Europska Unija - hrvatski - EMA (European Medicines Agency)

eco animal health europe limited - tylvalosin - Противоинфекционные za sistemsku upotrebu antibakterijski lijekovi za sistemsku upotrebu makrolidi - pheasants; chicken; turkeys; pigs - pigstreatment i methaphylaxis svinja энзоотической upale pluća;liječenje svinjske пролиферативной энтеропатии (ileitis);liječenje i methaphylaxis dizenterija svinja. chickenstreatment i methaphylaxis respiratorne bolesti povezanih s галисептикум микоплазмоза kod pilića. pheasantstreatment respiratorne bolesti povezanih s галисептикум микоплазмы . turkeystreatment respiratorne bolesti povezanih s tylvalosin osjetljivih sojeva ornithobacterium rhinotracheale u purana.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

dr. theiss naturwaren gmbh, michelinstrasse 10, homburg, njemačka - biljni pripravak gavezove zeleni (0,5 - 0,7:1) koji se sastoji od 40% tekućeg ekstrakta gavezove zeleni (1,2 - 1,5:1), ekstrakcijsko otapalo: voda i 60% tekućeg ekstrakta iz ostatka tiještenja nakon vodene ekstrakcije gavezove zeleni (0,7 - 1,1:1), ekstrakcijsko otapalo: etanol 30 % (v/v) - krema - urbroj: 1 g kreme sadrži: 0,10 g biljnog pripravka gavezove zeleni (symphytum x uplandicum) (0,5 - 0,7:1), koji se sastoji od: 0,04 g tekućeg ekstrakta iz symphytum x uplandicum herba (gavezova zelen) (1,2 - 1,5:1), ekstrakcijsko otapalo: voda; 0,06 g tekućeg ekstrakta iz ostatka tiještenja nakon vodene ekstrakcije symphytum x uplandicum herba (gavezova zelen) (0,7 - 1,1:1), ekstrakcijsko otapalo: etanol 30 % (v/v).

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

fresenius kabi d.o.o., radnička cesta 37a, zagreb, hrvatska - visoko pročišćeno riblje ulje glicerol pročišćeni fosfatidi iz jaja - emulzija za infuziju - 10% - urbroj: 100 ml emulzije sadrži 10,0 g visoko pročišćenog ribljeg ulja, 2,5 g glicerola i 1,2 g pročišćenih fosfatida iz jaja

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

mark medical d.o.o., zagreb - ortopedski instrumenti

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olympus d.o.o., zagreb - elektrokirurški sustav koji se koristi u kirurgiji glave i vrata

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

olympus d.o.o. avenija većeslav holjevca 40 10000 zagreb -

Europska Unija - hrvatski - EMA (European Medicines Agency)

alexion europe sas - ravulizumab - hemoglobinuria, paroxysmal - selektivni imunosupresivi - paroxysmal nocturnal haemoglobinuria (pnh)ultomiris is indicated in the treatment of adult and paediatric patients with a body weight of 10 kg or above with pnh:- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months (see section 5. atypical haemolytic uremic syndrome (ahus)ultomiris is indicated in the treatment of patients with a body weight of 10 kg or above with ahus who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab (see section 5. generalized myasthenia gravis (gmg)ultomiris is indicated as an add-on to standard therapy for the treatment of adult patients with gmg who are anti-acetylcholine receptor (achr) antibody-positive. neuromyelitis optica spectrum disorder (nmosd)ultomiris is indicated in the treatment of adult patients with nmosd who are anti-aquaporin 4 (aqp4) antibody-positive (see section 5. ultomiris is indicated in the treatment of adult patients with paroxysmal nocturnal haemoglobinuria (pnh):- in patients with haemolysis with clinical symptom(s) indicative of high disease activity. - in patients who are clinically stable after having been treated with eculizumab for at least the past 6 months. ultomiris is indicated in the treatment of adult patients with atypical haemolytic uremic syndrome (ahus) who are complement inhibitor treatment-naïve or have received eculizumab for at least 3 months and have evidence of response to eculizumab.

Europska Unija - hrvatski - EMA (European Medicines Agency)

gilead sciences ireland uc - idelalisib - lymphoma, non-hodgkin; leukemia, lymphocytic, chronic, b-cell - antineoplastic agents, other antineoplastic agents - zydelig is indicated in combination with an anti‑cd20 monoclonal antibody (rituximab or ofatumumab) for the treatment of adult patients with chronic lymphocytic leukaemia (cll):who have received at least one prior therapy, oras first line treatment in the presence of 17p deletion or tp53 mutation in patients who are not eligible for any other therapies. zydelig is indicated as monotherapy for the treatment of adult patients with follicular lymphoma (fl) that is refractory to two prior lines of treatment.

Europska Unija - hrvatski - EMA (European Medicines Agency)

gilead sciences ireland uc - sacituzumab govitecan - breast neoplasms; triple negative breast neoplasms - antineoplastična sredstva - trodelvy as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic triple-negative breast cancer (mtnbc) who have received two or more prior systemic therapies, including at least one of them for advanced disease.

Europska Unija - hrvatski - EMA (European Medicines Agency)

astrazeneca ab - olaparib - neoplazme jajnika - antineoplastična sredstva - jajnika cancerlynparza prikazan kao monoterapija za:podržava liječenje odraslih bolesnika s поздними (figo faze iii i iv) u genima brca1/2-mutirani (зародышевой linije i/ili somatskih) brzorezni epitela jajnika, masterbatch cijevi ili primarni перитонеальный rak, koji u odgovor (potpuno ili djelomično) nakon završetka prve linije na bazi platine kemoterapije. maintenance treatment of adult patients with platinum sensitive relapsed high grade epithelial ovarian, fallopian tube, or primary peritoneal cancer who are in response (complete or partial) to platinum based chemotherapy. lynparza in combination with bevacizumab is indicated for the:maintenance treatment of adult patients with advanced (figo stages iii and iv) high-grade epithelial ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy in combination with bevacizumab and whose cancer is associated with homologous recombination deficiency (hrd) positive status defined by either a brca1/2 mutation and/or genomic instability (see section 5. breast cancerlynparza is indicated as:monotherapy or in combination with endocrine therapy for the adjuvant treatment of adult patients with germline brca1/2-mutations who have her2-negative, high risk early breast cancer previously treated with neoadjuvant or adjuvant chemotherapy (see sections 4. 2 i 5. monotherapy for the treatment of adult patients with germline brca1/2-mutations, who have her2 negative locally advanced or metastatic breast cancer. pacijenti moraju prethodno bile tretirane s антрациклина i таксана u (neo)adjuvantne ili метастатический, ako pacijenti nisu prikladni za tih postupaka (vidi odjeljak 5. pacijenti s receptore hormona (h)-pozitivnog raka dojke treba također razvili ili nakon pre-hormonska terapija, ili se smatraju neprikladnim za endokrine terapije. adenocarcinoma of the pancreaslynparza is indicated as:monotherapy for the maintenance treatment of adult patients with germline brca1/2-mutations who have metastatic adenocarcinoma of the pancreas and have not progressed after a minimum of 16 weeks of platinum treatment within a first-line chemotherapy regimen. prostate cancerlynparza is indicated as:monotherapy for the treatment of adult patients with metastatic castration-resistant prostate cancer (mcrpc) and brca1/2-mutations (germline and/or somatic) who have progressed following prior therapy that included a new hormonal agent. in combination with abiraterone and prednisone or prednisolone for the treatment of adult patients with mcrpc in whom chemotherapy is not clinically indicated (see section 5.