Europeiska unionen - svenska - EMA (European Medicines Agency)

laboratorios hipra, s.a. - mycoplasma hyopneumoniae, strain 7304 (nexhyon), expressing the capsid protein of porcine circovirus type 2a, inactivated - immunologicals for suidae, inactivated viral and inactivated bacterial vaccines - grisar - for the active immunisation of pigs:to reduce lung lesions associated with porcine enzootic pneumonia caused by mycoplasma hyopneumoniae. also, to reduce the incidence of these lesions (as observed in field studies). to reduce viraemia, virus load in lungs and lymphoid tissues and the duration of the viraemic period associated with diseases caused by porcine circovirus type 2 (pcv2). efficacy against pcv2 genotypes a, b and d has been demonstrated in field studies. to reduce culling rate and the loss of daily weight gain caused by mycoplasma hyopneumoniae and/or pcv2 related diseases (as observed at 6 months of age in field studies). mycoplasma hyopneumoniae: onset of immunity: 3 weeks after vaccinationduration of immunity: 23 weeks after vaccinationporcine circovirus type 2:onset of immunity: 2 weeks after vaccinationduration of immunity: 22 weeks after vaccinationin addition, a reduction in nasal and faecal shedding and the duration of nasal excretion of pcv2 was demonstrated in animals challenged at 4 weeks and at 22 weeks after vaccination.

Europeiska unionen - svenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, vildagliptin - diabetes mellitus, typ 2 - läkemedel som används vid 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 och 5. 1 för tillgänglig data på olika kombinationer).

Europeiska unionen - svenska - EMA (European Medicines Agency)

accord healthcare s.l.u. - metformin hydrochloride, sitagliptin hydrochloride monohydrate - diabetes mellitus, typ 2 - läkemedel som används vid diabetes - 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. - , trippel kombinationsterapi) som ett komplement till kost och motion hos patienter bristfälligt kontrollerad på deras maximal tolererad dos av metformin och en 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.

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandoz a/s - kandesartancilexetil - tablett - 16 mg - kandesartancilexetil 16 mg aktiv substans; laktosmonohydrat hjälpämne - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

actavis group ptc ehf. - kandesartancilexetil - tablett - 16 mg - kandesartancilexetil 16 mg aktiv substans; laktosmonohydrat hjälpämne - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandoz a/s - kandesartancilexetil - tablett - 32 mg - kandesartancilexetil 32 mg aktiv substans; laktosmonohydrat hjälpämne - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

actavis group ptc ehf. - kandesartancilexetil - tablett - 32 mg - laktosmonohydrat hjälpämne; kandesartancilexetil 32 mg aktiv substans - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandoz a/s - kandesartancilexetil - tablett - 4 mg - laktosmonohydrat hjälpämne; kandesartancilexetil 4 mg aktiv substans - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

actavis group ptc ehf. - kandesartancilexetil - tablett - 4 mg - kandesartancilexetil 4 mg aktiv substans; laktosmonohydrat hjälpämne - kandesartan

Sverige - svenska - Läkemedelsverket (Medical Products Agency)

sandoz a/s - kandesartancilexetil - tablett - 8 mg - laktosmonohydrat hjälpämne; kandesartancilexetil 8 mg aktiv substans - kandesartan