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SENATE AMENDED
PRIOR PRINTER'S NO. 3340
PRINTER'S NO. 3689
THE GENERAL ASSEMBLY OF PENNSYLVANIA
HOUSE BILL
No.
2069
Session of
2015
INTRODUCED BY FARRY, SAMUELSON, HENNESSEY, GROVE, YOUNGBLOOD,
BARRAR, COOK-ARTIS, V. BROWN, DeLUCA, BAKER, GALLOWAY,
WATSON, FREEMAN, DRISCOLL, QUIGLEY, GODSHALL, D. MILLER,
PHILLIPS-HILL, ROZZI, SAINATO, BULLOCK, MILLARD, SCHLOSSBERG,
STAATS, DiGIROLAMO, GIBBONS, D. COSTA, LONGIETTI, HARHAI,
DeLISSIO, RAVENSTAHL, THOMAS, GINGRICH, JOZWIAK, WHITE,
DAVIS, GILLEN, BRIGGS, BARBIN, NELSON AND MATZIE,
MAY 12, 2016
SENATOR BROOKS, AGING AND YOUTH, IN SENATE, AS AMENDED,
JUNE 30, 2016
AN ACT
Amending the act of August 26, 1971 (P.L.351, No.91), entitled
"An act providing for a State Lottery and administration
thereof; authorizing the creation of a State Lottery
Commission; prescribing its powers and duties; disposition of
funds; violations and penalties therefor; exemption of prizes
from State and local taxation and making an appropriation,"
in pharmaceutical assistance for the elderly, further
providing for definitions, for program generally and for
generic drugs, providing for medication synchronization,
further providing for the Pharmaceutical Assistance Contract
for the Elderly Needs Enhancement Tier (PACENET) and for
board and, providing for medication therapy management AND
FURTHER PROVIDING FOR COORDINATION OF BENEFITS.
The General Assembly of the Commonwealth of Pennsylvania
hereby enacts as follows:
Section 1. The definition of "board" in section 502 of the
act of August 26, 1971 (P.L.351, No.91), known as the State
Lottery Law, added November 21, 1996 (P.L.741, No.134), is
amended and the section is amended by adding definitions to
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read:
SECTION 1. THE DEFINITIONS OF "BOARD" AND "INCOME" IN
SECTION 502 OF THE ACT OF AUGUST 26, 1971 (P.L.351, NO.91),
KNOWN AS THE STATE LOTTERY LAW, ADDED NOVEMBER 21, 1996
(P.L.741, NO.134) AND REENACTED AND AMENDED FEBRUARY 7, 2014
(P.L.27, NO.12), ARE AMENDED AND THE SECTION IS AMENDED BY
ADDING DEFINITIONS TO READ:
Section 502. Definitions.
The following words and phrases when used in this chapter
shall have the meanings given to them in this section unless the
context clearly indicates otherwise:
* * *
"Board." The Pharmaceutical Assistance [Review] Advisory
Board.
* * *
"INCOME." ALL INCOME FROM WHATEVER SOURCE DERIVED,
INCLUDING, BUT NOT LIMITED TO, SALARIES, WAGES, BONUSES,
COMMISSIONS, INCOME FROM SELF-EMPLOYMENT, ALIMONY, SUPPORT
MONEY, CASH PUBLIC ASSISTANCE AND RELIEF, THE GROSS AMOUNT OF
ANY PENSIONS OR ANNUITIES, INCLUDING RAILROAD RETIREMENT
BENEFITS, ALL BENEFITS RECEIVED UNDER THE SOCIAL SECURITY ACT
(49 STAT. 620, 42 U.S.C. § 301 ET. SEQ.) NET OF AMOUNTS WITHHELD
FOR MEDICARE PART B PREMIUM PAYMENT, ALL BENEFITS RECEIVED UNDER
STATE UNEMPLOYMENT INSURANCE LAWS AND VETERANS' DISABILITY
PAYMENTS, ALL INTEREST RECEIVED FROM THE FEDERAL GOVERNMENT OR
ANY STATE GOVERNMENT OR ANY INSTRUMENTALITY OR POLITICAL
SUBDIVISION THEREOF, REALIZED CAPITAL GAINS, RENTALS, WORKMEN'S
COMPENSATION AND THE GROSS AMOUNT OF LOSS OF TIME INSURANCE
BENEFITS, LIFE INSURANCE BENEFITS AND PROCEEDS, EXCEPT THE FIRST
$10,000 OF THE TOTAL OF DEATH BENEFITS PAYMENTS, AND GIFTS OF
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CASH OR PROPERTY, OTHER THAN TRANSFERS BY GIFT BETWEEN MEMBERS
OF A HOUSEHOLD, IN EXCESS OF A TOTAL VALUE OF $300, BUT SHALL
NOT INCLUDE SURPLUS FOOD OR OTHER RELIEF IN KIND SUPPLIED BY A
GOVERNMENT AGENCY, THE PRINCIPAL AND ANY INTEREST ACCRUED FROM A
SAVINGS BOND OR PROPERTY TAX REBATE NOR SHALL THE TERM INCLUDE
ANY STATE VETERANS' BENEFIT PAYMENTS .
