Bill Text: NY A04823 | 2011-2012 | General Assembly | Introduced


Bill Title: Provides that drug utilization review and the preferred drug program shall not apply to certain drugs.

Spectrum: Moderate Partisan Bill (Democrat 4-1)

Status: (Introduced - Dead) 2012-09-04 - enacting clause stricken [A04823 Detail]

Download: New_York-2011-A04823-Introduced.html
                           S T A T E   O F   N E W   Y O R K
       ________________________________________________________________________
                                         4823
                              2011-2012 Regular Sessions
                                 I N  A S S E M B L Y
                                   February 8, 2011
                                      ___________
       Introduced  by  M.  of  A.  P. RIVERA  --  read once and referred to the
         Committee on Health
       AN ACT to amend the social services law and the public  health  law,  in
         relation to drug utilization review and the preferred drug program
         THE  PEOPLE OF THE STATE OF NEW YORK, REPRESENTED IN SENATE AND ASSEM-
       BLY, DO ENACT AS FOLLOWS:
    1    Section 1. Subdivision 4 of section 369-cc of the social services law,
    2  as added by section 39 of part C of chapter 58 of the laws of  2009,  is
    3  amended to read as follows:
    4    4.  (a)  The  commissioner,  through  the prospective DUR program, may
    5  require step therapy when there is more than  one  drug  appropriate  to
    6  treat  a  medical condition. The purpose of step therapy is to encourage
    7  the use of medically appropriate, cost effective drugs  when  clinically
    8  indicated  and to limit use of alternative drug therapies unless certain
    9  clinical requirements are met. The DUR board shall recommend  guidelines
   10  for  specific  diagnoses and therapy regimens within which practitioners
   11  may prescribe drugs without the requirement for prior  authorization  of
   12  those  drugs. In establishing these guidelines, the board shall consider
   13  clinical effectiveness, safety, and cost effectiveness.  Prior  authori-
   14  zation  under this paragraph shall be obtained under section two hundred
   15  seventy-three of the public health law.  IN ADDITION, THE  AUTHORITY  TO
   16  REQUIRE STEP THERAPY AS AUTHORIZED BY THIS PARAGRAPH SHALL NOT APPLY TO:
   17    (I) ATYPICAL ANTI-PSYCHOTICS;
   18    (II) ANTI-DEPRESSANTS;
   19    (III) ANTI-RETROVIRALS USED IN THE TREATMENT OF HIV/AIDS;
   20    (IV)  ANTI-REJECTION  DRUGS USED FOR THE TREATMENT OF ORGAN AND TISSUE
   21  TRANSPLANTS; AND
   22    (V) ANY OTHER THERAPEUTIC CLASS FOR THE TREATMENT OF MENTAL ILLNESS OR
   23  HIV/AIDS, RECOMMENDED BY THE DUR BOARD AND APPROVED BY THE COMMISSIONER.
   24    (b) The commissioner, through the prospective DUR  program,  may  from
   25  time  to time limit the quantity, frequency, and duration of drug thera-
   26  py, using guidelines developed by the DUR board.  The  DUR  board  shall
   27  develop clinical prescribing guidelines relating to quantity, frequency,
   28  and duration of drug therapy for the commissioner's use under this para-
        EXPLANATION--Matter in ITALICS (underscored) is new; matter in brackets
                             [ ] is old law to be omitted.
                                                                  LBD01204-01-1
       A. 4823                             2
    1  graph.  In establishing these guidelines, the board shall consider clin-
    2  ical effectiveness, safety, and cost effectiveness. Prior  authorization
    3  under  this paragraph shall be obtained under section two hundred seven-
