Union européenne - norvégien - EMA (European Medicines Agency)

janssen-cilag international n.v. - teclistamab - multippelt myelom - antineoplastiske midler - tecvayli is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least three prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti-cd38 antibody and have demonstrated disease progression on the last therapy.

Union européenne - norvégien - EMA (European Medicines Agency)

abbvie deutschland gmbh & co. kg - epcoritamab - lymphoma, large b-cell, diffuse - antineoplastiske midler - 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.

Norvège - norvégien - Statens legemiddelverk

teva gmbh - fingolimodhydroklorid - kapsel, hard - 0.5 mg

Union européenne - norvégien - EMA (European Medicines Agency)

janssen-cilag international n.v. - talquetamab - multippelt myelom - antineoplastiske midler - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Union européenne - norvégien - EMA (European Medicines Agency)

hra pharma rare diseases - ketoconazole - cushing syndrome - antimykotika for systemisk bruk - ketokonazol hra er indisert for behandling av endogent cushings syndrom hos voksne og ungdom over 12 år.

Union européenne - norvégien - EMA (European Medicines Agency)

biogen netherlands b.v. - natalizumab - multippel sklerose - selektive immunosuppressiva - 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 og 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.

Norvège - norvégien - Statens legemiddelverk

lohmann animal health gmbh & co kg - kyllinganemivirus (cav) stamme cux-1 - lyofilisat til bruk i drikkevann

Norvège - norvégien - Statens legemiddelverk

intervet international b.v. - bovint respiratorisk syncytialvirus, stamme ev 908, inaktivert / bovint parainfluensavirus 3, stamme sf-4 reisinger, helt, inaktivert / mannheimia haemolytica, serotype a1, stamme m4/1, inaktivert - injeksjonsvæske, suspensjon

Norvège - norvégien - Statens legemiddelverk

mundipharma as - oksykodonhydroklorid / naloksonhydrokloriddihydrat - depottablett - 5 mg / 2.5 mg

Norvège - norvégien - Statens legemiddelverk

mundipharma as - oksykodonhydroklorid / naloksonhydrokloriddihydrat - depottablett - 10 mg / 5 mg