Europska Unija - češki - 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).

Europska Unija - češki - EMA (European Medicines Agency)

biogen netherlands b.v. - diroximel fumarate (biib098) - roztroušená skleróza, relaps-remitentní - imunosupresiva - vumerity is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (see section 5. 1 for important information on the populations for which efficacy has been established).

Europska Unija - češki - EMA (European Medicines Agency)

mylan ireland limited - dimethyl fumarát - roztroušená skleróza, relaps-remitentní - imunosupresiva - dimethyl fumarate mylan is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Europska Unija - češki - EMA (European Medicines Agency)

zaklady farmafarmaceutyczne polpharma s.aceutyczne polpharma s.a. - dimethyl fumarát - roztroušená skleróza, relaps-remitentní - imunosupresiva - dimethyl fumarate polpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Europska Unija - češki - EMA (European Medicines Agency)

teva gmbh - dimethyl fumarát - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresiva - dimethyl fumarate teva is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Europska Unija - češki - EMA (European Medicines Agency)

accord healthcare s.l.u. - dimethyl fumarát - multiple sclerosis, relapsing-remitting; multiple sclerosis - imunosupresiva - dimethyl fumarate accord is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).

Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

aurovitas, spol. s r.o., praha array - 4127 aciklovir - tableta - 400mg - aciklovir

Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

zentiva a.s., bratislava array - 12 kyselina acetylsalicylovÁ; 223 kofein - tableta - 450mg/50mg - kyselina acetylsalicylovÁ, kombinace kromĚ psycholeptik

Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

belupo, s.r.o., bratislava array - 11745 alklometason-dipropionÁt - krém - 0,5mg/g - alklometason

Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

belupo, s.r.o., bratislava array - 11745 alklometason-dipropionÁt - mast - 0,5mg/g - alklometason