Report Adverse Event

Patient safety is a priority for Helsinn. We are committed to collect, analyse, and react upon any new information about the benefits and risks of our products. If you have information about a side effect or adverse reaction associated with any of our products, please let us know completing the form.

Helsinn is legally required to ensure that adverse events are traceable and available for follow-up. As a result, we must keep information about the reporter (i.e., the person reporting the occurred adverse event) to allow us to contact him/her once we have received the report, unless the reporter has expressly declined any follow-up contact. The personal data that we may collect when you report an adverse event is your: name; contact details (which may include your address, e-mail address, phone number or fax number); profession, and in case of healthcare professionals it may be asked also the clinic/institution name and address. All this information may determine any other further questions you could be asked about when you report an adverse event. It must be eventually defined the relationship between you and the subject of the adverse event.

Adverse events may also be reported to your national Health Authority as applicable according to national legislation.

The data you provide will be processed in full compliance with the applicable data protection laws. For further information please refer to the Pharmacovigilance Data Privacy Policy