Pharmacovigilance
Pharmacovigilance is the science and activities related to the detection, evaluation, prevention and understanding of adverse drug effects or any drug-related problems.
What should I report?
Any suspected adverse event:
- ADR (Adverse drug reaction)
- Suspected therapeutic failure
- Quality issue
- Medication error(s)
- Shortages
- Other
Where to notify?
Through the form available
below
- Include Form Button {see reference site, follow guideline color theme}
Who can notify?
All health professionals, as well as any citizen.
Medonefarma markets and distributes Mexican and US FDA approved medicines. This Pharmacovigilance adverse event reporting form is to assist in the notification of any medicines sold by Medonefarma and with supporting official invoice. Medonefarma recommends to report your adverse event directly to your physician, pharmacist and the producing medicine laboratory.