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The Role of Adverse Event Reporting in the FDA Response to ..:
Klontz, Karl C.
;
DeBeck, Heidi J.
;
LeBlanc, Pamela
...
Public Health Reports (1974-). 130 (2015) 5 - p. 526-532 , 2015
Link:
https://www.jstor.org/stable/43776211
RT Journal T1
The Role of Adverse Event Reporting in the FDA Response to a Multistate Outbreak of Liver Disease Associated with a Dietary Supplement
UL https://suche.suub.uni-bremen.de/peid=jstor-43776211&Exemplar=1&LAN=DE A1 Klontz, Karl C. A1 DeBeck, Heidi J. A1 LeBlanc, Pamela A1 Mogen, Kathryn M. A1 Wolpert, Beverly J. A1 Sabo, Jonathan L. A1 Salter, Monique A1 Seelman, Sharon L. A1 Lance, Susan E. A1 Monahan, Caitlin A1 Steigman, David S. A1 Gensheimer, Kathleen PB Association of Schools and Programs of Public Health YR 2015 SN 0033-3549 K1 Health sciences K1 Medical sciences K1 Nutritional science K1 Dietetics K1 Diet K1 Dietary supplements K1 Biological sciences K1 Biology K1 Anatomy K1 Digestive system K1 Liver K1 Medical conditions K1 Diseases K1 Digestive system diseases K1 Liver diseases K1 Health care industry K1 Health care administration K1 Physical trauma K1 Patient care K1 Medication administration K1 Political science K1 Government K1 Government agencies K1 Intelligence services K1 Surveillance K1 Law K1 Administrative law K1 Commercial law K1 Food law K1 Health and wellness K1 Public health JF Public Health Reports (1974-) VO 130 IS 5 SP 526 OP 532 LK http://dx.doi.org/https://www.jstor.org/stable/43776211 DO https://www.jstor.org/stable/43776211 SF ELIB - SuUB Bremen
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