Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka) Europese Unie - Fins - EMA (European Medicines Agency)

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

krka, d.d., novo mesto  - lenalidomide hydrochloride monohydrate - multiple myeloma; lymphoma, follicular - immunosuppressantit - multiple myelomalenalidomide krka d. novo mesto 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 d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto 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 d. novo mesto 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 d. novo mesto as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. lenalidomide krka d. novo mesto in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide krka d. novo mesto in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Europese Unie - Fins - 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 - immunosuppressantit - 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) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. 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 ja 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) on tarkoitettu aikuisille potilaille, joilla on aiemmin hoitamaton multippeli myelooma, jotka eivät ole oikeutettuja siirto. 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 ja 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).

Omnipaque 240 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 240 mg i/ml injektioneste, liuos

ge healthcare as - iohexol - injektioneste, liuos - 240 mg i/ml - joheksoli

Omnipaque 300 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 300 mg i/ml injektioneste, liuos

ge healthcare as - iohexol - injektioneste, liuos - 300 mg i/ml - joheksoli

Omnipaque 350 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 350 mg i/ml injektioneste, liuos

ge healthcare as - iohexol - injektioneste, liuos - 350 mg i/ml - joheksoli

Omnipaque 180 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 180 mg i/ml injektioneste, liuos

ge healthcare as - iohexol - injektioneste, liuos - 180 mg i/ml - joheksoli

Omnipaque 140 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 140 mg i/ml injektioneste, liuos

ge healthcare as - iohexol - injektioneste, liuos - 140 mg i/ml - joheksoli

OMNIPAQUE 200 mg I/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

omnipaque 200 mg i/ml injektioneste, liuos

amersham health as - iohexolum - injektioneste, liuos - 200 mg i/ml - joheksoli

Dentocaine 40 mg/ml / 0,005 mg/ml injektioneste, liuos Finland - Fins - Fimea (Suomen lääkevirasto)

dentocaine 40 mg/ml / 0,005 mg/ml injektioneste, liuos

inibsa dental s.l.u - articaine hydrochloride, adrenaline tartrate - injektioneste, liuos - 40 mg/ml / 0,005 mg/ml - artikaiini

Lenalidomide Mylan Europese Unie - Fins - EMA (European Medicines Agency)

lenalidomide mylan

mylan ireland limited - lenalidomidi - multiple myeloma - immunosuppressantit - multiple myelomalenalidomide mylan as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide mylan as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone is indicated for the treatment of adult patients with previously untreated multiple myeloma who are not eligible for transplant. lenalidomide mylan in combination with dexamethasone is indicated for the treatment of multiple myeloma in adult patients who have received at least one prior therapy. follicular lymphomalenalidomide mylan in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1-3a).