Den europeiske union - norsk - EMA (European Medicines Agency)

gilead sciences international ltd  - emtricitabine, rilpivirine hydrochloride, tenofovir disoproxil fumarate - hiv-infeksjoner - antivirale midler til systemisk bruk - eviplera er indisert for behandling av voksne infisert med humant immunsviktvirus type 1 (hiv-1) uten kjent mutasjoner tilknyttet motstand mot ikke-nukleosid revers transkriptase hemmer (nnrti) klassen, tenofovir eller emtricitabine, og med en viral last ≤ 100.000 hiv-1 rna kopier/ml. som med andre antiretrovirale legemidler, bør genotypic motstand tester og/eller historiske motstand data styre bruken av eviplera.

Den europeiske union - norsk - EMA (European Medicines Agency)

gilead sciences ireland uc - cobicistat - hiv-infeksjoner - antivirale midler til systemisk bruk - tybost is indicated as a pharmacokinetic enhancer of atazanavir 300 mg once daily or darunavir 800 mg once daily as part of antiretroviral combination therapy in human immunodeficiency virus-1 (hiv-1) infected adults and adolescents aged 12 years and older:weighing at least 35 kg co‑administered with atazanavir orweighing at least 40 kg co‑administered with darunavir.

Den europeiske union - norsk - EMA (European Medicines Agency)

kite pharma eu b.v. - axicabtagene ciloleucel - lymphoma, follicular; lymphoma, large b-cell, diffuse - antineoplastiske midler - 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.

Norge - norsk - Statens legemiddelverk

evolan pharma ab - aciklovir - hudstift - 5 %

Den europeiske union - norsk - EMA (European Medicines Agency)

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - antineoplastiske midler - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Den europeiske union - norsk - EMA (European Medicines Agency)

takeda manufacturing austria ag - octocog alfa - hemofili a - antihemoragika - behandling og profylakse av blødning hos pasienter med hemofili a (medfødt faktor viii-mangel). advate inneholder ikke von willebrand faktor i farmakologisk effektive mengder, og er derfor ikke indisert i genet for von willebrand disease.

Den europeiske union - norsk - EMA (European Medicines Agency)

helsinn birex pharmaceuticals ltd - netupitant, palonosetron hydrochloride - vomiting; neoplasms; nausea; cancer - antiemetika og antinauseants, - akynzeo er angitt i voksne for:forebygging av akutt og forsinket kvalme og oppkast forbundet med svært emetogenic cisplatin-basert kreft kjemoterapi. forebygging av akutt og forsinket kvalme og oppkast forbundet med moderat emetogenic kreft kjemoterapi.

Den europeiske union - norsk - EMA (European Medicines Agency)

viatris healthcare limited - imiquimod - condylomata acuminata; keratosis; keratosis, actinic; carcinoma, basal cell - antibiotika og kjemoterapeutiske midler til dermatologisk bruk - imiquimod cream is indicated for the topical treatment of :external genital and perianal warts (condylomata acuminata) in adults. small superficial basal cell carcinomas (sbccs) in adults. clinically typical, nonhyperkeratotic, nonhypertrophic actinic keratoses (aks) on the face or scalp in immunocompetent adult patients when size or number of lesions limit the efficacy and/or acceptability of cryotherapy and other topical treatment options are contraindicated or less appropriate.

Den europeiske union - norsk - EMA (European Medicines Agency)

sanofi b.v. - laronidase - mukopolysakkaridose i - andre alimentary tract and metabolism products, - aldurazyme er indikert for langsiktig enzym erstatning terapi hos pasienter med en bekreftet diagnose av mucopolysaccharidosis jeg (mps jeg; alfa-l-iduronidase mangel på) til å behandle nonneurological manifestasjoner av sykdommen.

Den europeiske union - norsk - EMA (European Medicines Agency)

mylan pharmaceuticals limited - amlodipine besilate, valsartan - hypertensjon - agenter som virker på renin-angiotensinsystemet - behandling av essensiell hypertensjon. amlodipine/valsartan mylan er indisert hos voksne hvis blodtrykket ikke er tilstrekkelig kontrollert på amlodipine eller valsartan monoterapi.