Pharmacovigilance

Pharmacovigilance

Pharmacovigilance is defined as the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other drug-related problems (WHO; 2002). It is the essential tool for the control and monitoring of medicines, as it enables the early detection of possible adverse effects, and also allows the perception of any anomaly in the therapeutic response.

What is an Adverse Event (AE)?

Any unintended medical occurrence (disease, symptom, signal or laboratory test abnormality) in a patient temporarily associated with the use of a pharmaceutical, whether or not having a causal relationship thereto.

The commitment of Pharmed Enterprises, LLC is to provide maximum efficacy and reliability, by potentiating benefits and minimizing possible risks. This implies permanent monitoring of our products both at their development stage and at their commercialization or extended use stage.

In order to report an adverse event or for any concern on safety issues of our medicines, you may contact us, both patients/consumers and healthcare professionals, in the following ways:

 

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