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Autor:
Hörl WH, Locatelli F, Haag Weber M, Ode M, Roth K, Lhotta K, Loipl J, Huspek M, Gstöttenbauer K, Karagyozova R, Monova D, Shikov P, Yovchev T, Bazeva P, Nenchev N, Charasse C, Bockreiss N, Buhl M, Dellanna F, Dragoun GP, Goller M, Klingbeil A, Knee J, Krallinger R, Menzer T, Perschon G, Toussaint K, Wichelhaus T, Kreuzer K, Brückner D, Leistikow F, Marsen T, Sacherer K, Zimmermann U, Kohnle M, Riedasch M, Brehm K, Vogt J, Morgenroth A, Herrnberger S, Zeh M, Dammerboer C, Hofmann T, Kraemer Guth A, Wilpert J, Pröschild F, Krämer B, Lang R, Zanker B, Lubrich Birkner I, Hemstege M, Jäkel D, Perino S, Riedl B, Assenmacher A, Albertazzi A, Colussi G, Garibotto G, Villa G, Gesualdo L, Triolo G, Cusi D, Gallieni M, Quarello F, Malberti F, Tarchini R, Di Iorio BR, Di Luca M, Bordoni E, Brunori G, Della Grotta F, Fracasso A, Guerrini E, Ragaiolo M, Costanzo R, Teatini U, Dimitrov S, Sikole A, Zabzun M, Janakievska P, Petrovska T, Rzanikoski T, Alceva M, Panova B, Daniewska D, Klatko W, Stryjewski D, Książek A, Kopecka Mechlińska L, Kędzierski P, Nowicki M, Szurkowski M, Papliński M, Trafny R, Kuczera M, Sokalski A, Rydzewski A, Liberek T, Uzar J, Bako GC, Ionescu D, Voiculescu M, Ardelean LC, Pitea IV, Demina L, Borsukov A, Marasaev V, Fedosseev A, Dudar I, Kolesnyk M, Kostynenko T, Kuchma I, Kuriata O, Lesovoy V, Martynyuk L, Nikonenko O., STEFONI, SERGIO
Publikováno v:
Clinical Nephrology. 78:24-32
HX575 was approved in the European Union in August 2007 as the first-ever biosimilar epoetin-α product. The present study extended the safety database on HX575 by monitoring adverse events (AEs) in clinical practice. Hemoglobin (Hb) levels and HX575