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Updated: May 1, 2026

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Published on: August 25, 2014
Teratogenic mechanisms associated with prenatal medication exposure
Marleen M H J van Gelder1, Iris A L M van Rooij1, Lolkje T W de Jong-van den Berg2
1Department for Health EvidenceRadboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
Medications during early pregnancy can cause birth defects through six main teratogenic mechanisms. Combining therapies may significantly increase risks for pregnant women.
Area of Science:
- Developmental toxicology
- Reproductive medicine
- Pharmacology
Background:
- Birth defects can arise from various exposures, notably medications taken during early pregnancy.
- Understanding teratogenic mechanisms is crucial for preventing congenital anomalies.
Purpose of the Study:
- To review the six principal teratogenic mechanisms associated with medication use in pregnancy.
- To highlight the implications of these mechanisms for research and clinical practice.
Main Methods:
- Literature review of teratogenic mechanisms.
- Synthesis of evidence from animal models and human studies.
- Analysis of the impact of multi-therapy on teratogenic risk.
Main Results:
- Identified six key teratogenic mechanisms: folate antagonism, neural crest cell disruption, endocrine disruption, oxidative stress, vascular disruption, and receptor/enzyme-mediated teratogenesis.
- Evidence for some mechanisms is primarily from animal models.
- Combined medication use may amplify teratogenic effects through shared pathways.
Conclusions:
- Knowledge of teratogenic mechanisms informs etiological and post-marketing surveillance.
- Findings have implications for prescribing practices for women of reproductive age.
- Multi-therapy poses a significantly increased risk for birth defects due to potential synergistic teratogenic mechanisms.
Related Concept Videos
Teratogenicity
Drug Toxicity: Dose-Dependent Reactions
Drug Toxicity: Risk factors
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Drug toxicity: Drug–Drug Interaction
Pharmacokinetics in Pediatric Patients: Drug Metabolism

