Strengthening the reporting of harms of all interventions in clinical trials
Med J Aust
.
2022 Nov 21;217(10):502-504.
doi: 10.5694/mja2.51755.
Epub 2022 Oct 26.
Authors
Christina Abdel Shaheed
1
,
Christopher G Maher
1
,
Ann-Mason Furmage
2
,
Tammy Hoffmann
3
,
Andrew J McLachlan
1
Affiliations
1
University of Sydney, Sydney, NSW.
2
Consumer Advisory Group, Royal Prince Alfred Hospital, Sydney, NSW.
3
Institute for Evidence-Based Healthcare, Bond University, Gold Coast, QLD.
PMID:
36287028
PMCID:
PMC9828512
DOI:
10.5694/mja2.51755
No abstract available
Keywords:
Adverse drug reactions; Adverse events; Clinical trials as topic.
MeSH terms
Adverse Drug Reaction Reporting Systems*
Drug-Related Side Effects and Adverse Reactions*
Humans