Ondansteron
General
- Type: antiemetics
- Dosage Forms: 4mg, 8mg
- Common Trade Names: Zofran
Adult Dosing
- Nausea/Vomiting: 4-8mg q4h, max 24mg a day
Pediatric Dosing
- Nausea/Vomiting: 0.1mg/kg IV q4h max dose at once:4-8mg, max 24mg
- Gastroenteritis - Vomiting
- 8 to 15 kg:
- 2mg orally disintegrating tablet dissolved orally as a single dose
- 15 to 30 kg:
- 4mg orally disintegrating tablet dissolved orally as a single dose
- Greater than 30 kg:
- 8mg orally disintegrating tablet dissolved orally as a single dose
- 8 to 15 kg:
Special Populations
- Pregnancy Rating: B
- Consider avoiding in 1st trimester; conflicting data regarding possible risk of teratogenicity
- Newer data argues that ondansetron is not the cause of birth defects[1]
- Lactation:safety unknown
- Renal Dosing:
- Adult: not defined
- Pediatric: not defined
- Hepatic Dosing: not defined
- Adult: not defined
- Pediatric: not defined
Contraindications
- Allergy to class/drug
- Congenital long QT syndrome
- Serotonin syndrome
Adverse Reactions
Serious
- bronchospasm
- steven-johnson syndrome
- QT prolongation
- torsades de pointes
- serotonin syndrome
- extrapyramidal symptoms
- blindness, transient
Common
- headache
- constipation
- fatigue
- hypoxia
- fever
- urinary retention
- agitation
Pharmacology
- Half-life: 4.6-5.7 hour
- Metabolism: liver
- Excretion: urine
- Mechanism of Action:selectively antagonizes serotonin 5-HT3 receptors
See Also
References
- ↑ Fejzo MS, et al. Ondansetron in pregnancy and risk of adverse fetal outcomes in the United States. Reprod Toxicol. 2016 Jul;62:87-91.