    4  ty-three of the public health law. Exceptions to any prior authorization
    5  imposed  as  a result of these guidelines shall include, but need not be
    6  limited to, provision for emergency circumstances where a medical condi-
    7  tion requires alleviation of severe pain or  which  threatens  to  cause
    8  disability  or  to  take a life if not promptly treated.  PRIOR AUTHORI-
    9  ZATION UNDER THIS PARAGRAPH SHALL BE OBTAINED PURSUANT  TO  SECTION  TWO
   10  HUNDRED  SEVENTY-THREE  OF  THE  PUBLIC  HEALTH  LAW.   IN ADDITION, THE
   11  AUTHORITY TO LIMIT THE QUANTITY, FREQUENCY AND DURATION OF DRUG  THERAPY
   12  AS AUTHORIZED BY THIS PARAGRAPH SHALL NOT APPLY TO:
   13    (I) ATYPICAL ANTI-PSYCHOTICS;
   14    (II) ANTI-DEPRESSANTS;
   15    (III) ANTI-RETROVIRALS USED IN THE TREATMENT OF HIV/AIDS;
   16    (IV)  ANTI-REJECTION  DRUGS USED FOR THE TREATMENT OF ORGAN AND TISSUE
   17  TRANSPLANTS; AND
   18    (V) ANY OTHER THERAPEUTIC CLASS FOR THE TREATMENT OF MENTAL ILLNESS OR
   19  HIV/AIDS, RECOMMENDED BY THE DUR BOARD AND APPROVED BY THE COMMISSIONER.
   20    S 2. Paragraph (b) of subdivision 11 of  section  272  of  the  public
   21  health  law,  as added by section 36 of part C of chapter 58 of the laws
   22  of 2009, is amended to read as follows:
   23    (b) (I) The commissioner may designate a  pharmaceutical  manufacturer
   24  as  one  with  whom  the commissioner is negotiating or has negotiated a
   25  manufacturer agreement, and all of the drugs it manufactures or  markets
   26  shall  be  included  in the preferred drug program. The commissioner may
   27  negotiate directly with a pharmaceutical manufacturer for rebates relat-
   28  ing to any or all of the drugs it manufactures or markets. A manufactur-
   29  er agreement shall designate any or all of  the  drugs  manufactured  or
   30  marketed  by  the  pharmaceutical manufacturer as being preferred or non
   31  preferred drugs. When a pharmaceutical manufacturer has been  designated
   32  by  the commissioner under this paragraph but has not reached a manufac-
   33  turer agreement with the pharmaceutical manufacturer, then  all  of  the
   34  drugs  manufactured or marketed by the pharmaceutical manufacturer shall
   35  be non preferred drugs. However,  notwithstanding  this  paragraph,  any
   36  drug  that  is selected to be on the preferred drug list under paragraph
   37  (b) of subdivision ten of this section on grounds  that  it  is  signif-
   38  icantly  more  clinically  effective  and  safer than other drugs in its
   39  therapeutic class shall be a preferred drug.
   40    (II) PRIOR AUTHORIZATION UNDER THIS PARAGRAPH SHALL BE OBTAINED PURSU-
   41  ANT TO THIS SECTION. IN ADDITION, THE AUTHORITY TO  DESIGNATE  DRUGS  AS
   42  PREFERRED  OR  NON PREFERRED PURSUANT TO AN AGREEMENT AUTHORIZED BY THIS
   43  PARAGRAPH SHALL NOT APPLY TO:
   44    (A) ATYPICAL ANTI-PSYCHOTICS;
   45    (B) ANTI-DEPRESSANTS;
   46    (C) ANTI-RETROVIRALS USED IN THE TREATMENT OF HIV/AIDS;
   47    (D) ANTI-REJECTION DRUGS USED FOR THE TREATMENT OF  ORGAN  AND  TISSUE
   48  TRANSPLANTS; AND
   49    (E) ANY OTHER THERAPEUTIC CLASS FOR THE TREATMENT OF MENTAL ILLNESS OR
   50  HIV/AIDS, RECOMMENDED BY THE DUR BOARD AND APPROVED BY THE COMMISSIONER.
   51    S  3. This act shall take effect immediately, provided that the amend-
   52  ments to section 272 of the public health law, made by  section  two  of
   53  this  act,  shall not affect the repeal of such section and shall expire
   54  and  be deemed repealed therewith.
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