US FDA approves updated Novartis Beovu® label, to include additional safety information

  • Novartis worked with US Food and Drug Administration (FDA) to update Beovu (brolucizumab) prescribing information to guide healthcare professionals in their treatment of wet AMD patients1
     
  • The update includes characterization of adverse events, retinal vasculitis and retinal vascular occlusion, as part of the spectrum of intraocular inflammation observed in the HAWK & HARRIER trials and noted in the original prescribing information1
     
  • Novartis has convened a fully dedicated team collaborating with …
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