* * *
"Medication synchronization." The coordination of
prescription drug filling or refilling by a pharmacy or
dispensing physician for a program participant taking two or
more medications for the purpose of improving medication
adherence.
"NADAC per unit." The current National Average Drug
Acquisition Cost per unit.
* * *
"STATE VETERANS' BENEFIT PAYMENTS." SERVICE-CONNECTED
COMPENSATION OR PAYMENTS PROVIDED TO A VETERAN OR AN UNMARRIED
SURVIVING SPOUSE OF A VETERAN BY A STATE AGENCY OR AUTHORIZED
UNDER STATE LAW.
"Wholesale acquisition cost." The cost of a dispensed drug
based upon the price published in a national drug pricing system
in current use by the Department of Aging as the wholesale
acquisition cost of a prescription drug in the most common
package size.
Section 2. Section 509(6) of the act, amended July 7, 2006
(P.L.1061, No.111), is amended and the section is amended by
adding a paragraph to read:
Section 509. Program generally.
The program shall include the following:
* * *
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[(6) The program payment shall be the lower of the
following amounts determined as follows:
(i) 88% of the average wholesale cost of the
prescription drug dispensed:
(A) with the addition of a dispensing fee of the
greater of:
(I) $4 per prescription; or
(II) the amount set by the department by
regulation;
(B) the subtraction of the copayment; and
(C) if required, the subtraction of the generic
differential; or
(ii) the pharmacy's usual charge for the drug
dispensed with the subtraction of the copayment and, if
required, the subtraction of the generic differential; or
(iii) if a generic drug, the most current Federal
upper payment limits established in the Medicaid Program
under 42 CFR § 447.332 (relating to upper limits for
multiple source drugs), plus a dispensing fee of $4 or
the amount set by the department by regulation, whichever
is greater minus the copayment. The department shall
update the average wholesale costs and the Federal upper
payment limits at least every 30 days.]
(6.1) If the NADAC per unit is available, the program
payment shall be the lower of the following amounts:
(i) the NADAC per unit:
(A) with the addition of a professional
dispensing fee of thirteen dollars per prescription;
and
(B) the subtraction of the copayment; or
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(ii) the pharmacy's usual and customary charge for
the drug dispensed with the subtraction of the copayment.
(6.2) If the NADAC per unit is unavailable, the program
payment shall be the lower of the following amounts:
(i) the wholesale acquisition cost plus 3.2%:
(A) with the addition of a professional
dispensing fee of thirteen dollars per prescription;
and
(B) the subtraction of the copayment; or
(iii) the pharmacy's usual and customary charge for
the drug dispensed with the subtraction of the copayment.
* * *
Section 3. Section 510(a) and (b) of the act, amended July
7, 2006 (P.L.1061, No.111), are amended to read:
Section 510. Generic drugs.
(a) In general.--Notwithstanding any other statute or
regulation, a brand name product shall be dispensed and not
substituted with an A-rated generic therapeutically equivalent
drug if it is less expensive to the program. If a less expensive
A-rated generic therapeutically equivalent drug is available for
dispensing to a claimant, the provider shall dispense the A-
rated generic therapeutically equivalent drug to the claimant.
The department shall reimburse providers based upon the most
current listing of [Federal upper payment limits established in
the Medicaid Program under 42 CFR § 447.332 (relating to upper
limits for multiple source drugs), plus a dispensing fee as set
forth in section 509(6). The department shall update the average
wholesale costs and the Federal upper payment limits on a
regular basis, at least every 30 days.] the NADAC per unit plus
a professional dispensing fee of $13 per prescription. The
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department shall not reimburse providers for brand name products
except in the following circumstances:
(1) There is no A-rated generic therapeutically
equivalent drug available on the market. This paragraph does
not apply to the lack of availability of an A-rated generic
therapeutically equivalent drug in the providing pharmacy
unless it can be shown to the department that the provider
made reasonable attempts to obtain the A-rated generic
therapeutically equivalent drug or that there was an
unforeseeable demand and depletion of the supply of the A-
rated generic therapeutically equivalent drug. In either
case, the department shall reimburse the provider for [88% of
the average wholesale cost] the NADAC per unit plus a
professional dispensing fee [based on the least expensive A-
rated generic therapeutically equivalent drug for the brand
drug dispensed] of $13 per prescription.
