I have some history working with the Adverse Event Reporting data. The API is nice, but it just exposes what they already offer in flat files .... stale data. Does it seem reasonable to you that the FDA runs a year behind on this data?

http://www.fda.gov/Drugs/GuidanceComplianceRegulatoryInforma...

They don't respond: https://twitter.com/statwonk/status/413355130461761536