Evropska unija - španščina - EMA (European Medicines Agency)

krka, d.d., novo mesto  - lenalidomide hydrochloride hydrate - multiple myeloma; lymphoma, follicular; myelodysplastic syndromes - inmunosupresores - 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) está indicado para el tratamiento de pacientes adultos no tratados previamente con mieloma múltiple que no son elegibles para el trasplante. 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).

Ekvador - španščina - Agencia Nacional de Regulación, Control y Vigilancia Sanitaria

celltrion, inc. corea, republica de - rituximab 10 mg/ml - concentrado para soluciÓn para perfusiÓn - cada ml contiene: rituximab 10 mg

Španija - španščina - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

reddy pharma iberia s.a. - bendamustina hidrocloruro - polvo para concentrado para soluciÓn para perfusiÓn - 100 mg - bendamustina hidrocloruro 100 mg - bendamustina

Španija - španščina - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

reddy pharma iberia s.a. - bendamustina hidrocloruro - concentrado para soluciÓn para perfusiÓn - 45 mg/ml inyectable 4 ml - bendamustina hidrocloruro 45 mg - bendamustina

Španija - španščina - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

altan pharmaceuticals sa - bendamustina hidrocloruro - concentrado para soluciÓn para perfusiÓn - 45 mg/ml inyectable 4 ml - bendamustina hidrocloruro 45 mg - bendamustina

Evropska unija - španščina - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - inmunosupresores selectivos - la colitis colitisentyvio está indicado para el tratamiento de pacientes adultos con moderada a gravemente activa la colitis ulcerosa que han tenido una respuesta inadecuada, perdió respuesta a, o eran intolerantes a la terapia convencional o un factor de necrosis tumoral alfa (tnfa), antagonista de la. la enfermedad de crohn diseaseentyvio está indicado para el tratamiento de pacientes adultos con moderada a gravemente activa la enfermedad de crohn que han tenido una respuesta inadecuada, perdió respuesta a, o eran intolerantes a la terapia convencional o un factor de necrosis tumoral alfa (tnfa), antagonista de la. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Evropska unija - španščina - EMA (European Medicines Agency)

laboratorios lesvi s.l. - fumarato de dimetilo - la esclerosis múltiple remitente-recurrente - inmunosupresores - dimethyl fumarate neuraxpharma is indicated for the treatment of adult patients with relapsing remitting multiple sclerosis.

Evropska unija - španščina - EMA (European Medicines Agency)

janssen-cilag international nv - ibrutinib - lymphoma, mantle-cell; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, protein kinase inhibitors - imbruvica as a single agent is indicated for the treatment of adult patients with relapsed or refractory mantle cell lymphoma (mcl). imbruvica as a single agent or in combination with rituximab or obinutuzumab or venetoclax is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll) (see section 5. imbruvica as a single agent or in combination with bendamustine and rituximab (br) is indicated for the treatment of adult patients with cll who have received at least one prior therapy. imbruvica as a single agent is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo immunotherapy. imbruvica in combination with rituximab is indicated for the treatment of adult patients with wm.

Evropska unija - španščina - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - avacopan - microscopic polyangiitis; wegener granulomatosis - inmunosupresores - tavneos, in combination with a rituximab or cyclophosphamide regimen, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (gpa) or microscopic polyangiitis (mpa).

Peru - španščina - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

farmindustria s.a. - clorhidrato de memantina; - tableta recubierta - por ; rituximab 100.000000 mcg; - rituximab