(2) An A-rated generic therapeutically equivalent drug
is deemed by the department, in consultation with a
utilization review committee, to have too narrow a
therapeutic index for safe and effective dispensing in the
community setting. The department shall notify providing
pharmacies of A-rated generic therapeutically equivalent
drugs that are identified pursuant to this paragraph on a
regular basis.
(3) The Department of Health has determined that a drug
shall not be recognized as an A-rated generic therapeutically
equivalent drug for purpose of substitution under section
5(b) of the act of November 24, 1976 (P.L.1163, No.259),
referred to as the Generic Equivalent Drug Law.
(4) At the time of dispensing, the provider has a
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prescription on which the brand name drug dispensed is billed
to the program by the provider at a usual and customary
charge which is equal to or less than the least expensive
usual and customary charge of any A-rated generic
therapeutically equivalent drug reasonably available on the
market to the provider.
(5) The brand name drug is less expensive to the
program.
(b) Generic not accepted.--If a claimant chooses not to
accept the A-rated generic therapeutically equivalent drug
required by subsection (a), the claimant shall be liable for the
copayment and [70% of the average wholesale cost of the brand
name drug] the NADAC per unit.
* * *
Section 4. The act is amended by adding a section to read:
Section 515.1. Medication synchronization.
(a) Prorated daily cost-sharing rate.--The program shall
permit and apply a prorated daily cost-sharing rate to
prescription drugs that are dispensed by a pharmacy for less
than a 30 days' supply if the pharmacist or prescriber
determines the fill or refill to be in the best interest of the
program participant and the program participant requests or
agrees to less than a 30 days' supply for the purpose of
medication synchronization.
(b) Denial of coverage prohibited.--
(1) The program may not deny coverage of a prescription
drug that is made in accordance with a plan among the health
plan, individual beneficiary or group plan, a practitioner
and a pharmacist for the purpose of medication
synchronization.
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(2) The program shall allow a pharmacy to override any
denial codes indicating that a prescription drug is being
refilled too soon for the purposes of medication
synchronization.
(c) Certain payment structures prohibited.--
(1) The program may not use payment structures
incorporating prorated dispensing fees.
(2) Dispensing fees for partially filled or refilled
prescriptions shall be paid in full for each prescription
drug dispensed, regardless of any prorated copayment for the
program participant or fee paid for alignment services.
Section 5. Section 519(b) AND (D) of the act, amended July
7, 2006 (P.L.1061, No.111), is ARE amended to read:
Section 519. The Pharmaceutical Assistance Contract for the
Elderly Needs Enhancement Tier.
* * *
(b) PACENET eligibility.--A person with an annual income of
not less than $14,500 and not more than [$23,500] $31,000 in the
case of a single person and of not less than $17,700 and not
more than [$31,500] $41,000 in the case of the combined income
of persons married to each other shall be eligible for enhanced
pharmaceutical assistance under this section. A person may, in
reporting income to the department, round the amount of each
source of income and the income total to the nearest whole
dollar, whereby any amount which is less than 50¢ is eliminated.
* * *
(D) COPAYMENT.--
(1) FOR CLAIMANTS UNDER THIS SECTION, THE COPAYMENT
SCHEDULE SHALL BE:
(I) [EIGHT] ELEVEN DOLLARS FOR NONINNOVATOR MULTIPLE
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SOURCE DRUGS AS DEFINED IN SECTION 702; OR
(II) [FIFTEEN] EIGHTEEN DOLLARS FOR SINGLE-SOURCE
DRUGS AND INNOVATOR MULTIPLE-SOURCE DRUGS AS DEFINED IN
SECTION 702.
(2) THE DEPARTMENT SHALL ANNUALLY CALCULATE THE
COPAYMENT SCHEDULES BASED ON THE PRESCRIPTION DRUGS AND
MEDICAL SUPPLIES CONSUMER PRICE INDEX. WHEN THE AGGREGATE
IMPACT OF THE PRESCRIPTION DRUGS AND MEDICAL SUPPLIES
CONSUMER PRICE INDEX EQUALS OR EXCEEDS $1, THE DEPARTMENT
SHALL ADJUST THE COPAYMENT SCHEDULES. EACH COPAYMENT SCHEDULE
SHALL NOT BE INCREASED BY MORE THAN $1 IN A CALENDAR YEAR.
