Principles
- High emetic risk (cisplatin, AC and others): four drugs — an NK1 antagonist, a 5-HT3 antagonist, dexamethasone and olanzapine [1, 2]. Olanzapine 10 mg reduced nausea over the five days after chemotherapy [3], and 5 mg was also effective with less sedation [4].
- Carboplatin AUC 4 or more: three drugs including an NK1 antagonist [1, 2].
- Moderate risk: a 5-HT3 antagonist plus dexamethasone on day 1 [1].
- Low risk: a single drug; minimal risk: no routine prophylaxis [1].
Common questions
What if nausea occurs despite prophylaxis?
For breakthrough nausea, give olanzapine if not already used, or a drug from another class, and step up prophylaxis by one level in the next cycle [1].
What is anticipatory nausea?
Nausea that starts before chemotherapy after a bad earlier experience; the best prevention is complete control from the first cycle, and lorazepam or behavioural therapy can help [1].
References
4 referencesShow all references, 3 with a study cardClose the reference list
Numbers in the text, such as [1], refer to these sources. Sources with a “Study card” button are summarised in the site’s evidence library.
- 1
- 2
- 3Olanzapine for the Prevention of Chemotherapy-Induced Nausea and Vomiting
- 4Olanzapine 5 mg plus standard antiemetic therapy for the prevention of chemotherapy-induced nausea and vomiting (J-FORCE): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial
This page is based on reputable scientific sources and was last updated on 27 October 2026. The content of this website is for educational and informational purposes only and does not replace consultation, diagnosis or treatment by a specialist physician. Consult your treating physician about any treatment decision.
Printed from the website; the full and up-to-date version: https://drdabiri.com/en/tools/antiemetic-regimen-cinv/