Day 2 | Saturday 5 July 2025, 8:30–14:30 CEST
Day 2 – Prostate Cancer
Plenary slides
Prescribing Information
XTANDI is indicated:
AE reporting information
NL: Reporting of suspected adverse reactions
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 national reporting system. Nederland: Nederlands Bijwerkingen Centrum Lareb;
Website: www.lareb.nl
UK: Adverse events should be reported.
Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for ‘MHRA yellow card’ in the Google Play Store or Apple App Store. Adverse events should also be reported to Astellas Pharma Ltd on 0800 783 5018
XTANDI is approved for use in multiple indications for the treatment of adult patients with advanced prostate cancer. Please refer to the specific marketing status for your country/market.
AE, adverse event; AI, artificial intelligence; CRPC, castration-resistant prostate cancer; DDI, drug-drug interaction; mHSPC, metastatic hormone-sensitive prostate cancer; nmHSPC, non-metastatic hormone-sensitive prostate cancer