AERS meaning in Governmental ?

Answer: What is Adverse Event Reporting System mean?

The FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and therapeutic biologic products. The FDA uses FAERS to monitor for new adverse events and medication errors that might occur with these products. It is a system that measures occasional harms from medications to ascertain whether the risk–benefit ratio is high enough to justify continued use of any particular drug and to identify correctable and preventable problems in health care delivery (such as need for retraining to prevent prescribing errors). The system interacts with several related systems including MedWatch and the Vaccine Adverse Event Reporting System. FAERS replaced legacy AERS system in Sep 2012.

reference

Full Form	Category
Agricultural Economics and Rural Sociology	Academic & Science
Atlantic Estuarine Research Society	Academic & Science
Association of Educators in Radiological Science	Academic & Science
Advanced Engineering and Research Associates	Academic & Science
Automated Earnings Reporting System	Accounts and Finance
Amlo (anti-money Laundering Office) Electronic Reporting System	Accounts and Finance
Aero Systems Engineering, Inc.	Business
Audit and Enterprise Risk Services	Business
Applied Education Research Scheme	Community
Applied Educational Research Scheme	Community
Adult Evaluation Review Services	General
Automated Election Results System	Governmental
Adult Evaluation and Review Services	Governmental
Adverse Event Reporting System	Governmental
Advanced Economic Research Systems	Governmental
Applied Energy Recovery Systems	Governmental
Acute Equine Respiratory Syndrome	Medical
Access/ Egress Roadway System	Military and Defence
Army Educational Requirements System	Military and Defence
Alaska Educational Radio System	Regional