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Updated: Dec 31, 2025

Behavioral Characterization of Pentylenetetrazole-induced Seizures: Moving Beyond the Racine Scale
Published on: July 8, 2025
Generalised tonic-clonic seizures on the subtherapeutic dose of olanzapine
Marium Mansoor1, Mohammad Hanif Mesiya2, Aisha Sanober Chachar2
1Psychiatry, Aga Khan University, Karachi, Pakistan mariumansoor@hotmail.com.
Abstract:
Olanzapine is a second-generation antipsychotic. Incidence of olanzapine-induced seizures (OIS) is low with monotherapy. Combination therapy with another antipsychotic, drug metabolism and old age are risk factors for OIS. Our patient was a 71-year-old man, admitted to the psychiatry unit. He was managed on the lines of bipolar affective disorder current episode depression and dementia. He was started on olanzapine 1.25 mg two times/day. The patient developed generalised tonic-clonic seizure that lasted for around two and a half minutes within 24 hours of olanzapine treatment. His electroencephalogram showed findings that were suggestive of mild slowing. Our case discusses the incidence of OIS on the subtherapeutic dose. This presentation involves multiple risk factors for OIS: a history of stroke, poststroke seizure, old age and cognitive impairment. Due to scarcity of evidence of OIS; mostly with recommended therapeutic dose range physicians may underestimate seizure risk at subtherapeutic doses.
Insights
Olanzapine can cause seizures even at low doses, especially in older adults with cognitive issues. This case highlights seizure risk with olanzapine (a second-generation antipsychotic) in elderly patients with multiple risk factors.
Area of Science:
- Neuroscience
- Psychopharmacology
- Clinical Neurology
Background:
- Olanzapine, a second-generation antipsychotic, is generally associated with a low incidence of seizures when used as monotherapy.
- Risk factors for olanzapine-induced seizures (OIS) include combination antipsychotic therapy, impaired drug metabolism, and advanced age.
Observation:
- A 71-year-old male patient with bipolar affective disorder, depression, and dementia was treated with a subtherapeutic dose of olanzapine (1.25 mg twice daily).
- Within 24 hours of initiating olanzapine, the patient experienced a generalized tonic-clonic seizure lasting approximately two and a half minutes.
- Electroencephalogram (EEG) revealed mild slowing, suggestive of a potential impact on brain activity.
Findings:
- This case report documents olanzapine-induced seizures (OIS) occurring at a subtherapeutic dosage, challenging the assumption that seizures are primarily linked to therapeutic ranges.
- The patient presented with multiple established risk factors for OIS, including advanced age, cognitive impairment, a history of stroke, and a prior post-stroke seizure.
Implications:
- Physicians may underestimate the risk of OIS at subtherapeutic doses due to the scarcity of evidence, particularly in patients with co-existing risk factors.
- This case underscores the importance of vigilant seizure risk assessment in elderly patients with cognitive impairment initiating olanzapine, even at reduced dosages.
- Further research is warranted to elucidate the precise mechanisms and dose-dependent seizure threshold of olanzapine in vulnerable patient populations.
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