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Drug-associated congenital anomalies of the external ear identified in the United States food and drug administration adverse event reporting system database

• Authors : Xinyu Li; Jiajia Hao; Datao Li

Subjects: Congenital anomalies; FAERS; Disproportionality analysis

• Source: Scientific Reports, Vol 14, Iss 1, Pp 1-9 (2024)

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Adverse drug events of denosumab: Data-mining based on the United States Food and Drug Administration Adverse Event Reporting System database.

• Authors : Shaohua LIU^1,2; Wangyan JIANG³; Jieru GUO⁴

• Source: Journal of Research in Pharmacy. 2024, Vol. 28 Issue 4, p1220-1230. 11p.

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Dietary Exposure to United States Food and Drug Administration-Approved Synthetic Food Colors in Children, Pregnant Women, and Women of Childbearing Age Living in the United States

• Authors : Bradman, Asa; Castorina, Rosemary; Thilakaratne, Ruwan

Subjects: Pediatric; Behavioral and Social Science; Nutrition

• Source: International Journal of Environmental Research and Public Health. 19(15)

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Disproportionality analysis of drug-induced dry mouth using data from the United States food and drug administration adverse event reporting system database

• Authors : Dan Xu; Hong Zhu; Meng Wu

Subjects: Dry mouth; FAERS; Disproportionality analysis

• Source: Heliyon, Vol 10, Iss 19, Pp e38561- (2024)

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Evaluating the accuracy of Chat Generative Pre-trained Transformer version 4 (ChatGPT-4) responses to United States Food and Drug Administration (FDA) frequently asked questions about dental amalgam

• Authors : Mehmet Buldur; Berkant Sezer

Subjects: Artificial intelligence; Public health; Dental amalgam

• Source: BMC Oral Health, Vol 24, Iss 1, Pp 1-12 (2024)

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Multifocal and Extended Depth of Focus Intraocular Lenses: A Comparison of Data from the United States Food and Drug Administration Premarket Approval Trials.

• Authors : Schallhorn, Julie M

Subjects: Biomedical and Clinical Sciences; Ophthalmology and Optometry; Eye Disease and Disorders of Vision

• Source: Journal of Refractive Surgery. 37(2)

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Assessment of safety profile of secukinumab in real-world scenario using United States food and drug administration adverse event reporting system database

• Authors : Vishnu Eshwar; Ashwin Kamath

Subjects: Medicine; Science

• Source: Scientific Reports, Vol 14, Iss 1, Pp 1-12 (2024)

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Suspected adverse drug reactions of rivaroxaban reported in the United States food and drug administration adverse event reporting system database: a pharmacovigilance study

• Authors : Jingying Wu; Jianru Wu; Biyu Tang

Subjects: suspected adverse event; disproportionality analysis; drug safety

• Source: Frontiers in Pharmacology, Vol 15 (2024)

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The drug risks of cilostazol: A pharmacovigilance study of FDA Adverse Event Reporting System database.

• Authors : Peng L; Qilu Hospital of Shandong University, Jinan, Shandong Province, China.; Li X

Subjects: Cilostazol*/Cilostazol*/Cilostazol*/adverse effects ; United States Food and Drug Administration* ; Adverse Drug Reaction Reporting Systems*/Adverse Drug Reaction Reporting Systems*/Adverse Drug Reaction Reporting Systems*/statistics & numerical data

• Source: PloS one [PLoS One] 2024 Dec 04; Vol. 19 (12), pp. e0314957. Date of Electronic Publication: 2024 Dec 04 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081

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Landscape of regulatory quantitative systems pharmacology submissions to the U.S. Food and Drug Administration: An update report.

• Authors : Bai JPF; Office of Clinical Pharmacology, Center for Drug Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA.; Liu G

Subjects: United States Food and Drug Administration* ; Drug Development*/Drug Development*/Drug Development*/methods ; Network Pharmacology*

• Source: CPT: pharmacometrics & systems pharmacology [CPT Pharmacometrics Syst Pharmacol] 2024 Dec; Vol. 13 (12), pp. 2102-2110. Date of Electronic Publication: 2024 Oct 18.Publisher: Wiley Country of Publication: United States NLM ID: 101580011 Publication Model:

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