Use of real-world evidence from healthcare utilization data to evaluate drug safety during pregnancy

Author:

Huybrechts Krista F.1ORCID,Bateman Brian T.12,Hernández-Díaz Sonia3

Affiliation:

1. Division of Pharmacoepidemiology and Pharmacoeconomics, Department of Medicine; Brigham and Women's Hospital and Harvard Medical School; Boston Massachusetts

2. Department of Anesthesiology, Perioperative and Pain Medicine; Brigham and Women's Hospital and Harvard Medical School; Boston Massachusetts

3. Department of Epidemiology; Harvard T.H. Chan School of Public Health; Boston Massachusetts

Funder

Eunice Kennedy Shriver National Institute of Child Health and Human Development

National Institute on Drug Abuse

National Institute of Mental Health

Publisher

Wiley

Subject

Pharmacology (medical),Epidemiology

Reference92 articles.

1. Increasing the participation of pregnant women in clinical trials;Heyrana;JAMA,2018

2. Hernandez-Diaz S. Pregnancy registries 2014 135 168

3. Food and Drug Administration Guidance for industry: establishing pregnancy exposure registries 2002 // http://www.fda.gov/ucm/groups/fdagov-public/@fdagov-drugs-gen/documents/document/ucm071639.pdf .

4. Systematic identification of drugs that cause birth defects—a new opportunity;Mitchell;N Engl J Med,2003

5. Harnessing the Medicaid Analytic eXtract (MAX) to evaluate medications in pregnancy: design considerations;Palmsten;PLoS ONE,2013

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