Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

bayer animal health gmbh 51368 leverkusen nemčija proizvajalec -

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

intervet international -

Evropska unija - slovenščina - EMA (European Medicines Agency)

acorda therapeutics ireland limited - levodopa - parkinsonova bolezen - anti-parkinsonska zdravila - inbrija je primerna za občasno zdravljenje epizodne motornih nihanja (off epizode) pri odraslih bolnikih s parkinsonovo boleznijo (pd), obdelan z levodopa/dope-decarboxylase zaviralec.

Evropska unija - slovenščina - EMA (European Medicines Agency)

bayer animal health gmbh - florfenicol, terbinafine hidroklorid, mometasone furoate - otologicals, kortikosteroidi in antiinfectives v kombinaciji - psi - za zdravljenje akutnih udarci otitis externa ali akutno exacerbations ponavljajočih se otitis, ki jih povzročajo mešane okužbe dovzetni sevov bakterije občutljive za florfenicol (staphylococcus pseudintermedius) in gliv, občutljiv na terbinafine (malassezia pachydermatis).

Evropska unija - slovenščina - EMA (European Medicines Agency)

mylan ireland limited - sugammadex sodium - neuromuskularna blokada - vsi drugi terapevtski izdelki - reversal of neuromuscular blockade induced by   rocuronium or vecuronium in adults. for the paediatric population: sugammadex is only recommended for routine reversal of rocuronium induced blockade in children and adolescents aged 2 to 17 years.

Evropska unija - slovenščina - EMA (European Medicines Agency)

accord healthcare s.l.u. - teriflunomide - multiplo sklerozo, recidivno-nakazila - imunosupresivi, selektivno imunosupresivi - teriflunomide accord is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Evropska unija - slovenščina - EMA (European Medicines Agency)

sanofi winthrop industrie - teriflunomide - multiple skleroza - selektivni imunosupresivi - aubagio is indicated for the treatment of adult patients and paediatric patients aged 10 years and older with relapsing remitting multiple sclerosis (ms) (please refer to section 5. 1 for important information on the population for which efficacy has been established).

Evropska unija - slovenščina - EMA (European Medicines Agency)

takeda pharma a/s - vedolizumab - colitis, ulcerative; crohn disease - selektivni imunosupresivi - ulcerozni colitisentyvio je indiciran za zdravljenje odraslih bolnikov z zmerno do močno aktivnim ulceroznim kolitisom, ki so imeli neustreznega odziva, izgubil odgovor da, ali so bili nestrpni, da bodisi konvencionalne terapije ali tumor nekroze faktor alfa (tnfa) antagonist. crohnova diseaseentyvio je indiciran za zdravljenje odraslih bolnikov z zmerno do hudo aktivno crohnovo boleznijo, ki so imeli neustreznega odziva, izgubil odgovor da, ali so bili nestrpni, da bodisi konvencionalne terapije ali tumor nekroze faktor alfa (tnfa) antagonist. pouchitisentyvio is indicated for the treatment of adult patients with moderately to severely active chronic pouchitis, who have undergone proctocolectomy and ileal pouch anal anastomosis for ulcerative colitis, and have had an inadequate response with or lost response to antibiotic therapy.

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

krka, d.d., novo mesto - terbinafin - tableta - terbinafin 250 mg / 1 tableta - terbinafin

Slovenija - slovenščina - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

krka, d.d., novo mesto - terbinafin - tableta - terbinafin 125 mg / 1 tableta - terbinafin