Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh  - risdiplam - mišična atrofija, hrbtenica - druga zdravila za motnje mišično-skeletnega sistema - evrysdi is indicated for the treatment of 5q spinal muscular atrophy (sma) in patients with a clinical diagnosis of sma type 1, type 2 or type 3 or with one to four smn2 copies.

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh - satralizumab - neuromyelitis optica - imunosupresivi - satralizumab (enspryng) is indicated as a monotherapy or in combination with immunosuppressive therapy (ist) for the treatment of neuromyelitis optica spectrum disorders (nmosd) in adult and adolescent patients from 12 years of age who are anti-aquaporin-4 igg (aqp4-igg) seropositive.

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh  - casirivimab, imdevimab - covid-19 virus infection - imunski sera in imunoglobulini, - ronapreve is indicated for:treatment of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19 (see section 4. prevention of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg (see section 4. the use of ronapreve should take into account information on the activity of ronapreve against viral variants of concern. glej poglavja 4. 4 in 5.

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh - mosunetuzumab - limfom, folikularni - antineoplastic agents, monoclonal antibodies - lunsumio as monotherapy is indicated for the treatment of adult patients with relapsed or refractory follicular lymphoma (fl) who have received at least two prior systemic therapies.

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh - faricimab - wet macular degeneration; macular edema; diabetes complications - oftalmologi - vabysmo is indicated for the treatment of adult patients with:neovascular (wet) age-related macular degeneration (namd),visual impairment due to diabetic macular oedema (dme).

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh  - glofitamab - lymphoma, large b-cell, diffuse - antineoplastična sredstva - columvi as monotherapy is indicated for the treatment of adult patients with relapsed or refractory diffuse large b cell lymphoma (dlbcl), after two or more lines of systemic therapy.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

actavis group ptc ehf. - mirtazapin - orodisperzibilna tableta - mirtazapin 30 mg / 1 tableta - mirtazapin

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

actavis group ptc ehf. - mirtazapin - orodisperzibilna tableta - mirtazapin 15 mg / 1 tableta - mirtazapin

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh - obinutuzumab - levkemija, limfocitna, kronična, b-celica - antineoplastična sredstva - kronično limfocitno levkemijo (cll)gazyvaro v kombinaciji z chlorambucil je indiciran za zdravljenje odraslih bolnikov s predhodno nezdravljenih kronično limfocitno levkemijo (cll) in z comorbidities česar so neprimerni za celoten odmerek fludarabine temelji terapije (glejte poglavje 5. folikularni limfom (fl)gazyvaro v kombinaciji s kemoterapijo, sledi gazyvaro vzdrževanje terapije pri pacientih, ki so dosegli odziv, ki je primerna za zdravljenje bolnikov s predhodno nezdravljenih napredno folikularni limfom. gazyvaro v kombinaciji z bendamustine sledi gazyvaro vzdrževanje je indiciran za zdravljenje bolnikov z folikularni limfom (fl), ki niso odzvali ali kdo napredoval med ali do 6 mesecev po zdravljenju z rituksimabom ali rituksimabom, ki vsebujejo režim.

Evropska unija - slovenščina - EMA (European Medicines Agency)

roche registration gmbh - ocrelizumab - multiple skleroza - imunosupresivi - zdravljenje odraslih bolnikov s ponavljajočo oblike multiple skleroze (rms) z aktivno boleznijo določi kliničnih ali slikanje funkcije. zdravljenje odraslih bolnikov z zgodnjim primarno progresivno multiplo sklerozo (ppms), v smislu bolezni, trajanje in stopnjo invalidnosti, in z imaging značilnosti značilno vnetno aktivnost.