The Ability and Tasks of Pharmacovigilance and Adverse Drug Events in India a Global Scenario

Abstract

Clinical trials are the first stage of pharmacovigilance, which continues until the medication is put on the market. Social media's introduction provides access to healthcare data that hasn't been vetted by conventional techniques of data collection. Enhancing clinical and scientific understanding of pharmacovigilance could be greatly aided by using natural language processing tools to retrieve patient reports of adverse medication occurrences from social media. Signal detection encompasses all side effects connected to a medication. The primary goal of the study is to extract information from the FAERS data, which includes both organized and unstructured patient information on prior adverse drug reactions. The study examines how the side effects of acetaminophen and ibuprofen are extracted and managed using the proper techniques.