Եվրոպական Միություն - դանիերեն - EMA (European Medicines Agency)

viiv healthcare b.v. - dolutegravir natrium, lamivudin - hiv infektioner - antivirale midler til systemisk anvendelse - dovato er indiceret til behandling af human immundefekt virus type 1 (hiv-1) infektion hos voksne og unge over 12 år, som vejer mindst 40 kg, og som er uden kendt eller formodet resistens over for integrase inhibitor klasse, eller lamivudin.

Դանիա - դանիերեն - Lægemiddelstyrelsen (Danish Medicines Agency)

fresenius kabi ab - natriumchlorid - infusionsvæske, opløsning - 9 mg/ml

Դանիա - դանիերեն - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - risedronatnatriumhemipentahydrat - filmovertrukne tabletter - 30 mg

Դանիա - դանիերեն - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - risedronatnatriumhemipentahydrat - filmovertrukne tabletter - 35 mg

Դանիա - դանիերեն - Lægemiddelstyrelsen (Danish Medicines Agency)

stada arzneimittel ag - risedronatnatriumhemipentahydrat - filmovertrukne tabletter - 5 mg

Եվրոպական Միություն - դանիերեն - EMA (European Medicines Agency)

merck sharp & dohme b.v. - peginterferon alfa-2b - hepatitis c kronisk - immunostimulants, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. der henvises til ribavirin og boceprevir produktresuméer (smpcs), når pegintron skal anvendes i kombination med disse lægemidler. adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. pegintron i kombination med ribavirin (bitherapy) er indiceret til behandling af chc-infektion hos voksne patienter, der er tidligere ubehandlet, herunder patienter med klinisk stabilt hiv co-infektion, og hos voksne patienter, der har undladt tidligere behandling med interferon-alfa (pegyleret eller non-pegyleret) og ribavirin kombination terapi eller alfa-interferon-monoterapi. interferon monoterapi, herunder pegintron, er indikeret primært i tilfælde af intolerance eller kontraindikation for ribavirin. der henvises til ribavirin spc, når pegintron er at blive brugt i kombination med ribavirin. paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna. når det besluttes ikke at udsætte behandlingen, indtil voksenalderen, det er vigtigt at overveje, at kombinationen af terapi-induceret vækst-hæmning, der kan være uoprettelige hos nogle patienter. beslutningen om at behandle en sag-for-sag. der henvises til ribavirin produktresumeet for kapsler eller oral opløsning, når pegintron er at blive brugt i kombination med ribavirin.

Եվրոպական Միություն - դանիերեն - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuri, paroxysmal - selektive immunosuppressiva - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Եվրոպական Միություն - դանիերեն - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - glecaprevir, pibrentasvir - hepatitis c kronisk - antivirale midler til systemisk anvendelse - maviret is indicated for the treatment of chronic hepatitis c virus (hcv) infection in adults and children aged 3 years and older. maviret coated granules is indicated for the treatment of chronic hepatitis c virus (hcv) infection in children 3 years and older.

Դանիա - դանիերեն - Lægemiddelstyrelsen (Danish Medicines Agency)

orion corporation - natriumvalproat - oral opløsning - 60 mg/ml

Եվրոպական Միություն - դանիերեն - EMA (European Medicines Agency)

alnylam netherlands b.v. - patisiran natrium - amyloidose, familiær - andre narkotika stoffer - onpattro er indiceret til behandling af arvelige transthyretin-medieret amyloidose (hattr amyloidose) hos voksne patienter med fase 1 eller fase 2 polyneuropati.