Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

atnahs pharma netherlands b.v. - solriamfetol hidroklorid - narcolepsy; sleep apnea, obstructive - psychoanaleptics, - sunosi pokazala da poboljšanje budnosti i smanjiti prekomjerna dnevna pospanost u odraslih bolesnika s narkolepsije (sa ili bez cataplexy). sunosi pokazala da poboljšanje budnosti i smanjiti prekomjerna dnevna pospanost (eds) kod odraslih pacijenata sa sindromom opstruktivna sleep apnea (osa), kod kojih je ЭЦП je nedovoljno obrađenih osnovnih osa terapija, kao što su kontinuirani pozitivni tlak u dišnim putevima (cpap stroj).

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

aimmune therapeutics ireland limited - defatted powder of arachis hypogaea l., semen (peanuts) - peanut hypersensitivity - allergens - palforzia is indicated for the treatment of patients aged 4 to 17 years with a confirmed diagnosis of peanut allergy. palforzia may be continued in patients 18 years of age and older. palforzia should be used in conjunction with a peanut-avoidant diet.

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

advicenne s.a. - potassium citrate monohydrated, potassium hydrogen carbonate - acidosis, renal tubular - mineral supplements - sibnayal is indicated for the treatment of distal renal tubular acidosis (drta) in adults, adolescents and children aged one year and older.

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

accord healthcare s.l.u. - sunitinib - gastrointestinal stromal tumors; carcinoma, renal cell; neuroendocrine tumors - antineoplastična sredstva - gastrointestinal stromal tumour (gist)sunitinib accord is indicated for the treatment of unresectable and/or metastatic malignant gastrointestinal stromal tumour (gist) in adults after failure of imatinib treatment due to resistance or intolerance. metastatic renal cell carcinoma (mrcc)sunitinib accord is indicated for the treatment of advanced/metastatic renal cell carcinoma (mrcc) in adults. pancreatic neuroendocrine tumours (pnet)sunitinib accord is indicated for the treatment of unresectable or metastatic, well-differentiated pancreatic neuroendocrine tumours (pnet) with disease progression in adults.

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

diurnal europe b.v. - hidrokortizon - adrenal hyperplasia, congenital - kortikosteroidi za sistemsku upotrebu - treatment of congenital adrenal hyperplasia (cah) in adolescents aged 12 years and over and adults.

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

vifor fresenius medical care renal pharma france - avacopan - microscopic polyangiitis; wegener granulomatosis - imunosupresivi - tavneos, in combination with a rituximab or cyclophosphamide regimen, is indicated for the treatment of adult patients with severe, active granulomatosis with polyangiitis (gpa) or microscopic polyangiitis (mpa).

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

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.

Avrupa Birliği - Hırvatça - EMA (European Medicines Agency)

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastična sredstva - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

alk-abelló a/s, boge allé 6-8, horsholm, danska - adrenalintartarat (epinefrintartarat) - otopina za injekciju u napunjenoj brizgalici - urbroj: 1 ml otopine sadrži 1 mg adrenalina (u obliku adrenalintartarata). pojedinačna doza od 0,15 ml otopine za injekciju sadrži 150 mikrograma adrenalina (u obliku adrenalintartarata).

Hırvatistan - Hırvatça - HALMED (Agencija za lijekove i medicinske proizvode)

alk-abelló a/s, boge allé 6-8, horsholm, danska - adrenalintartarat (epinefrintartarat) - otopina za injekciju u napunjenoj brizgalici - urbroj: 1 ml otopine sadrži 1 mg adrenalina (u obliku adrenalintartarata). pojedinačna doza od 0,30 ml otopine za injekciju sadrži 300 mikrograma adrenalina (u obliku adrenalintartarata).