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      Please email your AbbVie representative if you require any further information:

      Tom Dempsey
      Senior Product Specialist
      tom.dempsey@abbvie.com

      DUODOPA PRESCRIBING INFORMATION

       

      IE-DUOD-220039. Date of preparation: November 2022.

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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