Norveġja - Norveġiż - Statens legemiddelverk

orifarm as - insulin glargin - injeksjonsvæske, oppløsning - 100 e/ ml

Norveġja - Norveġiż - Statens legemiddelverk

amomed pharma gmbh - treprostinilnatrium - infusjonsvæske, oppløsning - 10 mg/ ml

Norveġja - Norveġiż - Statens legemiddelverk

amomed pharma gmbh - treprostinilnatrium - infusjonsvæske, oppløsning - 1 mg/ ml

Norveġja - Norveġiż - Statens legemiddelverk

amomed pharma gmbh - treprostinilnatrium - infusjonsvæske, oppløsning - 2.5 mg/ ml

Norveġja - Norveġiż - Statens legemiddelverk

amomed pharma gmbh - treprostinilnatrium - infusjonsvæske, oppløsning - 5 mg/ ml

Unjoni Ewropea - Norveġiż - EMA (European Medicines Agency)

sandoz gmbh - natalizumab - multiple sclerosis, relapsing-remitting; multiple sclerosis - immunsuppressive - 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 og 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.

Unjoni Ewropea - Norveġiż - EMA (European Medicines Agency)

janssen-cilag international n.v.    - rilpivirinhydroklorid - hiv-infeksjoner - antivirale midler til systemisk bruk - edurant, er i kombinasjon med andre antiretrovirale legemidler, indisert for behandling av humant immunsviktvirus type 1 (hiv‑1)-infeksjon i antiretroviral treatment‑naïve pasienter 12 år og eldre med en viral belastning ≤ 100.000 hiv‑1 rna kopier/ml. som med andre antiretroviral legemidler, genotypic motstand testing som bør styre bruken av edurant.

Unjoni Ewropea - Norveġiż - EMA (European Medicines Agency)

novo nordisk a/s - insulin aspart - sukkersyke - drugs used in diabetes, insulins and analogues for injection, fast-acting - behandling av diabetes mellitus hos voksne, ungdom og barn i alderen 1 år og over.

Unjoni Ewropea - Norveġiż - EMA (European Medicines Agency)

janssen-cilag international nv - ibrutinib - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.

Unjoni Ewropea - Norveġiż - EMA (European Medicines Agency)

janssen-cilag international nv - etravirine - hiv-infeksjoner - non-nucleoside reverse transcriptase inhibitors, antivirals for systemic use - intelence, sammen med en økt protease hemmer og andre antiretrovirale legemidler, er indisert for behandling av menneske-immunsvikt-virus-type-1 (hiv-1) infeksjon hos antiretroviral behandling-erfarne voksne pasienter og i antiretroviral behandling-erfarne pediatriske pasienter fra seks år gammel. denne indikatoren er basert på uke-48 analyser fra to fase-iii studier i svært pretreated pasienter hvor intelence ble undersøkt i kombinasjon med en optimalisert bakgrunn regime (obr) som inkluderte darunavir/ritonavir. indikasjon i paediatric pasienter er basert på 48-uke analyser av én arm, fase ii studie i antiretroviral behandling-erfarne paediatric pasienter.