Definition Of Medication Error Reporting
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Drug Event AlgorithmRecommendations / StatementsFor Consumers About Medication Errors What is a Medication Error? The Council defines a "medication error" as follows: "A medication definition of medication error in nursing error is any preventable event that may cause or
Medication Error Reporting Form
lead to inappropriate medication use or patient harm while the medication is in the medication error reporting procedure control of the health care professional, patient, or consumer. Such events may be related to professional practice, health care products, procedures, and systems, medication error reporting format including prescribing, order communication, product labeling, packaging, and nomenclature, compounding, dispensing, distribution, administration, education, monitoring, and use." The Council urges medication errors researchers, software developers, and institutions to use this standard definition to identify errors. NAN Alert The National Alert Network (NAN) publishes the alerts from the
Medication Error Reporting In Nursing Homes Identifying Targets For Patient Safety Improvement
National Medication Errors Reporting Program. NAN encourages the sharing and reporting of medication errors, so that lessons learned can be used to increase the safety of the medication use system. September 15, 2016 Observe for possible fluid leakage when preparing parenteral syringes Subscribe Archive Popular links Definition Taxonomy Dangerous Abbreviations Upcoming Meetings There is no meeting avaiable. Previous Meetings Report Medication ErrorsISMP Medication Errors Reporting Program (MERP) Go U.S. Food and Drug Administration's MedWatch Reporting Program © 2016 National Coordinating Council for Medication Error Reporting and Prevention. All Rights Reserved. *Permission is hereby granted to reproduce information contained herein provided that such reproduction shall not modify the text and shall include the copyright notice appearing on the pages from which it was copied. This copyright statement will change to the new year after the 1st of every year.
Drug Event AlgorithmRecommendations / StatementsFor Consumers 20 Years of Medication Safety Advocacy Read about NCC MERP's advancements in promoting safe medication use in its Anniversary Report. Medication Error Index Learn how NCC MERP helps the health care industry track medication error reporting categories and classify medication errors through the Medication Error Index. Consumer Information for Safe medication error reporting and prevention Medication Use Visit our Consumer Information for Safe Medication Use page to learn how you may help to
Medication Error Reporting A Survey Of Nursing Staff
decrease the number of preventable deaths caused by medication errors. The National Coordinating Council for Medication Error Reporting and Prevention (NCC MERP) is an independent body composed of 27 national organizations. http://www.nccmerp.org/about-medication-errors In 1995, the United States Pharmacopeial Convention (USP) spearheaded the formation of the National Coordinating Council for Medication Error Reporting and Prevention: Leading national health care organizations are meeting, collaborating, and cooperating to address the interdisciplinary causes of errors and to promote the safe use of medications. USP is a founding member and the Secretariat for NCC MERP. Medication Errors Definition What is http://www.nccmerp.org/ a Medication Error? See Definition Taxonomy Provides a standard language and structure when analyzing medication error reports. See Taxonomy Index NCC MERP adopted a Medication Error Index that classifies an error according to the severity of the outcome. See Category Index NAN Alert The National Alert Network (NAN) publishes the alerts from the National Medication Errors Reporting Program. NAN encourages the sharing and reporting of medication errors, so that lessons learned can be used to increase the safety of the medication use system. September 15, 2016 Observe for possible fluid leakage when preparing parenteral syringes Subscribe Archive Upcoming Meetings There is no meeting avaiable. Previous Meetings Report Medication ErrorsISMP Medication Errors Reporting Program (MERP) Go U.S. Food and Drug Administration's MedWatch Reporting Program © 2016 National Coordinating Council for Medication Error Reporting and Prevention. All Rights Reserved. *Permission is hereby granted to reproduce information contained herein provided that such reproduction shall not modify the text and shall include the copyright notice appearing on the pages from which it was copied. This copyright statement will change to the new year after the 1st of every year.
Home Food Drugs Medical Devices Radiation-Emitting Products Vaccines, Blood & Biologics Animal & Veterinary Cosmetics Tobacco Products http://www.fda.gov/drugs/drugsafety/medicationerrors/ 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 Prevention and Analysis (DMEPA) reviews medication error reports on marketed human drugs including prescription drugs, generic drugs, and over-the-counter medication error 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 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 medication error reporting 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, there are cases of adverse events where a name of a marketed product is identified as a source of confusion and error. Therefore, we continue to encourage healthcare providers, patients and consumers to report all medication errors to MedWatch so that we can be made aware of potential problems related to drug names and the Agency can provide effective interventions that