What type of information does the events class in clinical data capture include?

The events class in clinical data capture primarily includes information regarding adverse events and medical history. This class is crucial for monitoring patient safety and understanding how a treatment affects participants during a clinical trial.

Adverse events refer to any unwanted or harmful reactions that patients may experience while undergoing treatment, which must be documented to assess the safety profile of the investigated intervention. Additionally, collecting data on participants' medical histories is important for determining how these variables might influence the outcome of the study.

While patient contact information, laboratory test results, and treatment schedules are essential for managing studies, they are not the focus of the events class. Instead, the events class specifically captures clinical events that can impact the efficacy and safety evaluations of the clinical trial, making it fundamental in the context of clinical data reporting and analysis.