Unión Europea - español - EMA (European Medicines Agency)

takeda manufacturing austria ag - proteína c humana - purpura fulminans; protein c deficiency - agentes antitrombóticos - ceprotin is indicated for prophylaxis and treatment of  purpura fulminans  coumarin-induced skin necrosis and venous thrombotic events in patients with severe congenital protein c deficiency.

Unión Europea - español - 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.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - brentuximab vedotin - lymphoma, non-hodgkin; hodgkin disease - agentes antineoplásicos - hodgkin lymphomaadcetris is indicated for adult patients with previously untreated cd30+ stage iv hodgkin lymphoma (hl) in combination with doxorubicin, vinblastine and dacarbazine (avd). adcetris is indicated for the treatment of adult patients with cd30+ hl at increased risk of relapse or progression following autologous stem cell transplant (asct). adcetris is indicated for the treatment of adult patients with relapsed or refractory cd30+ hodgkin lymphoma (hl):following asct, orfollowing at least two prior therapies when asct or multi-agent chemotherapy is not a treatment option. systemic anaplastic large cell lymphomaadcetris in combination with cyclophosphamide, doxorubicin and prednisone (chp) is indicated for adult patients with previously untreated systemic anaplastic large cell lymphoma (salcl). adcetris is indicated for the treatment of adult patients with relapsed or refractory salcl. cutaneous t cell lymphomaadcetris is indicated for the treatment of adult patients with cd30+ cutaneous t cell lymphoma (ctcl) after at least 1 prior systemic therapy.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - alogliptin, la pioglitazona - diabetes mellitus, tipo 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - incresync is indicated as a second- or third-line treatment in adult patients aged 18 years and older with type-2 diabetes mellitus: , as an adjunct to diet and exercise to improve glycaemic control in adult patients (particularly overweight patients) inadequately controlled on pioglitazone alone, and for whom metformin is inappropriate due to contraindications or intolerance;, in combination with metformin (i. terapia de combinación triple) como complemento a la dieta y el ejercicio para mejorar el control glucémico en pacientes adultos (particularmente en pacientes con sobrepeso) que no están adecuadamente controladas en su máxima dosis tolerada de metformina y la pioglitazona. además, incresync puede ser utilizado para reemplazar las tabletas de alogliptin and pioglitazone en los pacientes adultos mayores de 18 años con diabetes mellitus de tipo 2 que ya están siendo tratados con esta combinación. después de la iniciación de la terapia con incresync, los pacientes deben ser revisados después de tres a seis meses para evaluar la suficiencia de la respuesta al tratamiento (e. la reducción en hba1c). en los pacientes que no muestran una respuesta adecuada, incresync debe ser descontinuado. a la luz de los riesgos potenciales con la prolongada pioglitazona terapia, los médicos deben confirmar en posteriores revisiones de rutina que el beneficio de incresync se mantiene (véase la sección 4.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - fentanyl citrate - pain; cancer - analgésicos - instanyl está indicado para el tratamiento del dolor irruptivo en adultos que ya reciben terapia opioide de mantenimiento para el dolor crónico de cáncer. el dolor irruptivo es una exacerbación transitoria del dolor que ocurre en un contexto de dolor persistente controlado de otra manera.  patients receiving maintenance opioid therapy are those who are taking at least 60 mg of oral morphine daily, at least 25 micrograms of transdermal fentanyl per hour, at least 30 mg oxycodone daily, at least 8 mg of oral hydromorphone daily or an equianalgesic dose of another opioid for a week or longer.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - lanadelumab - angioedemas, hereditario - other hematological agents - takhzyro is indicated for routine prevention of recurrent attacks of hereditary angioedema (hae) in patients aged 2 years and older.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - brigatinib - carcinoma, pulmón no microcítico - agentes antineoplásicos - alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. alunbrig is indicated as monotherapy for the treatment of adult patients with anaplastic lymphoma kinase alkpositive advanced nsclc previously treated with crizotinib.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharmaceuticals international ag ireland branch - maribavir - infecciones por citomegalovirus - antivirales para uso sistémico - livtencity is indicated for the treatment of cytomegalovirus (cmv) infection and/or disease that are refractory (with or without resistance) to one or more prior therapies, including ganciclovir, valganciclovir, cidofovir or foscarnet in adult patients who have undergone a haematopoietic stem cell transplant (hsct) or solid organ transplant (sot). se debe dar consideración a las directrices oficiales sobre el uso adecuado de agentes antivirales.

Unión Europea - español - EMA (European Medicines Agency)

takeda pharma a/s - alogliptin benzoato, metformin hidrocloruro - diabetes mellitus, tipo 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - vipdomet is indicated in the treatment of adult patients aged 18 years and older with type-2 diabetes mellitus:as an adjunct to diet and exercise to improve glycaemic control in adult patients, inadequately controlled on their maximal tolerated dose of metformin alone, or those already being treated with the combination of alogliptin and metformin;in combination with pioglitazone (i. triple combination therapy) as an adjunct to diet and exercise in adult patients inadequately controlled on their maximal tolerated dose of metformin and pioglitazone;in combination with insulin (i. terapia de combinación triple) como complemento a la dieta y el ejercicio para mejorar el control glucémico en los pacientes cuando la insulina en una dosis estable y metformina por sí solos no proporcionan un adecuado control de la glucemia.

Perú - español - DIGEMID (Dirección General de Medicamentos, Insumos y Drogas)

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