get_visit_med75

Internal function used by <code>site_aggr()</code>.

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 

get_visit_med75 function

<dl><dt>df_pat</dt>
<dd>dataframe as returned by <code>pat_aggr()</code></dd>
<dt>method</dt>
<dd>character, one of c("med75", "med75_adj") defining method for
defining evaluation point visit_med75 (see details), Default: "med75_adj"</dd>
<dt>min_pat_pool</dt>
<dd>double, minimum ratio of available patients available for
sampling. Determines maximum visit_med75 value see Details. Default: 0.2</dd></dl>

Arguments

Get visit_med75. — get_visit_med75

<dl>

<dt>df_pat</dt>
<dd>dataframe as returned by <code>pat_aggr()</code></dd>


<dt>method</dt>
<dd>character, one of c("med75", "med75_adj") defining method for
defining evaluation point visit_med75 (see details), Default: "med75_adj"</dd>


<dt>min_pat_pool</dt>
<dd>double, minimum ratio of available patients available for
sampling. Determines maximum visit_med75 value see Details. Default: 0.2</dd>

</dl>

get_visit_med75: Get visit_med75.

Description

Usage

Value

Arguments