Unione Europea - ceco - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - imunosupresiva - 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) je indikován k léčbě dospělých pacientů s dříve neléčeným mnohočetným myelomem, kteří nejsou způsobilí pro transplantaci. 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 a 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) je indikován k léčbě dospělých pacientů s dříve neléčeným mnohočetným myelomem, kteří nejsou způsobilí pro transplantaci. 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 a 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).

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu; 992 norethisteron-acetÁt - potahovaná tableta - 1mg/0,5mg - norethisteron a estrogen

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu - potahovaná tableta - 1mg - estradiol

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu - potahovaná tableta - 2mg - estradiol

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 18026 lidskÝ glukagon - prášek a rozpouštědlo pro injekční roztok - 1mg - glukagon

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu; 992 norethisteron-acetÁt - potahovaná tableta - 2mg/1mg - norethisteron a estrogen

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu; 992 norethisteron-acetÁt; 13226 hemihydrÁt estradiolu - potahovaná tableta - 1mg+1mg/1mg - norethisteron a estrogen

Repubblica Ceca - ceco - SUKL (Státní ústav pro kontrolu léčiv)

novo nordisk a/s, bagsvaerd array - 13226 hemihydrÁt estradiolu; 13226 hemihydrÁt estradiolu; 992 norethisteron-acetÁt; 13226 hemihydrÁt estradiolu - potahovaná tableta - 2mg+2mg/1mg+1mg - norethisteron a estrogen

Unione Europea - ceco - EMA (European Medicines Agency)

novo nordisk a/s - inzulín detemir - diabetes mellitus - léky užívané při diabetu - léčba diabetes mellitus u dospělých, dospívajících a dětí ve věku 1 roku a starší.

Unione Europea - ceco - EMA (European Medicines Agency)

novo nordisk a/s - inzulin aspart - diabetes mellitus - léky užívané při diabetu - novorapid je indikován k léčbě diabetes mellitus u dospělých, dospívajících a dětí ve věku od 1 roku.