REPORT ADVERSE EVENTS (healthcare professionals in the UK or Ireland)
For the UK, reporting forms and information can be found at yellowcard.mhra.gov.uk. Adverse events in the UK should also be reported to Amicus on 08082346864 or via email to drugsafety@amicusrx.com
For Ireland, adverse events should be reported to the Pharmacovigilance Unit at the Health Products Regulatory Authority (HPRA) at www.hpra.ie. Adverse events in Ireland should also be reported to Amicus on 1800936230 or via email to drugsafety@amicusrx.com

REPORTING OF SIDE EFFECTS (patients and public in the UK or Ireland)
If you experience any side effects, talk to your doctor, pharmacist or nurse. This includes any possible side effects that are not listed in the patient information leaflet in the medication box. In the UK, you can also report side effects directly via the yellow card scheme at: yellowcard.mhra.gov.uk. In Ireland, you can also report side effects directly to the Health Products Regulatory Agency (HPRA) at: www.hpra.ie. By reporting side effects you can help provide more information on the safety of this medicine.