修订日志请参阅本政策末尾的重要提醒,了解重要的监管和法律信息。描述以下是需要事先授权的生物学和非生物学疾病改良的抗毛药(DMARD):tocilizumab(actemra®),adalimumab(humira®),adalimimAb-abab-afzb(abrilada™) P(Hulio®),Adalimumab-Adaz(Hyrimoz®),Adalimumab-aacf(idacio®),adalimumab-ryvk(ymlandi®b-a),adalimumab ry™),英澳,secukinumab(cosentyx®),eTanercept(enbrel®),vedolizumab(entyasstekinizum®mab-srlf(imuldosa™),infrifiximab-dyyb(fiffectra® Ab-Mrkz(Omvohteil®),Umab-aauz(Otulfi®),Ustekinumab-ttwe(Pyzchiva®),英夫利昔单抗(Remicade®),英夫利克斯莫比(Remicade®) N(Simponi®,SimponiAria®),risankizumab-rzaa(Skyrizi®),Deucravacitinib(Sotyktu™),uStekinumab(stelara®),ustekinumab-stba(seqeyma®®®)® ®),Natalizumab-sztn(Tyruko®),Natalizumab(Tysabri®),Etrasimod(Velsipity™),Ustekinumab-auub(Wezlana™),Tofacitinib-rjankinib-rjank®U®,Xeljanz™),Xeljanz™),OzAniMod(Zepos)(Zepos)(Zepos)。 FDA 批准适应症
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