from:
[email protected]
to: me
date: Thu, Aug 4, 2016 at 5:07 PM
subject: MedWatch confirmation message.
Dear Reporter:
Thank you for submitting your report to MedWatch, the FDA Safety Information and Adverse Event Reporting Program.
This acknowledgment confirms that your report was received. Reports are added to a post marketing safety database with similar reports and reviewed by the FDA's post marketing safety staff. Voluntary reports are essential for ensuring the continued safety of FDA-regulated products. One or two well documented case reports may provide an early signal of unexpected problems and lead to additional evaluation. This may result in FDA regulatory actions that improve the safety of the products used in patient care each day.
You will only be contacted for follow-up by FDA if additional information on this report is needed in our evaluation process.
Again, thank you for taking the time to submit your report. If you have any questions, please send them to:
[email protected] .
Sincerely yours,
MedWatch
