[1] NOTE:  As provided in LFC policy, this report is intended only for use by the standing finance committees of the legislature.  The Legislative Finance Committee does not assume responsibility for the accuracy of the information in this report when used in any other situation.

 

Only the most recent FIR version (in HTML & Adobe PDF formats) is available on the Legislative Website.  The Adobe PDF version includes all attachments, whereas the HTML version does not.  Previously issued FIRs and attachments may be obtained from the LFC’s office in Suite 101 of the State Capitol Building North.

 

 

F I S C A L   I M P A C T   R E P O R T

 

 

 

SPONSOR:

Feldman

 

DATE TYPED:

02/01/02

 

HB

 

 

SHORT TITLE:

Pharmaceutical Supplemental Rebate Act

 

SB

253

 

 

ANALYST:

Dunbar

 

APPROPRIATION

 

Appropriation Contained

Estimated Additional Impact

Recurring

or Non-Rec

Fund

Affected

FY02

FY03

FY02

FY03

 

 

 

 

$0.1    See Narrative

Recurring

General Fund

 

(Parenthesis ( ) Indicate Expenditure Decreases)

 

Relates to HB264, SB226, HB200, SB091, HJM41, SB238, SJM23, HB149, SB263, HJM021,

     SJM35, SJM22, and SB118

 

 

SOURCES OF INFORMATION

 

Responses Received

Department of Health (DOH)

Human Services Department (HSD)

Attorney General (AG)

Health Policy Commission (HPC)

 

SUMMARY

 

     Synopsis of Bill

 

Senate Bill 253 enacts the Pharmaceutical Supplemental Rebate Act.  This Act requires a formulary or preferred drug list to provide medically appropriate drug therapies for patients.  The bill also provides for negotiated discount prices or rebates from drug manufacturers or labelers. Rebates and/or discounts will be greater than those required under Federal law.  Manufacturers who fail to negotiate such rebates will be placed on a prior authorization list.  Savings from this program must be reported to the Legislative Health and Human Services annually.  The Human Services Department must seek any necessary waivers of Federal law or rules to implement this Act.

 

 

 

 

 

     Significant Issues

 

This Bill is similar to laws successfully implemented in Florida and Michigan.  The AG reports that the pharmaceutical industry trade association, Pharma, has an apparent policy of mounting judicial challenges to all state programs designed to reduce the cost of prescription drugs.  Pharma’s challenges in Florida and Michigan have been unsuccessful.  Significant issues include whether the Department of Human Services has the necessary administrative capacity and expertise to implement the program.

 

The AG is uneasy as to whether the terms of the current Medicaid Managed Care contracts would transfer any resultant savings to the benefit of the managed care companies and not to a reduction in Medicaid costs.

 

FISCAL IMPLICATIONS

 

The bill does not contain an appropriation. (See administrative implications below)

 

ADMINISTRATIVE IMPLICATIONS

 

Medical Assistance Division (MAD) currently has one Pharmacist managing the Medicaid Drug Program, and another managing the Medicaid Drug Rebate Program.  The division also employs a medical director.

 

HSD indicates that currently, the Medicaid program requires prior authorization for very few drugs, and the Medicaid pharmacist using relatively broad criteria does all authorizations.  HSD believes that SB 253 would vastly increase the number of drugs requiring prior authorization.

 

Supplemental rebates and other drug discounts have not been negotiated in the past.  If SB 253 is enacted into law, additional staff may be required.

 

Employing a drug formulary would require the creation of a Pharmacy and Therapeutics (P&T) Committee as outlined in the Social Security Act, Section 1927. 

 

RELATIONSHIP

 

 

 

 

OTHER SUBSTANTIVE ISSUES

 

HPC reports that prescription drug spending in the United States has grown more than 10% per year since 1995, placing financial pressure on private and public programs.  Such spending is likely to rise 15% - 18% through the year 20045.  Medicaid expenditures from 1997 to 2000 grew at an average annual rate of 18.1%6.

 

HSD anticipates confusion in the Medicaid drug program if the formulary restrictions, which would be established pursuant to SB 253 are not aggressively communicated, and if medical providers do not proactively seek them out.

 

The bill could require renegotiation of the state’s current contract with Express Scripts to accommodate all state –managed drug programs.

 

BD/ar


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