pat_aggr

Internal function used by <code>site_aggr()</code> and
<code>plot_visit_med75()</code>, adds the maximum visit for each patient.

Monitoring of Adverse Event (AE) reporting in clinical trials is
important for patient safety. Sites that are under-reporting AEs can be detected
using Bootstrap-based simulations that simulate overall AE reporting. Based on the
simulation an AE under-reporting probability is assigned to each site in a
given trial (Koneswarakantha 2021 <doi:10.1007/s40264-020-01011-5>).

Bjoern Koneswarakantha

simaerep

Find Clinical Trial Sites Under-Reporting Adverse Events

F. Hoffmann-La Roche Ltd 

pat_aggr function

<dl><dt>df_visit</dt>
<dd>dataframe</dd></dl>

Arguments

Aggregate visit to patient level. — pat_aggr

<dl>

<dt>df_visit</dt>
<dd>dataframe</dd>

</dl>

pat_aggr: Aggregate visit to patient level.

Description

Usage

Value

Arguments