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Get the free Drug Utilization R eview Board - Oklahoma.gov

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** PUBLIC DISCLOSURE COPY **990OMB No. 15450047Return of Organization Exempt From Income TaxForm (Rev. January 2020)Under section 501(c), 527, or 4947(a)(1) of the Internal Revenue Code (except private
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01
Gather all necessary information about the patient such as medical history, current medications, and any known drug allergies.
02
Review the patient's prescribed medications and compare them to their medical history to ensure they are appropriate and safe.
03
Analyze the patient's drug therapy to identify any potential issues such as drug interactions, duplications, or inappropriate dosages.
04
Develop recommendations based on the findings of the drug utilization review and communicate them to the prescriber for follow-up action.
05
Document the results of the drug utilization review and any recommendations made for future reference and auditing purposes.

Who needs drug utilization r eview?

01
Patients who are taking multiple medications from different healthcare providers.
02
Healthcare providers who want to ensure the safety and effectiveness of their patient's drug therapy.
03
Healthcare facilities looking to improve patient outcomes and reduce medication errors.
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Drug utilization review (DUR) is a process aimed at ensuring that prescribed medications are appropriate, safe, and effective for patients based on their clinical data and treatment needs.
Healthcare providers, including pharmacists and physicians, along with healthcare organizations that administer medication therapies, are typically required to file drug utilization reviews.
To fill out a drug utilization review, one must gather patient information, including medical history and current medications, and complete a standardized DUR form that assesses medication appropriateness and adherence to guidelines.
The purpose of drug utilization review is to improve the quality of patient care by ensuring judicious use of medications, reducing adverse drug events, and promoting optimal therapeutic outcomes.
Information that must be reported typically includes patient demographics, medication names and dosages, indications for use, prescribing physician details, and any noted interactions or contraindications.
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