Lenalidomide Krka (previously Lenalidomide Krka d.d. Novo mesto) Europese Unie - Nederlands - 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) is geïndiceerd voor de behandeling van volwassen patiënten met eerder behandelde multipel myeloom die niet in aanmerking komen voor transplantatie. 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 en 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) is geïndiceerd voor de behandeling van volwassen patiënten met eerder behandelde multipel myeloom die niet in aanmerking komen voor transplantatie. 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 en 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).

Lenalidomide Accord Europese Unie - Nederlands - EMA (European Medicines Agency)

lenalidomide accord

accord healthcare s.l.u. - lenalidomide - multiple myeloma - immunosuppressiva - multiple myelomalenalidomide accord as monotherapy is indicated for the maintenance treatment of adult patients with newly diagnosed multiple myeloma who have undergone autologous stem cell transplantation. lenalidomide accord as combination therapy with dexamethasone, or bortezomib and dexamethasone, or melphalan and prednisone (see section 4. 2) is geïndiceerd voor de behandeling van volwassen patiënten met eerder behandelde multipel myeloom die niet in aanmerking komen voor transplantatie. lenalidomide akkoord in combinatie met dexamethason is geïndiceerd voor de behandeling van multipel myeloom bij volwassen patiënten die minstens één eerdere therapie. follicular lymphomalenalidomide accord in combination with rituximab (anti-cd20 antibody) is indicated for the treatment of adult patients with previously treated follicular lymphoma (grade 1 – 3a).

Lenalidomide EG 2.5 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 2.5 mg harde caps.

eg sa-nv - lenalidomide 2,5 mg - capsule, hard - 2,5 mg - lenalidomide 2.5 mg - lenalidomide

Lenalidomide EG 5 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 5 mg harde caps.

eg sa-nv - lenalidomide 5 mg - capsule, hard - 5 mg - lenalidomide 5 mg - lenalidomide

Lenalidomide EG 7.5 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 7.5 mg harde caps.

eg sa-nv - lenalidomide 7,5 mg - capsule, hard - 7,5 mg - lenalidomide 7.5 mg - lenalidomide

Lenalidomide EG 10 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 10 mg harde caps.

eg sa-nv - lenalidomide 10 mg - capsule, hard - 10 mg - lenalidomide 10 mg - lenalidomide

Lenalidomide EG 15 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 15 mg harde caps.

eg sa-nv - lenalidomide 15 mg - capsule, hard - 15 mg - lenalidomide 15 mg - lenalidomide

Lenalidomide EG 20 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 20 mg harde caps.

eg sa-nv - lenalidomide 20 mg - capsule, hard - 20 mg - lenalidomide 20 mg - lenalidomide

Lenalidomide EG 25 mg harde caps. België - Nederlands - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

lenalidomide eg 25 mg harde caps.

eg sa-nv - lenalidomide 25 mg - capsule, hard - 25 mg - lenalidomide 25 mg - lenalidomide

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

lenalidomide mylan

mylan ireland limited - lenalidomide - multiple myeloma - immunosuppressiva - 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).