Endo Adverse Event Reporting

Welcome to Endo Adverse Event Reporting

If you experience an adverse event from one of our drugs, tell your healthcare provider and then report it to us.

Please report as much relevant information as possible. At a minimum, you will need to provide the following:

• Initials, sex, age, or date of birth of the person who experienced the adverse event.
• The contact information of the person reporting the adverse event.
• A description of the adverse event, which can include the signs and symptoms experienced by the person.
• The name of the Endo product.

Please note that if you are involved in an Endo-sponsored clinical trial, adverse events should be reported to your study site.