All information you are about to see is related to a specific selected market, including the products’ portfolio, and therefore comply to different local regulations.

Pharmacovigilance

What is Pharmacovigilance?

Pharmacovigilance is a set of activities aimed at continuously evaluating all information relating to the safety of drugs, medical devices and all the products that Fidia has on the market.
In line with this general definition, the main objectives of Fidia’s Pharmacovigilance are:

To prevent any harm in humans using Fidia’s products;
To promote the safe and effective use of products, in particular, promptly communicating information on the safety of the products to patients, health professionals and the public.

What is an adverse event?

An adverse event is any undesirable experience associated with the use of a medical product in a patient.

What to do in case of an adverse event?

The reporting of adverse event is important to allow a continuous monitoring of its benefit / risk balance. Each country has laws governing the reporting of adverse event, therefore, if you experience adverse event with the use of any of our products, please contact your Physician.

How to report an Adverse Event to Fidia

If you are a healthcare professional or a patient seeking to report an adverse event, please call 1-866-749-2542 (option 3) to reach our Pharmacovigilance Team.