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This is your Novartis Ireland hub where you can access everything you need to support you and your patients in using our products and services. Here you'll find training materials, latest product information, and upcoming events and webinars.

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IE298087-1 | July 2024
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Medical Information Request

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.