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 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]
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 or by e-mail at [email protected]
Medical Queries:
Medical Information Service
For medical-scientific questions and for information about the products and their indications, please contact [email protected]