Pemazyre Europska Unija - češki - EMA (European Medicines Agency)

pemazyre

incyte biosciences distribution b.v. - pemigatinib - cholangiocarcinoma - antineoplastická činidla - pemazyre monotherapy is indicated for the treatment of adults with locally advanced or metastatic cholangiocarcinoma with a fibroblast growth factor receptor 2 (fgfr2) fusion or rearrangement that have progressed  after at least one prior line of systemic therapy.

Ponvory Europska Unija - češki - EMA (European Medicines Agency)

ponvory

janssen-cilag international n.v.    - ponesimod - roztroušená skleróza, relaps-remitentní - imunosupresiva - ponvory is indicated for the treatment of adult patients with relapsing forms of multiple sclerosis (rms) with active disease defined by clinical or imaging features.

Sondelbay Europska Unija - češki - EMA (European Medicines Agency)

sondelbay

accord healthcare s.l.u. - teriparatid - osteoporóza - vápníková homeostáza - sondelbay is indicated in adults. léčba osteoporózy u postmenopauzálních žen a u mužů se zvýšeným rizikem zlomenin. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. léčba osteoporózy spojené s trvalou terapií systémovými glukokortikoidy u žen a mužů se zvýšeným rizikem zlomenin.

Ebvallo Europska Unija - češki - EMA (European Medicines Agency)

ebvallo

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

Eladynos Europska Unija - češki - EMA (European Medicines Agency)

eladynos

theramex ireland limited - abaloparatide - osteoporosis, postmenopausal; osteoporosis - vápníková homeostáza - léčba osteoporózy u postmenopauzálních žen se zvýšeným rizikem zlomenin.

Teriparatide Sun Europska Unija - češki - EMA (European Medicines Agency)

teriparatide sun

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - vápníková homeostáza - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Kauliv Europska Unija - češki - EMA (European Medicines Agency)

kauliv

strides pharma (cyprus) limited - teriparatid - osteoporosis; osteoporosis, postmenopausal - vápníková homeostáza - kauliv is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Pedmarqsi Europska Unija - češki - EMA (European Medicines Agency)

pedmarqsi

fennec pharmaceuticals (eu) limited - sodium thiosulfate - ear diseases; ototoxicity - všechny ostatní terapeutické přípravky - pedmarqsi is indicated for the prevention of ototoxicity induced by cisplatin chemotherapy in patients 1 month to < 18 years of age with localised, non-metastatic, solid tumours.

ADDITIVA VITAMIN C ZITRONE 1000MG Šumivá tableta Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

additiva vitamin c zitrone 1000mg šumivá tableta

dr. b.scheffler gmbh, bergisch gladbach array - 102 kyselina askorbovÁ - Šumivá tableta - 1000mg - kyselina askorbovÁ (vitamin c)

AMINOPLASMAL B.BRAUN 5% E Infuzní roztok Češka Republika - češki - SUKL (Státní ústav pro kontrolu léčiv)

aminoplasmal b.braun 5% e infuzní roztok

b. braun melsungen ag, melsungen array - 790 isoleucin; 829 leucin; 851 lysin-hydrochlorid; 2445 methionin; 1117 fenylalanin; 1459 threonin; 1503 tryptofan; 1514 valin; 96 arginin; 717 histidin; 27 alanin; 55 glycin; 103 kyselina asparagovÁ; 665 kyselina glutamovÁ; 4147 prolin; 4717 serin; 1507 tyrosin; 1306 trihydrÁt natrium-acetÁtu; 2458 hydroxid sodnÝ; 1170 kalium-acetÁt; 1322 chlorid sodnÝ; 856 hexahydrÁt chloridu hoŘeČnatÉho; 1341 dodekahydrÁt hydrogenfosforeČnanu sodnÉho - infuzní roztok - roztoky pro parenterÁlnÍ vÝŽivu, kombinace