Medication Error Reporting Software
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DataSetsGEO ProfilesGSSGTRHomoloGeneMedGenMeSHNCBI Web SiteNLM CatalogNucleotideOMIMPMCPopSetProbeProteinProtein ClustersPubChem BioAssayPubChem CompoundPubChem SubstancePubMedPubMed HealthSNPSparcleSRAStructureTaxonomyToolKitToolKitAllToolKitBookToolKitBookghUniGeneSearch termSearch Browse Titles Limits Advanced Help NCBI Bookshelf. A service of the National Library of Medicine, National medication error reporting categories Institutes of Health.Hughes RG, editor. Patient Safety and Quality: An Evidence-Based medication error reporting procedure Handbook for Nurses. Rockville (MD): Agency for Healthcare Research and Quality (US); 2008 Apr. Patient Safety and medication error reporting form Quality: An Evidence-Based Handbook for Nurses.Show detailsHughes RG, editor.Rockville (MD): Agency for Healthcare Research and Quality (US); 2008 Apr.ContentsSearch term < PrevNext > Chapter 35Error Reporting and medication error reporting format DisclosureZane Robinson Wolf; Ronda G. Hughes.Author InformationZane Robinson Wolf;1 Ronda G. Hughes.21 Zane Robinson Wolf, Ph.D., R.N., F.A.A.N., dean and professor, La Salle University School of Nursing and Health Sciences. E-mail: ude.ellasal@flow2 Ronda G. Hughes, Ph.D., M.H.S., R.N., senior health scientist administrator, Agency for Healthcare Research and Quality. E-mail: vog.shh.qrha@sehguH.adnoRBackgroundThis chapter examines reporting of health
Reporting Medication Errors In Nursing
care errors (e.g., verbal, written, or other form of communication and/or recording of near miss and patient safety events that generally involves some form of reporting system) and these events’ disclosure (e.g., communication of errors to patients and their families), including the ethical aspects of error-reporting mechanisms. The potential benefits of intrainstitutional and Web-based databases might assist nurses and other providers to prevent similar hazards and improve patient safety. Clinicians’ fears of lawsuits and their self-perceptions of incompetence could be dispelled by organizational cultures emphasizing safety rather than blame. This chapter focuses on the assertion that reporting errors that result in patient harm as well as seemingly trivial errors and near misses has the potential to strengthen processes of care and improve the quality of care afforded patients.Reporting ErrorsReporting errors is fundamental to error prevention. The focus on medical errors that followed the release of the Institute of Medicine’s (IOM) report To Err Is Human: Building a Safer Health System1 centered on the suggest
Event Reports (Incident Reports) Abuse & Neglect Reports Medication Error Reports
Describe The Difference Between Internal And External Reports
Witness Reports Therap Basic Management/Event Summaries Time Tracking Individual ncc merp medication error definition Services Plans Global ISP Template Library IPOP (Individual Plan of Protective Oversight and ncc merp taxonomy of medication errors Safeguards) Behavior Plans & Tracking T-Log (Nursing/Progress Notes) Therap Basic Secure Communications Demographics Activity Tracking/Audit Trails Notifications T-Notes Therap Calendar Caseworker Access https://www.ncbi.nlm.nih.gov/books/NBK2652/ Family Access Ger Resolution Advance Directives Therap Basic Health Tracking Applications Appointments Blood Glucose Height/Weight Immunization Infection Tracking Menses Respiratory Treatment Health Tracking Applications Seizures Skin Wounds Vital Signs Intake/Elimination Monthly and Detailed Reports Quarterly Nursing Reports Health Passport Lab Test Mobile Applications MAR https://www.therapservices.net/therap-basic/medication-error-reports/ (Medication Administration Records) Plus Electronic Health Records - EHR Billing/ Billing Plus ISP (Individual Service Program) Mobile TMS (Training Management System) Document Storage Personal Finance Letter Module Therap for States and Counties Employment Services and Supports Case Note Staff Ratio Tracking Pharmacy Interface States State Contracts (A-N) Alabama Arkansas California Idaho Kansas Montana Nebraska New Mexico State Contracts (N-W) North Dakota Oregon Puerto Rico South Carolina South Dakota Washington Wisconsin More States Alaska Arizona Colorado Connecticut Delaware District of Columbia Florida Georgia Hawaii Illinois Indiana Iowa More States Kentucky Louisiana Maine Maryland Massachusetts Michigan Mississippi Minnesota Missouri Nevada New Hampshire New Jersey More States New York North Carolina Ohio Oklahoma Pennsylvania Rhode Island Tennessee Texas Utah Vermont Virginia West Virginia Wyoming Conferences Webinars Videos Blogs Justin Brockie Certified Trainers Support
error or hazard to ISMP. If you are a CONSUMER, please click on the orange button below if you are ready to https://www.ismp.org/orderforms/reporterrortoismp.asp report an error or hazard. If you are a HEALTHCARE PRACTITIONER, you can report the error or hazard to ISMP using one of two secure methods: 1) Report to the ISMP National Medication Errors Reporting Program (MERP) or the ISMP National Vaccine Errors Reporting Program (VERP) These are confidential, voluntary reporting programs operated by ISMP to learn about the causes of medication and medication error vaccine errors. After you submit a report, ISMP staff will follow up with you to ask additional questions to clarify what went wrong and to identify the causes and factors that contributed to the reported event. The report will also be forwarded in confidence to the US Food and Drug Administration (FDA) and, when applicable, to product vendors to inform them about pharmaceutical medication error reporting labeling, packaging, and nomenclature issues that may cause errors by their design. Your name, contact information, and location will NOT be submitted to FDA or product vendors without your permission, and identifiable information will NOT be disclosed outside of ISMP. Click on the appropriate button below if you are ready to report an error or hazard to the ISMP MERP or ISMP VERP. Click here to learn more about ISMP reporting programs. 2) Report an adverse event to ISMP as a Patient Safety Organization (PSO) You may prefer to report an adverse medication or vaccine event to ISMP as a federally certified Patient Safety Organization (PSO). As a PSO, federal legal protection can be provided for certain patient safety information prepared within your patient safety evaluation system and submitted to ISMP. The protected information, called patient safety work product, includes information you provide about why the error happened or why the hazard exists, along with any further analysis of the event provided back to you by ISMP. The basic facts, whether written or observed, regarding what happened along with the patient’s medical/health records, are NO