Lacosamide and pregnancy: Data from spontaneous and solicited reports

Author:

Perucca Piero12ORCID,Bourikas Dimitrios3,Voinescu P. Emanuela4ORCID,Vadlamudi Lata56ORCID,Chellun Daya7,Kumke Thomas8,Werhahn Konrad J.8,Schmitz Bettina9

Affiliation:

1. Epilepsy Research Centre, Department of Medicine (Austin Health) University of Melbourne Melbourne Victoria Australia

2. Bladin‐Berkovic Comprehensive Epilepsy Program, Austin Health Melbourne Victoria Australia

3. UCB Pharma Alimos Greece

4. Brigham and Women's Hospital Harvard Medical School Boston Massachusetts USA

5. University of Queensland Centre for Clinical Research University of Queensland Herston Queensland Australia

6. Department of Neurology Royal Brisbane and Women's Hospital Herston Queensland Australia

7. UCB Pharma Braine‐l'Alleud Belgium

8. UCB Pharma Monheim am Rhein Germany

9. Vivantes Humboldt‐Klinikum Berlin Germany

Abstract

AbstractObjectiveIn pregnancy, it is important to balance the risks of uncontrolled epileptic seizures to the mother and fetus against the potential teratogenic effects of antiseizure medications. Data are limited on pregnancy outcomes among patients taking lacosamide (LCM), particularly when taken as monotherapy. The objective of this analysis was to evaluate the pregnancy outcomes of LCM‐exposed pregnancies.MethodsThis analysis included all reports in the UCB Pharma pharmacovigilance database of exposure to LCM during pregnancy from spontaneous sources (routine clinical settings) or solicited reports from interventional clinical studies and noninterventional postmarketing studies. Prospective and retrospective reports were analyzed separately.ResultsAt the data cutoff (August 31, 2021), there were 202 prospective pregnancy cases with maternal exposure to LCM and known outcomes. Among these cases, 44 (21.8%) patients received LCM monotherapy and 158 (78.2%) received LCM polytherapy. Most patients received LCM during the first trimester (LCM monotherapy: 39 [88.6%]; LCM polytherapy: 143 [90.5%]). From the prospective pregnancy cases with maternal LCM exposure, there were 204 reported outcomes (two twin pregnancies occurred in the polytherapy group). The proportion of live births was 84.1% (37/44) in patients who received LCM as monotherapy, and 76.3% (122/160) for LCM polytherapy. The overall proportion of abortions (for any reason) was 15.9% (7/44) with LCM monotherapy, and 22.5% (36/160) with LCM polytherapy. Congenital malformations were reported in 2.3% (1/44) of known pregnancy outcomes with maternal exposure to LCM monotherapy, and 6.9% (11/160) with polytherapy.SignificanceOur preliminary data do not raise major concerns on the use of LCM during pregnancy. Most pregnancies with LCM exposure resulted in healthy live births, and no new safety issues were identified. These findings should be interpreted with caution, as additional data are needed to fully evaluate the safety profile of LCM in pregnancy.

Funder

UCB Pharma

Publisher

Wiley

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1. Antiepileptic-drugs;Reactions Weekly;2024-06-08

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