This site is intended for healthcare professionals registered within the Republic of Ireland. If you are a member of the public, please click here.
Resources and Training
Welcome to the Resources and Training page. This is where you will find more information about resources and training relating to both Novartis products and therapy areas and further details on how to register for them.
Reporting of side effects
Reporting suspected adverse reactions after authorisation of the medicinal product is important. It allows continued monitoring of the benefit/risk profile of the medicinal product. All suspected adverse reactions should be reported to HPRA Pharmacovigilance, website www.hpra.ie. Adverse events can also be reported to Novartis preferably at www.novartis.com/report, by emailing [email protected] or by calling (01) 2080 612.
