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Podcast 1
Podcast 2
Podcast 3
Below is a recent Cardiology talk in the area of Hyperlipidaemia
Update on hyperlipidaemia for GPs, Practice Nurses & HCP's - Prof Tom Brett
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.
