Carmustine medac (previously Carmustine Obvius) यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

carmustine medac (previously carmustine obvius)

medac gesellschaft für klinische spezialpräparate mbh - la carmustina - hodgkin disease; lymphoma, non-hodgkin - agentes antineoplásicos - carmustine is indicated n adults in the following malignant neoplasms as a single agent or in combination with other antineoplastic agents and/or other therapeutic measures (radiotherapy, surgery): , brain tumours (glioblastoma, brain-stem gliomas, medulloblastoma, astrocytoma and ependymoma), brain metastases, secondary therapy in non-hodgkin’s lymphoma and hodgkin’s disease, as conditioning treatment prior to autologous haematopoietic progenitor cell transplantation (hpct) in malignant haematological diseases (hodgkin’s disease / non-hodgkin’s lymphoma).

Blenrep यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

blenrep

glaxosmithkline (ireland) limited - belantamab mafodotin - mieloma múltiple - agentes antineoplásicos - blenrep is indicated as monotherapy for the treatment of multiple myeloma in adult patients, who have received at least four prior therapies and whose disease is refractory to at least one proteasome inhibitor, one immunomodulatory agent, and an anti-cd38 monoclonal antibody, and who have demonstrated disease progression on the last therapy.

Dovprela (previously Pretomanid FGK) यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

dovprela (previously pretomanid fgk)

mylan ire healthcare limited - pretomanid - tuberculosis, resistente a múltiples fármacos - antimicobacterianos - dovprela is indicated in combination with bedaquiline and linezolid, in adults, for the treatment of pulmonary extensively drug resistant (xdr), or treatment-intolerant or nonresponsive multidrug-resistant (mdr) tuberculosis (tb). se debe dar consideración a las directrices oficiales sobre el uso adecuado de agentes antibacterianos.

Adakveo यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anemia, falciforme - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Cibinqo यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

cibinqo

pfizer europe ma eeig  - abrocitinib - dermatitis, atópica - otras preparaciones dermatológicas - cibinqo is indicated for the treatment of moderate-to-severe atopic dermatitis in adults who are candidates for systemic therapy.

Talvey यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

talvey

janssen-cilag international n.v. - talquetamab - mieloma múltiple - agentes antineoplásicos - talvey is indicated as monotherapy for the treatment of adult patients with relapsed and refractory multiple myeloma, who have received at least 3 prior therapies, including an immunomodulatory agent, a proteasome inhibitor, and an anti cd38 antibody and have demonstrated disease progression on the last therapy.

Bortezomib Accord यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

bortezomib accord

accord healthcare s.l.u. - bortezomib - mieloma múltiple - agentes antineoplásicos - el bortezomib acuerdo como monoterapia o en combinación con doxorubicina liposomal pegilada o dexametasona está indicado para el tratamiento de pacientes adultos con progresiva mieloma múltiple que han recibido al menos 1 antes de la terapia y que ya han sufrido o no son adecuados para el trasplante de células madre hematopoyéticas. el bortezomib acuerdo en combinación con melfalán y prednisona está indicado para el tratamiento de pacientes adultos no tratados previamente con mieloma múltiple que no son elegibles para la quimioterapia de dosis alta con trasplante de células madre hematopoyéticas. el bortezomib acuerdo en combinación con dexametasona, o con dexametasona y la talidomida, está indicado para el tratamiento de inducción de pacientes adultos no tratados previamente con mieloma múltiple que son elegibles para recibir altas dosis de quimioterapia con trasplante de células madre hematopoyéticas. el bortezomib acuerdo en combinación con rituximab, ciclofosfamida, doxorrubicina y prednisona está indicado para el tratamiento de pacientes adultos no tratados previamente con linfoma de células del manto que no son aptas para el trasplante de células madre hematopoyéticas.

Ninlaro यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

ninlaro

takeda pharma a/s - citrato de ixazomib - mieloma múltiple - agentes antineoplásicos - ninlaro en combinación con lenalidomida y dexametasona está indicado para el tratamiento de pacientes adultos con mieloma múltiple que han recibido al menos una terapia previa.

Wakix यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

wakix

bioprojet pharma - pitolisant - narcolepsia - otras drogas del sistema nervioso - wakix is indicated in adults, adolescents and children from the age of 6 years for the treatment of narcolepsy with or without cataplexy (see also section 5.

Sitagliptin / Metformin hydrochloride Mylan यूरोपीय संघ - स्पेनी - EMA (European Medicines Agency)

sitagliptin / metformin hydrochloride mylan

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabetes mellitus, tipo 2 - drogas usadas en diabetes - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride mylan is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride mylan is indicated in combination with a sulphonylurea (i. , terapia de combinación triple) como complemento a la dieta y ejercicio en pacientes inadecuadamente controlados en su máxima dosis tolerada de metformina y una sulfonilurea. sitagliptin/metformin hydrochloride mylan is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparg) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparg agonist. sitagliptin/metformin hydrochloride mylan is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.