Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva pharma b.v. - repaglinide - diabetes mellitus, tip 2 - drogi użati fid-dijabete - repaglinide huwa indikat fil-pazjenti bl-dijabete tat-tip-2 (mhux-insulina - dipendenti diabetes mellitus (niddm)) tagħhom hyperglycaemia jistgħu aktar jiġu kkontrollati b'mod sodisfaċenti minn dieta, piż tnaqqis u l-eżerċizzju. repaglinide huwa indikat ukoll flimkien ma 'metformin f'pazjenti b'dijabete tat-tip-2 li mhumiex ikkontrollati b'mod sodisfaċenti fuq metformin waħdu. il-kura għandha tinbeda bħala żieda mad-dieta u l-eżerċizzju biex ibaxxi l-glucose fid-demm fir-rigward ta'l-ikel.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

teva pharma b.v. - pioglitazone hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - pioglitazone is indicated in the treatment of type-2 diabetes mellitus as monotherapy: , in adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. , pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance. wara l-bidu tat-terapija b'pioglitazone, il-pazjenti għandhom jiġu riveduti wara 3 sa 6 xhur biex tevalwa l-adegwatezza tal-rispons għall-kura (e. it-tnaqqis fl-hba1c). f'pazjenti li jonqsu li juru rispons adegwat, pioglitazone għandu jitwaqqaf. fid-dawl tar-riskji potenzjali fit-tul mal-terapija, it-tobba għandhom jikkonfermaw fil-sussegwenti ta 'rutina reviżjonijiet li l-benefiċċju ta' pioglitazone jinżamm.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

eli lilly nederland b.v. - dulaglutide - diabetes mellitus, tip 2 - drugs used in diabetes, blood glucose lowering drugs, excl. insulins - trulicity is indicated for the treatment of patients 10 years and above with insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance or contraindicationsin addition to other medicinal products for the treatment of diabetes. għall-riżultati tal-istudju fir-rigward tal-kombinazzjonijiet, 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)

actavis group ptc ehf   - pioglitazone hydrochloride - diabetes mellitus, tip 2 - drogi użati fid-dijabete - pioglitazone is indicated as second or third line treatment of type 2 diabetes mellitus as described below:as monotherapyin adult patients (particularly overweight patients) inadequately controlled by diet and exercise for whom metformin is inappropriate because of contraindications or intolerance. as dual oral therapy in combination withmetformin, in adult patients (particularly overweight patients) with insufficient glycaemic control despite maximal tolerated dose of monotherapy with metformin. a sulphonylurea, only in adult patients who show intolerance to metformin or for whom metformin is contraindicated, with insufficient glycaemic control despite maximal tolerated dose of monotherapy with a sulphonylurea. as triple oral therapy in combination withmetformin and a sulphonylurea, in adult patients (particularly overweight patients) with insufficient glycaemic control despite dual oral therapy. pioglitazone is also indicated for combination with insulin in type 2 diabetes mellitus adult patients with insufficient glycaemic control on insulin for whom metformin is inappropriate because of contraindications or intolerance (see section 4. wara l-bidu tat-terapija b'pioglitazone, il-pazjenti għandhom jiġu riveduti wara 3 sa 6 xhur biex tevalwa l-adegwatezza tal-rispons għall-kura (e. it-tnaqqis fl-hba1c). f'pazjenti li jonqsu li juru rispons adegwat, pioglitazone għandu jitwaqqaf. fid-dawl tar-riskji potenzjali fit-tul mal-terapija, it-tobba għandhom jikkonfermaw fil-sussegwenti ta 'rutina reviżjonijiet li l-benefiċċju ta' pioglitazone huwa miżmum (ara sezzjoni 4.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

