Medication Error Classification
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Ismp Medication Error Classification
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Types Of Medication Errors In Hospitals
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Ismp Medication Error Categories
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Ncc Merp Taxonomy Of Medication Errors
67(6): 599–604. doi: 10.1111/j.1365-2125.2009.03415.xPMCID: PMC2723196Medication errors: definitions and classificationJeffrey K AronsonDepartment of Primary Health Care, Oxford, UKCorrespondence Dr Jeffrey K. Aronson, http://www.ahrq.gov/professionals/quality-patient-safety/patient-safety-resources/resources/match/matchtab6.html MA, DPhil, MBChB, FRCP, FBPharmacolS, FFPM (Hon), Department of Primary Health Care, Rosemary Rue Building, Old Road Campus, Headington, Oxford OX3 7LF, UK. Tel: +44 (0) 1865 289288 Fax: +44 (0) 1865 289287 E-mail: ku.ca.xo.mrahpnilc@nosnora.yerffejAuthor information ► Article notes ► Copyright and License http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2723196/ information ►Accepted 2009 Mar 18.Copyright Journal compilation © 2009 The British Pharmacological SocietyThis article has been cited by other articles in PMC.AbstractTo understand medication errors and to identify preventive strategies, we need to classify them and define the terms that describe them.The four main approaches to defining technical terms consider etymology, usage, previous definitions, and the Ramsey–Lewis method (based on an understanding of theory and practice).A medication error is ‘a failure in the treatment process that leads to, or has the potential to lead to, harm to the patient’.Prescribing faults, a subset of medication errors, should be distinguished from prescription errors. A prescribing fault is ‘a failure in the prescribing [decision-making] process that leads to, or has the potential to lead to, harm to the patient’. The c
Home Food Drugs Medical Devices Radiation-Emitting Products http://www.fda.gov/drugs/drugsafety/medicationerrors/ Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products Drugs Home Drugs Drug Safety and Availability Medication Errors Medication Errors Related to Drugs Share Tweet Linkedin Pin it More sharing options Linkedin Pin it Email Print Within the Center for Drug Evaluation and Research (CDER), the Division of medication error Medication Error Prevention and Analysis (DMEPA) reviews medication error reports on marketed human drugs including prescription drugs, generic drugs, and over-the-counter drugs. DMEPA uses the National Coordinating Council for Medication Error Reporting and Prevention (NCCMERP) definition of a medication error. Specifically, a medication error is "any preventable event that may of medication errors cause or lead to inappropriate medication use or patient harm while the medication is in the control of the health care professional, patient, or consumer. Such events may be related to professional practice, health care products, procedures, and systems, including prescribing; order communication; product labeling, packaging, and nomenclature; compounding; dispensing; distribution; administration; education; monitoring; and use."DMEPA includes a medication error prevention program staffed with healthcare professionals. Among their many duties, program staff review medication error reports sent to MedWatch, evaluate causality, and analyze the data to provide solutions to reduce the risk of medication errors to industry and others at FDA.Additionally, DMEPA prospectively reviews proprietary names, labeling, packaging, and product design prior to drug approval to help prevent medication errors.Although DMEPA encourages manufacturers to perform their due diligence when naming their drug products and we strive to avoid approving confusing proprietary names for drug products, the