two of the following agents: a vinca alkaloid, bleomycin and standard doxorubicin (or other anthracycline).

Europska Unija - estonski - EMA (European Medicines Agency)

tlc biopharmaceuticals b.v. - doksorubitsiini vesinikkloriid - breast neoplasms; ovarian neoplasms - antineoplastilised ained - ravi rinna-ja munasarjavähk.

Estonija - estonski - Ravimiamet

accord healthcare b.v. - mitomütsiin - intravesikaal-/süstelahuse pulber - 10mg 1tk; 10mg 5tk

Estonija - estonski - Ravimiamet

accord healthcare b.v. - mitomütsiin - intravesikaal-/süstelahuse pulber - 2mg 10tk; 2mg 5tk

Estonija - estonski - Ravimiamet

accord healthcare b.v. - mitomütsiin - süste-/infusioonilahuse pulber - 40mg 1tk; 40mg 5tk

Europska Unija - estonski - EMA (European Medicines Agency)

boehringer ingelheim international gmbh - telmisartan, amlodipine - hüpertensioon - reniini-angiotensiini süsteemi toimivad ained - ravi oluline hüpertensioon täiskasvanutel:add-therapytwynsta on näidustatud täiskasvanutel, kelle vererõhk ei ole adekvaatselt kontrollitav kohta amlodipine. asendamine therapyadult saavate patsientide telmisartan ja amlodipine alates eraldi tablette võib selle asemel saada tabletid twynsta sisaldavad sama komponendi doosid.