Sec. 716. Monitoring of adverse event data on dietary supplement use by members of the Armed Forces
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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. The modifications required by subsection
(a)shall ensure that the electronic health record system of the military health system— records adverse event report data regarding dietary supplement use by members of the Armed Forces; generates standard reports on adverse event data that can be aggregated for analysis; 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 provides for reporting of adverse event report data regarding dietary supplement use by members of the Armed Forces to the Food and Drug Administration. 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 reporting such data to the Food and Drug Administration. In this section: The term adverse event has the meaning given that term in section 761(a) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 379aa–1(a) ). The term dietary supplement has the meaning given that term in section 201(ff) of the Federal Food, Drug, and Cosmetic Act ( 21 U.S.C. 321(ff) ).
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- 21 USC 379aa–1(a)
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Sec. 716
Monitoring of adverse event data on dietary supplement use by members of the Armed Forces
Cite21 USC 379aa–1(a)
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