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1. Controlled-substance form: nurse can verify controlled substances at each change of shift. Monitor the receipts, administration, and disposal of a controlled substance.

2. Medication administration record (MAR). It document medication administered to a patient. It includes drug, dose, route of administration, frequency of administration, and the administration time. MAR lists patient's allergies and diagnoses. Yes, every time medication is administered to a patient , you need to update MAR.

3. Medication delivery record: provides accountability (held responsibility) for medication distribution between the pharmacy and hospital or LTF. It lists the medication found in a particular delivery for a patient.

4. Omnibus Budget Reconciliation Act 1990 is the law that require patient profile to be maintained. A patient profile identifies the patient by name, SSN, birth date, and gender. It provides billing information such as insurance (group number, patient's identification, patient's relationship to the cardholder), patient's medical history (current conditions), known allergies, and adverse reactions, listing of all medications (legend or OTC), the medication should have date, quantity, directions for use, and physician's name. list whether patient wants easy-open containers or use generic.

5. Physician order sheet (POS): List all physician's medication orders for a patients. Nondrug orders may include allergies, diagnoses, diet orders, directives, lab orders, and order for ancillary services (physical therapy, occupational therapy, respiratory therapy, speech therapy).

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Which U.S. agency sets the standards for the quality purity and safety of medications?

USP is a scientific nonprofit organization that sets public standards for identity, strength, quality and purity of medicines. USP standards are recognized in various provisions of the federal Food, Drug and Cosmetic Act (FDCA) and in laws, regulations and policies promulgated by states.

Which agency is responsible for monitoring medication purity?

The Food and Drug Administration (FDA), a regulatory agency within the Department of Health and Human Services, regulates the safety and effectiveness of drugs sold in the United States.

Which U.S. government agency is responsible for regulating medications quizlet?

Regulations giving authority to the U.S. Food and Drug Administration (FDA) to oversee the safety of food, drugs, and cosmetics.

Which federal action sets the standards for quality and requires proper medication labeling for preparations containing morphine?

The Pure Food and Drug Act required that products containing morphine indicate the quantity of the drug on their labels. The 1938 Food, Drug, and Cosmetic Act (FDCA) built on these rules by additionally requiring manufacturers to test their products for safety in human patients prior to approval.