Adakveo Unjoni Ewropea - Slovakk - EMA (European Medicines Agency)

adakveo

novartis europharm limited - crizanlizumab - anémia, kosáčiková bunka - other hematological agents - adakveo is indicated for the prevention of recurrent vaso occlusive crises (vocs) in sickle cell disease patients aged 16 years and older. it can be given as an add on therapy to hydroxyurea/hydroxycarbamide (hu/hc) or as monotherapy in patients for whom hu/hc is inappropriate or inadequate.

Kapruvia Unjoni Ewropea - Slovakk - EMA (European Medicines Agency)

kapruvia

vifor fresenius medical care renal pharma france - difelikefalin - pruritus - všetky ostatné terapeutické produkty - kapruvia is indicated for the treatment of moderate-to-severe pruritus associated with chronic kidney disease in adult patients on haemodialysis (see section 5.

Amyvid Unjoni Ewropea - Slovakk - EMA (European Medicines Agency)

amyvid

eli lilly nederland b.v. - florbetapir (18f) - radionuklidové zobrazovanie - diagnostické rádiofarmaká - tento liek je určený len na diagnostické účely. amyvid je radiopharmaceutical uvedené pre pozitrón emisnej tomografie (pet) zobrazovanie β-amyloid neuritic doska hustota v mozgy dospelých pacientov s kognitívnych schopností, ktoré sú hodnotené na alzheimerovej choroby (ad) a iné príčiny kognitívnych schopností. amyvid by mali byť použité v spojení s klinické hodnotenie. negatívne kontroly označuje riedke, alebo nie, plakety, čo nie je v súlade s diagnózou reklamy.

Sarclisa Unjoni Ewropea - Slovakk - EMA (European Medicines Agency)

sarclisa

sanofi winthrop industrie - isatuximab - viacnásobný myelóm - antineoplastické činidlá - sarclisa is indicated: in combination with pomalidomide and dexamethasone, for the treatment of adult patients with relapsed and refractory multiple myeloma (mm) who have received at least two prior therapies including lenalidomide and a proteasome inhibitor (pi) and have demonstrated disease progression on the last therapy. in combination with carfilzomib and dexamethasone, for the treatment of adult patients with multiple myeloma who have received at least one prior therapy (see section 5.

Pentasa Slovakkja - Slovakk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pentasa

ferring-léčiva, a.s., Česká republika - mesalazín - 29 - antirheumatica, antiphlogistica, antiuratica

Pentasa Slow release tablets 500 mg Slovakkja - Slovakk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pentasa slow release tablets 500 mg

ferring-léčiva, a.s., Česká republika - mesalazín - 29 - antirheumatica, antiphlogistica, antiuratica

Pentasa Sachet 2 g Slovakkja - Slovakk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pentasa sachet 2 g

ferring-léčiva, a.s., Česká republika - mesalazín - 29 - antirheumatica, antiphlogistica, antiuratica

Pentasa Slow release tablets 1 g Slovakkja - Slovakk - ŠÚKL (Štátny ústav pre kontrolu liečiv)

pentasa slow release tablets 1 g

ferring-léčiva, a.s., Česká republika - mesalazín - 29 - antirheumatica, antiphlogistica, antiuratica

Poteligeo Unjoni Ewropea - Slovakk - EMA (European Medicines Agency)

poteligeo

kyowa kirin holdings b.v. - mogamulizumab - sezary syndrome; mycosis fungoides - antineoplastické činidlá - poteligeo je indikovaný na liečbu dospelých pacientov s mycosis fungoides (mf) alebo sézary syndróm (ss), ktorí dostali aspoň jeden pred systémová terapia.