Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

astrazeneca ag - metformini hydrochloridum, dapagliflozinum - comprimés pelliculés - metformini hydrochloridum 500 mg, dapagliflozinum 5 mg ut dapagliflozinum propandiolum monohydricum, carmellosum natricum corresp. natrium 4.77 mg, hypromellosum, cellulosum microcristallinum, silica colloidalis hydrica, magnesii stearas, lactosum 48.00 mg, crospovidonum, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 110 0.69 mg, e 171, pro compresso obducto. - antidiabétique oral utilisé - synthetika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

astrazeneca ag - metformini hydrochloridum, dapagliflozinum - comprimés pelliculés - metformini hydrochloridum 500 mg, dapagliflozinum 10 mg ut dapagliflozinum propandiolum monohydricum, carmellosum natricum corresp. natrium 4.77 mg, hypromellosum, cellulosum microcristallinum, silica colloidalis hydrica, magnesii stearas, lactosum 48.00 mg, crospovidonum, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (rubrum), pro compresso obducto. - antidiabétique oral utilisé - synthetika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

astrazeneca ag - metformini hydrochloridum, dapagliflozinum - comprimés pelliculés - metformini hydrochloridum 1000 mg, dapagliflozinum 5 mg ut dapagliflozinum propandiolum monohydricum, carmellosum natricum corresp. natrium 4.75 mg, hypromellosum, cellulosum microcristallinum, silica colloidalis hydrica, magnesii stearas, lactosum 48.00 mg, crospovidonum, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (rubrum), pro compresso obducto. - antidiabétique oral utilisé - synthetika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

astrazeneca ag - metformini hydrochloridum, dapagliflozinum - comprimés pelliculés - metformini hydrochloridum 1000 mg, dapagliflozinum 10 mg ut dapagliflozinum propandiolum monohydricum, carmellosum natricum corresp. natrium 4.75 mg, hypromellosum, silica colloidalis hydrica, magnesii stearas, cellulosum microcristallinum, lactosum 48.00 mg, crospovidonum, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, e 171, e 172 (flavum), pro compresso obducto. - antidiabétique oral utilisé - synthetika

Suisse - français - Swissmedic (Swiss Agency for Therapeutic Products)

astrazeneca ag - dapagliflozinum, saxagliptinum - comprimés pelliculés - dapagliflozinum 10 mg ut dapagliflozinum propandiolum monohydricum, saxagliptinum 5 mg ut saxagliptini hydrochloridum, cellulosum microcristallinum, lactosum 40 mg, carmellosum natricum conexum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), macrogolum 3350, talcum, acidum hydrochloridum, natrii hydroxidum, e 171, e 172 (flavum), e 172 (rubrum), drucktinte: e 132, lacca, pro compresso obducto corresp. natrium max. 0.91 mg. - antidiabetikum - synthetika

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)

astrazeneca ab - la metformine chlorhydrate, la saxagliptine, dapagliflozin - diabète sucré, type 2 - les médicaments utilisés dans le diabète - qtrilmet est indiqué chez les adultes âgés de 18 ans et plus, atteints de diabète de type 2:améliorer le contrôle glycémique lorsque la metformine avec ou sans sulphonylurea (su) et la saxagliptine ou dapagliflozin ne donnent pas suffisamment de contrôle glycémique. quand déjà traités avec de la metformine et de la saxagliptine et de dapagliflozin.

Union européenne - français - EMA (European Medicines Agency)

mylan ireland limited - sitagliptin hydrochloride monohydrate, metformin hydrochloride - diabète sucré, type 2 - les médicaments utilisés dans le diabète - 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. 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 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.

Union européenne - français - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - diabète sucré, type 2 - les médicaments utilisés dans le diabète - 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 et 5. 1 pour les données disponibles sur différentes combinaisons).

Union européenne - français - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabète sucré, type 2 - les médicaments utilisés dans le diabète - for adult patients with type 2 diabetes mellitus:it 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. it 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. it 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. it 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.