Identification of Adverse Events  

What is identification of adverse events? 

Identification of adverse events refers to the process of detecting and documenting any harmful or unintended effects that occur as a result of using a medical treatment, drug, or medical device. These events can range from mild side effects to severe reactions that require medical intervention. The identification process is critical for ensuring patient safety and monitoring the ongoing risk profile of healthcare products. 

Why is identification of adverse events important? 

The identification of adverse events is a critical process in safeguarding public health. By detecting and addressing safety concerns early, healthcare providers can minimize patient risks, adjust treatment plans accordingly, and help ensure that medical products remain safe and effective for long-term use.