Pharmacovigilance is responsible for monitoring the safety of medicines from their development and throughout its life cycle. Performs activities for the detection, assessment, understanding and prevention of adverse events that may occur with the use of drugs.
Any drug has the potential to trigger adverse events, even those involved in a long process of research, development and manufacturing under strict quality conditions.
Pharmacovigilance is a shared responsibility of doctors, the pharmaceutical industry, health authorities and patients. The activities undertaken by the Pharmacovigilance favor the rational and safe use of medicines for the benefit of our health.
Therefore, although the probability of adverse events with the use of our medicines is low, we invite you to contact if you have any doubts about the safety of our products.
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