ZINNAT 125 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 125 mg

glaxowellcome uk ltd. - cefuroximum - compr. film. - 125mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 250 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 250 mg

glaxowellcome uk ltd. - cefuroximum - compr. film. - 250mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 500 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 500 mg

glaxowellcome uk ltd. - cefuroximum - compr. film. - 500mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 125 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 125 mg

glaxosmithkline trading services limited - irlanda - cefuroximum - compr. film. - 125mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 250 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 250 mg

glaxosmithkline trading services limited - irlanda - cefuroximum - compr. film. - 250mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 500 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 500 mg

glaxosmithkline trading services limited - irlanda - cefuroximum - compr. film. - 500mg - alte antibiotice betalactamice cefalosporine de generatia a ii-a

ZINNAT 125 mg/5 ml România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

zinnat 125 mg/5 ml

glaxosmithkline trading services limited - irlanda - cefuroximum - gran. pt. susp. orala - 125mg/5ml - alte antibiotice betalactamice cefalosporine de generatia a ii-a

Zolsketil pegylated liposomal Uniunea Europeană - română - EMA (European Medicines Agency)

zolsketil pegylated liposomal

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.

Caelyx pegylated liposomal Uniunea Europeană - română - EMA (European Medicines Agency)

caelyx pegylated liposomal

baxter holding b.v. - doxorubicină clorhidrat - sarcoma, kaposi; multiple myeloma; ovarian neoplasms; breast neoplasms - agenți antineoplazici - caelyx lipozomală polietilenglicată este indicat:ca monoterapie la pacienții cu cancer de sân metastatic, în cazul în care există un risc cardiac crescut;pentru tratamentul cancerului ovarian avansat la femeile care nu au reușit o primă linie de chimioterapie pe bază de platină regim;în asociere cu bortezomib pentru tratamentul mielomului multiplu progresiv la pacienții care au primit cel puțin un tratament anterior și care au suferit deja sau sunt improprii pentru transplant de măduvă osoasă;pentru tratamentul sida legate de sarcom kaposi (sk) la pacienții cu număr mic de celule cd4 (.

Celdoxome pegylated liposomal Uniunea Europeană - română - EMA (European Medicines Agency)

celdoxome pegylated liposomal

yes pharmaceutical development services gmbh - doxorubicină clorhidrat - breast neoplasms; ovarian neoplasms; multiple myeloma; sarcoma, kaposi - agenți antineoplazici - 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).