Objective: Signal detection by analyzing adverse event spontaneous report databases is used to monitor drug safety. One of the major spontaneous report databases is the FDA Adverse Event Reporting System (FAERS). Recently, the Japanese Adverse Drug Event Report database (JADER) was released. To com...
for more detail about the fda adverse event reporting system (faers), visit: the structured public labeling website, the basis of the data dictionary that they won’t share, whatever that means the national drug code directory, just in case you need to merge things with other things a sta...
Exploring the FDA Adverse Event Reporting System 40FAERS41 to Generate 系统标签: faers disease fda adverse monitoring hypotheses FDAAdverseEventReportingSystem(FAERS)GenerateHypothesesDiseaseMonitoringHongFangZhenqiangSuYupingWangAaronMillerZhichaoLiuPaulHowardWeidaTongScientificCoordination,NationalCenterToxicologicalRe...
Marimuthu, Sathiya PriyaSegal, Jodi B.Singh, SonalSpringer International PublishingDrug SafetyIyer G, Marimuthu SP, Segal JB, Singh S. An algorithm to identify generic drugs in the FDA adverse event reporting system. Drug Saf. 2017;40(9):799-808....
Pertuzumab is widely used for the treatment of HER2 + breast cancer. But its safety in the real world should be continuously monitored. So, we evaluated the safety of pertuzumab by pharmacovigilance analyze based on related adverse events (AEs) from the FDA Adverse Event Reporting System (...
The aim of this study was to identify ovary and uterus related adverse events (AEs) associated with statin use by analyzing data from FDA Adverse Event Reporting System (FAERS). We used OpenVigil 2.1 to query FAERS database. Ovary and uterus related AEs were defined by 383 Preferred Terms, ...
Therefore, we developed a custom dataset for this study derived from the FDA Adverse Event Reporting System (FAERS), a database of spontaneous adverse drug reaction reports maintained by the United States Food and Drug Administration (FDA). Here, we utilized the logistic matrix factorization (...
Taxane-associated adverse events were identified by the Medical Dictionary for Regulatory Activities Preferred Terms and analyzed and compared by mining the US Food and Drug Administration Adverse Event Reporting System pharmacovigilance database from January 2004 to December 2019.Reported adverse events,...
The FDA has made strides in improving transparency and data access, and has implemented tools to allow the pharmaceutical industry and the public to transform raw data into usable information. One of these tools is called the FDA Adverse Event Reporting System (FAERS) Public Dashboard. In this ...