Current through Register Vol. 30, No. 50, December 13, 2024
Section R4-25-603 - Prescribing and Dispensing RequirementsA podiatrist shall:
1. Not dispense schedule II controlled substances that are opioids.2. Not dispense a drug unless the drug is obtained from a manufacturer or distributor licensed in any state or jurisdiction;3. Ensure that a drug or device is dispensed only to a patient being treated by the podiatrist;4. Before dispensing a drug, provide a patient with a written prescription order that: a. Contains the following statement in bold type: "This prescription may be filled by the prescribing podiatrist or by a pharmacy of your choice," andb. Is signed by the podiatrist;5. Directly supervise each individual involved in preparing a drug that is dispensed;6. Ensure that a drug is: a. Dispensed in a prepackaged container or in a light resistant container with a consumer safety cap; andb. Labeled with the following information: i. The podiatrist's name, address, and telephone number;ii. The date the drug is dispensed;iii. The patient's name; andiv. The name, strength of the drug, and directions for the drug's use;7. Ensure that the original prescription order for a drug is countersigned and dated by the individual who prepared the drug for dispensing;8. Before a drug or device is dispensed to a patient: a. Review the drug or device to ensure compliance with the prescription order;b. Ensure the patient is informed of the following: i. The name of the drug or device,ii. Directions for taking the drug or using the device,iii. Precautions for the drug or device, andiv. Directions for storing the drug or device;9. Document in the medical record the following for each patient: a. Name of the drug or device dispensed,b. Strength of the drug dispensed,c. Date the drug or device is dispensed, andd. Therapeutic reasons for dispensing the drug or device;10. Maintain an inventory record for each drug that contains: c. Date the drug was received by the podiatrist,d. Amount of the drug received by the podiatrist,e. Name of the manufacturer and distributor of the drug, andf. A unique identifying number provided by the manufacturer or distributor of the drug;11. Store a drug in a locked cabinet or room and: a. Establish a written policy for access to the locked cabinet or room, andb. Make the written policy available to the Board or its authorized agent with within 72 hours of a Board request;12. Ensure that a drug is stored at temperatures recommended by the manufacturer of the drug; and13. Maintain a dispensing log, separate from the inventory record for each drug dispensed that includes the: e. Date the drug was dispensed, andf. The name and signature of the podiatrist who dispensed the drug.Ariz. Admin. Code § R4-25-603
Adopted effective July 27, 1995 (Supp. 95-3). Amended by final rulemaking at 9 A.A.R. 1846, effective July 19, 2003 (Supp. 03-2). Amended by final rulemaking at 26 A.A.R. 1501, effective 9/6/2020.