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The UPGx consortium received a grant of 14.5 million euros for the project. \u201cHorizon 2020\u201d is the largest research and innovation program of the European Union and aims to promote innovation and scientific excellence in Europe.<\/p>\n [\/et_pb_text][\/et_pb_column][et_pb_column type=”1_2″ _builder_version=”4.22.1″ _module_preset=”default” global_colors_info=”{}”][et_pb_image src=”https:\/\/pgxperts.com\/wp-content\/uploads\/2023\/09\/DNA_Medikamentenpass_Thumbnail_2.jpg” title_text=”DNA_Medikamentenpass_Thumbnail_2″ force_fullwidth=”on” _builder_version=”4.22.1″ _module_preset=”default” global_colors_info=”{}”][\/et_pb_image][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.26.0″ _module_preset=”default” custom_padding=”0px|||||” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.26.0″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_font_size=”18px” text_font_size_tablet=”17px” text_font_size_phone=”16px” text_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]The results of the study underline the importance of pharmacogenetic analysis for the prevention of adverse drug reactions and show that individualised medication based on the patient\u2019s genetic predisposition leads to better treatment outcomes. For PGXperts, this confirms the importance of our work and encourages us to continue our development efforts.[\/et_pb_text][\/et_pb_column][\/et_pb_row][et_pb_row _builder_version=”4.25.2″ _module_preset=”default” custom_margin=”|auto|0px|auto||” custom_padding=”0px||0px||false|false” global_colors_info=”{}”][et_pb_column type=”4_4″ _builder_version=”4.25.2″ _module_preset=”default” global_colors_info=”{}”][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” header_2_font=”|700|||||||” header_2_text_color=”#2495D0″ header_2_font_size=”18px” custom_margin=”||5px||false|false” custom_margin_tablet=”||5px||false|false” custom_margin_phone=”||10px||false|false” custom_margin_last_edited=”on|phone” custom_padding=”||0px|||” header_2_font_size_tablet=”17px” header_2_font_size_phone=”16px” header_2_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n [\/et_pb_text][et_pb_text _builder_version=”4.26.0″ _module_preset=”default” text_font_size=”18px” text_font_size_tablet=”17px” text_font_size_phone=”16px” text_font_size_last_edited=”on|phone” locked=”off” global_colors_info=”{}”]<\/p>\n With PGXperts InteractionCheck, interaction risks between drugs, active ingredients, foods and lifestyle habits as well as genetic variations can be identified in less than 1 minute. Interactions are clearly classified according to their severity and described in detail. The clear presentation of genetic interaction risks allows rapid identification of patients who could benefit from pharmacogenetic analysis. The InteractionCheck is available as a web application and for Android and iOS devices. It can thus be used both as an inpatient tool and on the road, for example, during home visits or emergency interventions.<\/span><\/p>\n For more information about the PGXperts InteractionCheck, please visit: www.pgxperts.com <\/a><\/p>\nPGXperts InteractionCheck – individualised medication with pharmacogenetic<\/h2>\n