Latanoprost exposure in pregnancy

Am J Ophthalmol. 2004 Aug;138(2):305-6. doi: 10.1016/j.ajo.2004.03.002.

Abstract

Purpose: To observe pregnancies exposed to latanoprost, a prostaglandin analog administered in the treatment of glaucoma. Its prescription is limited in pregnancy, because reproduction studies in animals report a high incidence of abortion and human investigations are not adequate. As a consequence it is classified as category C drug according to the United States Food and Drug Administration's use-in-pregnancy ratings.

Design: Observational study.

Methods: We collected data, referred to our Teratology Information Service, relative to latanoprost exposure in pregnancy. We followed by phone interviews women treated with latanoprost during the first trimester, and we evaluated whether there had been any adverse effects on the fetus.

Results: Eleven cases of latanoprost exposure in pregnancy were referred to our Teratology Information Service. One case was lost to follow-up, and one case was complicated by miscarriage. Nine cases had a complete follow-up without congenital anomalies.

Conclusions: Our series is too small to perform statistical significance; however, we found no evidence of adverse effects of latanoprost on pregnancy or neonatal outcomes.

MeSH terms

  • Abnormalities, Drug-Induced / etiology
  • Adult
  • Antihypertensive Agents / adverse effects
  • Antihypertensive Agents / therapeutic use*
  • Embryonic and Fetal Development / drug effects
  • Female
  • Glaucoma, Open-Angle / drug therapy*
  • Humans
  • Intraocular Pressure / drug effects
  • Latanoprost
  • Middle Aged
  • Ocular Hypertension / drug therapy
  • Pregnancy
  • Prenatal Exposure Delayed Effects
  • Prospective Studies
  • Prostaglandins F, Synthetic / adverse effects
  • Prostaglandins F, Synthetic / therapeutic use*

Substances

  • Antihypertensive Agents
  • Prostaglandins F, Synthetic
  • Latanoprost