has submitted comments to the FDA regarding the agency's estimated burden associated with adverse event reporting and recordkeeping for dietary supplements as required by the Dietary Supplement and Nonprescription Drug Consumer Protection Act (DSND-CPA), published in the Federal Register on March 23, 2012.
What does AE stand for?
AE stands for Adverse Event (clinical trials)
This definition appears very frequently and is found in the following Acronym Finder categories:
- Science, medicine, engineering, etc.
See other definitions of AE
We have 89 other meanings of AE in our Acronym Attic
- Adaptive Equipment (palliative care)
- Additional Entry (USPS)
- Address Extension (Sprint)
- Adjoint d'Enseignement (French: Teaching Assistant)
- Adult Entertainment
- Advanced Edition (software; various companies)
- Advanced Energy (various locations)
- Advanced Exchange
- Adverse Effect
- Adverse Event
Samples in periodicals archive:
Adverse Event Reporting News is devoted exclusively to coverage of Food and Drug Administration (FDA) and European Union (EU) requirements involving the reporting of adverse reactions with human drugs, biologics (such as vaccines), medical devises, and dietary supplements.
Long-term studies comparing the incidence of serious, clinically-significant upper GI adverse events in patients taking risedronate versus alendronate have not been performed.
KEY CONCEPTS * Patient Safety * Adverse Events * Medical Errors * Ensuring A Higher Quality of Care * National Center for Patient Safety Patient safety has moved to the front of the health care quality agenda after a recent report on patient safety by the Institute of Medicine's (IOM) Committee on Quality of Health Care in America.
The Food and Drug Administration (FDA), Center for Food Safety and Applied Nutrition (CFSAN), is currently developing a new, comprehensive system for tracking and analyzing adverse event reports involving foods, cosmetics and dietary supplements.