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

lenalidomide grindeks 5 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 6,032 mg - eq. lenalidomide 5 mg - capsule, hard - 5 mg - lenalidomide ammoniumchloride 6.032 mg - lenalidomide

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

lenalidomide grindeks 7.5 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 9,048 mg - eq. lenalidomide 7,5 mg - capsule, hard - 7,5 mg - lenalidomide ammoniumchloride 9.048 mg - lenalidomide

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

lenalidomide grindeks 10 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 12,064 mg - eq. lenalidomide 10 mg - capsule, hard - 10 mg - lenalidomide ammoniumchloride 12.064 mg - lenalidomide

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

lenalidomide grindeks 15 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 18,096 mg - eq. lenalidomide 15 mg - capsule, hard - 15 mg - lenalidomide ammoniumchloride 18.096 mg - lenalidomide

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

lenalidomide grindeks 20 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 24,128 mg - eq. lenalidomide 20 mg - capsule, hard - 20 mg - lenalidomide ammoniumchloride 24.128 mg - lenalidomide

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

lenalidomide grindeks 25 mg harde caps.

joint stock company grindeks - lenalidomide ammoniumchloride 30,16 mg - eq. lenalidomide 25 mg - capsule, hard - 25 mg - lenalidomide ammoniumchloride 30.16 mg - lenalidomide

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

lenalidomide krka d.d.

krka, d.d., novo mesto  - lenalidomide hydrochloride hydrate - multiple myeloma; lymphoma, follicular; myelodysplastic syndromes - immunosuppressiva - multiple myelomalenalidomide krka d. 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. 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 d. 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 d. 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. follicular lymphomalenalidomide krka d. 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).