Antiemetic · Drug monograph
Ondansetron: veterinary dose and monograph
Ondansetron is a veterinary antiemetic. 5-HT3 receptor antagonist — a central and peripheral antiemetic. Indications include refractory vomiting (parvovirus, pancreatitis, CKD); chemotherapy-induced nausea / vomiting; adjunct to maropitant for breakthrough vomiting. This monograph lists 4 reference doses for dogs, cats and primates, each with route, frequency and source.
At a glance
- Drug class
- Antiemetic
- Also known as
- Zofran, Emeset
- Species with doses
- Dogs, Cats and Primates
- General dose range
- 0.1–1 mg/kg IV q8–12h — check the species tables for the indication
- Routes
- IV
- Last reviewed
- 1 October 2026
Indications
- Refractory vomiting (parvovirus, pancreatitis, CKD)
- Chemotherapy-induced nausea / vomiting
- Adjunct to maropitant for breakthrough vomiting
Ondansetron dose by species
Doses are per administration unless stated. mg/kg doses scale with body weight; per-animal, per-quarter and infusion-rate doses are shown as the reference writes them.
Dogs
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| Antiemetic (general) | 0.1–0.5 mg/kg | IV | q6–12h (slow IV) | — |
| Chemotherapy-induced vomiting | 0.5–1 mg/kg | IV | 30 min before chemotherapy | — |
- Antiemetic (general): Papich 5e: vomiting from other causes 0.1–0.2 mg/kg slow IV q6–12h, increasing to 0.5 mg/kg if ineffective. Plumb’s p.909: 0.1–0.3 mg/kg slow IV q8–12h — dramatic results in parvovirus and pancreatitis (Tams 2007); 0.1–0.2 mg/kg IV q6–12h (Otto 2005); uraemia 0.6–1 mg/kg PO or IV q12h.
- Chemotherapy-induced vomiting: Papich 5e: 0.5–1 mg/kg IV or SC 30 min before IV cancer drugs. Plumb’s p.909 (Kent 2009): 0.1–0.5 mg/kg IV over 15 min q8h, or 0.5–1 mg/kg PO q8–12h. Oral bioavailability in dogs is under 10% (Papich).
Cats
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| Refractory vomiting / CKD nausea | 0.1–0.5 mg/kg | IV | q8–12h | — |
- Refractory vomiting / CKD nausea: Papich 5e: 0.5 mg/kg q8h SC, IV or PO (2 mg per cat — half a tablet — q8h is common); reduce to q12h with liver disease; CRI 0.5 mg/kg IV then 0.5 mg/kg/h. Plumb’s p.909: 0.5 mg/kg IV or PO twice daily (Trepanier 2010); intractable vomiting 0.1–0.15 mg/kg slow IV q6–12h (Scherk 2003).
Primates
| Indication | Dose | Route | Frequency | Duration |
|---|---|---|---|---|
| Antiemetic (monkeys, macaques) | 0.1–1 mg/kg | IV | q24h | — |
- Antiemetic (monkeys, macaques): Carpenter Exotic Animal Formulary 6th ed, Table 13-7 (p.710): monkeys 0.1 mg/kg slow IV q24h or 1 mg/kg SC q24h; macaques 4 mg/animal PO prophylaxis 30 min before. Sedation is a common side effect.
Contraindications
Known hypersensitivity. Use cautiously with other QT-prolonging drugs; reduce the dose in significant hepatic impairment.
Adverse effects
- Generally well tolerated
- Constipation, sedation (occasional)
- Rare QT prolongation at high IV doses
Drug interactions
- Apomorphine: a human patient given both developed SEVERE HYPOTENSION - the combination is contraindicated in humans. Relevant in small-animal practice, where apomorphine is the standard emetic
- Drugs affecting the QTc interval (amiodarone, cisapride, halothane, isoflurane, sotalol): theoretically additive QTc effects with possible serious arrhythmias
- Tramadol: in humans the combination may reduce the efficacy of BOTH drugs; veterinary significance unknown
Toxicity and overdose
Plumb's p.909: overdoses of up to 10x did not cause significant morbidity in human subjects; treat supportively if one occurs. The wide margin means the practical risks are the interactions rather than the dose - chiefly additive QTc prolongation with inhalational anaesthetics, and the masking of ileus or gastric distention noted under precautions.
Clinical pearls
- Layer with maropitant (different mechanism) for parvo / pancreatitis vomiting that breaks through single-agent therapy
- Plumb's p.909 flags an important blind spot: ondansetron may MASK ileus or gastric distention — it is not a substitute for nasogastric suction, so keep decompressing and imaging the vomiting patient
- Give slow IV — a rapid push can cause transient dysrhythmia
- Treats vomiting but not the cause — always pursue and address the primary disease
Mechanism of action
Plumb's p.909: 5-HT3 (serotonin type 3) receptor ANTAGONIST. 5-HT3 receptors sit peripherally on vagal nerve terminals and centrally in the chemoreceptor trigger zone (CTZ); Plumb's notes it is not clear whether ondansetron acts centrally, peripherally or both. This dual siting is why it works for chemotherapy- and toxin-driven vomiting that antihistaminic or dopaminergic antiemetics miss. No veterinary pharmacokinetic data was located; in humans it is well absorbed orally with some first-pass metabolism (bioavailability 50-60%), peak levels at about 2 hours, extensive hepatic metabolism and a 3-4 hour elimination half-life.
Formulations and products
- Ondansetron 2 mg/mL injection
- Ondansetron 4 mg tablet
- Ondansetron 8 mg tablet
Before you use this dose
Reference doses for veterinary professionals. Confirm the dose against the product label, the patient’s condition, current guidance and local regulations before use; the attending veterinarian remains responsible for every clinical decision.
Frequently asked questions
What is the dose of Ondansetron for dogs?
Reference doses for Ondansetron in dogs: 0.1–0.5 mg/kg IV q6–12h (slow IV) (Antiemetic (general)); 0.5–1 mg/kg IV 30 min before chemotherapy (Chemotherapy-induced vomiting). Confirm against the label and the patient before use.
What is the dose of Ondansetron for cats?
Reference doses for Ondansetron in cats: 0.1–0.5 mg/kg IV q8–12h (Refractory vomiting / CKD nausea). Confirm against the label and the patient before use.
What is the dose of Ondansetron for primates?
Reference doses for Ondansetron in primates: 0.1–1 mg/kg IV q24h (Antiemetic (monkeys, macaques)). Confirm against the label and the patient before use.
When should Ondansetron not be used?
Known hypersensitivity. Use cautiously with other QT-prolonging drugs; reduce the dose in significant hepatic impairment.
What are the side effects of Ondansetron in animals?
Generally well tolerated; Constipation, sedation (occasional); Rare QT prolongation at high IV doses.
Sources
- Plumb's Veterinary Drug Handbook
- Papich, Papich Handbook of Veterinary Drugs, 5th edition
- Carpenter, Exotic Animal Formulary
Last reviewed · VetMasterJi