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PUBMED FOR HANDHELDS

Journal Abstract Search


274 related items for PubMed ID: 15255086

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  • 2. Pharmacogenomic biomarker information in drug labels approved by the United States food and drug administration: prevalence of related drug use.
    Frueh FW, Amur S, Mummaneni P, Epstein RS, Aubert RE, DeLuca TM, Verbrugge RR, Burckart GJ, Lesko LJ.
    Pharmacotherapy; 2008 Aug; 28(8):992-8. PubMed ID: 18657016
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  • 3. A continuing black hole? The FDA boxed warning: an appeal to improve its clinical utility.
    Matlock A, Allan N, Wills B, Kang C, Leikin JB.
    Clin Toxicol (Phila); 2011 Jul; 49(6):443-7. PubMed ID: 21591886
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  • 4. FDA boxed warnings: how to prescribe drugs safely.
    O'Connor NR.
    Am Fam Physician; 2010 Feb 01; 81(3):298-303. PubMed ID: 20112888
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  • 5. "Black box" 101: How the Food and Drug Administration evaluates, communicates, and manages drug benefit/risk.
    Murphy S, Roberts R.
    J Allergy Clin Immunol; 2006 Jan 01; 117(1):34-9. PubMed ID: 16387581
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  • 6. Content and format of labeling for human prescription drugs; pregnancy labeling; public hearing--FDA. Notice of public hearing; request for comments.
    Fed Regist; 1997 Jul 31; 62(147):41061-3. PubMed ID: 10169832
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  • 13. Primary care physicians' use of FDA-approved prescription drug labels.
    Sullivan HW, O'Donoghue AC, Aikin KJ.
    J Am Board Fam Med; 2014 Jul 31; 27(5):694-8. PubMed ID: 25201939
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  • 15. Effects of Food and Drug Administration warnings on antidepressant use in a national sample.
    Olfson M, Marcus SC, Druss BG.
    Arch Gen Psychiatry; 2008 Jan 31; 65(1):94-101. PubMed ID: 18180433
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  • 16. Black box warning contraindicated comedications: concordance among three major drug interaction screening programs.
    Wang LM, Wong M, Lightwood JM, Cheng CM.
    Ann Pharmacother; 2010 Jan 31; 44(1):28-34. PubMed ID: 20040698
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  • 17. Measuring treatment impact: a review of patient-reported outcomes and other efficacy endpoints in approved product labels.
    Willke RJ, Burke LB, Erickson P.
    Control Clin Trials; 2004 Dec 31; 25(6):535-52. PubMed ID: 15588741
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  • 18. Requirements for submission of labeling for human prescription drugs and biologics in electronic format. Final rule.
    Food and Drug Administration, HHS.
    Fed Regist; 2003 Dec 11; 68(238):69009-20. PubMed ID: 14672084
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  • 19. The Physicians' Desk Reference. Problems and possible improvements.
    Cohen JS, Insel PA.
    Arch Intern Med; 1996 Jul 08; 156(13):1375-80. PubMed ID: 8678706
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