Adverse Event Reporting:
Physicians, other healthcare providers, and patients are encouraged to voluntarily report adverse events involving drugs or medical devices.
To make a report you can:
- In the US, visit www.fda.gov/medwatch or call 1-800-FDA-1088; or
- For QUTENZA, you may also call 1-877-900-6479 and select option 1, or press zero on your keypad to talk to an operator to direct your call.
Your contact information should only be entered if you wish to receive a response to your inquiry. Any information you care to submit will be governed by our Privacy Statement.