Eiropas Savienība - zviedru - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - dalbavancin hydrochloride - soft tissue infections; skin diseases, bacterial - antibakteriella medel för systemiskt bruk, - behandling av akuta bakteriella hud- och mjukdelsinfektioner (absssi) hos vuxna.

Eiropas Savienība - zviedru - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - upadacitinib - artrit, reumatoid - immunsuppressiva - 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.

Eiropas Savienība - zviedru - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastiska medel - tepkinly 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.

Zviedrija - zviedru - Läkemedelsverket (Medical Products Agency)

dr. august wolff gmbh & co arzneimittel - glykopyrroniumbromid - kräm - 2,2 mg/pumpning - glykopyrroniumbromid 2,7 mg aktiv substans; propylenglykol hjälpämne; cetostearylalkohol hjälpämne; bensylalkohol hjälpämne

Eiropas Savienība - zviedru - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - ombitasvir, paritaprevir, ritonavir - hepatit c, kronisk - antivirala medel för systemisk användning - viekirax indikeras i kombination med andra läkemedel för behandling av kronisk hepatit c (chc) hos vuxna. för hepatit c-virus (hcv) genotyp specifik aktivitet.

Eiropas Savienība - zviedru - EMA (European Medicines Agency)

abbvie deutschland gmbh co. kg - adalimumab - spondylitis, ankylosing; arthritis, juvenile rheumatoid; uveitis; colitis, ulcerative; psoriasis; arthritis, psoriatic; crohn disease; arthritis, rheumatoid - immunsuppressiva - se produktinformationsdokumentet.

Zviedrija - zviedru - Läkemedelsverket (Medical Products Agency)

medice arzneimittel pütter gmbh & co. kg - dexamfetaminsulfat - tablett - 20 mg - isomalt hjälpämne; dexamfetaminsulfat 20 mg aktiv substans

Zviedrija - zviedru - Läkemedelsverket (Medical Products Agency)

medice arzneimittel pütter gmbh & co. kg - dexamfetaminsulfat - tablett - 10 mg - isomalt hjälpämne; dexamfetaminsulfat 10 mg aktiv substans

Zviedrija - zviedru - Läkemedelsverket (Medical Products Agency)

denk pharma gmbh & co kg - amlodipinbesilat; valsartan - filmdragerad tablett - 5 mg/160 mg - amlodipinbesilat 6,95 mg aktiv substans; valsartan 160 mg aktiv substans

Zviedrija - zviedru - Läkemedelsverket (Medical Products Agency)

denk pharma gmbh & co kg - amlodipinbesilat; valsartan - filmdragerad tablett - 5 mg/80 mg - amlodipinbesilat 6,95 mg aktiv substans; valsartan 80 mg aktiv substans