Pregnancy Outcomes of Patients Exposed to Adalimumab in Japan
- PMID: 30304717
- PMCID: PMC6381873
- DOI: 10.1159/000493462
Pregnancy Outcomes of Patients Exposed to Adalimumab in Japan
Abstract
Background: This is the first retrospective report of pregnancy outcomes after exposure to adalimumab treatment in Japan.
Methods: Using the AbbVie safety database, we analyzed pregnancy outcome data from patients who received adalimumab treatment from April 16, 2008, to May 15, 2017.
Results: Data were extracted retrospectively for 74 pregnancies in 73 patients. More than half of the patients included in the study received adalimumab for the treatment of Crohn's disease (37.8%) or ulcerative colitis (20.3%), while 9.5% received adalimumab for rheumatoid arthritis. Of the 53 pregnancies with available outcome data, 45 newborns (45/53 [84.9%]) were delivered. Of these births, 30 were full-term, 2 were preterm, and 13 were unknown. Apgar scores were available for 11 of the 16 newborns whose mothers were exposed to adalimumab in the third trimester; all scores were within the normal range. Low birth weight was observed in 5 infants out of the 30 full-term deliveries. There were also 5 miscarriages (5/53 [9.4%]), 2 induced abortions (2/53 [3.8%]), and 1 stillbirth (1/53 [1.9%]). Eight maternal adverse events were observed in 5 pregnancies; no serious adverse events occurred.
Conclusion: Although safety concerns were inconclusive, these data do not report additional risk to pregnancy outcomes with adalimumab exposure.
Keywords: Adalimumab; Inflammatory bowel disease; Pregnancy; Rheumatoid arthritis; Safety.
© 2018 The Author(s) Published by S. Karger AG, Basel.
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