Patients vary in their biologicals reactions to pharmaceutical products. This is why not all adverse events (side effects, e.g. allergic reactions) associated with the use of pharmaceutical products can be detected during clinical development, not even by the most comprehensive clinical trials.

Capturing as many of these adverse reactions, however rare they may be, from worldwide sources is of paramount importance for continued patient and drug safety (pharmacovigilance).

In case you experience any adverse events following the administration of our product(s):

Report an adverse event: email: pv@mcpharma.com.tn

NB: All the information and personal data you share with us will be protected and kept confidential in line with our company standard operating procedures and applicable national data protection regulations