ADVERSE EVENT REPORTING


For the UK: 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 Actelion Pharmaceuticals UK Ltd on +44 (0)208 987 3333 or actdrugsafetyuk@its.jnj.com.

 

For IRL: Adverse events should be reported. Reporting forms and information can be found at www.hpra.ie.

Adverse events should also be reported to Actelion Pharmaceuticals UK Ltd on +44 (0)208 987 3333 or actdrugsafetyuk@its.jnj.com.

 

Clinical Trials

Actelion is committed to informing the medical community and the public about its clinical trials.  Click on the link below for more information.