Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

navidea biopharmaceuticals europe ltd. - tilmanocept - radionuklidno slikanje - otkrivanje tumora, dijagnostičkih радиофармпрепаратов - ovaj je lijek samo za dijagnostičku uporabu. lymphoseek меченных radioaktivnih izotopa je namijenjen za otkrivanje i интраоперационной vizualizacije psi limfnih čvorova, дренирующих primarni tumor kod odraslih pacijenata s rakom dojke, melanomom, ili lokalizirani karcinom pločastih stanica usne šupljine. vanjske vizualizacije i интраоперационной procjene može se izvesti uz pomoć uređaja detekcije gama .

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - monohidrat Имипенем, циластатин natrija, relebactam monohidrat - Грамотрицательные bakterijske infekcije - carbapenems, antibacterials for systemic use, - recarbrio is indicated for:- treatment of hospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap), in adults (see sections 4. 4 i 5. - treatment of bacteraemia that occurs in association with, or is suspected to be associated with hap or vap, in adults. - treatment of infections due to aerobic gram-negative organisms in adults with limited treatment options (see sections 4. 2, 4. 4 i 5. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

tesaro bio netherlands b.v. - rolapitant - vomiting; nausea; cancer - Противорвотные i antinauseants, - sprječavanje odgođene mučnine i povraćanja povezanih s visoko i umjereno emetogenom kemoterapijom raka kod odraslih osoba. varuby dao u sastav kombinirane terapije.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

uniqure biopharma b.v.  - alipogen tiparvovec - hyperlipoproteinemia type i - sredstva za modifikaciju lipida - glybera je indicirana za odrasle pacijente s dijagnozom obiteljskog deficita lipaze lipoproteina (lpld) i koji pate od teških ili višestrukih napada pankreatitisa unatoč ograničenjima prehrambenih masnoća. dijagnoza lpld mora biti potvrđena genetskim testiranjem. oznaka je ograničena na pacijente s detektabilnim razinama lpl proteina.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - sulfat ceftolozane, тазобактам natrija - bakterijske infekcije - antibakterijski lijekovi za sistemsku primjenu, - zerbaxa is indicated for the treatment of the following infections in adults:complicated intra abdominal infections;acute pyelonephritis;complicated urinary tract infections;hospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap). treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

sun pharmaceutical industries europe b.v. - sitagliptin fumarate, metformin hydrochloride - dijabetes mellitus, tip 2 - lijekovi koji se koriste u dijabetesu - for adult patients with type 2 diabetes mellitus:sitagliptin/metformin hydrochloride sun is indicated as an adjunct to diet and exercise to improve glycaemic control in patients inadequately controlled on their maximal tolerated dose of metformin alone or those already being treated with the combination of sitagliptin and metformin. sitagliptin/metformin hydrochloride sun is indicated in combination with a sulphonylurea (i. trostruki kombinovanu terapiju) kao dodatak prehrani i vježbe kod pacijenata, nedovoljno kontroliranim o njihovo maksimalno переносимой doze метформина i sulfonilurejom. sitagliptin/metformin hydrochloride sun is indicated as triple combination therapy with a peroxisome proliferator-activated receptor gamma (pparγ) agonist (i. , a thiazolidinedione) as an adjunct to diet and exercise in patients inadequately controlled on their maximal tolerated dose of metformin and a pparγ agonist. sitagliptin/metformin hydrochloride sun is also indicated as add-on to insulin (i. , triple combination therapy) as an adjunct to diet and exercise to improve glycaemic control in patients when stable dose of insulin and metformin alone do not provide adequate glycaemic control.

Korasia - Kroeshia - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

intervet international b.v., podružnica u republici hrvatskoj, heinzelova 62a, 10000 zagreb, hrvatska - živi, atenuirani virus zaraznog bronhitisa (soj 4-91) ≥3,6 log10 eid50 - liofilizat za resuspendiranje - kokoši

Umoja wa Ulaya - Kroeshia - 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.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

sanofi b.v. - clofarabine - prekursorska stanica limfoblastične leukemije-limfom - antineoplastična sredstva - liječenje akutne limfoblastične leukemije (all) u pedijatrijskih bolesnika koji imaju relapsed ili su vatrostalne nakon najmanje dva prethodnog režima i gdje nema drugih mogućnost liječenja predviđa da će rezultirati trajan odgovor. sigurnost i učinkovitost procijenjeni su u ispitivanjima bolesnika ≤ 21 godina kod početne dijagnoze.

Umoja wa Ulaya - Kroeshia - EMA (European Medicines Agency)

merck sharp & dohme b.v. - ertugliflozin l-pyroglutamic acid, metformin hydrochloride - dijabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - segluromet is indicated in adults aged 18 years and older with type 2 diabetes mellitus as an adjunct to diet and exercise to improve glycaemic control:in patients not adequately controlled on their maximally tolerated dose of metformin alonein patients on their maximally tolerated doses of metformin in addition to other medicinal products for the treatment of diabetesin patients already being treated with the combination of ertugliflozin and metformin as separate tablets.