The US Food and Drug Administration's Risk Evaluation and Mitigation Strategy (REMS) Program in Practice: Does It Really Inform Patients and Limit Risk?
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Veröffentlicht in: | American journal of kidney diseases 2012-05, Vol.59 (5), p.604-606 |
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container_title | American journal of kidney diseases |
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creator | Cohen, Robert A., MD, MSc Brown, Robert S., MD |
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doi_str_mv | 10.1053/j.ajkd.2011.12.008 |
format | Article |
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ispartof | American journal of kidney diseases, 2012-05, Vol.59 (5), p.604-606 |
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language | eng |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Chronic Disease Epoetin Alfa Erythropoietin - adverse effects Heart Failure - epidemiology Hematinics - adverse effects Humans Kidney Diseases - therapy Nephrology Patient Education as Topic - methods Physician-Patient Relations Recombinant Proteins - adverse effects Renal Dialysis Risk Assessment - methods Risk Factors Risk Management Stroke - epidemiology United States United States Food and Drug Administration |
title | The US Food and Drug Administration's Risk Evaluation and Mitigation Strategy (REMS) Program in Practice: Does It Really Inform Patients and Limit Risk? |
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