Adverse Event Reports
What Is An Adverse Event Report?
The FDA Adverse Event Reporting System (FAERS) is a database that contains adverse event reports, medication error reports and product quality complaints resulting in adverse events that were submitted to FDA. The database is designed to support the FDA’s post-marketing safety surveillance program for drug and therapeutic biologic products.
What is drugadverseeventreports.com?
The company behind this company, Walnut St. Labs, is a data services company that seeks to make important datasets accessible to more people. The openFDA data is a rich source of insight into pharmaceutical drugs. This site aims to simplify access to the data.
The Latest Reports
Showing 151–160 of 160 results
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Fabrazyme Adverse Event Report 2018
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Klonopin Adverse Event Report 2018
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Xanax Adverse Event Report 2018
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Ritalin Adverse Event Report 2018
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Lunesta Adverse Event Report 2018
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Demerol Adverse Event Report 2018
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Ambien Adverse Event Report 2018
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Adderall Adverse Event Report 2018
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Xarelto Adverse Event Report 2018
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Oxycontin Adverse Event Report 2018
$19.99