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Comparative safety of prescribed Esketamine and ketamine in relation to renal and urinary disorders: A pharmacovigilance perspective.

Stefania Chiappini, Amira Guirguis, Nicolò Schifano, John Corkery, Francesco Semeraro, Alessio Mosca, Giacomo d'Andrea, Gabriele Duccio Papanti, Davide Arillotta, Giuseppe Floresta, Giovanni Martinotti, Fabrizio Schifano

Progress in Neuro-Psychopharmacology and Biological Psychiatry January 10, 2025 DOI: 10.1016/j.pnpbp.2024.111213 (opens in new tab)

Study at a glance

AI-extracted from the abstract
Characteristics Pharmacovigilance analysis Peer reviewed
Population Adverse event reports in the FDA Adverse Events Reporting System (FAERS) for esketamine, ketamine, quetiapine, aripiprazole, olanzapine, risperidone, citalopram, escitalopram, paroxetine, fluoxetine, sertraline, duloxetine, venlafaxine, amitriptyline, and clomipramine
Interventions esketamine ketamine quetiapine aripiprazole olanzapine risperidone citalopram escitalopram paroxetine fluoxetine sertraline duloxetine venlafaxine amitriptyline clomipramine
Topics Esketamine Ketamine
Keywords Pharmacovigilance Urological safety Drug surveillance Medication safety Bladder safety Urological complications Esketamine spravato Antidepress
Citations 12
Key points Esketamine had lower or comparable odds of renal and urinary disorders compared to other antidepressants and antipsychotics, while ketamine had higher odds.

Abstract

Intranasal esketamine, approved with oral antidepressants for adults with treatment-resistant depression (TRD), is the S-enantiomer of ketamine and has higher potency and affinity for N-Methyl-d-Aspartate receptors. Administered intranasally, it offers rapid absorption and onset, essential for severe depressive symptoms or suicidal impulses. Comparative studies on esketamine and ketamine's urological safety profiles show esketamine has lower or comparable risks of renal and urinary disorders. Ketamine, however, has documented cases of nephrotoxicity and severe urological issues in recreational users. The study aims to further evaluate and compare these profiles against other antidepressants and antipsychotics using the Food and Drug Administration (FDA) Adverse Events Reporting System (FAERS) data. ADR cases were reported to the FDA up to May 12, 2024, being drugs listed including esketamine, ketamine, quetiapine, aripiprazole, olanzapine, risperidone, citalopram, escitalopram, paroxetine, fluoxetine, sertraline, duloxetine, venlafaxine, amitriptyline, and clomipramine. Risperidone showed the highest ADRs (107,418) and serious cases (71,515), with significant renal and urinary disorders reported, including acute kidney injury and urinary incontinence. Olanzapine, quetiapine, and aripiprazole also had high serious ADRs. Venlafaxine and fluoxetine were notable among antidepressants for acute kidney injury. Esketamine and ketamine were associated with lower urinary tract symptoms and nephrolithiasis. Disproportionality analysis revealed ketamine had higher odds of renal and urinary disorders compared to other drug classes, while esketamine had lower or comparable odds. The data suggest a relatively favorable tolerability profile for these drugs, especially esketamine. However, the results highlight the necessity for more extensive studies to evaluate long-term safety and optimize treatment protocols.

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