Steglatro Europska Unija - hrvatski - EMA (European Medicines Agency)

steglatro

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic kiselina - dijabetes mellitus, tip 2 - drugs used in diabetes, sodium-glucose co-transporter 2 (sglt2) inhibitors - steglatro prikazan u odraslih osoba u dobi od 18 godina i stariji sa dijabetesom tipa 2 kao dodatak prehrani i fizičke vježbe za poboljšanje glikemijski kontrole:kao monoterapija kod bolesnika za koje primjena метформина se smatra da je neprimjereno zbog netolerancije ili kontraindikacija. osim drugih lijekova za liječenje šećerne bolesti.

Pifeltro Europska Unija - hrvatski - EMA (European Medicines Agency)

pifeltro

merck sharp & dohme b.v. - doravirine - hiv infekcije - antivirusni lijekovi za sustavnu uporabu - pifeltro is indicated, in combination with other antiretroviral medicinal products, for the treatment of adults, and adolescents aged 12 years and older weighing at least 35 kg infected with hiv 1 without past or present evidence of resistance to the nnrti class.

Ervebo Europska Unija - hrvatski - EMA (European Medicines Agency)

ervebo

merck sharp & dohme b.v.  - рекомбинантный virus везикулярного стоматита (soj indiana) s brisanje koverti glikoprotein, zamijenjen zair ebole (soj киквите 1995) površinski glikoprotein - Геморрагическая groznice ebole - cjepiva - ervebo is indicated for active immunization of individuals 1 year of age or older to protect against ebola virus disease (evd) caused by zaire ebola virus. korištenje ervebo moraju biti u skladu sa službenim preporukama.

Vaxneuvance Europska Unija - hrvatski - EMA (European Medicines Agency)

vaxneuvance

merck sharp & dohme b.v.  - pneumococcal polysaccharide conjugate vaccine (adsorbed) - pneumococcal infekcije - pneumococcus, purified polysaccharides antigen conjugated - vaxneuvance is indicated for active immunisation for the prevention of invasive disease, pneumonia and acute otitis media caused by streptococcus pneumoniae in infants, children and adolescents from 6 weeks to less than 18 years of age. vaxneuvance is indicated for active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. pogledajte odjeljke 4. 4 i 5. 1 za informacije o zaštiti od specifičnih pneumokoknih serotipova. the use of vaxneuvance should be in accordance with official recommendations.

Teriparatide Sun Europska Unija - hrvatski - EMA (European Medicines Agency)

teriparatide sun

sun pharmaceutical industries europe b.v. - teriparatid - osteoporosis; osteoporosis, postmenopausal - homeostaza kalcija - 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.

Lyfnua Europska Unija - hrvatski - EMA (European Medicines Agency)

lyfnua

merck sharp & dohme b.v. - gefapixant - cough - kašalj i hladno pripremanje - lyfnua is indicated in adults for the treatment of refractory or unexplained chronic cough.

Ayvakyt Europska Unija - hrvatski - EMA (European Medicines Agency)

ayvakyt

blueprint medicines (netherlands) b.v. - avapritinib - tumori gastrointestinalnog stroma - drugi antitumorski lijekovi, inhibitori протеинкиназы - ayvakyt is indicated as monotherapy for the treatment of adult patients with unresectable or metastatic gastrointestinal stromal tumours (gist) harbouring the platelet-derived growth factor receptor alpha (pdgfra) d842v mutation.

Fabrazyme Europska Unija - hrvatski - EMA (European Medicines Agency)

fabrazyme

sanofi b.v. - agalsidaza beta - fabry-ovu bolest - drugi gastrointestinalni trakt i metabolizam, lijekovi, - fabrazyme je indiciran za dugoročnu zamjensku enzimsku terapiju u bolesnika s potvrđenom dijagnozom fabryove bolesti (nedostatak α-galaktozidaze-a).

Myozyme Europska Unija - hrvatski - EMA (European Medicines Agency)

myozyme

sanofi b.v. - alglukozidaza alfa - vrsta ii za skladištenje glikogena - drugi gastrointestinalni trakt i metabolizam, lijekovi, - myozyme je indiciran za dugoročnu zamjensku enzimsku terapiju (ert) u bolesnika s potvrđenom dijagnozom bolesti pompe (nedostatak kiselina-a-glukozidaza). u bolesnika s kasnim početkom bolesti Помпе dokaz učinkovitosti ograničena.

Elzonris Europska Unija - hrvatski - EMA (European Medicines Agency)

elzonris

stemline therapeutics b.v. - tagraxofusp - lymphoma - antineoplastična sredstva - elzonris is indicated as monotherapy for the first-line treatment of adult patients with blastic plasmacytoid dendritic cell neoplasm (bpdcn).