Report an Adverse
Event/Product Complaint

Purdue Pharma routinely collects and analyzes safety information on our products, including reports from healthcare professionals and patients about adverse events and product complaints. We submit safety reports as appropriate to the U.S. Food and Drug Administration (FDA), which reviews these reports and, when necessary, takes steps to alert healthcare professionals of emerging safety concerns.

This process helps to ensure that healthcare professionals have up-to-date information, so you can make informed decisions when prescribing or recommending a Purdue product.

The prescription and illicit opioid abuse crisis is a multifaceted public health challenge, and as a manufacturer of prescription opioids, we have a responsibility to join the fight. At Purdue we are committed to lead our industry in helping address our nation's prescription and illicit opioid abuse crisis.

There is more to come – as we continue to work with partners and experts to deliver solutions. Below you will find additional information about our efforts.

Read our open letter about the opioid crisis.