Brief ReportBrief Report
Primary Care Physicians' Use of FDA-Approved Prescription Drug Labels
Helen W. Sullivan, Amie C. O'Donoghue and Kathryn J. Aikin
The Journal of the American Board of Family
Medicine September 2014, 27 (5) 694-698; DOI: https://doi.org/10.3122/jabfm.2014.05.140039
Helen W. Sullivan
From the US Food and Drug Administration, Silver Spring, MD.
PhD, MPHAmie C. O'Donoghue
From the US Food and Drug Administration, Silver Spring, MD.
PhDKathryn J. Aikin
From the US Food and Drug Administration, Silver Spring, MD.
PhDReferences
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FDA announces new prescription drug information format to improve patient safety. Silver Spring, MD: Food and Drug Administration; January 18, 2006. Available from: http://www.fda.gov/NewsEvents/Newsroom/PressAnnouncements/2006/ucm108579.htm. Accessed January 10, 2014.
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Code of federal regulations title 21. Food and drugs. Chapter I: Food and Drug Administration Department of Health and Human Services. Subchapter C–Drugs: general. Part 201: Labeling. Silver Spring, MD: US Food and Drug Administration; 2013.
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Requirements on content and format of labeling for human prescription drugs and biologics; requirements for prescription drug product labels; proposed rule. 21 CFR Part 201. Fed Regist 2000;65(247):81081–131.
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In this issue
The Journal of the American Board of Family
Medicine
Vol. 27, Issue 5
September-October 2014
Primary Care Physicians' Use of FDA-Approved Prescription Drug Labels
Helen W. Sullivan, Amie C. O'Donoghue, Kathryn J. Aikin
The Journal of the American Board of Family
Medicine Sep 2014, 27 (5) 694-698; DOI: 10.3122/jabfm.2014.05.140039
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