Skyrizi Europska Unija - hrvatski - 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.

Rinvoq Europska Unija - hrvatski - EMA (European Medicines Agency)

rinvoq

abbvie deutschland gmbh & co. kg - upadacitinib - artritis, reumatoidni - 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.

Exzolt Europska Unija - hrvatski - EMA (European Medicines Agency)

exzolt

intervet international b.v. - fluralaner - ektoparaciticidi, insekticidi i repelenti - piletina - liječenje infekcije crvenog buba (dermanyssus gallinae) peradi u uzgajivačima, uzgajivačima i slojevitim kokošima.

Febuksostat Stada 120 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

febuksostat stada 120 mg filmom obložene tablete

stada d.o.o., hercegovačka 14, zagreb, hrvatska - febuksostat hemihidrat - filmom obložena tableta - 120 mg - urbroj: jedna filmom obložena tableta sadrži 120 mg febuksostata (u obliku hemihidrata)

Febuksostat Stada 80 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

febuksostat stada 80 mg filmom obložene tablete

stada d.o.o., hercegovačka 14, zagreb, hrvatska - febuksostat hemihidrat - filmom obložena tableta - 80 mg - urbroj: jedna filmom obložena tableta sadrži 80 mg febuksostata (u obliku hemihidrata)

Sorafenib Mylan 200 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

sorafenib mylan 200 mg filmom obložene tablete

mylan ireland limited, unit 35/36 grange parade, baldoyle industrial estate, dublin 13, irska - sorafenibtosilat - filmom obložena tableta - 200 mg - urbroj: jedna filmom obložena tableta sadrži 200 mg sorafeniba (u obliku tosilata)

Segluromet Europska Unija - hrvatski - EMA (European Medicines Agency)

segluromet

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - dijabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.

Abakavir/Lamivudin Mylan Pharma 600 mg/300 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

abakavir/lamivudin mylan pharma 600 mg/300 mg filmom obložene tablete

mylan ireland limited, unit 35/36 grange parade, baldoyle industrial estate, dublin 13, irska - abakavirsulfat lamivudin - filmom obložena tableta - 600 mg + 300 mg - urbroj: jedna filmom obložena tableta sadrži 600 mg abakavira (u obliku abakavirsulfata) i 300 mg lamivudina

Sorafenib Sandoz 200 mg filmom obložene tablete Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

sorafenib sandoz 200 mg filmom obložene tablete

sandoz d.o.o., maksimirska 120, zagreb, hrvatska - sorafenibtosilat - filmom obložena tableta - 200 mg - urbroj: svaka filmom obložena tableta sadrži 200 mg sorafeniba (u obliku tosilata)