Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - l-amlodipina, valsartan - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. dafiro huwa indikat f'pazjenti li l-pressjoni tad-demm mhijiex ikkontrollata adegwatament bl-amlodipina jew valsartan monoterapija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

pfizer europe ma eeig - parecoxib sodium - uġigħ, wara l-operazzjoni - coxibs, antiinflammatory and antirheumatic products - għat-trattament għal żmien qasir ta 'uġigħ wara l-operazzjoni fl-adulti.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - sacubitril, valsartan - insuffiċjenza tal-qalb - antagonisti ta ' angiotensin ii, kombinazzjonijiet oħra, aġenti li jaġixxu fuq is-sistema renin-angiotensin - paediatric heart failureentresto is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction. adult heart failureentresto is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - valsartan, amlodipine (as amlodipine besilate) - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. exforge huwa indikat f'pazjenti li l-pressjoni tad-demm mhijiex ikkontrollata adegwatament bl-amlodipina jew valsartan monoterapija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm ltd - valsartan, amlodipine (as amlodipine besilate) - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'ipertensjoni essenzjali. imprida huwa indikat f'pazjenti li l-pressjoni tad-demm mhijiex ikkontrollata adegwatament bl-amlodipina jew valsartan monoterapija.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin - diabetes mellitus, tip 2 - drogi użati fid-dijabete - invokana is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise:as monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. for study results with respect to combination of therapies, effects on glycaemic control, cardiovascular and renal events, and the populations studied, see sections 4. 4, 4. 5 u 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm limited - sacubitril, valsartan - insuffiċjenza tal-qalb - aġenti li jaġixxu fuq is-sistema renin-angiotensin - paediatric heart failureneparvis is indicated in children and adolescents aged one year or older for treatment of symptomatic chronic heart failure with left ventricular systolic dysfunction (see section 5. adult heart failureneparvis is indicated in adult patients for treatment of symptomatic chronic heart failure with reduced ejection fraction (see section 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulina glargine - diabetes mellitus - drogi użati fid-dijabete - it-trattament tad-dijabete mellitus fl-adulti, l-adoloxxenti u t-tfal mill-età ta ' 6 snin.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

janssen-cilag international nv - canagliflozin, metformin hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - vokanamet huwa indikat f'adulti ta '18-il sena u akbar b'dijabete mellitus tip 2 bħala żieda mad-dieta u l-eżerċizzju biex itejjeb il-kontroll gliċemiku:f'pazjenti li mhumiex kontrollati sew fuq xieraq bl-felħu dożi ta' metformin alonein pazjenti fuq xieraq bl-felħu dożi ta 'metformin flimkien ma' oħrajn li jbaxxu glucose-prodotti mediċinali inkluża l-insulina, meta dawn ma jipprovdux kontroll gliċemiku adegwat. fil-pazjenti li diġà qegħdin jiġu kkurati b'kumbinazzjoni ta canagliflozin u metformin bħala separati tabletsfor-riżultati tal-istudju fir-rigward tal-kombinazzjoni ta ' terapiji, l-effetti fuq il-kontroll gliċemiku u episodji kardjovaskulari, u l-popolazzjonijiet studjati, ara sezzjonijiet 4. 4, 4. 5 u 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

biogen netherlands b.v. - dimetil fumarate - sklerosi multipla - immunosoppressanti - tecfidera is indicated for the treatment of adult and paediatric patients aged 13 years and older with relapsing remitting multiple sclerosis (rrms).