Eesti - eesti - Ravimiamet

v.m.d. - kolistiin - suukaudse lahuse pulber - 160mg 1g 100g 1tk; 160mg 1g 1000g 1tk

Eesti - eesti - Ravimiamet

sanofi-aventis estonia oÜ - spiramütsiin - õhukese polümeerikattega tablett - 3000000rÜ 10tk

Eesti - eesti - Ravimiamet

sanofi-aventis estonia oÜ - spiramütsiin - õhukese polümeerikattega tablett - 1500000rÜ 16tk

Eesti - eesti - Ravimiamet

sanofi-aventis zrt. - spiramütsiin - õhukese polümeerikattega tablett - 3000000rÜ 10tk

Eesti - eesti - Ravimiamet

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

Euroopa Liit - eesti - 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.

Eesti - eesti - 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

Euroopa Liit - eesti - 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.

Euroopa Liit - eesti - EMA (European Medicines Agency)

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

Eesti - eesti - Ravimiamet

medac gesellschaft für klinische spezialpräparate mbh - mitomütsiin - intravesikaallahuse pulber ja lahusti - 40mg 4tk; 40mg 5tk