Reporting adverse events and side effects is a regulatory obligation, and a commitment to our patients. It is essential to keeping drugs safe
The prevention of adverse events
"Pharmacogivilance is a regulatory requirement for all drug manufacturers. It's part of our commitment to patients and healthcare providers that they have the tools to determine the risk-benefit of the drug and use it appropriately."
If you are the person experiencing the side effect, in addition to filling this form it is very important that you refer to your doctor or healthcare provider directly.
For additional information, you may also contact PharmaMar at +34 91 234 34 34 or firstname.lastname@example.org.