Reporting suspected adverse drug reactions

The Yellow Card Scheme is run by the Medicines and Healthcare products Regulatory Agency (MHRA) and Commission on Human Medicine (CHM).

The scheme is used to collect information from health professionals and patients on suspected adverse drug reactions (ADRs). The continued success of the Yellow Card Scheme depends on your willingness to report suspected adverse drug reactions.

Both health professionals and patients can submit information through the Yellow Card website.

United Kingdom:
Adverse events should be reported. Reporting forms and information can be found at www.mhra.gov.uk/yellowcard
Adverse events should also be reported to Medical Information at Norgine Pharmaceuticals Ltd on 01895 826606 or MedInfo@norgine.com.

Ireland:
Adverse events should be reported. Reporting forms and information can be found at www.hpra.ie.
Adverse events should also be reported to Medical Information at Norgine Pharmaceuticals Ltd on +44 1895 826606 or MedInfo@norgine.com.