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The 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 therapeutic biologic products.
Founded in 1993, this system of voluntary reporting allows such information to be shared with the medical community or the general public. The system includes publicly available databases and online analysis tools for professionals. MedWatch also distributes information on medical recalls and other clinical safety communications via its platforms.
This is a list of online databases accessible via the ... Aviation Safety Reporting System; B. Bank of English ... Internet Off-Broadway Database; Internet Public ...
Last week, an agency official told Reuters about U.S plans to make public data collected by its surveillance system. Testing wastewater from sewers proved to be a powerful tool for detecting ...
Data mining techniques such as empirical Bayes methods can be used to improve the quality of data analysis. [5] The system was used in 1999 to identify a rotavirus vaccine that had an increased risk of a bowel obstruction condition , and confirmatory research led to the vaccine's use being suspended.
These databases collect genome sequences, annotate and analyze them, and provide public access. Some add curation of experimental literature to improve computed annotations. These databases may hold many species genomes, or a single model organism genome.
Strong safety signals of bicalutamide with interstitial lung disease have been observed in pharmacovigilance databases such as the FAERS and Japanese Adverse Drug Event Report (JADER) databases (e.g., ROR Tooltip reporting odds ratio = 9.2, 95% CI Tooltip confidence interval = 7.9–10.6; ROR = 8.2, 95% CI = 6.0–11.2).
ActiveReports; Actuate Corporation; BOARD; Business Objects; Cognos BI; Crystal Reports; CyberQuery; GoodData; I-net Crystal-Clear; InetSoft; Information Builders ...