Европейский союз - чешский - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride hydrate - multiple myeloma; lymphoma, follicular; myelodysplastic syndromes - imunosupresiva - multiple myelomalenalidomide krka d. 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 d. 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 d. 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 d. 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. follicular lymphomalenalidomide krka d. in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Европейский союз - чешский - EMA (European Medicines Agency)

krka, d.d., novo mesto - abirateron acetátu - prostatetické novotvary - endokrinní terapie - abiraterone krka is indicated with prednisone or prednisolone for:the treatment of newly diagnosed high risk metastatic hormone sensitive prostate cancer (mhspc) in adult men in combination with androgen deprivation therapy (adt) (see section 5. 1)the treatment of metastatic castration resistant prostate cancer (mcrpc) in adult men who are asymptomatic or mildly symptomatic after failure of androgen deprivation therapy in whom chemotherapy is not yet clinically indicated (see section 5. 1)the treatment of mcrpc in adult men whose disease has progressed on or after a docetaxel-based chemotherapy regimen.

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 100mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 140mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 20mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 50mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 70mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto slovinsko - 17512 dasatinib - potahovaná tableta - 80mg - dasatinib

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto array - 453 sodnÁ sŮl dexamethason-fosfÁtu - injekční/infuzní roztok - 4mg/ml - dexamethason

Чехия - чешский - SUKL (Státní ústav pro kontrolu léčiv)

krka, d.d., novo mesto, novo mesto array - 453 sodnÁ sŮl dexamethason-fosfÁtu - injekční/infuzní roztok - 8mg/2ml - dexamethason