PHARMACOVIGILANCE

Introduction: Knowledge about the toxicity derived from the use of medicines generates special attention among patients, prescribers, dispensers and regulatory authorities.
According to the definition of the WHO, Pharmacovigilance is the science and activities related to the detection, evaluation, understanding and prevention of the adverse effects of medicines or any other problem related to them.

What is an adverse event (AE)?

Any unfortunate medical event that may occur during treatment with a drug but does not necessarily have a causal relationship with that treatment. In this case, coincidence in time occurs without any suspicion of a causal relationship.

Report of Adverse Events

To report any adverse event related to any of our products, we appreciate you completing the available form below:

Patient's first and last name

Age

Gender

Weight

Treating Physician / Institution

Product name, presentation, and lot number

Description of the adverse effect (in as much detail as possible)

Phone

You can also contact directly: farmacovigilancia@biofactor.com.ar