SENATE DOCKET, NO. 306        FILED ON: 1/15/2013

SENATE  .  .  .  .  .  .  .  .  .  .  .  .  .  .  No. 1029

 

The Commonwealth of Massachusetts

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PRESENTED BY:

John F. Keenan

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To the Honorable Senate and House of Representatives of the Commonwealth of Massachusetts in General
Court assembled:

The undersigned legislators and/or citizens respectfully petition for the adoption of the accompanying bill:

An Act relative to prescription drug adverse event reporting..

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PETITION OF:

 

Name:

District/Address:

John F. Keenan

Norfolk and Plymouth

Daniel A. Wolf

Cape and Islands

Martin J. Walsh

13th Suffolk

James M. Murphy

4th Norfolk

Bruce E. Tarr

First Essex and Middlesex


SENATE DOCKET, NO. 306        FILED ON: 1/15/2013

SENATE  .  .  .  .  .  .  .  .  .  .  .  .  .  .  No. 1029

By Mr. Keenan, a petition (accompanied by bill, Senate, No. 1029) of John F. Keenan, Daniel A. Wolf, Martin J. Walsh, James M. Murphy and other members of the General Court for legislation relative to prescription drug adverse event reporting.  Public Health.

 

The Commonwealth of Massachusetts

 

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In the Year Two Thousand Thirteen

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An Act relative to prescription drug adverse event reporting..

 

Be it enacted by the Senate and House of Representatives in General Court assembled, and by the authority of the same, as follows:
 

SECTION 1. Chapter 38 of the General Laws is hereby amended by adding the following, which shall constitute section 16 of said chapter:-

Section 16. (a) The chief medical examiner shall file an adverse event report with the United States Food and Drug Administration any time the determined cause of death of an individual was due fully or in part to the ingestion of a Schedule II through VI controlled substance according to regulations promulgated by the Department of Public Health.  This report shall also be sent to the commissioner of the department of public health.

SECTION 2.  Section 24A of chapter 94C of the General Laws is hereby amended by adding the following new subsection:-

(l) Upon receiving a report of an overdose-related death from the chief medical examiner pursuant to section 16 of chapter 38 of the General Laws, the department shall investigate the prescription monitoring program record of the deceased individual.  In the annual report required by subsection (k) of this section, the department shall present information on any trends discovered through investigation of the prescription monitoring program records of individuals having suffered a fatal overdose in the preceding year, to include any indication of multiple deaths associated with a single prescriber.