Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - bortezomib - bortezomib

Unione Europea - italiano - EMA (European Medicines Agency)

koanaa healthcare gmbh - imatinib mesilato - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - agenti antineoplastici - imatinib koanaa is indicated for the treatment ofadult and paediatric patients with newly diagnosed philadelphia chromosome (bcr-abl) positive (ph+) chronic myeloid leukaemia (cml) for whom bone marrow transplantation is not considered as the first line of treatment. adult and paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis. adult and paediatric patients with newly diagnosed philadelphia chromosome positive acute lymphoblastic leukaemia (ph+ all) integrated with chemotherapy. adult patients with relapsed or refractory ph+ all as monotherapy. adult patients with myelodysplastic/myeloproliferative diseases (mds/mpd) associated with platelet-derived growth factor receptor (pdgfr) gene re-arrangements. adult patients with advanced hypereosinophilic syndrome (hes) and/or chronic eosinophilic leukaemia (cel) with fip1l1-pdgfrα rearrangement. the effect of imatinib on the outcome of bone marrow transplantation has not been determined. imatinib koanaa is indicated forthe treatment of adult patients with kit (cd 117) positive unresectable and/or metastatic malignant gastrointestinal stromal tumours (gist). the adjuvant treatment of adult patients who are at significant risk of relapse following resection of kit (cd117)-positive gist. i pazienti che hanno un basso o bassissimo rischio di recidiva non dovrebbero ricevere il trattamento adiuvante. the treatment of adult patients with unresectable dermatofibrosarcoma protuberans (dfsp) and adult patients with recurrent and/or metastatic dfsp who are not eligible for surgery. in adult and paediatric patients, the effectiveness of imatinib is based on overall haematological and cytogenetic response rates and progression-free survival in cml, on haematological and cytogenetic response rates in ph+ all, mds/mpd, on haematological response rates in hes/cel and on objective response rates in adult patients with unresectable and/or metastatic gist and dfsp and on recurrence-free survival in adjuvant gist. the experience with imatinib in patients with mds/mpd associated with pdgfr gene re-arrangements is very limited (see section 5. tranne che nel recente diagnosi di lmc in fase cronica, non ci sono studi clinici controllati che dimostrano un beneficio clinico o un aumento della sopravvivenza per queste malattie.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - melfalan - melfalan

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - talidomide - talidomide

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - sunitinib - sunitinib

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - capecitabina - capecitabina

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

koanaa healthcare gmbh - fingolimod - fingolimod

Italia - italiano - Ministero della Salute

intervet productions srl - kanamicina solfato acido, n-acetil-l-cisteina - kanamicina solfato acido - 7500000 unit? internazionali; n-acetil-l-cisteina - 7.5 grammo (i), kanamicina solfato acido - 7500000 unit? internazionali; n-acetil-l-cisteina - 7.5 grammo (i), kanamicina solfato acido - 7500000 unit? internazionali; n-acetil-l-cisteina - 7.5 grammo (i), kanamicina solfato acido - 7500000 unit? internazionali; n-acetil-l-cisteina - 7.5 grammo (i), n-acetil-l-cisteina - 7.5 g; kanamicina solfato acido - 7500000 ui, kanamicina solfato acido - 7500000 ui; n-acetil-l-cisteina - 7.5 g - combinations of antibacterials and other substances

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

f.i.r.m.a. s.p.a. - kanamicina - kanamicina

Italia - italiano - Ministero della Salute

intervet productions srl - kanamicina, kanamicina solfato acido - kanamicina solfato acido - 150000 ui/ml; kanamicina - nd, kanamicina - nd ; kanamicina solfato acido - 150000 ui/ml - kanamycin