Dexafast 2 mg/ml România - română - ICBMV (Institutul pentru Controlul Produselor Biologice si Medicamentelor de Uz Veterinar)

dexafast 2 mg/ml

livisto int'l s.l., spania - dexametazonă - soluţie injectabilă - alte medicamente - bovine, cabaline, câini, pisici, porcine - cabaline, bovine, porcine, câini, pisici - tratamentul afecțiunilor inflamatorii sau alergice. bovine - inducerea parturiției. tratamentul cetozei primare. cabaline - tratamentul artritei, bursitei sau tenosinovitei.

Corticen 2 mg/ml România - română - ICBMV (Institutul pentru Controlul Produselor Biologice si Medicamentelor de Uz Veterinar)

corticen 2 mg/ml

univete, s.a., portugalia - dexametazona sodiu fosfat - soluţie injectabilă - hormonale - bovine, cabaline, câini, pisici, porcine - cai, bovine, porci, câini și pisici - tratamentul proceselor inflamatorii sau alergice. bovine - inducerea parturiției. tratamentul cetozei primare. cai - tratamentul artritelor, bursitelor sau sinovitelor.

Lenalidomide Krka d.d. Novo mesto (previously Lenalidomide Krka) Uniunea Europeană - română - 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 - imunosupresoare - 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) este indicat pentru tratamentul pacienților adulți cu mielom multiplu netratați anterior, care nu sunt eligibili pentru transplant. 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) este indicat pentru tratamentul pacienților adulți cu mielom multiplu netratați anterior, care nu sunt eligibili pentru transplant. 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) Uniunea Europeană - română - 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 - imunosupresoare - 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) este indicat pentru tratamentul pacienților adulți cu mielom multiplu netratați anterior, care nu sunt eligibili pentru transplant. 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 și 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) este indicat pentru tratamentul pacienților adulți cu mielom multiplu netratați anterior, care nu sunt eligibili pentru transplant. 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 și 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).

Darzalex Uniunea Europeană - română - EMA (European Medicines Agency)

darzalex

janssen-cilag international n.v. - daratumumab - mielom multiplu - monoclonal antibodies and antibody drug conjugates, antineoplastic agents - multiple myelomadarzalex is indicated: in combination with lenalidomide and dexamethasone or with bortezomib, melphalan and prednisone for the treatment of adult patients with newly diagnosed multiple myeloma who are ineligible for autologous stem cell transplant. în asociere cu bortezomib, talidomida și dexametazona, pentru tratamentul pacienților adulți diagnosticați recent cu mielom multiplu care sunt eligibili pentru transplant autolog de celule stem. în asociere cu lenalidomidă și dexametazonă, sau bortezomib și dexametazonă, pentru tratamentul pacienților adulți cu mielom multiplu care au primit cel puțin un tratament anterior. in combination with pomalidomide and dexamethasone for the treatment of adult patients with multiple myeloma who have received one prior therapy containing a proteasome inhibitor and lenalidomide and were lenalidomide refractory, or who have received at least two prior therapies that included lenalidomide and a proteasome inhibitor and have demonstrated disease progression on or after the last therapy (see section 5. ca monoterapie pentru tratamentul pacienților adulți cu recidivat și refractar mielom multiplu, înainte de a căror terapie a inclus un inhibitor proteazomal și un agent imunomodulator și care au demonstrat progresia bolii în ultima terapie. al amyloidosisdarzalex is indicated in combination with cyclophosphamide, bortezomib and dexamethasone for the treatment of adult patients with newly diagnosed systemic light chain (al) amyloidosis.

Kyprolis Uniunea Europeană - română - EMA (European Medicines Agency)

kyprolis

amgen europe b.v. - carfilzomib - mielom multiplu - agenți antineoplazici - kyprolis in combination with daratumumab and dexamethasone, with lenalidomide and dexamethasone, or with dexamethasone alone is indicated for the treatment of adult patients with multiple myeloma who have received at least one prior therapy.

DEXAMETAZONA KRKA 4 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dexametazona krka 4 mg

krka, d.d., novo mesto - slovenia - dexamethasonum - compr. - 4mg - corticosteroizi sistemici glucocorticoizi

DEXAMETAZONA KRKA 8 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dexametazona krka 8 mg

krka, d.d., novo mesto - slovenia - dexamethasonum - compr. - 8mg - corticosteroizi sistemici glucocorticoizi

DEXAMETAZONA KRKA 20 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dexametazona krka 20 mg

krka, d.d., novo mesto - slovenia - dexamethasonum - compr. - 20mg - corticosteroizi sistemici glucocorticoizi

DEXAMETAZONA KRKA 40 mg România - română - ANMDM (Agentia Nationala a Medicamentului si a Dispozitivelor Medicale)

dexametazona krka 40 mg

krka, d.d., novo mesto - slovenia - dexamethasonum - compr. - 40mg - corticosteroizi sistemici glucocorticoizi