Pharmacovigilance

Pharmacovigilance is responsible for monitoring the safety of medicines from their development and throughout their life cycle. It performs activities for the detection, assessment, understanding and prevention of adverse events that may occur with the use of medicines.

Any drug has the potential to trigger adverse events, even those involving a long process of development, research and manufacturing under rigorous quality conditions.

Pharmacovigilance is a responsibility shared by healthcare professionals, the pharmaceutical industry, health authorities and patients. The activities carried out by Pharmacovigilance favor the rational and safe use of medicines for the benefit of our health.

Therefore, we invite you to contact us if you have any questions about the safety of our products.

The information provided will be kept confidential.

*Privacy policy for pharmacovigilance and medical information queries