I am a healthcare professional in the UK or Ireland
I am a patient who has been prescribed Pombiliti®▼+ Opfolda® in the UK or Ireland
I am not a healthcare professional in the UK or Ireland or a patient prescribed Pombiliti®▼+ Opfolda® in the UK or Ireland
REPORTING ADVERSE EVENTS (healthcare professionals in the UK or Ireland)
Adverse events should be reported.
In the UK, reporting forms and information can be found at yellowcard.mhra.gov.uk. Adverse events should also be reported to Amicus on 0808 234 6864 or via email to drugsafety@amicusrx.com.
In Ireland, reporting forms and information can be found at www.hpra.ie. Adverse events in Ireland should also be reported to Amicus on 1800936230 or via email to drugsafety@amicusrx.com.
REPORTING SIDE EFFECTS (patients and public in the UK or Ireland)
If you get any side effects, talk to your doctor, pharmacist, or nurse. This includes any possible side effects not listed in the Patient Leaflet. You can also report side effects directly through the national reporting system.
In the UK, you can report side effects directly via the yellow card scheme at: yellowcard.mhra.gov.uk. Adverse events should also be reported to Amicus on 0808 234 6864 or via email to drugsafety@amicusrx.com.
In Ireland, you can report side effects directly to the Health Products Regulatory Agency (HPRA) at: www.hpra.ie. Adverse events should also be reported to Amicus on 1800936230 or via email to drugsafety@amicusrx.com.
Amicus will only use your details to contact you about your suspected side effect. By reporting side effects, you can help provide more information on the safety of this medicine.
▼ This medicine is subject to additional monitoring. This will allow quick identification of new safety information. You can help by reporting any side effects you may get. See above for how to report side effects.