Belgique - français - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

monrol europe s.r.l. - pertechnétate sodique de technetium (tc 99m) 8,3 gbq - 33,9 gbq; molybdate sodique (mo-99) 10 gbq - 40 gbq - générateur radiopharmaceutique - 10-40 gbq - molybdate sodique (mo-99); pertechnétate sodique de technetium (tc 99m) - technetium (99mtc) pertechnetate

Belgique - français - AFMPS (Agence Fédérale des Médicaments et des Produits de Santé)

monrol europe s.r.l. - chlorure de lutétium (lu-177) 40 gbq/ml - solution de précurseur radiopharmaceutique - other therapeutic radiopharmaceuticals

Union européenne - français - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - diabète sucré, type 2 - les médicaments utilisés dans le diabète - 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. triple thérapie de combinaison) en complément d'un régime alimentaire et l'exercice chez les patients insuffisamment contrôlés sur leur dose maximale tolérée de metformine et une sulphonylurea. 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.

Union européenne - français - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - diabète sucré, type 2 - les médicaments utilisés dans le diabète - for adult patients with type 2 diabetes mellitus, sitagliptin sun is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. a thiazolidinedione) when use of a pparγ agonist is appropriate and when diet and exercise plus the pparγ agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a pparγ agonist and metformin when use of a pparγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin sun is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Union européenne - français - EMA (European Medicines Agency)

glaxosmithkline dungarvan limited - esoméprazole - reflux gastro-oesophagien - inhibiteurs de pompe à protons - nexium control est indiqué pour le traitement à court terme des symptômes de reflux (e. brûlures d'estomac et régurgitation acide) chez les adultes.

Union européenne - français - EMA (European Medicines Agency)

takeda gmbh - pantoprazole - reflux gastro-oesophagien - inhibiteurs de pompe à protons - traitement à court terme des symptômes de reflux (e. brûlures d'estomac, régurgitation acide) chez les adultes.

Union européenne - français - EMA (European Medicines Agency)

takeda gmbh - pantoprazole - reflux gastro-oesophagien - inhibiteurs de pompe à protons - traitement à court terme des symptômes de reflux (e. brûlures d'estomac, régurgitation acide) chez les adultes.