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Adverse Event Reporting


Adverse event reporting is the process of identifying, monitoring, and documenting negative or unexpected effects resulting from the use of a medication or medical product. These reports play a crucial role in monitoring drug safety, assessing potential risks, and minimizing potential hazards.

How to Report a Side Effect?

To report an adverse event or reaction related to BMED Pharmaceuticals products, you may complete the TÜFAM reporting form and submit it to 'bmed.pv@pleksus.com.tr' or contact us by calling +90 531 433 67 36.