Quality of reporting of adverse events in clinical trials of covid-19 drugs: systematic review.
- DOI
- 10.1136/bmjmed-2022-000352
- Published
- 2023
- Container
- BMJ medicine
- Publisher
- Not recorded
- Open access
- yes
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limited evidence Score 45/100 under policy 1.0.0. This is a metadata assessment, not a judgment of the paper's conclusions.
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Cite this work
BibTeX
@article{allodium:10.1136/bmjmed-2022-000352,
title = {Quality of reporting of adverse events in clinical trials of covid-19 drugs: systematic review.},
author = {Madi K and Flumian C and Olivier P and Sommet A and Montastruc F},
year = {2023},
journal = {BMJ medicine},
doi = {10.1136/bmjmed-2022-000352},
url = {https://doi.org/10.1136/bmjmed-2022-000352}
}RIS
TY - JOUR TI - Quality of reporting of adverse events in clinical trials of covid-19 drugs: systematic review. AU - Madi K AU - Flumian C AU - Olivier P AU - Sommet A AU - Montastruc F PY - 2023 JO - BMJ medicine DO - 10.1136/bmjmed-2022-000352 UR - https://doi.org/10.1136/bmjmed-2022-000352 ER -
APA
K, M., C, F., P, O., A, S., & F, M. (2023). Quality of reporting of adverse events in clinical trials of covid-19 drugs: systematic review.. BMJ medicine. https://doi.org/10.1136/bmjmed-2022-000352
Source records
- pubmed · retrieved 2026-09-26T22:13:51.999Z