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# Ondem (ondansetron)
## Overview
Ondansetron is a selective 5-HT3 receptor antagonist that inhibits nausea and vomiting by blocking serotonin receptors both peripherally on vagal nerve terminals and centrally in the chemoreceptor trigger zone.
## Primary Indications
* Prevention of chemotherapy-induced nausea and vomiting (CINV).
* Prevention/treatment of postoperative nausea and vomiting (PONV).
* Prevention of nausea and vomiting associated with radiotherapy.
## Adult Dosing
* **CINV (Highly Emetogenic):** 24 mg orally 30 minutes before chemotherapy.
* **CINV (Moderately Emetogenic):** 8 mg orally every 12 hours, starting 30 minutes before chemotherapy; continue for 1–2 days post-chemo.
* **PONV:** 16 mg orally 1 hour before induction of anesthesia; alternatively, 4 mg IV/IM administered at induction or postoperatively.
## Pediatric Dosing
* **CINV (Ages 4–11):** 4 mg orally 30 minutes before chemotherapy, then 4 mg 4 and 8 hours after the first dose, then 4 mg every 8 hours for 1–2 days.
* **PONV (Ages 1 month–12 years):** Weight-based dosing: 0.1 mg/kg (up to 4 mg) IV administered preoperatively or postoperatively.
* *Note: Dosing can vary by institutional protocol; always verify pediatric weight-based orders.*
## Dose Adjustments
* **Hepatic Impairment:** Maximum dose of 8 mg/day in patients with severe hepatic impairment (Child-Pugh score ≥10).
* **Renal Impairment:** No dosage adjustment required.
## Contraindications
* Known hypersensitivity to ondansetron or other 5-HT3 receptor antagonists.
* Concomitant use of apomorphine (risk of profound hypotension and loss of consciousness).
* Congenital long QT syndrome.
## Adverse Effects
* **Common:** Headache, constipation, malaise, fatigue, diarrhea.
* **Serious:** QT interval prolongation (dose-dependent), Torsades de Pointes, serotonin syndrome (when used with other serotonergic agents), and anaphylaxis.
## Key Drug Interactions
* **QT Prolonging Agents:** Increased risk of cardiac arrhythmias (e.g., amiodarone, citalopram, antipsychotics).
* **Serotonergic Agents:** Increased risk of serotonin syndrome (e.g., SSRIs, SNRIs, MAOIs, tramadol).
* **CYP2D6/3A4 Inducers:** May decrease ondansetron plasma concentrations (e.g., rifampin, phenytoin).
## Monitoring
* **ECG:** Consider monitoring in patients with electrolyte abnormalities (hypokalemia/hypomagnesemia), congestive heart failure, or those taking other QT-prolonging medications.
* **Clinical:** Monitor for signs of serotonin syndrome (agitation, tachycardia, hyperreflexia).
* **Hydration:** Monitor fluid/electrolyte status if vomiting persists.
## Clinical Pearls
* **QT Risk:** Single IV doses should not exceed 16 mg.
* **Administration:** Orally disintegrating tablets (ODT) should be placed on the tongue and allowed to dissolve; they are not intended for administration via enteral tubes.
* **Efficacy:** Ondansetron is highly effective for chemotherapy and postoperative nausea but is less effective for nausea caused by motion sickness or delayed-phase CINV compared to other agents (e.g., NK1 antagonists).
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*Disclaimer: This information is for educational purposes only. Always verify current prescribing information, institutional protocols, and patient-specific factors via reliable resources such as Lexicomp or the official FDA package insert before prescribing or administering medication.*