エストニア - エストニア語 - Ravimiamet

g.l. pharma gmbh - pantoprasool - gastroresistentne tablett - 40mg 20tk; 40mg 28tk; 40mg 7tk; 40mg 50tk; 40mg 30tk; 40mg 60tk; 40mg 56tk

エストニア - エストニア語 - Ravimiamet

pfizer enterprises sarl - karboplatiin - infusioonilahuse kontsentraat - 10mg 1ml 15ml 1tk; 10mg 1ml 5ml 1tk; 10mg 1ml 45ml 1tk

エストニア - エストニア語 - Ravimiamet

krka d.d. novo mesto - luuderohuleht - siirup - 7mg 1ml 150ml 1tk

エストニア - エストニア語 - Ravimiamet

zentiva k.s. - sorafeniib - õhukese polümeerikattega tablett - 200mg 112tk

欧州連合 - エストニア語 - EMA (European Medicines Agency)

ucb pharma s.a.   - fenfluramine hydrochloride - epilepsies, myoclonic - antiepileptics, - treatment of seizures associated with dravet syndrome as an add-on therapy to other antiepileptic medicines for patients 2 years of age and older. fintepla is indicated for the treatment of seizures associated with dravet syndrome and lennox-gastaut syndrome as an add-on therapy to other anti-epileptic medicines for patients 2 years of age and older.

エストニア - エストニア語 - Ravimiamet

lv system service sia - sorafeniib - õhukese polümeerikattega tablett - 200mg 112tk

欧州連合 - エストニア語 - EMA (European Medicines Agency)

accord healthcare s.l.u. - sorafenib tosilate - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastilised ained - hepatocellular carcinomasorafenib accord is indicated for the treatment of hepatocellular carcinoma (see section 5. renal cell carcinomasorafenib accord is indicated for the treatment of patients with advanced renal cell carcinoma who have failed prior interferon-alpha or interleukin-2 based therapy or are considered unsuitable for such therapy.

欧州連合 - エストニア語 - EMA (European Medicines Agency)

pierre fabre medicament - tabelecleucel - lymphoproliferative disorders - ebvallo is indicated as monotherapy for treatment of adult and paediatric patients 2 years of age and older with relapsed or refractory epstein-barr virus positive post-transplant lymphoproliferative disease (ebv+ ptld) who have received at least one prior therapy. for solid organ transplant patients, prior therapy includes chemotherapy unless chemotherapy is inappropriate.

欧州連合 - エストニア語 - EMA (European Medicines Agency)

bayer ag - sorafeniib - carcinoma, hepatocellular; carcinoma, renal cell - antineoplastilised ained - hepatotsellulaarne carcinomanexavar on näidustatud ravi hepatotsellulaarne kartsinoom. neeru-cell carcinomanexavar on näidustatud patsientide raviks kaugelearenenud neerurakuline vähk, kes ei ole suutnud enne interferoon-alfa või interleukiin-2 põhinev ravi või peetakse sobi selline ravi. liigendatud kilpnäärme carcinomanexavar on näidustatud patsientide ravi järk-järguline, lokaalselt kaugelearenenud või metastaatilise, liigendatud (papillary/follikulaarne/hürthle cell) kilpnäärme kartsinoom, tulekindlad, et radioaktiivse joodi.

欧州連合 - エストニア語 - EMA (European Medicines Agency)

glaxosmithkline biologicals s.a. - split gripiviirus, inaktiveeritud, mis sisaldab antigeeni: a / vietnam / 1194/2004 (h5n1) nagu tüvi (nibrg-14) - influenza, human; immunization; disease outbreaks - vaktsiinid - aktiivne immuniseerimine gripiviiruse a viiruse h5n1 alatüübi vastu. see näidustus põhineb immunogenicity andmeid tervisliku teemasid, alates vanusest 18 aastat aastast pärast manustamist kaks annust vaktsiini, mis on valmistatud a/vietnam/1194/2004 nibrg-14 (h5n1) (vt lõik 5. prepandemic gripi vaktsiin (h5n1) (split virion, inaktiveeritud, adjuvanted) glaxosmithkline biologicals 3. 75 µg tuleks kasutada vastavalt euroopa liidu arendus.