Łotwa - łotewski - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - metformīna hidrohlorīds - apvalkotā tablete - 850 mg

Łotwa - łotewski - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - metformīna hidrohlorīds - apvalkotā tablete - 500 mg

Łotwa - łotewski - Zāļu valsts aģentūra

aurobindo pharma (malta) limited, malta - metformīna hidrohlorīds - apvalkotās tabletes - 1000 mg

Łotwa - łotewski - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - kvetiapīns - ilgstošās darbības tablete - 200 mg

Łotwa - łotewski - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - kvetiapīns - ilgstošās darbības tablete - 300 mg

Łotwa - łotewski - Zāļu valsts aģentūra

accord healthcare b.v., netherlands - kvetiapīns - ilgstošās darbības tablete - 400 mg

Łotwa - łotewski - Zāļu valsts aģentūra

alvogen ipco s.a.r.l, luxembourg - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg

Łotwa - łotewski - Zāļu valsts aģentūra

teva b.v., netherlands - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg

Łotwa - łotewski - Zāļu valsts aģentūra

actavis group ptc ehf., iceland - bortezomibs - pulveris injekciju šķīduma pagatavošanai - 3,5 mg

Unia Europejska - łotewski - EMA (European Medicines Agency)

koanaa healthcare gmbh - imatinib mesilate - leukemia, myelogenous, chronic, bcr-abl positive; precursor cell lymphoblastic leukemia-lymphoma; myelodysplastic-myeloproliferative diseases; hypereosinophilic syndrome; dermatofibrosarcoma; gastrointestinal stromal tumors - antineoplastiski līdzekļi - 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. pacienti, kuriem ir ar zemu vai ļoti zemu atkārtošanās risku, nevajadzētu saņemt palīgvielu ārstēšana. 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. izņemot tikko diagnosticēta cml hroniskā fāzē, nav kontrolētos pētījumos, kas liecina par klīnisko ieguvumu vai palielina izdzīvošanas šo slimību.