Adverse Events Reporting

Adverse Events Reporting [1]

Adverse Event Reporting:

Suspected Adverse Drug Reactions (side effects) and medication errors may be reported using the Medicines Authority ADR reporting form, which is available online at
http://www.medicinesauthority.gov.mt/adrportal [2] and sent by post or email to; P: Pharmacovigilance Section at Post-Licensing Directorate, Medicines Authority, Sir Temi Zammit
Buildings, Malta Life Sciences Park, San Gwann. SGN 3000. E: [email protected] [3]

Healthcare Professionals may also report any adverse events associated with the use of Novartis products to Novartis Pharma Services Inc., Representative Office, Malta, by phone on +356 21222872, online on https://www.novartis.com/report [4] or by e-mail at [email protected] [5]

Medical Queries:

Medical Information Service

For medical-scientific questions and for information about the products and their indications, please contact [email protected] [6]