EMA conferma la sospensione dell’AIC di tutti i medicinali a base di ranitidina nell’UE
Italiano
Mon, 21 Sep 2020 00:00:00 -0400
Three of the recalls, which BD announced on Aug. 4, 2020, have been designated as Class I recalls by the U.S. Food and Drug Administration (FDA), which means that FDA has determined that there is a reasonable probability that the use of the product will cause serious adverse health consequences or d
Summary of opinion: Gamifant,emapalumab, 23/07/2020, Negative
Summary of opinion: Yervoy,ipilimumab, 17/09/2020, Positive
Summary of opinion: Zejula,niraparib, 17/09/2020, Positive
Summary of opinion: Obiltoxaximab SFL,obiltoxaximab, 17/09/2020, Positive
Summary of opinion: Lynparza,olaparib, 17/09/2020, Positive
Summary of opinion: Orfadin,nitisinone, 17/09/2020, Positive
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