Cuba - español - CECMED (Autoridad Reguladora de Medicamentos, Equipos y Dispositivos Médicos)

laboratorios khandelwal pvt. ltd., plot b-1, maharashtra, india. - clorhidrato de irinotecan - solución concentrada para infusión iv. - 20,0 mg/ml

Unión Europea - español - EMA (European Medicines Agency)

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.

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

regiomedica gmbh - irinotecan hidrocloruro trihidrato - excipientes: sorbitol,hidroxido de sodio (e-524) - otros agentes antineoplÁsicos - otros agentes antineoplásicos - irinotecán

Cuba - español - CECMED (Autoridad Reguladora de Medicamentos, Equipos y Dispositivos Médicos)

naprod life sciences pvt. ltd. planta g-17/1,maharashtra, india. - clorhidrato de irinotecán - solución para infusión iv - 20 mg/ml

Cuba - español - CECMED (Autoridad Reguladora de Medicamentos, Equipos y Dispositivos Médicos)

fresenius kabi oncology limited, baddi 1 y baddi 2,solan, india. - clorhidrato de irinotecán - concentrado para infusión iv - 20 mg/ml

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

almirall, s.a. - irinotecan hidrocloruro trihidrato - excipientes: sorbitol,hidroxido de sodio (e-524) - otros agentes antineoplÁsicos - otros agentes antineoplásicos - irinotecán

España - español - AEMPS (Agencia Española de Medicamentos y Productos Sanitarios)

almirall, s.a. - irinotecan hidrocloruro trihidrato - excipientes: sorbitol,hidroxido de sodio (e-524) - otros agentes antineoplÁsicos - otros agentes antineoplásicos - irinotecán

Unión Europea - español - EMA (European Medicines Agency)

les laboratoires servier - irinotecan anhydrous free-base - neoplasias pancreáticas - agentes antineoplásicos - tratamiento del adenocarcinoma metastásico del páncreas, en combinación con 5 fluorouracilo (5 fu) y leucovorina (lv), en pacientes adultos que han progresado después de la terapia basada en gemcitabina.

Unión Europea - español - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - diabetes mellitus, tipo 2 - drogas usadas en diabetes - vildagliptin/metformin hydrochloride accord is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:- in patients who are inadequately controlled with metformin hydrochloride alone. - in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. - in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 y 5. 1 para datos disponibles sobre diferentes combinaciones).

Unión Europea - español - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - diabetes mellitus, tipo 2 - drogas usadas en diabetes - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun 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 sun 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 sun is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. sitagliptin/metformin hydrochloride sun 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.