Danska - danščina - Lægemiddelstyrelsen (Danish Medicines Agency)

orion corporation - quetiapin fumarat - depottabletter - 150 mg

Danska - danščina - Lægemiddelstyrelsen (Danish Medicines Agency)

orion corporation - quetiapin fumarat - depottabletter - 200 mg

Danska - danščina - Lægemiddelstyrelsen (Danish Medicines Agency)

orion corporation - quetiapin fumarat - depottabletter - 300 mg

Danska - danščina - Lægemiddelstyrelsen (Danish Medicines Agency)

orion corporation - quetiapin fumarat - depottabletter - 400 mg

Evropska unija - danščina - EMA (European Medicines Agency)

eli lilly nederland b.v. - abemaciclib - bryst neoplasmer - antineoplastiske midler - early breast cancerverzenios in combination with endocrine therapy is indicated for the adjuvant treatment of adult patients with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative, node positive early breast cancer at high risk of recurrence (see section 5. in pre or perimenopausal women, aromatase inhibitor endocrine therapy should be combined with a luteinising hormone-releasing hormone (lhrh) agonist. advanced or metastatic breast cancerverzenios is indicated for the treatment of women with hormone receptor (hr) positive, human epidermal growth factor receptor 2 (her2) negative locally advanced or metastatic breast cancer in combination with an aromatase inhibitor or fulvestrant as initial endocrine-based therapy, or in women who have received prior endocrine therapy. in pre- or perimenopausal women, the endocrine therapy should be combined with a lhrh agonist.

Evropska unija - danščina - EMA (European Medicines Agency)

bayer ag - larotrectinib sulfat - abdominal neoplasmer - antineoplastiske midler - vitrakvi som monoterapi er indiceret til behandling af voksne og pædiatriske patienter med solide tumorer, hvor der vises en neurotrophic receptor tyrosin kinase (ntrk) gen fusion,der har en sygdom, der er lokalt avanceret, metastatisk eller hvor kirurgisk resektion er sandsynligvis resultere i alvorlig sygelighed, andwho har ingen tilfredsstillende behandling valg.

Evropska unija - danščina - EMA (European Medicines Agency)

ab science - masitinib - bukspyttkjertel-neoplasmer - protein kinase hæmmere - behandling af ikke resectable lokalt fremskreden eller metastatisk kræft i bugspytkirtlen.

Evropska unija - danščina - EMA (European Medicines Agency)

masitinib - gastrointestinale stromale tumorer - protein kinase hæmmere - behandling af inoperabel og/eller metastatisk maligne gastrointestinale stromale tumor (gist).

Evropska unija - danščina - EMA (European Medicines Agency)

gilead sciences ireland uc, galapagos nv - filgotinib maleate - arthritis, reumatoid - immunosuppressiva - rheumatoid arthritisjyseleca 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). jyseleca may be used as monotherapy or in combination with methotrexate (mtx). ulcerative colitisjyseleca is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic agent.

Evropska unija - danščina - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - cytomegalovirusinfektioner - antivirale midler til systemisk anvendelse - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). det bør overvejes at officielle vejledning om hensigtsmæssig brug af antivirale agenter.