Adverse event reporting
Clinigen has a regulatory responsibility to monitor the safety of medicines. This applies to the drugs we market, as well as those used in clinical trials or global access programs.
Are you a healthcare professional?
To report an adverse event or adverse drug reaction, please download and complete the reporting form below. Please return the form to us by fax or e-mail as indicated at the top of the form.
Are you a patient?
If you are a patient, you should always ask your doctor for medical advice about any unwanted effects of treatment. However, you can also report an adverse event or adverse drug reaction using the form below.