Pharmacovigilance

The excellence of our contribution entails competence and sense of responsibility.
Pharmacovigilance plays an important role in collecting and evaluating information on adverse drug reactions. Thus, PLS PHARMA, in compliance with what is legally established, actively and attentively exercises the collection and respective treatment of adverse reactions related to its medicinal products.
Do you wish to report an adverse reaction of a medicinal product from PLS Pharma?
Fill out the form below and click on “Send” .
How is the National Pharmacovigilance System regulated? 
According to Decree-law 242/2002, of the 5th of November. 
What is an adverse drug reaction?
The WHO defines adverse drug reaction as " Any response to a drug which is noxious and unintended, and which occurs at doses normally used in man for prophylaxis, diagnosis, or therapy of disease, or for the modification of physiological function".
How to report an adverse drug reaction for one of PLS Pharma´s medicinal products? 
Contact the health professional that monitors your therapy, or you may do it here directly.

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