نتائج البحث

Exploratory disproportionality analysis of potentially drug-induced eosinophilic pneumonia using United States Food and Drug Administration adverse event reporting system.

• Authors : Kamath A; Department of Pharmacology, Kasturba Medical College Mangalore, Manipal Academy of Higher Education, Manipal, Karnataka, India. .

Subjects: Adverse Drug Reaction Reporting Systems*/Adverse Drug Reaction Reporting Systems*/Adverse Drug Reaction Reporting Systems*/statistics & numerical data ; United States Food and Drug Administration* ; Pulmonary Eosinophilia*/Pulmonary Eosinophilia*/Pulmonary Eosinophilia*/chemically induced

• Source: Scientific reports [Sci Rep] 2025 Jan 09; Vol. 15 (1), pp. 1455. Date of Electronic Publication: 2025 Jan 09.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Strength of clinical evidence supporting the United States Food and Drug Administration Accelerated Approvals from 2015 to 2022.

• Authors : Zhang X; Peking University First Hospital, Beijing, China.; Clinical Research Institute, Institute of Advanced Clinical Medicine, Peking University, Beijing, China.

Subjects: United States Food and Drug Administration* ; Drug Approval*; United States

• Source: BMC medicine [BMC Med] 2024 Dec 18; Vol. 22 (1), pp. 587. Date of Electronic Publication: 2024 Dec 18.Publisher: BioMed Central Country of Publication: England NLM ID: 101190723 Publication Model: Electronic Cited Medium: Internet ISSN: 1741-7015

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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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Recent Use of Novel Data Streams During Foodborne Illness Cluster Investigations by the United States Food and Drug Administration: Qualitative Review

• Authors : Michael C Bazaco; Christina K Carstens; Tiffany Greenlee

Subjects: Public aspects of medicine; RA1-1270

• Source: JMIR Public Health and Surveillance, Vol 11, Pp e58797-e58797 (2025)

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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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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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Analysis of the measurements used as potency tests for the 31 US FDA-approved cell therapy products.

• Authors : Simon CG Jr; Biosystems & Biomaterials Division, National Institute of Standards & Technology (NIST), Gaithersburg, MD, USA. .; Bozenhardt EH

Subjects: United States Food and Drug Administration* ; Cell- and Tissue-Based Therapy*; United States

• Source: Journal of translational medicine [J Transl Med] 2025 Mar 04; Vol. 23 (1), pp. 259. Date of Electronic Publication: 2025 Mar 04.Publisher: BioMed Central Country of Publication: England NLM ID: 101190741 Publication Model: Electronic Cited Medium: Internet ISSN: 1479-5876

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Oseltamivir-induced hepatotoxicity: A retrospective analysis of the FDA adverse event reporting system.

• Authors : Yu L; College of Traditional Chinese Medicine of Chongqing Medical University, Chongqing, China.; Xiang Q

Subjects: Oseltamivir*/Oseltamivir*/Oseltamivir*/adverse effects ; Chemical and Drug Induced Liver Injury*/Chemical and Drug Induced Liver Injury*/Chemical and Drug Induced Liver Injury*/epidemiology ; Chemical and Drug Induced Liver Injury*/Chemical and Drug Induced Liver Injury*/Chemical and Drug Induced Liver Injury*/etiology

• Source: PloS one [PLoS One] 2025 Feb 25; Vol. 20 (2), pp. e0314970. Date of Electronic Publication: 2025 Feb 25 (Print Publication: 2025).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081

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Disproportionality analysis of Raynaud's phenomenon associated with calcitonin gene-related peptide inhibitors using the Food and Drug Administration adverse event reporting system.

• Authors : Lee N; College of Pharmacy, Daegu Catholic University, 13-13, Hayang-ro, Hayang-eup, Gyeongsan, Gyeongbuk, 38430, Republic of Korea.; Ok JH

Subjects: Raynaud Disease*/Raynaud Disease*/Raynaud Disease*/chemically induced ; Raynaud Disease*/Raynaud Disease*/Raynaud Disease*/epidemiology ; United States Food and Drug Administration*

• Source: Scientific reports [Sci Rep] 2025 Feb 15; Vol. 15 (1), pp. 5675. Date of Electronic Publication: 2025 Feb 15.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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