PROFESSIONAL VERSION

Effect of Reproductive Treatment on the Fetus or Neonate in Animals

Full Review: Jul 2026 ByTheresa Beachler, DVM, PhD, DACT, Veterinary Diagnostic and Production Animal Medicine, College of Veterinary Medicine, Iowa State University | Peer reviewed byMelissa A. Mercer, DVM, PhD, DACVIM-LA, DACVCP, University of California, Davis
Last updated: Jul 2026
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An important component of reproductive pharmacology is the effect that treatment with a medication administered to pregnant dams or to lactating, nursing dams has on the fetus or neonate. Many factors influence the ability of a drug to cross the placenta, including placental architecture of the particular species. In general, drugs that are lipid-soluble, nonionized, and of low molecular weight cross the placenta readily.

The potential effects of pharmacotherapeutics on pregnancy and neonatal development are being increasingly studied in domestic animals; frequently, however, inferences must be made from studies in other animal species or in humans. Many drugs are known to be teratogenic during pregnancy; these should be avoided (see the table ).

Table
Table

Pregnant humans should handle with care many drugs intended for animals, especially those that are known to cause pregnancy loss, that induce premature delivery, or that are teratogenic. Whenever possible, handling of these drugs should avoided. The recommendation is to consult the National Institute for Occupational Safety and Health (NIOSH) List of Hazardous Drugs in Healthcare Settings and to follow the FDA's labeling instructions for medications with known risks for pregnancy, lactation, and females and males of reproductive potential.

Any administration of medication to lactating animals requires consideration of excretion of the drug or its metabolites in milk and of the effects on suckling neonates. Research on how the exposure of mothers to various medications affects nursing neonates has been limited, and inferences are frequently made from possible effects known in humans.

Pearls & Pitfalls

  • Any administration of medication to lactating animals requires consideration of excretion of the drug or its metabolites in milk and of the effects on suckling neonates.

The National Institute of Child Health and Human Development's Drugs and Lactation Database (LactMed) provides information about known effects in humans and animals from exposure during nursing or milk consumption. Milk produced for human consumption must be free of potentially harmful residues, and all relevant laws and regulations regarding usage and appropriate withdrawal times should be followed.

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