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Home > Drug Safety > Pharmacovigilance

Pharmacovigilance

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October 8, 2025 (Updated on: October 27, 2025)
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According to the World Health Organization (WHO), pharmacovigilance describes the science and efforts behind drug safety. This includes drug testing in clinical trials and the monitoring of side effects.

In the United States, the Food and Drug Administration (FDA) is the primary authority for pharmacovigilance, while the Centers for Disease Control and Prevention (CDC) monitors vaccine safety, and the National Institutes of Health (NIH) performs additional research on drug safety.

DISCLAIMER: MedShadow provides information and resources related to medications, their effects, and potential side effects. However, it is important to note that we are not a substitute for professional medical advice, diagnosis, or treatment. The content on our site is intended for educational and informational purposes only. Individuals dealing with medical conditions or symptoms should seek guidance from a licensed healthcare professional, such as a physician or pharmacist, who can provide personalized medical advice tailored to their specific circumstances.

While we strive to ensure the accuracy and reliability of the information presented on MedShadow, we cannot guarantee its completeness or suitability for any particular individual’s medical needs. Therefore, we strongly encourage users to consult with qualified healthcare professionals regarding any health-related concerns or decisions. By accessing and using MedShadow, you acknowledge and agree that the information provided on the site is not a substitute for professional medical advice and that you should always consult with a qualified healthcare provider for any medical concerns.

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