European Union - Estonian - EMA (European Medicines Agency)

astellas pharma europe b.v. - gilteritinib dietüülfumaraat - leukeemia, müeloidne, äge - antineoplastilised ained - xospata on näidustatud monotherapy raviks täiskasvanud patsientidel, kes on taastekkinud või tulekindlad ägeda müeloidse leukeemia (aml), mille flt3 mutatsioon.

European Union - Estonian - EMA (European Medicines Agency)

insmed netherlands b.v. - amikacin sulfate - hingamisteede infektsioonid - antibacterials süsteemseks kasutamiseks, - arikayce liposomal is indicated for the treatment of non-tuberculous mycobacterial (ntm) lung infections caused by mycobacterium avium complex (mac) in adults with limited treatment options who do not have cystic fibrosis.

European Union - Estonian - EMA (European Medicines Agency)

roche registration gmbh  - pralsetinib - kartsinoom, mitteväikerakk-kopsu - antineoplastilised ained - gavreto is indicated as monotherapy for the treatment of adult patients with rearranged during transfection (ret) fusion-positive advanced non-small cell lung cancer (nsclc) not previously treated with a ret inhibitor.

European Union - Estonian - EMA (European Medicines Agency)

stemline therapeutics b.v. - elacestrant - rinnanäärmed - endokriinset ravi - orserdu monotherapy is indicated for the treatment of postmenopausal women, and men, with estrogen receptor (er) positive, her2-negative, locally advanced or metastatic breast cancer with an activating esr1 mutation who have disease progression following at least one line of endocrine therapy including a cdk 4/6 inhibitor.

European Union - Estonian - EMA (European Medicines Agency)

daiichi sankyo europe gmbh - quizartinib dihydrochloride - leukeemia, müeloid - antineoplastic agents, protein kinase inhibitors - vanflyta is indicated in combination with standard cytarabine and anthracycline induction and standard cytarabine consolidation chemotherapy, followed by vanflyta single-agent maintenance therapy for adult patients with newly diagnosed acute myeloid leukaemia (aml) that is flt3-itd positive.

European Union - Estonian - EMA (European Medicines Agency)

recordati rare diseases - karglumhape - amino acid metabolism, inborn errors; propionic acidemia - muud alimentary seedetrakti ja ainevahetust tooted, - carbaglu on näidustatud ravi:hyperammonaemia tõttu n-acetylglutamate-synthase esmane puudus;hyperammonaemia tõttu isovaleric acidaemia;hyperammonaemia tõttu methymalonic acidaemia;hyperammonaemia tõttu propioonhappe acidaemia.

Estonia - Estonian - Ravimiamet

aurobindo pharma (malta) limited - piperatsilliin+tasobaktaam - infusioonilahuse pulber - 2000mg+250mg 12tk; 2000mg+250mg 1tk; 2000mg+250mg 10tk

Estonia - Estonian - Ravimiamet

actavis group ptc ehf. - piperatsilliin+tasobaktaam - süste-/infusioonilahuse pulber - 2000mg+250mg 12tk; 2000mg+250mg 1tk

Estonia - Estonian - Ravimiamet

actavis group ptc ehf. - piperatsilliin+tasobaktaam - süste-/infusioonilahuse pulber - 4000mg+500mg 1tk

European Union - Estonian - EMA (European Medicines Agency)

merck sharp & dohme b.v. - peginterferoon alfa-2b - c-hepatiit, krooniline - immunostimulants, - adults (tritherapy)pegintron in combination with ribavirin and boceprevir (tritherapy) is indicated for the treatment of chronic-hepatitis-c (chc) genotype-1 infection in adult patients (18 years of age and older) with compensated liver disease who are previously untreated or who have failed previous therapy. palun vaadake ribavirin ja boceprevir ravimi omaduste kokkuvõtted (smpcs) kui pegintron on kasutada koos nende ravimitega. adults (bitherapy and monotherapy)pegintron is indicated for the treatment of adult patients (18 years of age and older) with chc who are positive for hepatitis-c-virus rna (hcv-rna), including patients with compensated cirrhosis and / or co-infected with clinically stable hiv. pegintron koos ribavirin (bitherapy) on näidustatud ravi chc nakkuse täiskasvanud patsientidel, kes on eelnevalt ravimata, sealhulgas patsientidel, kellel on kliiniliselt stabiilne hiv-nakkus ja täiskasvanud patsientidel, kes on jätnud eelnev ravi interferoon-alfa (pegylated või mitte-pegylated) ja ribavirin kombinatsiooni teraapia või interferoon-alfa monotherapy. interferoon monotherapy, sh pegintron on näidustatud peamiselt juhul, talumatus või vastunäidustus, et ribavirin. palun vaadake ribavirin ravimi omaduste kokkuvõte, kui pegintron on kasutada koos ribavirin. paediatric population (bitherapy)pegintron is indicated in a combination regimen with ribavirin for the treatment of children three years of age and older and adolescents who have chc, previously untreated, without liver decompensation, and who are positive for hcv-rna. kui otsustatakse, et ei ravi edasi lükata, kuni täiskasvanueani, on tähtis arvestada, et kombineeritud ravi tingitud majanduskasvu pidurdumine, mis võib olla pöördumatu mõnedel patsientidel. otsus ravida, tuleb teha iga juhtumi puhul eraldi. palun vaadake ribavirin ravimi omaduste kokkuvõte kapslite või suukaudse lahuse kui pegintron on kasutada koos ribavirin.