Humira Evropska unija - slovenščina - EMA (European Medicines Agency)

humira

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - imunosupresivi - prosimo, glejte dokument o izdelku.

Constella Evropska unija - slovenščina - EMA (European Medicines Agency)

constella

abbvie deutschland gmbh & co. kg - linaklotid - sindrom razdražljivega črevesa - zdravila za zaprtje - constella je indicirana za simptomatsko zdravljenje zmernega do hudega sindroma razdražljivega črevesja z zaprtjem (ibs-c) pri odraslih.

Lumigan Evropska unija - slovenščina - EMA (European Medicines Agency)

lumigan

abbvie deutschland gmbh & co. kg - bimatoprost - glaucoma, open-angle; ocular hypertension - prostaglandin analogues, ophthalmologicals - zmanjšanje zvišanega očesnega tlaka pri kroničnem glavkomu odprtega zakotja in očesni hipertenziji (kot monoterapija ali kot dodatno zdravljenje zaviralcev beta).

Kaletra Evropska unija - slovenščina - EMA (European Medicines Agency)

kaletra

abbvie deutschland gmbh co. kg - lopinavir, ritonavir - okužbe z virusom hiv - antivirals for systemic use, protease inhibitors - zdravilo kaletra je indicirano v kombinaciji z drugimi protiretrovirusnimi zdravili za zdravljenje odraslih, mladostnikov in otrok, starih od 14 dni ali več, z virusom humane imunske pomanjkljivosti (hiv-1). izbira kaletra za zdravljenje protease inhibitor izkušeni hiv-1 okuženih bolnikov, ki mora temeljiti na posameznih virusnih odpornost testiranje in zdravljenje zgodovina bolnikov.

Maviret Evropska unija - slovenščina - EMA (European Medicines Agency)

maviret

abbvie deutschland gmbh co. kg - glecaprevir, pibrentasvir - hepatitis c, kronični - antivirusi za sistemsko uporabo - 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.

Rinvoq Evropska unija - slovenščina - EMA (European Medicines Agency)

rinvoq

abbvie deutschland gmbh & co. kg - upadacitinib - artritis, revmatoidni - imunosupresivi - rheumatoid arthritisrinvoq 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). rinvoq may be used as monotherapy or in combination with methotrexate. psoriatic arthritisrinvoq is indicated for the treatment of active psoriatic arthritis in adult patients who have responded inadequately to, or who are intolerant to one or more dmards. rinvoq may be used as monotherapy or in combination with methotrexate. axial spondyloarthritisnon-radiographic axial spondyloarthritis (nr-axspa)rinvoq is indicated for the treatment of active non-radiographic axial spondyloarthritis in adult patients with objective signs of inflammation as indicated by elevated c-reactive protein (crp) and/or magnetic resonance imaging (mri), who have responded inadequately to nonsteroidal anti-inflammatory drugs (nsaids). ankylosing spondylitis (as, radiographic axial spondyloarthritis)rinvoq is indicated for the treatment of active ankylosing spondylitis in adult patients who have responded inadequately to conventional therapy. atopic dermatitisrinvoq is indicated for the treatment of moderate to severe atopic dermatitis in adults and adolescents 12 years and older who are candidates for systemic therapy. ulcerative colitisrinvoq is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.  crohn’s diseaserinvoq is indicated for the treatment of adult patients with moderately to severely active crohn’s disease who have had an inadequate response, lost response or were intolerant to either conventional therapy or a biologic agent.

Ganfort Evropska unija - slovenščina - EMA (European Medicines Agency)

ganfort

abbvie deutschland gmbh & co. kg - bimatoprost, timolol - glaucoma, open-angle; ocular hypertension - oftalmologi - zmanjšanje intraokularnega tlaka (iop) pri bolnikih z glavkomom odprtega zakotja ali očesno hipertenzijo, ki se premalo odzivajo na topične beta blokatorje ali analoge prostaglandinov.

Norvir Evropska unija - slovenščina - EMA (European Medicines Agency)

norvir

abbvie deutschland gmbh co. kg - ritonavir - okužbe z virusom hiv - antivirusi za sistemsko uporabo - ritonavir je indiciran v kombinaciji z drugimi protiretrovirusnimi zdravili za zdravljenje bolnikov, okuženih s hiv-1 (odrasli in otroci, stari dve leti ali več).

Xydalba Evropska unija - slovenščina - EMA (European Medicines Agency)

xydalba

abbvie deutschland gmbh & co. kg - dalbavancin hydrochloride - soft tissue infections; skin diseases, bacterial - antibacterials za sistemsko uporabo, - zdravljenje, akutna bakterijska kože in strukturo kožo okužb (absssi) pri odraslih.

Skyrizi Evropska unija - slovenščina - EMA (European Medicines Agency)

skyrizi

abbvie deutschland gmbh & co. kg - risankizumab - psoriasis; arthritis, psoriatic - imunosupresivi - plaque psoriasisskyrizi is indicated for the treatment of moderate to severe plaque psoriasis in adults who are candidates for systemic therapy. psoriatic arthritisskyrizi, alone or in combination with methotrexate (mtx), is indicated for the treatment of active psoriatic arthritis in adults who have had an inadequate response or who have been intolerant to one or more disease-modifying antirheumatic drugs (dmards). crohn's diseaseskyrizi is indicated for the treatment of adult patients with moderately to severely active crohn's disease who have had an inadequate response to, lost response to, or were intolerant to conventional therapy or a biologic therapy.