Pharmacovigilance, as defined by the World Health Organization (WHO), is “the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.”

Adverse Drug Reaction

An adverse reaction is a response to a medicinal product which is noxious and unintended. This includes adverse reactions which arise from:

  • the use of a medicinal product within the terms of the marketing authorization;
  • the use outside the terms of the marketing authorization, including overdose, off-label use, misuse, abuse and medication errors;
  • occupational exposure.

How to, and to whom, report an adverse reaction

If you wish to directly notify Kedrion about a suspected adverse reaction related to our drugs, please fill in the form below:



EN: Pharmacovigilance
Qualification *
Gender (M/F)
Has the adverse event stopped?
How bad was the adverse event?
How is the adverse event now?

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