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      • This website is for Irish Healthcare Professionals only

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      SmPC

      *Oral tablet.
      †Administer intravenously. Dose may be split as 100 mg and 900 mg on Days 1 and 2 of Cycle 1, respectively. Graphic not to scale. Each cycle is 28 days.


      Dosing overview 

      Dosing overview is available on page 2 and 3 by clicking on download of Dosing and Administration Guide below 

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      Reference: 1. VENCLYXTO® Summary of Product Characteristics, available at www.medicines.ie 

      IE-VNCCLL-220035 | Date of preparation: July 2022

      CLICK HERE FOR FULL VENCLYXTO® (venetoclax) PRESCRIBING INFORMATION
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      Reporting an Adverse Event: Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk balance of the medicinal product. Healthcare professionals are asked to report any suspected adverse reactions via Health Products Regulatory Authority (HPRA) Pharmacovigilance. www.hpra.ie.

       

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      Date of Preparation: July 2022 | IE-ABBV-220078