Actrapid Európska únia - dánčina - EMA (European Medicines Agency)

actrapid

novo nordisk a/s - humant insulin - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus.

Monotard Európska únia - dánčina - EMA (European Medicines Agency)

monotard

novo nordisk a/s - insulin human - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus.

Ultratard Európska únia - dánčina - EMA (European Medicines Agency)

ultratard

novo nordisk a/s - insulin human - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus.

Velosulin Európska únia - dánčina - EMA (European Medicines Agency)

velosulin

novo nordisk a/s - insulin human - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus.

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Európska únia - dánčina - EMA (European Medicines Agency)

lenalidomide krka (previously lenalidomide krka d.d. novo mesto)

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; myelodysplastic syndromes; lymphoma, follicular; lymphoma, mantle-cell - immunosuppressiva - multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) er indiceret til behandling af voksne patienter med tidligere ubehandlet myelomatose, der ikke er berettiget til transplantation. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 og 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a). multiple myelomalenalidomide krka as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide krka as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) er indiceret til behandling af voksne patienter med tidligere ubehandlet myelomatose, der ikke er berettiget til transplantation. lenalidomide krka in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. myelodysplastic syndromeslenalidomide krka as monotherapy is indicated for the treatment of adult patients with transfusion-dependent anemia due to low- or intermediate-1-risk myelodysplastic syndromes associated with an isolated deletion 5q cytogenetic abnormality when other therapeutic options are insufficient or inadequate. mantle cell lymphomalenalidomide krka as monotherapy is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (see sections 4. 4 og 5. follicular lymphomalenalidomide krka in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Novomate 277,8 mg/ml pulver og solvens til injektionsvæske, suspension Dánsko - dánčina - Lægemiddelstyrelsen (Danish Medicines Agency)

novomate 277,8 mg/ml pulver og solvens til injektionsvæske, suspension

lohmann pharma herstellung gmbh - penethamathydroiodid - pulver og solvens til injektionsvæske, suspension - 277,8 mg/ml - kvæg

Levemir Európska únia - dánčina - EMA (European Medicines Agency)

levemir

novo nordisk a/s - insulin detemir - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus hos voksne, unge og børn i alderen 1 år og derover.

Actraphane Európska únia - dánčina - EMA (European Medicines Agency)

actraphane

novo nordisk a/s - insulin human - diabetes mellitus - narkotika anvendt i diabetes - behandling af diabetes mellitus.