Table 1.
Drug | FDA Pregnancy Risk Categories * | Observations |
---|---|---|
Cyclosporine | C | Preferred Conventional |
Metotrexate | X | Contraindicated (3 months drug-free interval before conception) |
Acitretin | X | Contraindicated (3 years drug-free interval before conception) |
Dimethyl-fumarate | C | Contraindicated |
Apremilast | C | Contraindicated |
Anti-TNF-alpha | B | Certolizumab Pegol: preferred biologic |
Anti IL-12/23 | B | Stopping in the second and third trimesters |
Anti IL-17 | B (Secukinumab) N/A (Ixekizumab; Brodalumab) |
Stopping in the second and third trimesters Limited available data on use in pregnant women are insufficient to inform a drug-associated risk of adverse developmental outcomes |
Anti IL-23 | N/A | Limited available data on use in pregnant women are insufficient to inform a drug-associated risk of adverse developmental outcomes |
FDA: Food and Drug Administration; TNF: Tumour Necrosis Factor; IL: Interleukin; N/A: Not Available; * FDA Category of Drug Evidence: A: Adequate, well-controlled studies in pregnant women do not show any risk to the fetus in the first trimester; B: Animal studies did not demonstrate risk to the fetus; no well-controlled studies in humans exist; or animal studies demonstrated risk, but well-controlled studies in pregnant women do not demonstrate adverse effects on the fetus; C: Animal studies demonstrate risk to the fetus (this category also applies to drugs for which no animal or well-controlled studies in humans exist); D: There is evidence of risk to the fetus with these drugs, but their benefits may outweigh risks; X: There is positive evidence of risk that outweighs any possible benefit.