União Europeia - esloveno - EMA (European Medicines Agency)

mylan ireland limited - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastična sredstva - azacitidine mylan is indicated for the treatment of adult patients who are not eligible for haematopoietic stem cell transplantation (hsct) with:intermediate 2 and high risk myelodysplastic syndromes (mds) according to the international prognostic scoring system (ipss),chronic myelomonocytic leukaemia (cmml) with 10 29% marrow blasts without myeloproliferative disorder,acute myeloid leukaemia (aml) with 20 30% blasts and multi lineage dysplasia, according to world health organisation (who) classification,aml with > 30% marrow blasts according to the who classification.

União Europeia - esloveno - EMA (European Medicines Agency)

accord healthcare s.l.u. - azacitidin - myelodysplastic syndromes; leukemia, myelomonocytic, chronic; leukemia, myeloid, acute - antineoplastična sredstva - azacitidine soglasju je indicirano za zdravljenje odraslih bolnikih, ki niso primerni za haematopoietic stem cell presaditev (hsct) z:- intermediate-2 in visokim tveganjem myelodysplastic sindromov (mds) je v skladu z mednarodnim prognostic sistem točkovanja (ipss),- kronično myelomonocytic levkemijo (cmml) z 10-29 % mozga eksplozije brez myeloproliferative motnje,- akutno mieloično levkemijo (aml) z 20-30 % blastov in multi-rodbine displazija, po ocenah svetovne zdravstvene organizacije (who), in razvrščanje,- aml s >30% mozgu eksplozije glede na razvrstitev, ki.

União Europeia - esloveno - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - karcinom, pljučni pljuč - antineoplastična sredstva - rybrevant as monotherapy is indicated for treatment of adult patients with locally advanced or metastatic non-small cell lung cancer (nsclc) with activating epidermal growth factor receptor (egfr) exon 20 insertion mutations, after failure of platinum-based chemotherapy.

União Europeia - esloveno - EMA (European Medicines Agency)

pfizer europe ma eeig - pneumococcal polysaccharide serotype 1, pneumococcal polysaccharide serotype 3, pneumococcal polysaccharide serotype 4, pneumococcal polysaccharide serotype 5, pneumococcal polysaccharide serotype 6a, pneumococcal polysaccharide serotype 6b, pneumococcal polysaccharide serotype 7f, pneumococcal polysaccharide serotype 8, pneumococcal polysaccharide serotype 9v, pneumococcal polysaccharide serotype 10a, pneumococcal polysaccharide serotype 11a, pneumococcal polysaccharide serotype 12f, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 15b, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 22f, pneumococcal polysaccharide serotype 23f, pneumococcal polysaccharide serotype 33f - pnevmokokne okužbe - cepiva - active immunisation for the prevention of invasive disease and pneumonia caused by streptococcus pneumoniae in individuals 18 years of age and older. glej poglavja 4. 4 in 5. 1 za informacije o zaščiti proti specifičnim pnevmokoknim serotipom. apexxnar should be used in accordance with official recommendations. .

Eslovênia - esloveno - JAZMP (Javna agencija RS za zdravila in medicinske pripomočke)

levonorgestrel - intrauterini dostavni sistem - levonorgestrel 52 mg / 1 sistem - plastični maternični vložki z dodatkom progestogenov

União Europeia - esloveno - EMA (European Medicines Agency)

sanofi b.v. - laronidaza - mucopolisaharidoza i - drugi zdravljene bolezni prebavil in presnove izdelki, - aldurazyme je označen za dolgoročno encim nadomestno zdravljenje pri bolnikih s potrjeno diagnozo mucopolysaccharidosis i (mps i; alfa-l-iduronidase pomanjkljivost) za zdravljenje nonneurological manifestacije bolezni.

União Europeia - esloveno - EMA (European Medicines Agency)

pharmaxis europe limited - manitol - cistična fibroza - kašelj in hladni pripravki - bronchitol je primerna za zdravljenje cistična fibroza (cf) pri odraslih, starih 18 let in več kot dodatna terapija za najboljši standard oskrbe.

União Europeia - esloveno - EMA (European Medicines Agency)

neuraxpharm pharmaceuticals s.l. - midazolam - epilepsija - psiholeptiki - zdravljenje dolgotrajno, akutno, krčevito zasegi pri dojenčkih, malčkih, otrocih in mladostnikih (od treh mesecev do manj kot 18 let). buccolam se sme uporabiti le starši / skrbniki, kjer bolnik je bila diagnosticirana, da imajo epilepsijo. za dojenčke med tri in šest mesecev starosti, zdravljenje mora biti v bolnišnici nastavitev pri spremljanju, je mogoče, in reanimacijo oprema je na voljo.

União Europeia - esloveno - EMA (European Medicines Agency)

mylan dura gmbh - clopidogrel (as hydrochloride) - peripheral vascular diseases; stroke; myocardial infarction - antitrombotična sredstva - clopidogrel je navedeno pri odraslih za preprečevanje atherothrombotic dogodkov v:bolnike, ki trpijo za miokardni infarkt (od nekaj dni do manj kot 35 dni), ischaemic kap (od 7 dni do manj kot 6 mesecev) ali sedež periferne arterijske bolezni.

União Europeia - esloveno - EMA (European Medicines Agency)

teva pharma b.v. - clopidogrel (as hydrochloride) - peripheral vascular diseases; acute coronary syndrome; myocardial infarction; stroke - antitrombotična sredstva - clopidogrel je navedeno pri odraslih za preprečevanje atherothrombotic dogodkov v:bolnike, ki trpijo za miokardni infarkt (od nekaj dni do manj kot 35 dni), ischaemic kap (od 7 dni do manj kot 6 mesecev) ali sedež periferne arterijske bolezni. patients suffering from acute coronary syndrome:non-st segment elevation acute coronary syndrome (unstable angina or non-q-wave myocardial infarction), including patients undergoing a stent placement following percutaneous coronary intervention, in combination with acetylsalicylic acid (asa). st segmentu višinskih akutni miokardni infarkt, v kombinaciji s asa v medicinsko zdravljenih bolnikih, ki izpolnjujejo pogoje za thrombolytic terapija. za nadaljnje informacije, prosimo, preberite razdelek 5.