Drug pregnancy categories

This categorization system has been superseded by the 2015 FDA Pregnancy and Lactation Labeling Rule

Background

The FDA previously assigned letter categories to medications based on their potential for risk to the fetus
New drugs approved after the 2015 PLLR will not be assigned a pregnancy category.^[1]

Category	Interpretation	Details
A	Human studies show no risk	Adequate, well-controlled studies in pregnant women have not shown an increased risk of fetal abnormalities to the fetus in any trimester of pregnancy
B	No evidence of risk in studies	Animal studies have revealed no evidence of harm to the fetus, however, there are no adequate and well-controlled studies in pregnant women. OR Animal studies have shown an adverse effect, but adequate and well-controlled studies in pregnant women have failed to demonstrate a risk to the fetus in any trimester.
C	Risk cannot be ruled out	Animal studies have shown an adverse effect and there are no adequate and well-controlled studies in pregnant women. OR No animal studies have been conducted and there are no adequate and well-controlled studies in pregnant women.
D	Positive evidence of risk	Adequate well-controlled or observational studies in pregnant women have demonstrated a risk to the fetus. However, the benefits of therapy may outweigh the potential risk. For example, the drug may be acceptable if needed in a life-threatening situation or serious disease for which safer drugs cannot be used or are ineffective.
X	Contraindicated in pregnancy	Adequate well-controlled or observational studies in animals or pregnant women have demonstrated positive evidence of fetal abnormalities or risks. The use of the product is contraindicated in women who are or may become pregnant.

Includes most medications not listed elsewhere here

↑ Brucker MC, King TL. The 2015 US Food and Drug Administration Pregnancy and Lactation Labeling Rule. J Midwifery Womens Health. 2017;62(3):308-316. doi:10.1111/jmwh.12611

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