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Test code: 15142

This assay tests for levetiracetam, an anticonvulsant medication used to control certain types of seizures in patients with epilepsy.  Levetiracetam is a prescribed drug that helps prevent partial onset or focal, myoclonic, and tonic-clonic seizures.

It is marketed under the trade names Keppra® and Keppra XR® (extended release). It is an effective seizure drug because it has a wider therapeutic range than many existing first-generation seizure medications. It is also associated with fewer severe adverse effects and does not interact with as many other drugs. Common adverse effects include weakness, infection, and drowsiness.1 Some symptoms of toxicity include extreme drowsiness, agitation, aggression, hallucinations, lack of coordination, rash, and numbness, tingling, or burning in the hands or feet.1

The laboratory test is a quantitative assay that reports measured serum levels of levetiracetam in mcg/mL. Levetiracetam serum level testing is important because it can help verify and optimize desired dosage for the patient, verify patient adherence to prescription criteria, detect occurrence of toxicity from overdose, and help monitor the impact of recent health changes that affect drug clearance or kidney function.

Once steady state has been reached, blood specimens can be collected 0.5 to 1 hour before the next oral dose (trough).

Note: After onset of treatment, steady state is typically reached in 2 days for adults and in 1 to 2 days for children. The elimination half-life is 6 to 8 hours in adults with epilepsy, 5 to 7 hours in children with epilepsy, and 10 to 11 hours in elderly volunteers.2

The therapeutic range of levetiracetam is generally 10.0 to 40.0 mcg/mL (mg/L) for trough collections.3, A trough blood concentration >46 µg/mL may be toxic; however, toxic levels are not well established.4 Results should be interpreted in the context of the clinical picture, including evidence of drug effectiveness and/or toxicity.

Most people with blood levels within the therapeutic range will respond to the drug without excessive adverse effects. However, individual responses can vary,  and some patients may require dosages outside of the established range to effectively control seizures and/or limit adverse effects. Dosage is considered adequate if the patient has no recurrent seizures and no significant adverse effects.

A levetiracetam concentration above or below the therapeutic range may indicate that the patient is not taking the drug as prescribed. Additionally, high concentrations may be a sign of impaired renal function, if the drug is not optimally cleared through the kidneys.

References

  1. Keppra® [package insert]. Smyrna, GA: UCB, Inc; 2009. http://www.accessdata.fda.gov/drugsatfda_docs/label/2009/021035s078s080,021505s021s024lbl.pdf
  2. Dasgupta A, Krasowski MD, eds. Therapeutic Drug Monitoring Data: A Concise Guide. 4th ed. Academic Press; 2020.
  3. Hiemke C, Bergemann N, Clement HW, et al., Consensus guidelines for therapeutic drug monitoring in neuropsychopharmacology: update 2017. Pharmacopsychiatry. 2018;51(1-02): 9-62. doi:10.1055/s-0043-116492
  4. Patsalos PN. Clinical pharmacokinetics of levetiracetam. Clin Pharmacokinet. 2004;43(11):707-724. doi:10.2165/00003088-200443110-00002


This FAQ is provided for informational purposes only and is not intended as medical advice. Test selection and interpretation, diagnosis, and patient management decisions should be based on the clinician’s education, clinical expertise, and assessment of the patient.

 

Document FAQS.180 Version: 2

Version 2: Effective 05/05/2026 to present

Version 1: Effective 10/08/2019 to 05/05/2026
Version 0: Effective 10/26/2016 to 10/08/2019