Jakavi Evropská unie - čeština - EMA (European Medicines Agency)

jakavi

novartis europharm limited - ruxolitinib (jako fosfát) - myeloproliferative disorders; polycythemia vera; graft vs host disease - antineoplastická činidla - myelofibrosis (mf)jakavi is indicated for the treatment of disease related splenomegaly or symptoms in adult patients with primary myelofibrosis (also known as chronic idiopathic myelofibrosis), post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis. po polycytemii vera (pv)přípravek jakavi je indikován k léčbě dospělých pacientů s po polycytemii vera, kteří jsou rezistentní na léčbu nebo s intolerancí hydroxymočovina. graft versus host disease (gvhd)jakavi is indicated for the treatment of patients aged 12 years and older with acute graft versus host disease or chronic graft versus host disease who have inadequate response to corticosteroids or other systemic therapies (see section 5.

Opzelura Evropská unie - čeština - EMA (European Medicines Agency)

opzelura

incyte biosciences distribution b.v. - ruxolitinib phosphate - vitiligo - ostatní dermatologické přípravky - opzelura is indicated for the treatment of non-segmental vitiligo with facial involvement in adults and adolescents from 12 years of age.

Inrebic Evropská unie - čeština - EMA (European Medicines Agency)

inrebic

bristol myers squibb pharma eeig - fedratinib dihydrochloride monohydrate - myeloproliferative disorders; primary myelofibrosis - antineoplastická činidla - inrebic is indicated for the treatment of disease-related splenomegaly or symptoms in adult patients with primary myelofibrosis, post polycythaemia vera myelofibrosis or post essential thrombocythaemia myelofibrosis who are janus associated kinase (jak) inhibitor naïve or have been treated with ruxolitinib.

Yescarta Evropská unie - čeština - EMA (European Medicines Agency)

yescarta

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastická činidla - yescarta is indicated for the treatment of adult patients with diffuse large b cell lymphoma (dlbcl) and high-grade b-cell lymphoma (hgbl) that relapses within 12 months from completion of, or is refractory to, first-line chemoimmunotherapy. yescarta is indicated for the treatment of adult patients with relapsed or refractory (r/r) dlbcl and primary mediastinal large b cell lymphoma (pmbcl), after two or more lines of systemic therapy. yescarta is indicated for the treatment of adult patients with r/r follicular lymphoma (fl) after three or more lines of systemic therapy.

SPORANOX 10MG/ML Perorální roztok Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

sporanox 10mg/ml perorální roztok

janssen-cilag s.r.o., praha array - 9219 itrakonazol - perorální roztok - 10mg/ml - itrakonazol

Olumiant Evropská unie - čeština - EMA (European Medicines Agency)

olumiant

eli lilly nederland b.v. - baricitinib - artritida, revmatoidní - imunosupresiva - rheumatoid arthritisbaricitinib is indicated for the treatment of moderate to severe active rheumatoid arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more disease modifying anti rheumatic drugs (dmards). olumiant může být použit jako monoterapie nebo v kombinaci s methotrexátem. atopic dermatitisolumiant is indicated for the treatment of moderate to severe atopic dermatitis in adult and paediatric patients 2 years of age and older who are candidates for systemic therapy. alopecia areatabaricitinib is indicated for the treatment of severe alopecia areata in adult patients (see section 5. juvenile idiopathic arthritisbaricitinib is indicated for the treatment of active juvenile idiopathic arthritis in patients 2 years of age and older who have had an inadequate response or intolerance to one or more prior conventional synthetic or biologic dmards:- polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [rf+] or negative [rf-], extended oligoarticular),- enthesitis related arthritis, and- juvenile psoriatic arthritis. baricitinib may be used as monotherapy or in combination with methotrexate.

PROKANAZOL 100MG Tvrdá tobolka Česká republika - čeština - SUKL (Státní ústav pro kontrolu léčiv)

prokanazol 100mg tvrdá tobolka

pro.med.cs praha a.s. array - 9219 itrakonazol - tvrdá tobolka - 100mg - itrakonazol