S.Amdt. 1560Senate114th Congress (2015-2017)2nd degree
S.Amdt. 1560
Sponsored by
Sen. Richard Blumenthal (D-CT)
Submitted June 3, 2015
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Senate amendment submitted
June 3, 2015
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Senate amendment submitted
June 3, 2015
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Senate amendment submitted
June 3, 2015
Text
Submitted
SA 1560. Mr. BLUMENTHAL (for himself and Mr. Durbin) submitted an amendment intended to be proposed to amendment SA 1463 proposed by Mr. McCain to the bill H.R. 1735, to authorize appropriations for fiscal year 2016 for military activities of the Department of Defense and for military construction, to prescribe military personnel strengths for such fiscal year, and for other purposes; which was ordered to lie on the table; as follows: At the end of subtitle B of title VII, add the following: SEC. 721. MONITORING OF ADVERSE EVENT DATA ON DIETARY SUPPLEMENT USE BY MEMBERS OF THE ARMED FORCES. (a) In General.--The Secretary of Defense shall modify the electronic health record system of the military health system to include data regarding the use by members of the Armed Forces of dietary supplements and adverse events with respect to dietary supplements. (b) Requirements.--The modifications required by subsection (a) shall ensure that the electronic health record system of the military health system-- (1) records adverse event report data regarding dietary supplement use by members of the Armed Forces; (2) generates standard reports on adverse event data that can be aggregated for analysis; (3) issues automated alerts to signal a significant change in adverse event reporting or to signal a risk of interaction with a medication or other treatment; and (4) is interoperable with the MedWatch form of the Food and Drug Administration (as described in section 760(d) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379aa(d))). (c) Outreach.--The Secretary shall conduct outreach to health care providers in the military health system to educate such providers on the importance of entering adverse event report data regarding dietary supplement use by members of the Armed Forces into the electronic health record system of the military health system and the MedWatch form described in subsection (b)(4). (d) Definitions.--In this section: (1) Adverse event.--The term ``adverse event'' has the meaning given such term in section 761(a) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 379aa-1(a)). (2) Dietary supplement.--The term ``dietary supplement'' has the meaning given such term in section 201(ff) of the Federal Food, Drug, and Cosmetic Act (21 U.S.C. 321(ff)). ______