FDA Adverse Event Reporting System
Description: The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA.
Cross-references: https://github.com/NCATSTranslator/Translator-All/wiki/FAERS
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Edge Type Validation
This section shows the validation of edge types in this knowledge source against the recognized biolink schema patterns.
201,810
Recognized Edges
( 99.9 %)
Recognized Edges
( 99.9 %)
202
Unrecognized Edges
( 0.1 %)
Unrecognized Edges
( 0.1 %)
