Levetiracetam Interaction with Direct Oral Anticoagulants: A Pharmacovigilance Study

• Published in: CNS drugs 2023-12, Vol.37 (12), p.1111-1121
• Main Authors: Abou Kaoud, Mohammed, Nissan, Ran, Segev, Amitai, Sabbag, Avi, Orion, David, Maor, Elad
• Format: Article
• Language: English
• Subjects: Administration, Oral; Age; Anticoagulants; Anticoagulants - adverse effects; Anticonvulsants; Atrial Fibrillation - drug therapy; Carbamazepine; Convulsions & seizures; Drug interactions; Epilepsy; Etiracetam; Hemorrhage; Humans; Ischemia; Ischemic Stroke - drug therapy; Levetiracetam - adverse effects; Medicine; Medicine & Public Health; Mortality; Neurology; Neurosciences; Older people; Original Research Article; P-Glycoprotein; Patients; Pharmacotherapy; Pharmacovigilance; Psychiatry; Psychopharmacology; Pyridones - adverse effects; Regression analysis; Retrospective Studies; Stroke
• ISSN: 1172-7047; 1179-1934
• DOI: 10.1007/s40263-023-01052-1

Background Levetiracetam is widely used in post-stroke epilepsy. However, it is suspected to possess P-glycoprotein (P-gp) induction properties, and therefore, a potentially significant interaction with direct oral anticoagulants (DOACs). We aimed to search for ischemic stroke signals with levetiracetam and the DOACs. Methods In this retrospective pharmacovigilance study, we used the FAERS database to identify ischemic stroke events associated with DOACs and concomitant use of levetiracetam. We evaluated disproportionate reporting by the adjusted reporting odds ratio (adjROR) and the lower bound of the shrinkage 95% confidence interval. When shrinkage is positive, an increased risk of a specific adverse event occurrence is emphasized over the sum of the individual risks when these same drugs are used separately. Results We identified 1841 (1.5%), 3731 (5.3%), 338 (4.9%), and 1723 (1.3%) ischemic stroke reports with apixaban, dabigatran, edoxaban, and rivaroxaban, respectively. The adjROR of the interaction effect was 3.57 (95% CI 2.81–4.58) between DOACs and levetiracetam. The shrinkage analysis detected an interaction between each of the DOACs and levetiracetam. The logistic model and shrinkage analysis failed to detect an interaction when queried for hemorrhagic stroke. A significant signal in the classical enzyme inducer, carbamazepine, strengthened our results (adjROR; 8.47, 95% CI 5.37–13.36). Conclusions Our study shows a strong signal for the levetiracetam interaction with the DOACs. Our findings suggest implementation of a drug monitoring strategy.