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simaerep: Find Clinical Trial Sites Under-Reporting Adverse Events
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>).
| Version: |
0.5.0 |
| Depends: |
R (≥ 4.0), ggplot2 |
| Imports: |
dplyr (≥ 1.0.0), tidyr (≥ 1.1.0), magrittr, purrr, rlang, stringr, forcats, cowplot, RColorBrewer, furrr (≥ 0.2.1), progressr, knitr, tibble |
| Suggests: |
testthat, devtools, pkgdown, spelling, haven, vdiffr, lintr |
| Published: |
2024-04-03 |
| Author: |
Bjoern Koneswarakantha
 [aut, cre,
cph],
F. Hoffmann-La Roche Ltd [cph] |
| Maintainer: |
Bjoern Koneswarakantha <bjoern.koneswarakantha at roche.com> |
| License: |
MIT + file LICENSE |
| URL: |
https://openpharma.github.io/simaerep/,
https://github.com/openpharma/simaerep |
| NeedsCompilation: |
no |
| Language: |
en-US |
| Materials: |
README NEWS |
| CRAN checks: |
simaerep results |
Documentation:
Downloads:
Linking:
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https://CRAN.R-project.org/package=simaerep
to link to this page.
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
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