Europska Unija - hrvatski - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - Šećerna bolest - lijekovi koji se koriste u dijabetesu - diabetes mellitus gdje je potrebno liječenje inzulinom. insuman rapid je pogodan za liječenje hiperglikemijsku komu i ketoacidoza, kao i za postizanje unaprijed, intra - i postoperativna stabilizacija u bolesnika sa šećernom bolešću.

Europska Unija - hrvatski - EMA (European Medicines Agency)

sanofi-aventis deutschland gmbh - insulin human - Šećerna bolest - lijekovi koji se koriste u dijabetesu - diabetes mellitus gdje je potrebno liječenje inzulinom. inzulin ljudske winthrop rapid je pogodan za liječenje hiperglikemijsku komu i ketoacidoza, kao i za postizanje unaprijed, intra - i postoperativna stabilizacija u bolesnika sa šećernom bolešću.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer europe ma eeig - crizotinib - karcinom, ne-malih stanica pluća - antineoplastična sredstva - xalkori as monotherapy is indicated for:the first‑line treatment of adults with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with previously treated anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc)the treatment of adults with ros1‑positive advanced non‑small cell lung cancer (nsclc)the treatment of paediatric patients (age ≥6 to.

Europska Unija - hrvatski - 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 9v, pneumococcal polysaccharide serotype 14, pneumococcal polysaccharide serotype 18c, pneumococcal polysaccharide serotype 19a, pneumococcal polysaccharide serotype 19f, pneumococcal polysaccharide serotype 23f - pneumococcal infections; immunization - cjepiva - aktivna imunizacija za prevenciju invazivnih bolesti, pneumonije i akutnog otitis medija uzrokovana streptococcus pneumoniae kod dojenčadi, djece i adolescenata od 6 tjedana do 17 godina starosti. aktivna imunizacija za sprječavanje invazivnih bolesti uzrokovane streptococcus pneumoniae kod odraslih ≥18 godina i starije. pogledajte odjeljke 4. 4 i 5. 1 za informacije o zaštiti od specifičnih pneumokoknih serotipova. korištenje Превенар 13 mora biti definiran na temelju službenih preporuka, uzimajući u obzir rizik od invazivnih bolesti u različitim dobnim skupinama, leži u osnovi srodne bolesti, kao i varijabilnost серотипа za epidemiologiju u različitim zemljopisnim područjima.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer europe ma eeig - Пегвисомант - acromegaly - hipofiza i hipotalamusni hormoni i analozi - liječenje odraslih bolesnika s akromegalija koji su imali neadekvatan odgovor na operacije i/ili radioterapije, u kojima odgovarajući tretman s pomoću analoga somatostatina ne normalizirati razinu igf-ja sam koncentracije ili ne tolerira. liječenje odraslih bolesnika s akromegalija koji su imali neadekvatan odgovor na operacije i/ili radioterapije, u kojima odgovarajući tretman s pomoću analoga somatostatina ne normalizirati razinu igf -ja sam koncentracije ili ne tolerira.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer ireland pharmaceuticals - avibactam sodium, ceftazidime pentahydrate - pneumonia, bacterial; soft tissue infections; pneumonia; urinary tract infections; gram-negative bacterial infections - antibakterijski lijekovi za sistemsku primjenu, - zavicefta is indicated in adults and paediatric patients aged 3 months and older for the treatment of the following infections:complicated intra-abdominal infection (ciai)complicated urinary tract infection (cuti), including pyelonephritishospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap)treatment of patients with bacteraemia that occurs in association with, or is suspected to be associated with, any of the infections listed above. zavicefta is also indicated for the treatment of infections due to aerobic gram-negative organisms in adults and paediatric patients aged 3 months and older with limited treatment options. treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer europe ma eeig - talazoparib - neoplazme dojki - antineoplastična sredstva - talzenna prikazan kao monoterapija za liječenje odraslih bolesnika s зародышевой linije gena brca1/2 mutacije, koje imaju her2 negativan lokalno-održao ili метастатического raka dojke . patients should have been previously treated with an anthracycline and/or a taxane in the (neo)adjuvant, locally advanced or metastatic setting unless patients were not suitable for these treatments. pacijenti s receptore hormona (h)-pozitivan rak dojke moraju biti obrađene do эндокринно-terapija, ili se smatraju neprikladnim za endokrine terapije na temelju.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer europe ma eeig - lorlatinib - karcinom, ne-malih stanica pluća - antineoplastic agents, protein kinase inhibitors - lorviqua as monotherapy is indicated for the treatment of adult patients with anaplastic lymphoma kinase (alk)‑positive advanced non‑small cell lung cancer (nsclc) previously not treated with an alk inhibitor. lorviqua as monotherapy is indicated for the treatment of adult patients with alk‑positive advanced nsclc whose disease has progressed after:alectinib or ceritinib as the first alk tyrosine kinase inhibitor (tki) therapy; orcrizotinib and at least one other alk tki.

Europska Unija - hrvatski - EMA (European Medicines Agency)

roche registration gmbh  - casirivimab, imdevimab - covid-19 virus infection - imuni serumi i homologna, - ronapreve is indicated for:treatment of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg who do not require supplemental oxygen and who are at increased risk of progressing to severe covid-19 (see section 4. prevention of covid-19 in adults and adolescents aged 12 years and older weighing at least 40 kg (see section 4. the use of ronapreve should take into account information on the activity of ronapreve against viral variants of concern. pogledajte odjeljke 4. 4 i 5.

Europska Unija - hrvatski - EMA (European Medicines Agency)

janssen-cilag international n.v.    - amivantamab - karcinom, ne-malih stanica pluća - 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.