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    • This website is for Irish Healthcare Professionals only

      Report 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 the  Health Products Regulatory Authority (HPRA) Pharmacovigilance www.hpra.ie

      Date of preparation: August 2020 IE-ABBV-200186