2012 -- H 7650 | |
======= | |
LC01727 | |
======= | |
STATE OF RHODE ISLAND | |
| |
IN GENERAL ASSEMBLY | |
| |
JANUARY SESSION, A.D. 2012 | |
| |
____________ | |
| |
A N A C T | |
RELATING TO HUMAN SERVICES - MEDICAL ASSISTANCE | |
|
      |
|
      |
     Introduced By: Representative Arthur J. Corvese | |
     Date Introduced: February 16, 2012 | |
     Referred To: House Health, Education & Welfare | |
It is enacted by the General Assembly as follows: | |
1-1 |
     SECTION 1. Section 40-8-24 of the General Laws in Chapter 40-8 entitled "Medical |
1-2 |
Assistance" is hereby amended to read as follows: |
1-3 |
     40-8-24. Less expensive alternative medications. -- (a) For pharmaceutical purchases |
1-4 |
eligible for reimbursement under the Medicaid state plan, the department shall encourage the |
1-5 |
substitution of generic drugs which are therapeutically equivalent and interchangeable with |
1-6 |
specific brand name drugs in accordance with section 21-31-16.1 and related regulations of the |
1-7 |
department of health, except in the event that a brand name is determined by the director to be |
1-8 |
less costly to the state than the equivalent generic. Calculation of comparative drug costs shall |
1-9 |
include consideration of the amount paid by the state to the pharmacy for a drug under the current |
1-10 |
retail pharmacy reimbursement formula, less any discounts or rebates, including those paid |
1-11 |
pursuant to federal Medicaid law during the previous calendar quarter, and inclusive of all |
1-12 |
dispensing fees. |
1-13 |
     (b) The department shall not require a beneficiary to use, prior to using a brand name |
1-14 |
prescription drug prescribed by a licensed prescriber, any alternative brand name prescription |
1-15 |
drug or over-the-counter drugs. |
1-16 |
     (c) The department may require a beneficiary to use, prior to using a brand name |
1-17 |
prescription drug prescribed by a licensed prescriber, a therapeutically equivalent generic drug, |
1-18 |
unless, pursuant to sections 5-19.1-19, 5-37-18.1 and 21-31-15(b), the prescriber indicates “brand |
1-19 |
name necessary” on the prescription form, or if the prescriber gives oral directions to that effect |
1-20 |
to the dispensing pharmacist. |
2-1 |
     SECTION 2. This act shall take effect on July 1, 2012. |
      | |
======= | |
LC01727 | |
======= | |
EXPLANATION | |
BY THE LEGISLATIVE COUNCIL | |
OF | |
A N A C T | |
RELATING TO HUMAN SERVICES - MEDICAL ASSISTANCE | |
*** | |
3-1 |
     This act would prevent the department of human services from requiring a Medicaid |
3-2 |
beneficiary to use an alternative brand name prescription drug or over-the-counter drug prior to |
3-3 |
using a brand name prescription drug prescribed by a licensed physician. |
3-4 |
     This act would take effect on July 1, 2012. |
      | |
======= | |
LC01727 | |
======= |