Vyndaqel Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

vyndaqel

pfizer europe ma eeig - tafamidis - amiloidozė - kiti nervų sistemos vaistai - vyndaqel skirtas gydyti suaugusiems pacientams, sergantiems 1 etapas simptominis polineuropatija atidėti periferinių nervų pakenkimas amiloidozė transthyretin.

Mepsevii Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

mepsevii

ultragenyx germany gmbh - vestronidase alfa - mucopolysaccharidosis vii - fermentai - mepsevii fluorouracilu ir folino ne neurologiniai požymiai mucopolysaccharidosis vii (mps vii; sly sindromas).

Nyxthracis (previously Obiltoxaximab SFL) Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

nyxthracis (previously obiltoxaximab sfl)

sfl pharmaceuticals deutschland gmbh - nyxthracis - anthrax - imuninės serumai ir imunoglobulinai, - obiltoxaximab sfl is indicated in combination with appropriate antibacterial drugs in all age groups for treatment of inhalational anthrax due to bacillus anthracis (see section 5. obiltoxaximab sfl is indicated in all age groups for post-exposure prophylaxis of inhalational anthrax when alternative therapies are not appropriate or are not available (see section 5.

Evkeeza Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

evkeeza

ultragenyx germany gmbh - evinacumab - hipercholesterolemija - lipidą keičiančios medžiagos - evkeeza is indicated as an adjunct to diet and other low-density lipoprotein-cholesterol (ldl-c) lowering therapies for the treatment of adult and adolescent patients aged 12 years and older with homozygous familial hypercholesterolaemia (hofh).

Voraxaze Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

voraxaze

serb sas - glucarpidase - metabolic side effects of drugs and substances - visi kiti gydomieji produktai - voraxaze is indicated to reduce toxic plasma methotrexate concentration in adults and children (aged 28 days and older) with delayed methotrexate elimination or at risk of methotrexate toxicity.

Nulibry Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

nulibry

tmc pharma (eu) limited - fosdenopterin hydrobromide dihydrate - metal metabolism, inborn errors - kiti virškinimo trakto ir metabolizmo produktus, - nulibry is indicated for the treatment of patients with molybdenum cofactor deficiency (mocd) type a.

Livmarli Europos Sąjunga - lietuvių - EMA (European Medicines Agency)

livmarli

mirum pharmaceuticals international b.v. - maralixibat chloride - alagille syndrome - other drugs for bile therapy - livmarli is indicated for the treatment of cholestatic pruritus in patients with alagille syndrome (algs) 2 months of age and older.

Furosemide Accord Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

furosemide accord

accord healthcare b.v. - furozemidas - injekcinis ar infuzinis tirpalas - 10 mg/ml - furosemide

Furosemide Norameda Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

furosemide norameda

norameda, uab - furozemidas - injekcinis ar infuzinis tirpalas - 10 mg/ml - furosemide

Epirubicin Accord Lietuva - lietuvių - SMCA (Valstybinė vaistų kontrolės tarnyba)

epirubicin accord

accord healthcare b.v. - epirubicino hidrochloridas - injekcinis ar infuzinis tirpalas - 2 mg/ml - epirubicin