Key result
Newer anti-seizure medications are linked to rhabdomyolysis, with levetiracetam showing ~8-fold higher odds.
Why the study?
Few real-world studies have shown a clear association between newer-generation anti-seizure medications and rhabdomyolysis.
Are newer-generation anti-seizure medications associated with an increased risk of rhabdomyolysis?
Observational (n=1,130)
Are newer-generation anti-seizure medications associated with an increased risk of rhabdomyolysis?
Odds Ratio: 8.01 (95% CI 7.26–8.84)
Newer-generation anti-seizure medications, particularly levetiracetam, are associated with a significant risk of rhabdomyolysis, highlighting the need for early recognition of symptoms.
May signal rhabdomyolysis risk with newer ASMs; leaves open need for prospective confirmation before practice change.
Objective: Rhabdomyolysis is a potentially fatal adverse reaction mostly triggered by certain medications. Few real-world studies have shown a clear association between newer-generation anti-seizure medications (ASMs) and rhabdomyolysis. We sought to quantify the risk and evaluate the clinical features and management of rhabdomyolysis associated with newer-generation ASMs. Methods: Data were retrieved from the US FDA Adverse Event Reporting System database (FAERS) from 2018 to 2022 on newer-generation ASMs to identify rhabdomyolysis events, and disproportionality analyses were conducted by estimating the reporting odds ratios (RORs) and corresponding 95% confidence intervals (CIs). Furthermore, case reports from 2012 to 31 December 2022 on newer-generation ASMs-induced rhabdomyolysis were retrieved for retrospective analysis. Results: A total of 1,130 rhabdomyolysis reports from the FAERS database were considered. Levetiracetam had the greatest proportion and the highest positive signal values of rhabdomyolysis. The RORs (95% CIs) for newer-generation ASMs were, in descending order, levetiracetam 8.01 (7.26–8.84), lamotrigine 3.78 (3.25–4.40), oxcarbazepine 3.47 (2.53–4.75), pregabalin 2.75 (2.43–3.12), lacosamide 1.85 (1.29–2.65), topiramate 1.64 (1.25–2.15), and gabapentin 1.32 (1.13–1.55). Twenty-six case reports showed evidence of rhabdomyolysis, and levetiracetam (65.4%) was the most frequently reported agent. The median age was 32 years; typical initial symptoms included muscle weakness (34.8%), myalgia (34.8%), backache (17.4%), fatigue (13.0%) and leg pain (8.7%). The median time to onset of rhabdomyolysis was 2 days. All cases had elevated creatine phosphokinase (CPK), and some cases were accompanied by elevated creatinine (57.1%) and myoglobinuria (53.8%). Cessation of ASMs could lead to complete clinical remission. The median time for creatine phosphokinase (CPK) normalization was 8 days. Conclusion: This study identified 7 newer-generation ASMs with significant rhabdomyolysis reporting associations. Prescribers should be more aware of this risk and teach patients to recognize rhabdomyolysis signs/symptoms early.
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Deng et al. (2023) conducted an observational in Rhabdomyolysis (n=1,130). Newer-generation anti-seizure medications (e.g., levetiracetam) was evaluated on Rhabdomyolysis reporting odds ratio (ROR 8.01, 95% CI 7.26-8.84). Newer-generation anti-seizure medications were associated with rhabdomyolysis, with levetiracetam showing the highest reporting odds ratio (ROR 8.01; 95% CI 7.26-8.84).
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