This process screens all adverse events by performing a Cochran-Mantel-Haenszel exact test on all 2 x 2 tables constructed from event resolution and treatment arm. Resolution is computed directly from the end time of an adverse event and the end time of the trial, or from a resolution time window that you specify.
Refer to the AE Incidence Screen report description, keeping in mind the following important process differences in contrast with the example:
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output (including tab names) reflects adverse event resolution (resolution status is determined by Determine Resolved / Not Resolved Status using:), rather than incidence
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Time Windows for Start of AE replaces Trial Time Windows
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Dot Plot: Click
 to create a dot plot for selected terms or for all terms that fall under selected groups, with rates of adverse events by treatment, the relative risk, the risk difference, and the odds ratio presented. |
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Relative Risk Plot: Click
 to create a relative risk plot and table for selected terms or for all terms that fall under selected groups, with rates of adverse events by treatment, the log2(relative risk) and unadjusted 95% confidence intervals (Multiple Testing Method is not applied) presented. |
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Odds Ratio Plot: Click
 to create a plot that shows the ratio of the odds for exhibiting a selected event/intervention to the odds for those who do not exhibit the event/intervention and it can be used to estimate the relative risk when the probability of positive response is small. |
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Contingency Analysis: Click
 to create the typical treatment by event contingency table for selected terms or for all terms that fall under selected groups. |
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Venn Diagram: Click
 to create a Venn diagram for up to five selected terms or for terms that fall under selected groups, to show the co-occurrence of adverse events within study subject. |
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Tabulate: Click
 to create a table for selected terms or for all terms that fall under selected groups, showing the co-occurrence of adverse events within study subject. You can further modify the tables to show additional summary statistics. |
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Click
 to view the associated data tables. Refer to View Data for more information. |
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Click
 to generate a standardized pdf- or rtf-formatted report containing the plots and charts of selected sections. |
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Click
 to take notes, and store them in a central location. Refer to Add Notes for more information. |
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Click
 to read user-generated notes. Refer to View Notes for more information. |
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Click the arrow to reopen the completed process dialog used to generate this output.
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Note: For information about how treatment emergent adverse events (TEAEs) are defined in JMP Clinical, please refer to Determining If an Event Is a Treatment Emergent Adverse Event.