MabCampath Eiropas Savienība - slovāku - EMA (European Medicines Agency)

mabcampath

genzyme europe b.v. - alemtuzumab - leukémia, lymfocytárna, chronická, b-bunka - antineoplastické činidlá - mabcampath je indikovaný na liečbu pacientov s b-buniek lymfatickou leukémiou (bcll) pre koho fludarabín kombinácia chemoterapie nie je vhodné.

RECTODELT 100 mg Slovākija - slovāku - ŠÚKL (Štátny ústav pre kontrolu liečiv)

rectodelt 100 mg

trommsdorff gmbh and co. kg, nemecko - prednizón - 56 - hormona (lieČiva s hormonÁlnou aktivitou)

Jext 150 mikrogramov Slovākija - slovāku - ŠÚKL (Štátny ústav pre kontrolu liečiv)

jext 150 mikrogramov

alk-abelló a/s, dánsko - epinefrín (adrenalín) - 41 - cardiaca

Jext 300 mikrogramov Slovākija - slovāku - ŠÚKL (Štátny ústav pre kontrolu liečiv)

jext 300 mikrogramov

alk-abelló a/s, dánsko - epinefrín (adrenalín) - 41 - cardiaca

Teriparatide Sun Eiropas Savienība - slovāku - EMA (European Medicines Agency)

teriparatide sun

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - homeostáza vápnika - teriparatide sun is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

Kauliv Eiropas Savienība - slovāku - EMA (European Medicines Agency)

kauliv

strides pharma (cyprus) limited - teriparatid - osteoporosis; osteoporosis, postmenopausal - homeostáza vápnika - kauliv is indicated in adults. treatment of osteoporosis in postmenopausal women and in men at increased risk of fracture (see section 5. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures has been demonstrated. treatment of osteoporosis associated with sustained systemic glucocorticoid therapy in women and men at increased risk for fracture (see section 5.

BindRen Eiropas Savienība - slovāku - EMA (European Medicines Agency)

bindren

mitsubishi pharma europe ltd - colestilan - hyperfosfatémie - lieky na liečbu hyperkaliémie a hyperfosfatémie - liečba hyperfosfatémie u dospelých pacientov s chronickou chorobou obličiek v štádiu 5, ktorí dostávajú hemodialýzu alebo peritoneálnu dialýzu.

Edistride Eiropas Savienība - slovāku - EMA (European Medicines Agency)

edistride

astrazeneca ab - dapagliflozín propándiol monohydrát - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - lieky používané pri cukrovke - 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. okrem iných liekov na liečbu diabetes mellitus 2. typu. 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 a 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 Eiropas Savienība - slovāku - EMA (European Medicines Agency)

forxiga

astrazeneca ab - dapagliflozín propándiol monohydrát - diabetes mellitus, type 2; heart failure, systolic; heart failure; renal insufficiency, chronic - lieky používané pri cukrovke - 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. okrem iných liekov na liečbu diabetes mellitus 2. typu. 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 a 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.

Renvela Eiropas Savienība - slovāku - EMA (European Medicines Agency)

renvela

sanofi b.v. - sevelamer karbonátu - hyperphosphatemia; renal dialysis - všetky ostatné terapeutické produkty - renvela je indikovaná na kontrolu hyperfosfatémie u dospelých pacientov, ktorí dostávajú hemodialýzu alebo peritoneálnu dialýzu. renvela je tiež indikovaný na zastavenie hyperphosphataemia u dospelých pacientov s chronickým ochorením obličiek nie na dialýzu s fosforu v sére ≥ 1. 78 mmol/l. renvela by mali byť použité v rámci viacerých terapeutický prístup, ktoré by mohli obsahovať vápnik doplnok, 1,25-dihydroxy vitamín d3, alebo jeden z jeho analógy ovládať vývoj obličiek ochorenia kostí.