Ondansetron

Generic name
Ondansetron
Brand name
ATC Code
A04AA01

Ondansetron

Dosages
Side effects in children
Warnings & precautions in children
Contra-indications in children

Interactions
PK
Renal impairment
References

Pharmacokinetics in children

The following pharmacokinetic parameters have been observed following intravenous administration (Zofran SPC) (Mondick et al. 2010, Spahr-Schopfer et al. 1995):

Post operatieve nausea and vomiting (PONV):

Age n= t½ (hr) Cl (l/hr/kg) Vd (l/kg)
1-4 months 19 6,7 0,40 3,5
5-24 months 22 2,9 0,58 2,3
3-12 years 21 2,9 0,44 1,65

Chemotherapy induced nausea and vomiting (CINV) :

Age n= t½ (hr) Cl (l/hr/kg) Vd (l/kg)
1-48 months 115 4,9 0,58 3,65
4-18 years 21 2,8 0,60 1,9

 

dose recommendation of formulary compared to licensed use (on-label versus off-label)

No information is present at this moment.

Available formulations

No information is present at this moment.

Dosages

Go to:

Nausea and vomiting in low emetogenic chemotherapy
  • Oral
  • Intravenous
    • 1 month up to 18 years
      [4] [22] [26] [29] [30]
      • 10 mg/m²/dose, once only. Max single dose: 8 mg/dose.
        • A second dose of 5 mg/m2 can be administerred if needed.
        • 10 mg/m2 is similar to 0,3 mg/kg
Nausea and vomiting in moderate to high emetogenic chemotherapy
  • Intravenous
    • 1 month up to 18 years
      [4] [22] [26] [29] [30]
      • 15 mg/m²/day in 3 doses. Max single dose: 16 mg/dose.
        • 15 mg/m2/day is equivalent to 0,45 mg/kg/day
        • Give 15 minutes before the course of medication.
  • Oral
    • 1 month up to 18 years
      [4] [22] [23] [26] [29] [30]
      • 15 mg/m²/day in 3 doses. Max single dose: 8 mg/dose.
        • 15 mg/m2/day is equivalent to 0,45 mg/kg/day
        • Give 15 minutes before the course of medication.
Nausea and vomiting, post-operative
  • Oral
    • 0 years up to 3 years
      • 1 mg/dose, as required, max. 3x daily with a dosing interval of 4 hours.
    • 3 years up to 11 years
      • 2 mg/dose, as required, max. 3x daily with a dosing interval of 4 hours.
    • 11 years up to 18 years
      • 4 mg/dose, as required, max. 3x daily with a dosing interval of 4 hours.
    • 1 month up to 18 years
      [24] [25] [27] [28] [31] [33]
      • 0.1 mg/kg/dose, as required, max. 3x daily with a dosing interval of 4 hours. Max single dose: 4 mg/dose.
      • Oral administration only if intravenous use is not possible or preferred. 

  • Intravenous
Acute gastroenteritis with vomiting and dehydration

Renal impaiment in children > 3 months

GFR ≥10 ml/min/1.73m2: Dose adjustment not required.

GFR <10 ml/min/1.73m2: A general recommendation on dose adjustment cannot be provided.

The complete list of all undesirable drug reactions can be found in the national Summary of Product Characteristics (SmPC) – click here

Side effects in children

QT extension (Trivedi et al. 2016). 

The complete list of all contra-indications can be found in the national Summary of Product Characteristics (SmPC) – click here

Contra-indications

No information available on specific contra indications in children.

The complete list of all warnings and precautions can be found in the national Summary of Product Characteristics (SmPC) – click here

Warnings & precautions in children

Paediatric patients receiving ondansetron in combination with hepatotoxic chemotherapeutic agents should be monitored closely for impaired liver function.

Studies in adults show that ondansetron in doses of > 32 mg/dose can cause a dose-dependent extension of the QT interval, potentially leading to cardiac dysrhythmia, including torsades de pointes. Publications by Brenner (2016) Nathan (2011) and McKechnie (2010) describe prolongation of the QT interval leading to heart rhythm abnormalities in children with a heart defect/congenital long QT-interval syndrome. Using ondansetron must be avoided in children with a congenital long QT syndrome. Caution is needed when there are risk factors for prolongation of the QT interval: Hypopotassemia; impaired renal function; diabetes mellitus; combined use with drugs that prolong the QTc-interval or that increase the bloodconcentration; high doses; pre-existing prolonged QTc-interval or long QTc-interval syndrome.  If risk factors are present a ECG should be performed prior to the start of therapy.

A lethal reaction on ondansetron has been described in a case report on a child with comorbid malignant hyperthermia (Gener 2010)

Interactions

The complete list of all interactions can be found in the national Summary of Product Characteristics (SmPC) – click here

ANTIEMETICS AND ANTINAUSEANTS

This pages provides a list of drugs from the same ATC class for comparison. This does not necessarily mean that these drugs are interchangeable.

Serotonin (5HT3) antagonists
A04AA02
A04AA05
Other antiemetics
A04AD12

References

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  3. Carter B. et al, Antiemetic treatment for acute gastroenteritis in children: an updated Cochrane systematic review with meta-analysis and mixed treatment comparison in a Bayesian framework, BMJ Open, 2012, Jul 19;2(4)
  4. Van de Wetering, MD., Werkboek Supportive Care, www.skion.nl, 2017
  5. Alhashimi D, et al, Antiemetics for reducing vomiting related to acute gastroenteritis in children and adolescents, Cochrane Database Syst Rev, 2009, Apr 15;(2), CD005506
  6. Roslund G, et al, The role of oral ondansetron in children with vomiting as a result of acute gastritis/gastroenteritis who have failed oral rehydration therapy: a randomized controlled trial., Ann Emerg Med, 2008, Jul;52(1), 22-29
  7. Lincke, CR, Ondansetron tegen braken bij acute gastro-enteritis, Farmacother Kind, 2010, 1, 12-8
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  12. Ramsook C, et al, A randomized clinical trial comparing oral ondansetron with placebo in children with vomiting from acute gastroenteritis, Ann Emerg Med, 2002, Apr;39(4), 397-403
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  14. Nathan AT, et al, Implications of anesthesia in children with long QT syndrome, Anesth Analg, 2011 , May;112(5):, 1163-8
  15. McKechnie K et al, Ventricular tachycardia after ondansetron administration in a child with undiagnosed long QT syndrome, Can J Anaesth, 2010, May;57(5), 453-7
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  29. Jain, S., et al , A randomized, open-label non-inferiority study to compare palonosetron and ondansetron for prevention of acute chemotherapy-induced vomiting in children with cancer receiving moderate or high emetogenic chemotherapy, Support Care Cancer, 2018, 26(9), 3091-3097
  30. Tan, J., et al. , Palonosetron is nonsuperior to ondansetron in acute phase but provides superior antiemetic control in delayed phase for pediatric patients administered highly emetogenic chemotherapy., Pediatr Blood Cancer, 2018, 65 (2)
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Changes

Therapeutic Drug Monitoring


Overdose