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

qutavina

eurogenerics holdings b.v. - teriparatid - osteoporoza - homeostaza kalcija - qutavina is indicated in adults. liječenje osteoporoze u žena u postmenopauzi i muškaraca pri povećanom riziku od loma. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. liječenje osteoporoze, povezan sa stalnim sistemsku terapiju s glukokortikoidi, kod žena i muškaraca pod povećanim rizikom prijeloma.

Lantan Viatris 500 mg tablete za žvakanje Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

lantan viatris 500 mg tablete za žvakanje

viatris limited, damastown industrial park, mulhuddart, dublin, irska - lantan karbonat - tableta za žvakanje - 500 mg - urbroj: jedna tableta za žvakanje od 500 mg sadrži količinu lantan karbonat oktahidrata ekvivalentnu 500 mg lantana

ATECTURA Breezhaler 125 µg/1 kapsula+ 127,5 µg/1 kapsula prašak za inhalaciju, tvrda kapsula Bosna i Hercegovina - hrvatski - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

atectura breezhaler 125 µg/1 kapsula+ 127,5 µg/1 kapsula prašak za inhalaciju, tvrda kapsula

novartis ba d.o.o. - indakaterol, mometazon - prašak za inhalaciju, tvrda kapsula - 125 µg/1 kapsula+ 127,5 µg/1 kapsula - 1 tvrda kapsula, praška za inhalaciju sadrži: 150 µg indakaterola (u obliku acetata) i 160 µg mometazon furoata. jedna isporučena doza (doza koja izađe iz nastavka za usta inhalera) sadrži 125 µg indakaterola (acetata) i 127,5 µg mometazon furoata.

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

voraxaze

serb sas - glucarpidase - metabolic side effects of drugs and substances - svi ostali terapeutski proizvodi - 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.

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

brukinsa

beigene ireland ltd - zanubrutinib - waldenstrom macroglobulinemia - antineoplastična sredstva - brukinsa as monotherapy is indicated for the treatment of adult patients with waldenström’s macroglobulinaemia (wm) who have received at least one prior therapy, or in first line treatment for patients unsuitable for chemo-immunotherapy. brukinsa as monotherapy is indicated for the treatment of adult patients with marginal zone lymphoma (mzl) who have received at least one prior anti-cd20-based therapy. brukinsa as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukemia (cll).

Phytocyst oralne kapi, otopina Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

phytocyst oralne kapi, otopina

alpen pharma gmbh, steinenfeld 3, zell am harmersbach, njemačka - tekući ekstrakt (1:1,5 &ndash 2,1) iz mješavine zlatničine zeleni, zeleni guščarskog petoprsta i zeleni poljske preslice (4,2:1,4 : 1), ekstrakcijsko otapalo: etanol 50% (v/v) - oralne kapi, otopina - urbroj: 10 ml (= 9,5 g) phytocyst oralnih kapi, otopine sadrži: 7,9 ml tekućeg ekstrakta (1 : 1,5 – 2,1) iz mješavine solidago gigantea ait. i/ili solidago canadensis l., herba (zlatničina zelen), potentilla anserina l., herba (zelen guščarskog petoprsta) i equisetum arvense l., herba (zelen poljske preslice) (4,2 : 1,4 : 1). ekstrakcijsko otapalo: etanol 50 % v/v 30 kapi jednako je 1,3 ml otopine

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

sondelbay

accord healthcare s.l.u. - teriparatid - osteoporoza - homeostaza kalcija - sondelbay is indicated in adults. liječenje osteoporoze u žena u postmenopauzi i muškaraca pri povećanom riziku od loma. in postmenopausal women, a significant reduction in the incidence of vertebral and non-vertebral fractures but not hip fractures have been demonstrated. liječenje osteoporoze, povezan sa stalnim sistemsku terapiju s glukokortikoidi, kod žena i muškaraca pod povećanim rizikom prijeloma.

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

kauliv

strides pharma (cyprus) limited - teriparatid - osteoporosis; osteoporosis, postmenopausal - homeostaza kalcija - 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.

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

kapruvia

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