Link: https://www.fda.gov/drugs/drug-approvals-and-databases/fda-adverse-event-reporting-system-faers
Description: WebFDA Adverse Event Reporting System supports the FDA's post-marketing safety surveillance program for all marketed drug and therapeutic biologic products.
DA: 23 PA: 26 MOZ Rank: 70
Link: https://www.fda.gov/drugs/questions-and-answers-fdas-adverse-event-reporting-system-faers/fda-adverse-event-reporting-system-faers-public-dashboard
Description: WebDec 7, 2023 · The intention of this tool is to expand access of FAERS data to the general public to search for information related to human adverse events reported to the FDA by the pharmaceutical industry ...
DA: 55 PA: 85 MOZ Rank: 24
Link: https://www.fda.gov/drugs/surveillance/questions-and-answers-fdas-adverse-event-reporting-system-faers
Description: WebThe 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 ...
DA: 66 PA: 85 MOZ Rank: 45
Link: https://open.fda.gov/data/faers/
Description: WebAbout FAERS. The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to...
DA: 88 PA: 86 MOZ Rank: 29
Link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4194268/
Description: WebThe FAERS is a database that supports the FDA's post-marketing drug-safety monitoring efforts . The database contains valuable information about AEs, medication errors, patient demographics, and more. Since its inception, millions’ cases have been reported to the FAERS by manufacturers, health-care professionals, and consumers.
DA: 51 PA: 13 MOZ Rank: 79
Link: https://en.wikipedia.org/wiki/FDA_Adverse_Event_Reporting_System
Description: WebThe FDA Adverse Event Reporting System (FAERS or AERS) is a computerized information database designed to support the U.S. Food and Drug Administration's (FDA) postmarketing safety surveillance program for all approved drug and …
DA: 86 PA: 7 MOZ Rank: 28
Link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431724/
Description: WebAug 23, 2018 · The FDA’s Adverse Event Reporting System (FDA AERS or FAERS) is one such database which contains reports of adverse events (AEs) associated with drugs, biologics, and certain other medicinal products. 1 The FDA received more than 1.8 million new AE reports in 2017, and the number of reports in FAERS exceeds 15.9 million. 1 …
DA: 5 PA: 98 MOZ Rank: 36
Link: https://fis.fda.gov/extensions/FPD-FAQ/FPD-FAQ.html
Description: WebThe FAERS public dashboard is a new, user-friendly and interactive web-based tool that was created to give the public the ability to query the FDA FAERS database and improve transparency. The data presented in the FAERS public …
DA: 83 PA: 89 MOZ Rank: 32
Link: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8954498/
Description: WebFeb 23, 2022 · FAERS is a database for the spontaneous reporting of adverse events and medication errors involving human drugs and therapeutic biological products [ 13 ]. Currently, the FDA receives over 1 million adverse-event and medication error reports of drug or biological product use annually, making it one of the largest pharmacovigilant …
DA: 32 PA: 68 MOZ Rank: 36
Link: https://open.fda.gov/apis/drug/event/
Description: WebDrug Adverse Event Overview. The openFDA drug adverse event API returns data that has been collected from the FDA Adverse Event Reporting System (FAERS), a database that contains information on adverse event and medication error reports submitted to FDA. Drug Indication.
DA: 7 PA: 6 MOZ Rank: 59