Shows odds (ROR or PRR) of reporting an adverse event (AE) and its statistical significance (adjusted p-value) for selected column. Points on the top right indicate increased risk for the AE in the context of the selected target. Points on the top left indicate decreased risk for the AE in the context of the selected target.
Includes AEs with adjusted p < 0.05 and |log2(ROR/PRR)| ≥ 1 in at least one facet.
This dashboard allows you to explore and visualize adverse event (AE) data related to GLP-1 RA therapies. Use the Visualizations tab to interact with the data.
The data used in this dashboard is sourced from the FDA Adverse Event Reporting System (FAERS). We have processed and cleaned the data to provide meaningful insights into GLP-1 RA treatment related adverse events.