Invokana 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

invokana

janssen-cilag international nv - kanagliflozinas - cukrinis diabetas, 2 tipas - narkotikai, vartojami diabetu - 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 ir 5.

Suliqua 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

suliqua

sanofi winthrop industrie - insulin glargine, lixisenatide - cukrinis diabetas, 2 tipas - narkotikai, vartojami diabetu - 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.

Edistride 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

edistride

astrazeneca ab - dapagliflozino propanedilo monohidratas - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - narkotikai, vartojami diabetu - type 2 diabetes mellitusedistride is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. be kitų vaistų, skirtų gydyti 2 tipo cukrinis diabetas. 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 ir 5. heart failureedistride is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseedistride is indicated in adults for the treatment of chronic kidney disease.

Forxiga 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

forxiga

astrazeneca ab - dapagliflozino propanedilo monohidratas - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - narkotikai, vartojami diabetu - type 2 diabetes mellitusforxiga is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exerciseas monotherapy when metformin is considered inappropriate due to intolerance. be kitų vaistų, skirtų gydyti 2 tipo cukrinis diabetas. 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 ir 5. heart failureforxiga is indicated in adults for the treatment of symptomatic chronic heart failure. chronic kidney diseaseforxiga is indicated in adults for the treatment of chronic kidney disease.

Dapagliflozin Viatris 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

dapagliflozin viatris

viatris limited - dapagliflozin - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - narkotikai, vartojami diabetu - type 2 diabetes mellitusdapagliflozin viatris is indicated in adults and children aged 10 years and above for the treatment of insufficiently controlled type 2 diabetes mellitus as an adjunct to diet and exercise- as monotherapy when metformin is considered inappropriate due to intolerance. - in addition to other medicinal products for the treatment of type 2 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 ir 5. heart failuredapagliflozin viatris is indicated in adults for the treatment of symptomatic chronic heart failure with reduced ejection fraction. chronic kidney diseasedapagliflozin viatris is indicated in adults for the treatment of chronic kidney disease.

Enerzair Breezhaler 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

enerzair breezhaler

novartis europharm limited - indacaterol, glycopyrronium bromide, mometasone - astma - vaistai nuo obstrukcinių kvėpavimo takų ligų, - enerzair breezhaler is indicated as a maintenance treatment of asthma in adult patients not adequately controlled with a maintenance combination of a long acting beta2 agonist and a high dose of an inhaled corticosteroid who experienced one or more asthma exacerbations in the previous year.

Zimbus Breezhaler 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

zimbus breezhaler

novartis europharm limited - glycopyrronium bromide, indacaterol (acetate), mometasone furoate - astma - vaistai nuo obstrukcinių kvėpavimo takų ligų, - maintenance treatment of asthma in adults whose disease is not adequately controlled.

Procoralan 欧盟 - 立陶宛文 - EMA (European Medicines Agency)

procoralan

les laboratoires servier - ivabradino hidrochloridas - angina pectoris; heart failure - Širdies terapija - simptominis lėtinės stabiliosios krūtinės anginos ivabradinas yra skirtas simptominiam stabiliosios krūtinės anginos – širdies vainikinių arterijų liga suaugusiems pacientams normalus sinusinis ritmas ir širdies susitraukimų dažnis ≥ 70 k/min. ivabradine is indicated :in adults unable to tolerate or with a contraindication to the use of beta-blockersor in combination with beta-blockers in patients inadequately controlled with an optimal beta-blocker dose. gydymas lėtinio širdies nepakankamumo gydymą ivabradinu nurodomas lėtinio širdies nepakankamumo ii nyha iv klasės su sistoline pacientams – sinusinis ritmas ir kurių širdies susitraukimų dažnis yra ≥ 75 susitraukimai per minutę, kartu su standartiniu gydymu, įskaitant gydymą beta receptorių blokatoriais arba kada gydymą beta receptorių blokatoriais yra kontraindikuotini arba netoleruojami.

TSEFALEN 500 mg, plėvele dengtos tabletės šunims 立陶宛 - 立陶宛文 - SMCA (Valstybinė vaistų kontrolės tarnyba)

tsefalen 500 mg, plėvele dengtos tabletės šunims

icf srl industrija chimica fine (italija) - tabletės - glaskragujevca.netvienoje tabletėje yra: cefaleksino (cefaleksino monohidrato) - 500,0 mg; pagalbinių medžiagų. - Šunims gydyti, sergantiems cefaleksinui jautrių bakterijų sukeltomis kvėpavimo takų, šlapimo ir lyties takų, odos, vietinėmis minkštųjų audinių bei virškinimo trakto infekcinėmis ligomis.

TSEFALEN 1 000 mg, plėvele dengtos tabletės šunims 立陶宛 - 立陶宛文 - SMCA (Valstybinė vaistų kontrolės tarnyba)

tsefalen 1 000 mg, plėvele dengtos tabletės šunims

icf srl industrija chimica fine (italija) - tabletės - lanoxin lanoxin vienoje tabletėje yra: cefaleksino (cefaleksino monohidrato) - 1000,0 mg; pagalbinių medžiagų. - Šunims gydyti, sergantiems cefaleksinui jautrių bakterijų sukeltomis kvėpavimo takų, šlapimo ir lyties takų, odos, vietinėmis minkštųjų audinių bei virškinimo trakto infekcinėmis ligomis.