Fusicutan Plus 20 mg/g + 1 mg/g krema ক্রোয়েশিয়া - ক্রোয়েশীয় - HALMED (Agencija za lijekove i medicinske proizvode)

fusicutan plus 20 mg/g + 1 mg/g krema

mibe pharmaceuticals d.o.o., zavrtnica 17, zagreb, hrvatska - fusidatna kiselina hemihidrat, betametazonvalerat - krema - 20 mg/g + 1 mg/g - urbroj: 1 g kreme sadrži 20,4 mg fusidatne kiseline 0,5 h2o (ekvivalentno 20 mg fusidatne kiseline) i 1,214 mg betametazonvalerata (ekvivalentno 1 mg betametazona)

Isaderm 5 mg/g + 1 mg/g, gel za pse ক্রোয়েশিয়া - ক্রোয়েশীয় - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

isaderm 5 mg/g + 1 mg/g, gel za pse

dechra veterinary products a/s, mekuvuj 9, 7171 uldum, danska - fusidatna kiselina; betametazon (u obliku valerata) - gel - kortikosteroidi, kombinacije s antibioticima - pasa

OTOMAX ক্রোয়েশিয়া - ক্রোয়েশীয় - Ministarstvo poljoprivrede, Uprava za Veterinarstvo i sigurnost hrane

otomax

intervet international bv - podružnica u rh, ivana lučića 2a, 10000 zagreb, republika hrvatska - gentamicin u obliku gentamicinsulfata ; betametazon u obliku betametazonvalerata; klotrimazol - kapi za uho, suspenzija - pasa

Yondelis ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

yondelis

pharma mar s.a. - trabectedin - ovarian neoplasms; sarcoma - antineoplastična sredstva - yondelis je indiciran za liječenje bolesnika s naprednim sarkom mekog tkiva, nakon neuspjeha anatraciklinima, i ili nezgodan za primanje tih agenata su. podaci o učinkovitosti temelje se uglavnom na bolesnika s liposarkom i leiomyosarcomom. Йонделис u kombinaciji s пегилированным липосомальным doksorubicin (fpga) indiciran za liječenje pacijenata s relaps платино osjetljivi raka jajnika .

Competact ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

competact

cheplapharm arzneimittel gmbh - pioglitazone, metformin hidroklorid - dijabetes mellitus, tip 2 - lijekovi koji se koriste u dijabetesu - competact is indicated in the treatment of type 2 diabetes mellitus patients, particularly overweight patients, who are unable to achieve sufficient glycaemic control at their maximally tolerated dose of oral metformin alone.

Eucreas ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

eucreas

novartis europharm limited - вилдаглиптин, metformin hidroklorid - dijabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - eucreas is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control.

Evra ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

evra

gedeon richter plc. - norelgestromin, ethinyl estradiol - kontracepcija - spolni hormoni i modulatori genitalnog sustava, - Ženska kontracepcija. evra je namijenjen za žene u fertilnoj dobi. sigurnost i efikasnost je instaliran kod žena u dobi od 18 do 45 godina.

Glubrava ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

glubrava

takeda pharma a/s - метформина hidroklorid пиоглитазона hidroklorid - dijabetes mellitus, tip 2 - lijekovi koji se koriste u dijabetesu - glubrava je indicirana kao druga linija liječenja tipa 2 šećerne bolesti u odraslih bolesnika, osobito prekomjernom tjelesnom težinom, koji ne mogu postići zadovoljavajuću kontrolu glikemije u maksimalno podnošljivoj dozi peroralnim metforminom. nakon početka terapije s пиоглитазоном, pacijenti moraju biti revidiran nakon tri do šest mjeseci, za procjenu adekvatnosti odgovora na liječenje (e. smanjenje pokazatelja hba1c). kod bolesnika koji ne pokazuju adekvatan odgovor treba da se ukine pioglitazone. u svjetlu potencijalnih rizika za dugotrajno liječenje, propisane lijekove treba potvrditi u kasnijim rutinske inspekcije da dobro pioglitazone sprema.

Icandra (previously Vildagliptin / metformin hydrochloride Novartis) ইউরোপীয় ইউনিয়ন - ক্রোয়েশীয় - EMA (European Medicines Agency)

icandra (previously vildagliptin / metformin hydrochloride novartis)

novartis europharm limited - вилдаглиптин, metformin hidroklorid - dijabetes mellitus, tip 2 - drugs used in diabetes, combinations of oral blood glucose lowering drugs - icandra is indicated as an adjunct to diet and exercise to improve glycaemic control in adults with type 2 diabetes mellitus:in patients who are inadequately controlled with metformin hydrochloride alone. in patients who are already being treated with the combination of vildagliptin and metformin hydrochloride, as separate tablets. in combination with other medicinal products for the treatment of diabetes, including insulin, when these do not provide adequate glycaemic control (see sections 4. 4, 4. 5 i 5. 1 za dostupne podatke o različitim kombinacijama).