REPORT A SUSPECTED ADVERSE EVENT

Our Privacy Notice outlines how ViiV Healthcare handles the processing of personal information when dealing with your enquiry, complaint or adverse event report.

Thank you for choosing to report a suspected adverse event​

For Belgium: Please report adverse events to the Belgian Centre for Pharmacovigilance for medicines for Human use of the Federal Agency for Medicines and Health Products via adr@afmps.be or via www.notifieruneffetindesirable.be or to ViiV HealthCare srl/bv 010/ 85 65 00.

For Luxembourg: Please report adverse events to the Centre Régional de Pharmacovigilance de Nancy or Division de la pharmacie et des médicaments de la Direction de la santé via www.guichet.lu/pharmacovigilance or to ViiV Healthcare srl/bv +32 10 85 65 00.

PM-BE-HVX-WCNT-230001 - June 2023