Harm and the potential for harm from medical care is pervasive and well-documented. Much of the safety literature has historically focused on physical harm, but the Agency for Healthcare Research and ...
Please provide your email address to receive an email when new articles are posted on . The FDA Adverse Event Reporting System will now host daily publications, instead of quarterly. The agency’s goal ...
Adverse Drug Event Reporting: The Roles of Consumers and Health-Care Professionals: Workshop Summary
Active surveillance systems screen claims data and notify healthcare providers who then determine if follow-up or adverse event reporting is required. These systems can scan for known adverse events ...
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