Radiopharmaceutical Adverse Events and Product Defects reporting

All serious adverse events should always be reported via the MHRA and CHM (Commission on Human Medicines) portals:
 
YELLOW CARDS:  for serious pharmaceutical adverse events; see
http://www.mhra.gov.uk/Safetyinformation/Reportingsafetyproblems/Reporting
suspectedadversedrugreactions/index.htm
 
BLUE CARDS: for medical devices adverse incidents; see
http://www.mhra.gov.uk/Safetyinformation/Reportingsafetyproblems/Devices/index.htm
 
BNMS professional-led database for non-critical adverse events and product defects,  can be found here:
 
 http://www.bnms.org.uk/adverse-event/defect-reporting/adverse-event-reporting-information.html