Unione Europea - italiano - EMA (European Medicines Agency)

biogen netherlands b.v. - natalizumab - sclerosi multipla - immunosoppressori selettivi - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 e 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Unione Europea - italiano - EMA (European Medicines Agency)

sanofi winthrop industrie - aflibercept - neoplasie colorettali - agenti antineoplastici - trattamento del carcinoma del colon-retto metastatico (mcrc).

Unione Europea - italiano - EMA (European Medicines Agency)

otsuka pharmaceutical netherlands b.v. - brexpiprazole - schizofrenia - psicolettici - il trattamento della schizofrenia.

Unione Europea - italiano - EMA (European Medicines Agency)

lipomed gmbh - deferiprone - iron overload; beta-thalassemia - tutti gli altri prodotti terapeutici - deferiprone lipomed in monoterapia è indicato per il trattamento del sovraccarico di ferro nei pazienti con talassemia major, mentre la terapia di chelazione è controindicata o inadeguata. deferiprone lipomed in combinazione con un altro chelante è indicato nei pazienti con talassemia major, quando la monoterapia con qualsiasi agente chelante del ferro è inefficace, o quando la prevenzione o il trattamento di conseguenze pericolose per la vita del sovraccarico di ferro giustifica rapida o per la cpu correzione.

Unione Europea - italiano - EMA (European Medicines Agency)

swedish orphan biovitrum ab (publ) - avatrombopag maleate - trombocitopenia - antiemorragici - doptelet è indicato per il trattamento della trombocitopenia grave, in pazienti adulti con malattia cronica di fegato che sono in programma di sottoporsi a una procedura invasiva. doptelet is indicated for the treatment of primary chronic immune thrombocytopenia (itp) in adult patients who are refractory to other treatments (e. corticosteroidi, immunoglobuline).

Unione Europea - italiano - EMA (European Medicines Agency)

instituto grifols s.a. - fostamatinib disodium - trombocitopenia - altre sistemica hemostatics - tavlesse è indicato per il trattamento di malattie croniche trombocitopenia immune (itp) in pazienti adulti che sono refrattari ad altri trattamenti.

Unione Europea - italiano - EMA (European Medicines Agency)

bristol-myers squibb pharma eeig - ozanimod hydrochloride - multiple sclerosis, relapsing-remitting; colitis, ulcerative - immunosoppressori - multiple sclerosiszeposia is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis (rrms) with active disease as defined by clinical or imaging features. ulcerative colitiszeposia is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis (uc) who have had an inadequate response, lost response, or were intolerant to either conventional therapy or a biologic agent.

Unione Europea - italiano - EMA (European Medicines Agency)

stemline therapeutics b.v. - selinexor - mieloma multiplo - agenti antineoplastici - nexpovio is indicatedin combination with bortezomib and dexamethasone for the treatment of adult patients with multiple myeloma who have received at least one prior therapy. in combination with dexamethasone for the treatment of multiple myeloma in adult patients who have received at least four prior therapies and whose disease is refractory to at least two proteasome inhibitors, two immunomodulatory agents and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Italia - italiano - AIFA (Agenzia Italiana del Farmaco)

sun pharmaceutical industries (europe) b.v. - lenalidomide - lenalidomide

Unione Europea - italiano - EMA (European Medicines Agency)

horizon therapeutics ireland dac - inebilizumab - neuromyelitis optica - immunosoppressori - uplizna is indicated as monotherapy for the treatment of adult patients with neuromyelitis optica spectrum disorders (nmosd) who are anti-aquaporin 4 immunoglobulin g (aqp4-igg) seropositive (see section 5.