Dejene, Sara Z. BS∗; Funk, Michele Jonsson PhD∗; Pate, Virginia MS∗; Wu, Jennifer M. MD, MPH†
From the ∗Department of Epidemiology, Gillings School of Global Public Health
†Department of Obstetrics and Gynecology, School of Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC.
Correspondence: Sara Z. Dejene, BS. E-mail: [email protected].
This article was published online ahead of print on September 30, 2021.
Funding for this project was supplied by the following sources: S.Z.D. receives tuition and stipend support from the Center for Pharmacoepidemiology in the UNC Department of Epidemiology and the North Carolina Translational and Clinical Sciences Institute (current member companies include GlaxoSmithKline, AbbVie, Boehringer Ingelheim, UCB BioSciences, and Takeda). M.J.F. receives salary support from the Center for Pharmacoepidemiology in the UNC Department of Epidemiology (current members: GlaxoSmithKline, AbbVie, Boehringer Ingelheim, UCB BioSciences, Takeda) and consulting fees via UNC from GlaxoSmithKline. The project described was supported by the National Center for Advancing Translational Sciences and the National Institutes of Health through grant award number ULTR002489. The database infrastructure used for this project was funded by the Pharmacoepidemiology Gillings Innovation Lab for the Population-Based Evaluation of Drug Benefits and Harms in Older US Adults (GIL200811.0010); the Center for Pharmacoepidemiology, Department of Epidemiology, UNC Gillings School of Global Public Health; the CER Strategic Initiative of UNC’s Clinical Translational Science Award (UL1TR002489); the Cecil G. Sheps Center for Health Services Research, UNC; and the UNC School of Medicine. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health. None of the authors have any conflicts of interest to declare with respect to this work.
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