Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Eiropas Savienība - latviešu - EMA (European Medicines Agency)

lenalidomide krka (previously lenalidomide krka d.d. novo mesto)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - imūnsupresanti - multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) ir norādīts ārstēšanai pieaugušiem pacientiem ar iepriekš neārstētiem multiplā mieloma, kas nav tiesīgi transplantātu. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 un 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) ir norādīts ārstēšanai pieaugušiem pacientiem ar iepriekš neārstētiem multiplā mieloma, kas nav tiesīgi transplantātu. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 un 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Ventilastin Novolizer 100 mikrogrami/devā inhalācijas pulveris Latvija - latviešu - Zāļu valsts aģentūra

ventilastin novolizer 100 mikrogrami/devā inhalācijas pulveris

meda pharma gmbh & co.kg, germany - salbutamols - inhalācijas pulveris - 100 µg/devā

Fortulin Novolizer 12 mikrogrami/izsmidzinājumā inhalācijas pulveris Latvija - latviešu - Zāļu valsts aģentūra

fortulin novolizer 12 mikrogrami/izsmidzinājumā inhalācijas pulveris

meda pharma, sia, latvija - formoterola fumarāta dihidrāts - inhalācijas pulveris - 12 mikrogrami/izsmidzinājumā

Fortulin Novolizer 6 mikrogrami/izsmidzinājumā inhalācijas pulveris Latvija - latviešu - Zāļu valsts aģentūra

fortulin novolizer 6 mikrogrami/izsmidzinājumā inhalācijas pulveris

meda pharma, sia, latvija - formoterola fumarāta dihidrāts - inhalācijas pulveris - 6 mikrogrami/izsmidzinājumā

Naklofen 50 mg zarnās šķīstošās tabletes Latvija - latviešu - Zāļu valsts aģentūra

naklofen 50 mg zarnās šķīstošās tabletes

krka, d.d., novo mesto, slovenia - diklofenaka nātrija sāls - zarnās šķīstošā tablete - 50 mg

Naklofen 11,6 mg/g gels Latvija - latviešu - Zāļu valsts aģentūra

naklofen 11,6 mg/g gels

krka, d.d., novo mesto, slovenia - diklofenaka dietilamīna sāls - gels - 11,6 mg/g