DIPROSALIC 0,64 mg+30 mg/g România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

diprosalic 0,64 mg+30 mg/g

schering-plough labo n.v. - belgia - combinatii (betamethasonum +acid salicyilicum) - unguent - 0,64 mg+30 mg/g - corticosteroizi alte combinatii corticosteroizi cu potenta mare in alte combinatii

XEOMIN 100 UNITATI România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

xeomin 100 unitati

merz pharma gmbh & co. kgaa - germania - toxina botulinica de tip a unui - pulb. pt. sol. inj. - 100 unitati - miorelaxante periferice alte miorelaxante cu actiune periferica

XEOMIN 50 UNITATI România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

xeomin 50 unitati

merz pharma gmbh & co. kgaa - germania - toxina botulinica de tip a unui - pulb. pt. sol. inj. - 50 unitati - miorelaxante periferice alte miorelaxante cu actiune periferica

XEOMIN 200 UNITATI România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

xeomin 200 unitati

merz pharma gmbh & co. kgaa - germania - toxina botulinica de tip a unui - pulb. pt. sol. inj. - 200unitati - miorelaxante periferice alte miorelaxante cu actiune periferica

Imatinib Actavis Uniunea Europeană - română - EMA (European Medicines Agency)

imatinib actavis

actavis group ptc ehf - imatinib - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma - protein kinase inhibitors, antineoplastic agents - imatinib actavis is indicated for the treatment of: , 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;, paediatric patients with ph+ cml in chronic phase after failure of interferon-alpha therapy, or in accelerated phase or blast crisis;, adult patients with ph+ cml in blast crisis;, adult 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-pdgfr rearrangement;, 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. , efectul de imatinib pe rezultatul de transplantul de măduvă osoasă nu a fost determinată. imatinib actavis is indicated for: , 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 dfsp. experiența cu imatinib la pacienții cu mds/mpd asociate cu genei fcdp-re-aranjamente este foarte limitat. nu există studii controlate care să demonstreze un beneficiu clinic sau a crescut de supraviețuire pentru aceste boli.