Lyxumia Uni Eropa - Latvi - EMA (European Medicines Agency)

lyxumia

sanofi winthrop industrie - lixisenatide - cukura diabēts, 2. tips - drugs used in diabetes, glucagon-like peptide-1 (glp-1) analogues - lyxumia is indicated for the treatment of adults with type 2 diabetes mellitus to achieve glycaemic control in combination with oral glucose lowering medicinal products and/or basal insulin when these, together with diet and exercise, do not provide adequate glycaemic control.

Xultophy Uni Eropa - Latvi - EMA (European Medicines Agency)

xultophy

novo nordisk a/s - insulīna degludec, liraglutide - cukura diabēts, 2. tips - cukura diabēts - xultophy tiek norādīts ārstēšanai pieaugušajiem ar 2. tipa cukura diabētu, lai uzlabotu glycaemic kontrole apvienojumā ar mutisku glikozes pazemina medikamentu, kad šie atsevišķi vai kombinācijā ar glp-1 receptoru agonists vai bazālo insulīna nesniedz atbilstošu glycaemic kontroles.

Tysabri Uni Eropa - Latvi - EMA (European Medicines Agency)

tysabri

biogen netherlands b.v. - natalizumab - multiplā skleroze - selective immunosuppressants - tysabri is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis for the following patient groups: , patients with highly active disease activity despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 un 5. 1), , or, patients with rapidly evolving severe relapsing remitting multiple sclerosis defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain mri or a significant increase in t2 lesion load as compared to a previous recent mri.

Libtayo Uni Eropa - Latvi - EMA (European Medicines Agency)

libtayo

regeneron ireland designated activity company (dac) - cemiplimab - karcinoma, švamšā šūna - antineoplastiski līdzekļi - cutaneous squamous cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with metastatic or locally advanced cutaneous squamous cell carcinoma (mcscc or lacscc) who are not candidates for curative surgery or curative radiation. basal cell carcinomalibtayo as monotherapy is indicated for the treatment of adult patients with locally advanced or metastatic basal cell carcinoma (labcc or mbcc) who have progressed on or are intolerant to a hedgehog pathway inhibitor (hhi). non-small cell lung cancerlibtayo as monotherapy is indicated for the first-line treatment of adult patients with non-small cell lung cancer (nsclc) expressing pd-l1 (in ≥ 50% tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. libtayo in combination with platinum‐based chemotherapy is indicated for the first‐line treatment of adult patients with nsclc expressing pd-l1 (in ≥ 1% of tumour cells), with no egfr, alk or ros1 aberrations, who have:locally advanced nsclc who are not candidates for definitive chemoradiation, ormetastatic nsclc. cervical cancerlibtayo as monotherapy is indicated for the treatment of adult patients with recurrent or metastatic cervical cancer and disease progression on or after platinum-based chemotherapy.

Tyruko Uni Eropa - Latvi - EMA (European Medicines Agency)

tyruko

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - imūnsupresanti - tyruko is indicated as single disease modifying therapy in adults with highly active relapsing remitting multiple sclerosis (rrms) for the following patient groups: patients with highly active disease despite a full and adequate course of treatment with at least one disease modifying therapy (dmt) (for exceptions and information about washout periods see sections 4. 4 un 5. 1), or, patients with rapidly evolving severe rrms defined by 2 or more disabling relapses in one year, and with 1 or more gadolinium enhancing lesions on brain magnetic resonance imaging (mri) or a significant increase in t2 lesion load as compared to a previous recent mri.

Dasatinib Norameda 20 mg apvalkotās tabletes Latvia - Latvi - Zāļu valsts aģentūra

dasatinib norameda 20 mg apvalkotās tabletes

norameda uab, lithuania - dasatinibs - apvalkotā tablete - 20 mg

Dasatinib Norameda 50 mg apvalkotās tabletes Latvia - Latvi - Zāļu valsts aģentūra

dasatinib norameda 50 mg apvalkotās tabletes

norameda uab, lithuania - dasatinibs - apvalkotā tablete - 50 mg

Dasatinib Norameda 70 mg apvalkotās tabletes Latvia - Latvi - Zāļu valsts aģentūra

dasatinib norameda 70 mg apvalkotās tabletes

norameda uab, lithuania - dasatinibs - apvalkotā tablete - 70 mg

Quetiapine Accord 150 mg ilgstošās darbības tabletes Latvia - Latvi - Zāļu valsts aģentūra

quetiapine accord 150 mg ilgstošās darbības tabletes

accord healthcare b.v., netherlands - kvetiapīns - ilgstošās darbības tablete - 150 mg

Zenadea 2 mg/0,03 mg apvalkotās tabletes Latvia - Latvi - Zāļu valsts aģentūra

zenadea 2 mg/0,03 mg apvalkotās tabletes

zentiva, k.s., czech republic - dienogestum, ethinylestradiolum - apvalkotā tablete - 2 mg/0,03 mg