Data for HTN Pulmenoary ADE Reports

The data used in this study have been curated from multiple publicly available data sources for hypertensive patients, including the FDA’s Adverse Event Reporting System (FAERS), which houses all ADEs reported to the FDA by pharmaceutical companies, healthcare providers, and consumers. The data, including the hypertension dataset, is updated quarterly by the FDA and currently includes reports submitted from the first quarter of 2004 to the last quarter of 2019. This dataset focuses on drugs and their ADEs but includes additional data such as disease, drug, and demographic information as well as information related to patient outcome.