Drug makers' adverse event reports are often incomplete, US report finds
- PMID: 25652561
- DOI: 10.1136/bmj.h651
Drug makers' adverse event reports are often incomplete, US report finds
Similar articles
-
Miscategorization of Deaths in the US Food and Drug Administration Adverse Events Database.JAMA Intern Med. 2020 Jan 1;180(1):147-148. doi: 10.1001/jamainternmed.2019.4030. JAMA Intern Med. 2020. PMID: 31589249 Free PMC article.
-
Food and Drug Administration Adverse Event Reports of Retinal Vascular Occlusions Associated With Phosphodiesterase Type 5 Inhibitor Use.J Neuroophthalmol. 2016 Dec;36(4):480-481. doi: 10.1097/WNO.0000000000000450. J Neuroophthalmol. 2016. PMID: 27851718 No abstract available.
-
Evaluating the completeness and accuracy of MedWatch data.Am J Ther. 2014 Nov-Dec;21(6):442-6. doi: 10.1097/MJT.0b013e318262316f. Am J Ther. 2014. PMID: 23011177
-
[Safety of medicinal products and reporting of adverse drug reactions].Neurol Neurochir Pol. 2004 Nov-Dec;38(6):503-10. Neurol Neurochir Pol. 2004. PMID: 15654675 Review. Polish.
-
Role of postmarketing surveillance in contemporary medicine.Annu Rev Med. 2011;62:1-10. doi: 10.1146/annurev-med-060309-164311. Annu Rev Med. 2011. PMID: 20809798 Review.
Cited by
-
Comparison of the Completeness of Spontaneously Reported Adverse Drug Reactions by Consumers, Healthcare Professionals, and Pharmaceutical Companies: An Evaluation of Databases From Two High-Income Countries.Pharmacol Res Perspect. 2025 Aug;13(4):e70164. doi: 10.1002/prp2.70164. Pharmacol Res Perspect. 2025. PMID: 40778745 Free PMC article.
-
Lack of essential information in spontaneous reports of adverse drug reactions in Catalonia-a restraint to the potentiality for signal detection.Eur J Clin Pharmacol. 2017 Jun;73(6):751-758. doi: 10.1007/s00228-017-2223-5. Epub 2017 Mar 1. Eur J Clin Pharmacol. 2017. PMID: 28251276
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Medical