Tennessee § 53-10-204 - Substitution authorized — Instructions of prescriber.

§ 53-10-204. Substitution authorized — Instructions of prescriber.

The prescriber shall allow for substitution with a generic equivalent of a brand name drug or drug product under all circumstances, unless: The prescriber determines the medical necessity of a brand name drug or drug product due to: An adverse reaction previously experienced by the patient to a generic equivalent; A generic equivalent has previously been demonstrated as ineffective for the patient; or Any other clinically based prescriber determined need; A generic equivalent is not available; or Section 53-10-210 concerning notification to the patient and the prescriber have not been complied with in instances involving an anti-epileptic drug. If the prescriber determines a brand name drug or drug product is medically necessary for a patient, the prescriber shall, in the prescriber's own handwriting, place the instruction showing intent upon the prescription at the time it is prepared and issued. For the purposes of this subsection (b), instructions showing intent may include, but not be limited to, the following language: “Brand name medically necessary”, “dispense as written”, “medically necessary”, “brand name”, “no generic”; Any abbreviation of the language in subdivision (b)(1); or Any other prescriber handwritten notation, such as circling a preprinted instruction to dispense as written on the prescription order, that clearly conveys the intent that a brand name is necessary for this patient. If the prescriber determines a brand name drug or drug product is medically necessary for a patient and that prescription order is issued verbally, the prescriber shall alert the pharmacist that use of the brand name drug or drug product is medically necessary for the patient. If the prescriber determines a brand name drug or drug product is medically necessary for a patient and that prescription order is issued by the prescriber in the form of an electronic prescription order or facsimile prescription order, the prescriber shall place, or cause to be placed, the proper instruction on the electronic prescription order or facsimile prescription order prior to it being transmitted to the pharmacist. Nothing in this section shall be construed to prevent a prescriber from informing a patient of the prescriber's professional opinion as to the capabilities, effectiveness and acceptability of any drug. Acts 2005, ch. 434, § 6; 2006, ch. 564, §§ 1, 2; 2007, ch. 370, § 2. Compiler's Notes. Former part 2, §§ 53-10-201 — 53-10-206 (Acts 1977, ch. 66, §§ 1-5, 9; T.C.A., §§ 52-1221 — 52-1226; Acts 1986, ch. 505, § 1; 1992, ch. 539, § 1; 1995, ch. 474, § 1), concerning substitution of generic drugs, was repealed by Acts 2005, ch. 434, § 2, effective June 17, 2005. For provisions on affordable drugs, see this part 2. Acts 2007. ch. 370, § 3 provided that the general assembly finds, determines and declares that the act is necessary for the immediate preservation of the public peace, health and safety. Cross-References. Affordable health insurance for the uninsured, title 56, ch. 7, part 6. Medical Assistance Act, title 71, ch. 5, part 1. Prescription drug programs, title 71, ch. 2, part 5. Pharmaceutical connection program, title 71, ch. 5, part 5. Volunteer Rx discount drug program, title 56, ch. 57, part 1.