Gastroenterology Hub is intended for healthcare professionals working in the Republic of Ireland only.
From infographics to vignettes and other downloadable materials, explore a range of resources to aid your patient discussions and help your patients better understand their IBD and Entyvio
Adverse Events should be reported to the Pharmacovigilance Unit at the Health Products Regulatory Authority. Reporting forms and information can be found at: www.hpra.ie. Adverse events should also be reported to Takeda at: AE.GBR-IRL@takeda.com.