Section 6. Section 520 of the act, amended or added November
21, 1996 (P.L.741, No.134) and November 26, 2003 (P.L.212,
No.37), is amended to read:
Section 520. Board.
(a) Establishment.--The Pharmaceutical Assistance [Review]
Advisory Board is continued to ensure that the program is
providing and continues to provide the assistance intended in a
fiscally responsible manner without excessively hampering the
pharmaceutical industry.
(b) Composition.--The board shall be comprised of the
following [eight] persons:
(1) The Secretary of Aging, who shall serve as its
chairman.
(2) The Secretary of Revenue.
(3) The Secretary of Health.
(4) [Five] Nine public members[, one appointed by the
President pro tempore of the Senate, one appointed by the
Minority Leader of the Senate, one appointed by the Speaker
of the House of Representatives, one appointed by the
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Minority Leader of the House of Representatives and one
appointed by the Governor. Those appointed by the legislative
officers shall include two senior citizens who have not been
a part of the pharmaceutical industry to serve as consumer
advocates, one representative of the pharmaceutical industry
and one practicing Pennsylvania pharmacist. The individual
appointed by the Governor must be a physician. A public
member who misses two consecutive meetings without good cause
acceptable to the chairman shall be replaced by the
appointing authority.] appointed as follows:
(i) Four practicing Pennsylvania pharmacists whose
names are jointly submitted by the Pennsylvania
Pharmacists Association and the Pennsylvania Association
of Chain Drug Stores and then appointed by the following:
(A) One member appointed by the President pro
tempore of the Senate.
(B) one member appointed by the Minority Leader
of the Senate.
(C) One member appointed by the Speaker of the
House of Representatives.
(D) One member appointed by the Minority Leader
of the House of Representatives.
(ii) Five individuals appointed by the Governor
which include the following:
(A) One representative from the pharmaceutical
industry.
(B) Four senior citizens who have not been a
part of the pharmaceutical industry, two of whom may
be senior advocates.
(5) Should a board vacancy not be filled by the
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appointing authority within 60 days, the power to appoint an
individual to the vacancy shall be given to the Secretary of
Aging.
(c) Review.--Using the annual report submitted by the
department pursuant to section 2102 and other appropriate data
sources, the board shall conduct an annual review. The board
shall develop recommendations concerning any changes in the
level of copayment, deductible or in the level of fees paid to
participating pharmacists. The board shall review the
department's therapeutic drug utilization review program on an
ongoing basis. The board may also recommend other changes in the
structure of the program and direct the department to enter into
discussions with the private contractor concerning amendments to
the contract, or the department may enter into such discussion
if it deems necessary. The copayment or deductible schedule
shall only be adjusted on an annual basis.
(c.1) Powers and duties.--The board shall advise on the
following:
(1) The development and implementation of the department
proposals for medication synchronization and medication
therapy management programs and reimbursement methodologies.
(2) Adjustment of the dispensing fee, as needed.
(3) Cost-of-living adjustment increases for medication
synchronization, medication therapy management and the
dispensing fee.
(d) Meetings.--The board shall meet at least two times per
year and not more than four times per year.
Section 7. The act is amended by adding a section to read:
Section 522.1. Medication therapy management.
PACE shall, in consultation with the board, develop a
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proposal for a medication therapy management program by using
retail community pharmacies enrolled in the program. PACE, in
consultation with the board, shall submit the proposal to the
General Assembly no later than one year after the effective date
of this section.
SECTION 8. SECTION 534(B)(4) OF THE ACT, ADDED JULY 7, 2006
(P.L.1061, NO.111), IS REPEALED:
SECTION 534. COORDINATION OF BENEFITS.
* * *
(B) SPECIFIC COORDINATION PROVISIONS.--THE FOLLOWING
PROVISIONS SHALL APPLY TO CLAIMANTS WHO ARE ALSO PART D
ENROLLEES:
* * *
[(4) PART D ENROLLEES ENROLLED IN PACENET SHALL PAY THE
PART D PREMIUMS CHARGED BY THEIR PDP OR, WITH RESPECT TO THE
PRESCRIPTION DRUG PLAN, MEDICARE ADVANTAGE PRESCRIPTION DRUG
PLAN AND THE PROGRAM SHALL PAY ANY COPAYMENTS IN EXCESS OF
THOSE SET FORTH IN SECTION 519.]
* * *
Section 8 9. This act shall take effect immediately.
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