Select Your Location

Please confirm your Location to route your request to the responsible local team.

Which INCYTE product does your adverse event relate to?*

Please provide as many details as possible as well as indication.

* Mandatory

Please provide an accurate description of the adverse event, including symptoms, if the medication was interrupted, any other concomitant medication used or any special circumstances (i.e., treatment during pregnancy), along with dates, if available.

* Mandatory


Mandatory Field

Please provide information on the medical history, including any diseases or medical conditions, medical procedures, and medications taken.

* Mandatory




Privacy Policy:

Incyte processes personal information about you, such as your full name, business contact information, specialty, any personal information you will need to provide while submitting an enquiry, reporting an adverse event or reporting a product quality complaint and with your explicit consent, to communicate with you about any type of medical-scientific information or educational material.

Depending on your location, you may have the right to access, delete, restrict, edit, move or object to the use of your personal information. Depending on your location, you also have the right to lodge a complaint with the data protection authority at your place of residence or work.

You can learn more about Incyte’s privacy practices by visiting incyte.com/privacy-policy. By accessing this link, you can learn about the types of personal information we collect, how we use it, whether collection and processing is optional, the sources of the personal information we process, how it is shared, where it is stored or transferred to, how long we keep it and contact information for Incyte, Incyte’s data protection officer and your supervisory authority.

Please contact privacy@incyte.com if you have any questions, concerns or wish to exercise your rights.


* Mandatory

Healthcare professionals are asked to report any suspected adverse reactions via the national reporting system. Please see the details of the national reporting systems in the EU on this link; https://www.ema.europa.eu/en/documents/template-form/qrd-appendix-v-adverse-drug-reaction-reporting-details_en.docx
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