Short Description: Adverse events are medical occurrences when a drug available in the market results in an unwanted effect on patients. Pharmaceutical companies are required to report such incidents to FDA for further evaluation of the drug, as a part of the FDA regulatory system.

Adverse events are medical occurrences when a drug available in the market results in an unwanted effect on patients. Pharmaceutical companies are required to report such incidents to FDA for further evaluation of the drug, as a part of the FDA regulatory system. These companies face challenges in identification of sentiments and differentiating severe & non-severe events from patient’s data. Artificial Intelligence techniques like NLP, Machine Learning, take the Adverse Events Reporting System to the next level. View this infographic to know how.

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