Seizures After Pediatric Vilazodone Ingestion: A Case Series
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Published on: September 20, 2024
Insights
Vilazodone, an antidepressant, can cause serious toxicity in children, including seizures. Accidental ingestion requires immediate medical attention to prevent severe neurological complications.
Area of Science:
- Pharmacology
- Pediatric Toxicology
Background:
- Vilazodone hydrochloride, approved in 2011 for major depressive disorder, is a novel antidepressant with a dual mechanism: selective serotonin reuptake inhibition and 5-HT1A receptor partial agonism.
- It is not approved for pediatric use, and data on its toxicity in children are scarce.
Observation:
- This report details two pediatric cases of vilazodone ingestion leading to significant toxicity.
- One child experienced refractory status epilepticus, while the other had transient seizure activity.
- Both required intensive management with benzodiazepines and, in one case, barbiturates.
Findings:
- Pediatric vilazodone ingestions can result in severe neurological events, including seizures.
- The existing literature, including these new cases, highlights a pattern of seizure activity following accidental vilazodone exposure in children.
Implications:
- Healthcare providers and families should be aware of the potential dangers of pediatric vilazodone ingestion.
- Vigilance and prompt medical intervention are crucial for managing toxicity in young children exposed to vilazodone.
Abstract:
Vilazodone hydrochloride is the first member in a new class of antidepressants called indolealkylamines and was approved for use in the United States in 2011 for major depressive disorder. It has a combined mechanism of action of a selective serotonin reuptake inhibitor and a partial agonist of serotonin 5-HT1A receptors. It has not been approved for use in the pediatric population, and toxicity from exploratory vilazodone ingestion has been rarely described to date. We describe 2 children with laboratory-confirmed vilazodone ingestions that led to significant toxicity including refractory status epilepticus in 1 patient and likely transient seizure activity in the other. Both patients required multiple doses of benzodiazepines; in the more severe case, barbiturates were added to control seizure activity. These children returned to baseline and had no prolonged neurologic complications. Pediatric experience with vilazodone is limited; however, the literature demonstrates 3 additional case reports of children experiencing seizure after vilazodone ingestion. With the 2 new cases presented here, it seems prudent to educate prescribers and families of the potential dangers of ingestion of vilazodone tablets by young children.
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