The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2023. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2021. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2020. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2022. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2019. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to FDA (U.S. Food and Drug Administration) in 2018. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.
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The FDA Adverse Event Reporting System (FAERS) contains information on medication errors, quality complaints and drug-related adverse events that were submitted to the FDA (U.S. Food and Drug Administration) in 2023. The Demographics dataset contains patient demographic and administrative information, a single record for each event report.