Adverse Event Reporting

Reporting suspected adverse drug reactions

The Yellow Card Scheme is run by the Medicines and Healthcare products

Regulatory Agency (MHRA) and Commission on Human Medicines (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.

Adverse events should be reported. Reporting forms and information can be found at

Adverse events should also be reported to Internis on 01271 334 609