North Dakota Medication Data Form - Medication Error and Near Miss Classification

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US-02260BG
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This form is a generic example that may be referred to when preparing such a form for your particular state. It is for illustrative purposes only. Local laws should be consulted to determine any specific requirements for such a form in a particular jurisdiction.

The North Dakota Medication Data Form — Medication Error and Near Miss Classification is a comprehensive tool designed to accurately capture and categorize medication errors and near misses that occur within the state of North Dakota. This form plays a crucial role in monitoring and analyzing medication-related incidents, aiming to improve medication safety and patient care. Keywords: North Dakota, medication data form, medication error, near miss classification, monitoring, analyzing, medication safety, patient care. This standardized form enables healthcare facilities, including hospitals, clinics, and pharmacies, to report any medication errors or near misses that have taken place. Its purpose is to gather detailed information about these incidents to identify patterns, causes, and potential areas of improvement. By capturing data on medication errors, which refers to preventable events that may cause harm to patients, the form helps healthcare providers understand the underlying causes and implement corrective measures. Near misses, on the other hand, are events that do not result in harm but have the potential to cause harm if circumstances were slightly different. Thus, reporting near misses allows for proactive identification and prevention of future errors. The North Dakota Medication Data Form — Medication Error and Near Miss Classification is often divided into multiple sections, categorizing incidents based on various factors. These sections may include: 1. Patient Information: This section collects data such as patient demographics, age, gender, and medical conditions. This information helps in better understanding the patient population affected by medication errors and near misses. 2. Incident Description: Here, healthcare providers provide a narrative description of the event, including the type of error or near miss, medication involved, dosage, route of administration, and any contributing factors. Gathering this level of detail is essential for accurate incident classification and analysis. 3. Categorization and Classification: This segment of the form allows healthcare providers to classify the incident based on standardized categories, such as wrong medication, incorrect dose, unauthorized medication, omission of medication, or wrong administration route. Classification options may vary depending on the specific version or revision of the form being used. 4. Contributing Factors: In this section, healthcare providers identify underlying factors that contributed to the error or near miss. These can include system failures, lack of staff training, miscommunication, or equipment issues. Analyzing contributing factors helps in pinpointing areas where process improvements can be made to prevent future incidents. 5. Preventive Measures: The form often includes a section to document any actions taken to prevent similar incidents from occurring in the future. This may involve changes in protocols, additional training, or system enhancements. The North Dakota Medication Data Form — Medication Error and Near Miss Classification serves as a valuable tool in enhancing medication safety across healthcare facilities in North Dakota. By encouraging comprehensive incident reporting, analysis, and improvement initiatives, this form contributes to the continuous enhancement of patient care and the reduction of medication-related errors and near misses.

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The ASHP classifies errors as prescribing error, dispensing error, omission error, wrong time error, unauthorized drug error, improper dose error, wrong dosage-form error, wrong drug-preparation error, wrong administration-technique error, deteriorated drug error, monitoring error, compliance error, and other ...

Health care professionals and consumers have the opportunity to report the occurrence of medication errors to a variety of organizations. Examples include the Institute of Safe Medication Practices (ISMP) and the Food and Drug Administration (FDA). These organizations collectively review error submissions.

Write a note in the medical record documenting what happened, the impact on the patient, treatment provided, and results. You can include who was told about it, what they were told, and when.

Near-misses can be classified as belonging to category B of the NCC MERP classification. Near-misses do not reach the patient, but can still potentially cause harm. In 1 emergency department, the rate of an error occurring but not reaching the patient was 11.8%.

Draw a single line through the erroneous entry and write the time, date, and your name. Identify the reason for the correction. Include the rationale in your notation; for example, ?mistaken entry, wrong medication name written.? Follow facility policy when adding late information.

A medication error is defined as "any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is in the control of the healthcare professional, patient, or consumer,? ing to the National Coordinating Council for Medication Error Reporting and Prevention.

The FDA Adverse Event Reporting System (FAERS) is a database that contains information on adverse event and medication error reports submitted to FDA. The database is designed to support the FDA's post-marketing safety surveillance program for drug and therapeutic biologic products.

Medication error procedures: Immediately notify the supervisor and physician. Follow agency policy to notify appropriate professionals. Know and follow your facility's policy for medication errors. Complete a medication error report in ance with regulations and agency policies.

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Feb 6, 2023 — The GER Event Report along with the GER Event Type form (e.g. medication error, injury, etc.) must be completed and submitted together. The ... Jul 11, 2015 — DATAFORM 3 Medication Error and Near Miss Classification Form.I will be completing the task(s) listed on the EPCSP Procedure and Training form as the extended personal care ... Report of all medication errors or omissions. Aug 29, 2018 — If that individual is not available, the medication error or near miss will be reported to the manager and the Medication Reporting Form for  ... Jan 19, 2018 — ... in book or electronic data form (available in the pharmacy or online) which ... the medical director, drugs must be obtained from a North Dakota. by KJ Jones · 2008 · Cited by 8 — The limited availability of pharmacists in CAHs limits pharmacists' ability to intercept medication errors before reaching the patient (e.g., near-miss errors); ... This survey collected information about the number of medication errors and near-misses reported in the year prior to joining the project, the extent to ... The ADE Action Plan identifies efforts to date to measure and prevent ADEs, and promote medication safety. In addition, this plan outlines future opportunities ... This Program Report for the year April 2010-March 2011of the Healthcare SafetyZone®. (HCSZ) Portal, in part with the North Dakota Critical Access Hospital ... This Program Report for the year April 2010-March 2011of the Healthcare SafetyZone®. (HCSZ) Portal, in part with the North Dakota Critical Access Hospital ...

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North Dakota Medication Data Form - Medication Error and Near Miss Classification