Europska Unija - hrvatski - 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.

Europska Unija - hrvatski - EMA (European Medicines Agency)

octapharma ab - simoktookog alfa - hemofilija a - antihemorrhagics - liječenje i profilaksu krvarenja u bolesnika s hemofilijom a (nedostatak kongenitalnog faktora viii). vihuma može se koristiti za sve dobne skupine.

Europska Unija - hrvatski - EMA (European Medicines Agency)

swedish orphan biovitrum international ab - nitisinone - tyrosinemias - drugi gastrointestinalni trakt i metabolizam, lijekovi, - hereditary tyrosinemia type 1 (ht 1)orfadin is indicated for the treatment of adult and paediatric (in any age range) patients with confirmed diagnosis of hereditary tyrosinemia type 1 (ht 1) in combination with dietary restriction of tyrosine and phenylalanine. alkaptonuria (aku)orfadin is indicated for the treatment of adult patients with alkaptonuria (aku).

Europska Unija - hrvatski - EMA (European Medicines Agency)

eisai gmbh - Эрибулин - breast neoplasms; liposarcoma - antineoplastična sredstva - halavenova monoterapija je indicirana za liječenje bolesnika s lokalno naprednim ili metastatskim karcinomom dojke koji su napredovali nakon najmanje jednog kemoterapijskog režima za naprednu bolest (vidjeti odjeljak 5. prije terapije trebalo je uključiti antraciklin i taksan osim ako pacijenti nisu prikladni za ove tretmane. halaven indiciran za liječenje odraslih bolesnika s operirati липосаркома, koji je dobio do антрациклин-sadrži terapije (ako je neupotrebljiv) za održao ili метастатического bolesti (vidi odjeljak 5.

Europska Unija - hrvatski - EMA (European Medicines Agency)

astrazeneca ab - acalabrutinib - leukemija, limfocitna, kronična, b-stanica - antineoplastic agents, protein kinase inhibitors, - calquence as monotherapy or in combination with obinutuzumab is indicated for the treatment of adult patients with previously untreated chronic lymphocytic leukaemia (cll). calquence as monotherapy is indicated for the treatment of adult patients with chronic lymphocytic leukaemia (cll) who have received at least one prior therapy.

Europska Unija - hrvatski - EMA (European Medicines Agency)

astrazeneca ab - tezepelumab - astma - lijekovi za opstruktivne plućne bolesti dišnih putova, - tezspire is indicated as an add-on maintenance treatment in adults and adolescents 12 years and older with severe asthma who are inadequately controlled despite high dose inhaled corticosteroids plus another medicinal product for maintenance treatment.

Europska Unija - hrvatski - EMA (European Medicines Agency)

astrazeneca ab - fulvestrant od - neoplazme dojki - endokrini terapija, anti-estrogeni - faslodex is indicated , as monotherapy for the treatment of estrogen receptor positive, locally advanced or metastatic breast cancer in postmenopausal women:, , not previously treated with endocrine therapy, or, with disease relapse on or after adjuvant antiestrogen therapy, or disease progression on antiestrogen therapy. , , , in combination with palbociclib for the treatment of hormone receptor (hr)-positive, human epidermal growth factor receptor 2 (her2)-negative locally advanced or metastatic breast cancer in women who have received prior endocrine therapy. u pre - ili perimenopauzi, u sveobuhvatnoj liječenju s palbociclib treba kombinirati s luteinizirajućeg hormona releasing hormon (lhrh) agonist.

Europska Unija - hrvatski - EMA (European Medicines Agency)

merck sharp & dohme b.v.  - sulfat ceftolozane, тазобактам natrija - bakterijske infekcije - antibakterijski lijekovi za sistemsku primjenu, - zerbaxa is indicated for the treatment of the following infections in adults:complicated intra abdominal infections;acute pyelonephritis;complicated urinary tract infections;hospital-acquired pneumonia (hap), including ventilator associated pneumonia (vap). treba uzeti u obzir formalne preporuke za odgovarajuće korištenje antibakterijskih posrednika.

Europska Unija - hrvatski - EMA (European Medicines Agency)

pfizer ireland pharmaceuticals - fosamil цефтаролин - community-acquired infections; skin diseases, infectious; pneumonia - antibakterijski lijekovi za sistemsku primjenu, - zinforo is indicated for the treatment of the following infections in neonates, infants, children, adolescents and adults: , complicated skin and soft tissue infections (cssti), community-acquired pneumonia (cap) , consideration should be given to official guidance on the appropriate use of antibacterial agents.

Hrvatska - hrvatski - HALMED (Agencija za lijekove i medicinske proizvode)

sedana medical ab, vendevägen 89, danderyd, Švedska - izofluran - para inhalata, tekućina - urbroj: izofuran 100% v/v