Texas Statutes
Subchapter A. Prescription and Substitution Requirements
Section 562.0141. Transplant Immunosuppressant Drug Product Selection Prohibited

Sec. 562.0141. TRANSPLANT IMMUNOSUPPRESSANT DRUG PRODUCT SELECTION PROHIBITED. (a) In this section:
(1) "Immunosuppressant drug" means any drug prescribed for immunosuppressant therapy following a transplant.
(2) "Interchange" means the substitution of one version of the same immunosuppressant drug, including a generic version for the prescribed brand, a brand version for the prescribed generic version, a generic version by one manufacturer for a generic version by a different manufacturer, a different formulation of the prescribed immunosuppressant drug, or a different immunosuppressant drug for the immunosuppressant drug originally prescribed.
(b) A pharmacist may not interchange an immunosuppressant drug or formulation of an immunosuppressant drug, brand or generic, for the treatment of a patient following a transplant without prior consent to the interchange from the prescribing practitioner.
(c) To comply with Subsection (b), a pharmacist shall notify a prescribing practitioner orally or electronically to secure permission to interchange an immunosuppressant drug or formulation of an immunosuppressant drug, brand or generic. The practitioner's authorization or denial of authorization must be documented by the pharmacist and by the practitioner.
(d) If a pharmacist does not have the same drug product by the same manufacturer in stock to refill the prescription, or if the practitioner is unavailable to give authorization, the pharmacist may dispense a drug product that is generically equivalent if the pharmacist, before dispensing the generally equivalent drug product:
(1) notifies and receives consent from the patient, at the time the prescription is dispensed, to substitute the prescribed drug product; and
(2) notifies the prescribing practitioner of the drug product substitution orally or electronically at the earliest reasonable time, but not later than 24 hours after dispensing the prescription.
(e) This section is only effective subject to the conditions established by Section 562.0142.
Added by Acts 2007, 80th Leg., R.S., Ch. 385 (S.B. 625), Sec. 2, eff. June 15, 2007.

Structure Texas Statutes

Texas Statutes

Occupations Code

Title 3 - Health Professions

Subtitle J - Pharmacy and Pharmacists

Chapter 562 - Practice by License Holder

Subchapter A. Prescription and Substitution Requirements

Section 562.001. Definitions

Section 562.002. Legislative Intent

Section 562.003. Disclosure of Price; Patient's Option

Section 562.004. Prescription Transmitted Orally by Practitioner

Section 562.005. Record of Dispensed Drug or Biological Product

Section 562.0051. Communication Regarding Certain Dispensed Biological Products

Section 562.006. Label

Section 562.0061. Other Prescription Information

Section 562.0062. Required Statement Regarding Medication Disposal

Section 562.007. Refills

Section 562.008. Generic Equivalent or Interchangeable Biological Product Authorized

Section 562.009. Requirements Concerning Selection of Generically Equivalent Drug or Interchangeable Biological Product

Section 562.010. Responsibility Concerning Generically Equivalent Drug or Interchangeable Biological Product; Liability

Section 562.011. Restriction on Selection of and Charging for Generically Equivalent Drug or Interchangeable Biological Product

Section 562.012. Substitution of Dosage Form Permitted

Section 562.013. Applicability of Subchapter

Section 562.014. Narrow Therapeutic Index Drugs

Section 562.0141. Transplant Immunosuppressant Drug Product Selection Prohibited

Section 562.0142. Adoption of Rules

Section 562.015. Dispensing Directive; Compliance With Federal Law

Section 562.016. List of Approved Interchangeable Biological Products