Data Mining of the Public Version of the FDA Adverse Event Reporting System
The US Food and Drug Administration (FDA) Adverse Event Reporting System (FAERS, formerly AERS) is a database that contains information on adverse event and medication error reports submitted to the FDA. Besides those from manufacturers, reports can be submitted from health care professionals and th...
| Main Authors: | , , , |
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| Format: | Online |
| Language: | English |
| Published: |
Ivyspring International Publisher
2013
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3689877/ |