Drug-induced torsades de pointes: Disproportionality analysis of the United States Food and Drug Administration adverse event reporting system. [PDF]
Front Cardiovasc Med, 2022 Wu Z, Zhou P, He N, Zhai S.
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A Toxic Mouthful: the Misalignment of Dental Mercury Regulations [PDF]
, 2013 Mercury amalgam dental fillings have been used for over one hundred and fifty years in hundreds of millions of patients around the world. In the past two decades, scientific evidence has shown that mercury fillings have harmful effects on human health ...
McGrath, Kaitlin
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Doxycycline use and adverse pregnancy or neonatal outcomes: A descriptive study using the United States Food and Drug Administration Adverse Event Reporting System database. [PDF]
Health Sci Rep, 2022 Kaundinnyayana S, Kamath A.
europepmc +1 more source
Comparison of Good Clinical Practice Inspection Processes for Marketing Applications Between the United States Food and Drug Administration and the European Medicines Agency. [PDF]
Ther Innov Regul Sci, 2023 Ayalew K +11 more
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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. [PDF]
Int J Environ Res Public Health, 2022 Bradman A +7 more
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Evaluation of the EVO/EVO+ Sphere and Toric Visian ICL: Six Month Results from the United States Food and Drug Administration Clinical Trial. [PDF]
Clin Ophthalmol, 2022 Packer M.
europepmc +1 more source
Assessment of pancreatitis associated with tocilizumab use using the United States Food and Drug Administration Adverse Event Reporting System database. [PDF]
Sci Rep, 2021 Kamath A, Acharya SD, Rao RR, Ullal SD.
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Adverse events related to total ankle replacement devices: an analysis of reports to the United States Food and Drug Administration. [PDF]
Int Orthop, 2021 Mahmoud K +3 more
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PharmaceuticsDrug development costs can be significantly reduced if proven “platform” technologies are allowed to be used without having to validate their use. The most recent US Food and Drug Administration (FDA) guideline brings more clarity, as well as a greater focus on the most complex technologies that can now be used for faster drug development.
openaire +3 more sources
National Analysis of Adverse Events Involving Distal Radius Plate Systems Reported to the United States Food and Drug Administration. [PDF]
CureusAhmad M +5 more
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