 United States Food and Drug Administration
"United States Food and Drug Administration" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
An agency of the PUBLIC HEALTH SERVICE concerned with the overall planning, promoting, and administering of programs pertaining to maintaining standards of quality of foods, drugs, therapeutic devices, etc.
| Descriptor ID |
D014486
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| MeSH Number(s) |
I01.409.137.500.600.650.760 N03.540.348.500.500.600.650.760
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| Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "United States Food and Drug Administration".
Below are MeSH descriptors whose meaning is more specific than "United States Food and Drug Administration".
This graph shows the total number of publications written about "United States Food and Drug Administration" by people in UAMS Profiles by year, and whether "United States Food and Drug Administration" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2025 | 0 | 1 | 1 | | 2024 | 3 | 0 | 3 | | 2022 | 0 | 2 | 2 | | 2021 | 0 | 4 | 4 | | 2020 | 2 | 4 | 6 | | 2019 | 0 | 1 | 1 | | 2018 | 0 | 2 | 2 | | 2016 | 0 | 1 | 1 | | 2014 | 1 | 1 | 2 | | 2013 | 0 | 1 | 1 | | 2012 | 0 | 1 | 1 | | 2011 | 0 | 1 | 1 | | 2010 | 0 | 5 | 5 | | 2008 | 0 | 1 | 1 | | 2007 | 0 | 3 | 3 | | 2006 | 1 | 1 | 2 | | 2005 | 0 | 6 | 6 | | 2004 | 0 | 1 | 1 | | 2002 | 0 | 2 | 2 | | 2001 | 1 | 0 | 1 | | 1999 | 0 | 1 | 1 | | 1996 | 0 | 1 | 1 | | 1995 | 0 | 1 | 1 | | 1994 | 1 | 1 | 2 |
To return to the timeline, click here.
Below are the most recent publications written about "United States Food and Drug Administration" by people in Profiles over the past ten years.
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Rabin RL, Altman MC, Arshad SH, Beger RD, Frischmeyer-Guerrerio PA, Goleva E, Hamilton RG, Khurana Hershey GK, Shamji MH, Sampson HA, Santos AF, Shreffler WG, Togias A, Vieths S, Wambre E, Wenzel SE, Hise K, Lee J, Tripathi A, Slater JE. Biomarker-driven drug development for allergic diseases and asthma: An FDA public workshop. J Allergy Clin Immunol. 2025 Jun; 155(6):1753-1766.
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Wallace TC, Koturbash I. DSHEA 1994 - Celebrating 30 Years of Dietary Supplement Regulation in the United States. J Diet Suppl. 2025; 22(1):1-8.
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Patel T, Chen C, Al Hadidi S, Kadry Y, Sridhara R, Purcell E, Wisch L, Retzlaff J, Foti M, Pazdur R, Kluetz P, Gao J. Reflections and Roadmaps: Career Development beyond the FDA-AACR Oncology Educational Fellowship. Clin Cancer Res. 2024 Aug 01; 30(15):3144-3146.
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Wolfe KH, Pierce VM, Humphries RM. How New Regulation of Laboratory-Developed Antimicrobial Susceptibility Tests Will Affect Infectious Diseases Clinical Practice. Clin Infect Dis. 2024 05 15; 78(5):1140-1147.
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Tobacyk J, Parks BJ, Lovelady N, Brents LK. Qualitative content analysis of public responses to an FDA inquiry on the impact of scheduling changes to kratom. Int J Drug Policy. 2022 10; 108:103817.
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Yan J, Datta S, Kesselman A, Malhotra A, Scherer K, Wadhwa V. Adverse Events Associated with New Nitinol Venous-Labeled Stents: A Review of the FDA MAUDE Database. J Vasc Interv Radiol. 2022 10; 33(10):1261-1263.
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Rick JW, Lio P, Hsiao JL, Shi VY. Response to: "Special editorial: When prescribing Janus kinase inhibitors for dermatologic conditions, be mindful of the Food and Drug Administration's September 1, 2021, data safety communication". J Am Acad Dermatol. 2022 07; 87(1):e33-e34.
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Ramai D, DeLuca M, Facciorusso A, Ofosu A, Girotra M, Tabibian JH, Rodrigues-Pinto E, Adler DG, Barakat MT. Analysis of Reported Adverse Events With Colonic Stents: An FDA MAUDE Database Study. J Clin Gastroenterol. 2022 10 01; 56(9):784-786.
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Al Hadidi S. The Use of Modified Surrogate End Points in Cancer Clinical Trials. Cancer Invest. 2022 01; 40(1):14-16.
