Ondansetron

Ondansetron

Ondansetron (Zofran, Zuplenz)

Mechanism of action

Anti-emetic medication.

Selectively antagonises the serotonin 5-HT3 receptor. This receptor, located peripherally on vagal afferents as well as centrally in the chemoreceptor trigger zone (CTZ) of the area postrema, is responsible for vomiting reflex. 

Indications and dose

Pharmacokinetics

Onset of action

  • Peroral: 30 minutes; peak effect: 40 minutes
  • Intravenous: rapid; peak effect: 10 minutes

Duration of action: 4 hours

Half-life of elimination: 3–4 hours

Metabolism: Hepatic

Elimination: Kidneys, Faeces

Directions for administration

In patients with moderate to severe hepatic impairment a total daily dose of 8 mg should not be exceeded.

Slow bolus should be administered over at least 30 seconds. 

Medicinal forms

Tablets – 2 mg, 4 mg, 8 mg

Oral solution – 4 mg/5 ml, 8 mg/5 ml

Solution for Injection/Infusion – 2 mg/ml

  • 1 vial = 4 ml (8 mg)

Side-effects

Dizziness, headache, constipation 

QT interval prolongation

Bradycardia

Chest pain with or without ST segment depression

Flushing

Serotonin syndrome 

References

  1. https://www.medicines.org.uk/emc/search?q=ondansetron
  2. Ondansetron: Uses, Interactions, Mechanism of Action | DrugBank Online
  3. Pharm 101: Ondansetron • LITFL
  4. Ondansetron - an overview | ScienceDirect Topics