Remedies needed to address the pathology in reporting adverse reactions and Food and Drug Administration use of reports
- PMID: 12534769
- PMCID: PMC1494800
- DOI: 10.1046/j.1525-1497.2003.t01-1-21115.x
Remedies needed to address the pathology in reporting adverse reactions and Food and Drug Administration use of reports
Comment on
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Adverse drug event monitoring at the Food and Drug Administration.J Gen Intern Med. 2003 Jan;18(1):57-60. doi: 10.1046/j.1525-1497.2003.20130.x. J Gen Intern Med. 2003. PMID: 12534765 Free PMC article.
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Measuring errors and adverse events in health care.J Gen Intern Med. 2003 Jan;18(1):61-7. doi: 10.1046/j.1525-1497.2003.20147.x. J Gen Intern Med. 2003. PMID: 12534766 Free PMC article.
References
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- Scott HD, Thacher-Renshaw A, Rosenbaum SE, et al. Physician reporting of adverse drug reactions. Results of the Rhode Island Adverse Drug Reaction Reporting Project. JAMA. 1990;263:1785–8. - PubMed
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- Lurie P, Sasich LD. Safety of FDA-approved drugs. JAMA. 1999;282:2297–8. - PubMed
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- Who owns the FDA? The drug industry or the people? BMJ. 2002. 555–6, 561, 592–595.
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