How do we get access to US FDA files containing Adverse Event Reports

The 1996 amendments to the Freedom of Information Act (FOIA) mandate publicly accessible "electronic reading rooms" with agency FOIA response materials and other information routinely available to the public, with electronic search and indexing features.Before submitting a FOIA request, we need to check to see if the information we are looking for is already available on FDA's Web site. We can use our search engine to find what you're looking for.