What are the adverse events reporting procedures? All Healthcare Professionals are required to follow their country specific legal requirements and local guidelines for the reporting of adverse events. 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 GlaxoSmithKline Pharmaceuticals s.a./n.v. via be.medinfo@gsk.com. UK: Adverse events should be reported. Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/ or search for MHRA Yellowcard in the Google Play or Apple App store. Adverse events should also be reported to GlaxoSmithKline on +44 (0) 800 221 441 or UKSafety@gsk.com. Other countries: Please follow https://www.gsk.com/en-gb/contact-us/report-a-possible-side-effect/ |