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Wolf J, Abzug MJ, Wattier RL, Sue PK, Vora SB, Zachariah P, Dulek DE, Waghmare A, Olivero R, Downes KJ, James SH, Pinninti SG, Yarbrough A, Aldrich ML, MacBrayne CE, Soma VL, Grapentine SP, Oliveira CR, Hayes M, Kimberlin DW, Jones SB, Bio LL, Morton TH, Hankins JS, Maron GM, Timberlake K, Young JL, Orscheln RC, Schwenk HT, Goldman DL, Groves HE, Huskins WC, Rajapakse NS, Lamb GS, Tribble AC, Lloyd EC, Hersh AL, Thorell EA, Ratner AJ, Chiotos K, Nakamura MM. Initial Guidance on Use of Monoclonal Antibody Therapy for Treatment of Coronavirus Disease 2019 in Children and Adolescents. J Pediatric Infect Dis Soc. 2021 May 28; 10(5):629-634.
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Fishbein H, Bauer D, Yu Q, Mermelstein R, Jones D, Miller A, Harrell M, Loukas A, Sterling K, Colip B, Mittl B. Harmonizing Cigar Survey Data Across Tobacco Centers of Regulatory Science, Center for Tobacco Products, and Population Assessment of Tobacco and Health Studies: The Cigar Collaborative Research Group. Nicotine Tob Res. 2021 01 07; 23(1):212-218.
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Chen Z, Liu X, Hogan W, Shenkman E, Bian J. Applications of artificial intelligence in drug development using real-world data. Drug Discov Today. 2021 05; 26(5):1256-1264.
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Weston S, Coleman CM, Haupt R, Logue J, Matthews K, Li Y, Reyes HM, Weiss SR, Frieman MB. Broad Anti-coronavirus Activity of Food and Drug Administration-Approved Drugs against SARS-CoV-2 In Vitro and SARS-CoV In Vivo. J Virol. 2020 10 14; 94(21).
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Fagan P, Eissenberg T, Jones DM, Cohen JE, Nez Henderson P, Clanton MS. The First 10 Years: Reflecting on Opportunities and Challenges of the Tobacco Products Scientific Advisory Committee of the United States Food and Drug Administration. J Leg Med. 2020 Jul-Dec; 40(3-4):293-320.
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Al Hadidi S, Mims M, Miller-Chism CN, Kamble R. Participation of African American Persons in Clinical Trials Supporting U.S. Food and Drug Administration Approval of Cancer Drugs. Ann Intern Med. 2020 08 18; 173(4):320-322.
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Walker LA, Koturbash I, Kingston R, ElSohly MA, Yates CR, Gurley BJ, Khan I. Cannabidiol (CBD) in Dietary Supplements: Perspectives on Science, Safety, and Potential Regulatory Approaches. J Diet Suppl. 2020; 17(5):493-502.
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Stevens D, Claborn MK, Gildon BL, Kessler TL, Walker C. Onasemnogene Abeparvovec-xioi: Gene Therapy for Spinal Muscular Atrophy. Ann Pharmacother. 2020 10; 54(10):1001-1009.
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Inselman A, Liu F, Wang C, Shi Q, Pang L, Mattes W, White M, Lyn-Cook B, Rosas-Hernandez H, Cuevas E, Lantz S, Imam S, Ali S, Petibone DM, Shemansky JM, Xiong R, Wang Y, Tripathi P, Cao X, Heflich RH, Slikker W. Dr. Daniel Acosta and In Vitro toxicology at the U.S. Food and Drug Administration's National Center for Toxicological Research. Toxicol In Vitro. 2020 Apr; 64:104471.
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Deer T, Kim P, Pope JE, Hayek S, McDowell G, Mekhail N, Diwan S, Saulino M, Moeschler S, Schultz D, Gritsenko K, Prager J, Peterson EA, Staats P, Poree L, Fishman MA, Vallejo R, Calodney A, Slavin K, de Leon Cassadala O, Levy R, Buvanendran A, Sitzman BT, Sayed D, Ferrante FM, Kloth D, Gilligan CJ, Kapural L, Kloster DR, Leong M, Rosenow JM, Lamer TJ, Stearns L. Physician Guidance on the Use of Off-Labeled Drugs in Intrathecal Drug Delivery Systems for Chronic Pain. Neuromodulation. 2019 10; 22(7):765-768.
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Garza M, Seker E, Zozus M. Development of Data Validation Rules for Therapeutic Area Standard Data Elements in Four Mental Health Domains to Improve the Quality of FDA Submissions. Stud Health Technol Inform. 2019; 257:125-132.
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Klyn NAM, Kleindienst Robler S, Alfakir R, Nielsen DW, Griffith JW, Carlson DL, Lundy L, Dhar S, Zapala DA. A Retrospective Estimate of Ear Disease Detection Using the "Red Flags" in a Clinical Sample. Ear Hear. 2018 Sep-Oct; 39(5):1035-1038.
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McElfish PA, Purvis RS, Stewart MK, James L, Kim Yeary KH, Long CR. Health Research Funding Agencies' Policies, Recommendations, and Tools for Dissemination. Prog Community Health Partnersh. 2018; 12(4):473-482.
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Hill KD, Goldstein BH, Angtuaco MJ, Chu PY, Fleming GA. Post-market surveillance to detect adverse events associated with Melody? valve implantation. Cardiol Young. 2017 Aug; 27(6):1090-1097.
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