accord healthcare s.l.u. - ivabradine hydrochloride - angina pectoris; heart failure - terapija kardijaka - kura sintomatika ta kronika stabbli, anġina pectorisivabradine huwa indikat għat-trattament tas-sintomi ta ' angina pectoris kronika stabbli fil-mard tal-arterji koronarji adulti b'ritmu sinusali normali u rata tal-qalb ≥ 70 bpm. ivabradine huwa indikat :- fl-adulti li ma jistgħux jittolleraw jew bil-kontra-indikazzjoni għall-użu tal-imblokkaturi tar-riċetturi beta jew flimkien ma ' beta blockers f'pazjenti mhux ikkontrollati adegwatament bil-aħjar beta-blocker-doża. it-trattament tal-qalb kroniku failureivabradine huwa indikat f'insuffiċjenza kronika tal-qalb nyha ii-iv tal-klassi b'disfunzjoni sistolika, fil-pazjenti fl-sinus ritmiku u li d-rata tal-qalb huwa ≥ 75 bpm, f'kombinazzjoni ma ' terapija standard, inklużi l-beta-blockers jew meta beta-blockers huwa kontra-indikati jew mhux ittollerati. (ara sezzjoni 5.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

astrazeneca ab - saxagliptin - diabetes mellitus, tip 2 - drogi użati fid-dijabete - add-on combination therapyonglyza is indicated in adult patients aged 18 years and older with type-2 diabetes mellitus 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 metformin alone, with diet and exercise, does not provide adequate glycaemic control;in combination with a sulphonylurea, when the sulphonylurea alone, with diet and exercise, does not provide adequate glycaemic control in patients for whom use of metformin is considered inappropriate;in combination with a thiazolidinedione, when the thiazolidinedione alone with diet and exercise, does not provide adequate glycaemic control in patients for whom use of a thiazolidinedione is considered appropriate;as triple oral therapy:in combination with metformin plus a sulphonylurea when this regimen alone, with diet and exercise, does not provide adequate glycaemic control;as combination therapy with insulin (with or without metformin), when this regimen alone, with diet and exercise, does not provide adequate glycaemic control.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

krka, d.d., novo mesto - repaglinide - diabetes mellitus, tip 2 - drogi użati fid-dijabete - repaglinide huwa indikat fil-pazjenti bl-dijabete tat-tip-2 (mhux-insulina - dipendenti diabetes mellitus (niddm)) tagħhom hyperglycaemia jistgħu aktar jiġu kkontrollati b'mod sodisfaċenti minn dieta, piż tnaqqis u l-eżerċizzju. il-kura għandha tinbeda bħala żieda mad-dieta u l-eżerċizzju biex ibaxxi l-glucose fid-demm fir-rigward ta'l-ikel.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm ltd. - aliskiren, għall-idroklorotijażide - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'pressjoni għolja essenzjali fl-adulti. riprazo hct huwa indikat f'pazjenti li l-pressjoni tad-demm ma tkunx ikkontrollata sew b'aliskiren jew hydrochlorothiazide użati waħidhom. rirpozo hct huwa indikat bħala terapija ta 'sostituzzjoni f'pazjenti li jkunu kontrollati sew b'aliskiren u hydrochlorothiazide, mogħtija flimkien, bl-istess livell ta' doża tat - taħlita.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

novartis europharm ltd. - aliskiren, għall-idroklorotijażide - pressjoni għolja - aġenti li jaġixxu fuq is-sistema renin-angiotensin - trattament ta 'pressjoni għolja essenzjali fl-adulti. sprimeo hct huwa indikat f'pazjenti li l-pressjoni tad-demm ma tkunx ikkontrollata sew b'aliskiren jew hydrochlorothiazide użati waħidhom. sprimeo hct huwa indikat bħala terapija ta 'sostituzzjoni f'pazjenti li jkunu kontrollati sew b'aliskiren u hydrochlorothiazide, mogħtija flimkien, bl-istess livell ta' doża tat - taħlita.

Unjoni Ewropea - Malti - EMA (European Medicines Agency)

sanofi winthrop industrie - l-insulina glargine, lixisenatide - diabetes mellitus, tip 2 - drogi użati fid-dijabete - suliqua is indicated for the treatment of adults with insufficiently controlled type 2 diabetes mellitus to improve glycaemic control as an adjunct to diet and exercise in addition to metformin with or without sglt-2 inhibitors.