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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
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)
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.
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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