Խորվաթիա - խորվաթերեն - HALMED (Agencija za lijekove i medicinske proizvode)

teva gmbh, graf-arco-str. 3, ulm, njemačka - fampridin - tableta s produljenim oslobađanjem - urbroj: jedna tableta s produljenim oslobađanjem sadrži 10 mg fampridina

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate - dijabetes mellitus, tip 2 - lijekovi koji se koriste u dijabetesu - for adult patients with type 2 diabetes mellitus, sitagliptin sun is indicated to improve glycaemic control:as monotherapy:- in patients inadequately controlled by diet and exercise alone and for whom metformin is inappropriate due to contraindications or intolerance. as dual oral therapy in combination with:- metformin when diet and exercise plus metformin alone do not provide adequate glycaemic control. - a sulphonylurea when diet and exercise plus maximal tolerated dose of a sulphonylurea alone do not provide adequate glycaemic control and when metformin is inappropriate due to contraindications or intolerance. - a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. a thiazolidinedione) when use of a pparγ agonist is appropriate and when diet and exercise plus the pparγ agonist alone do not provide adequate glycaemic control. as triple oral therapy in combination with:- a sulphonylurea and metformin when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. - a pparγ agonist and metformin when use of a pparγ agonist is appropriate and when diet and exercise plus dual therapy with these medicinal products do not provide adequate glycaemic control. sitagliptin sun is also indicated as add-on to insulin (with or without metformin) when diet and exercise plus stable dose of insulin do not provide adequate glycaemic control.

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

amivas ireland ltd - artesunate - malarija - antiprotozoals - artesunate amivas is indicated for the initial treatment of severe malaria in adults and children. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje противомалярийных posrednika.

Բոսնիա և Հերցեգովինա - խորվաթերեն - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

medicopharmacia d.o.o. sarajevo - ibandronska kiselina - film tableta - 50 mg/1 tableta - 1 film tableta sadrži: 50 mg ibandronska kiselina (u obliku ibandronatnatrijum, monohidrata)

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

ptc therapeutics international limited - eladocagene exuparvovec - metabolizam aminokiselina, urođene pogreške - enzymes, other alimentary tract and metabolism products - upstaza is indicated for the treatment of patients aged 18 months and older with a clinical, molecular, and genetically confirmed diagnosis of aromatic l amino acid decarboxylase (aadc) deficiency with a severe phenotype (see section 5.

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

sanofi b.v. - sutimlimab - hemolysis; anemia, hemolytic, autoimmune - imunosupresivi - enjaymo is indicated for the treatment of haemolytic anaemia in adult patients with cold agglutinin disease (cad).

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

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.

Բոսնիա և Հերցեգովինա - խորվաթերեն - Agencija za lijekove i medicinska sredstva Bosne i Hercegovine (Агенција за лијекове и медицинска средства Босне и Херцеговине)

roche d.o.o.roche ltd. - risdiplam - prašak za oralnu otopinu - 0,75 mg/1 ml - 1 bočica sa 2 g praška za oralnu otopinu sadrži 60 mg risdiplama (1 ml rekonstituirane otopine sadrži 0,75 mg risdiplama)

Եվրոպական Միություն - խորվաթերեն - EMA (European Medicines Agency)

eli lilly nederland b.v. - mirikizumab - kolitis, ulcerativni - imunosupresivi - omvoh is indicated for the treatment of adult patients with moderately to severely active ulcerative colitis who have had an inadequate response with, lost response to, or were intolerant to either conventional therapy or a biologic treatment.

Չեռնոգորիա - խորվաթերեն - CInMED-Institut za ljekove i medicinska sredstva Crne Gore

dio stranog druŠtva "krka d.d. novo mesto" slovenija - predstavniŠtvo podgorica - eksemestan - film tableta - 25mg