Table 1.
Drug | FDA riska | Transplacental passage | Human teratogenicity | Fetal/neonatal adverse effects | Long-term effects in offspring | Impairment of fertility |
Non-steroidal anti-inflammatory drugs | B/D | Yes | No | In late pregnancy, constriction of the ductus arteriosus, reduction of renal blood flow | Not studied | Cases of inhibition of follicle rupture |
Prednisone | B | Limited | Increase in oral clefts | Rare (cataract, adrenal insufficiency, infection) | Not studied | Not studied |
Dexamethasone | C | Yes | Not reportedb | Neurodevelopmental abnormalities | Not studied | Not studied |
Betamethasone | C | Yes | Not reportedb | Neurodevelopmental abnormalities ? | Not studied | Not studied |
Bisphosphonates | C | Not studied | Not reported | Two cases of hypocalcaemia in the newborn infant | Not studied | Not studied |
Details and references are given in the text. aThe United States Food and Drug Administration (FDA) pregnancy risk categories are as follows: A, no risk in controlled clinical studies in humans; B, human data reassuring or when absent, animal studies show no risk; C, human data are lacking; animal studies show risk or are not done; D, positive evidence of risk, benefit may outweigh; X, contraindicated during pregnancy. bNo indication for maternal use in the first trimester.