Skip to content
MedsAcross

Fixed-dose combination

Fosnetupitant and Palonosetron

Also known as fosnetupitant, palonosetron hydrochloride
Available on requestCold chain
Presentations
1
Brands
1
Manufacturers
1
Available from stock
0

Fosnetupitant and Palonosetron is a fixed-dose combination medicine. It is available as injection for intravenous use. MedsAcross supplies Fosnetupitant and Palonosetron for export from India to licensed hospitals, importers and physicians acting for named patients, with the documents each country requires.

Information from the US FDA prescribing information, retrieved 12 November 2026. Not yet medically reviewed.How we review

Key facts

Pharmacological class
Serotonin-3 Receptor Antagonist, Serotonin 3 Receptor Antagonists
US FDA first approval
19 April 2018
EU status
Not recorded
Orphan designation
Not recorded
WHO essential medicine
Not recorded
India (CDSCO)
Not yet confirmed against CDSCO approval lists
Routes
Intravenous
Dosage forms
Injection
Fixed-dose combination of
Fosnetupitant, Palonosetron

Clinical information

From the regulator-approved product information. Each section names its source.

Uses

AKYNZEO capsules is indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of cancer chemotherapy, including, but not limited to, highly emetogenic chemotherapy. AKYNZEO capsules is a combination of palonosetron and netupitant: palonosetron prevents nausea and vomiting during the acute phase and netupitant prevents nausea and vomiting during both the acute and delayed phase after cancer chemotherapy. AKYNZEO for injection and AKYNZEO injection are indicated in combination with dexamethasone in adults for the prevention of acute and delayed nausea and vomiting associated with initial and repeat courses of highly emetogenic cancer chemotherapy.

Source: US FDA prescribing information

How it works

Netupitant is a selective antagonist of human substance P/neurokinin 1 (NK-1) receptors. Palonosetron is a 5-HT 3 receptor antagonist with a strong binding affinity for this receptor and little or no affinity for other receptors. Cancer chemotherapy may be associated with a high incidence of nausea and vomiting, particularly when certain agents, such as cisplatin, are used. 5-HT 3 receptors are located on the nerve terminals of the vagus in the periphery and centrally in the chemoreceptor trigger zone of the area postrema. Chemotherapeutic agents produce nausea and vomiting by stimulating the release of serotonin from the enterochromaffin cells of the small intestine. Serotonin then activates 5-HT 3 receptors located on vagal afferents to initiate the vomiting reflex.

Source: US FDA prescribing information

Dosing overview

Recommended Dosage AKYNZEO capsules: The recommended dosage is one AKYNZEO capsule administered 1 hour prior to the start of chemotherapy, with or without food. Preparation and Administration AKYNZEO injection is supplied either as a Ready-to-Use (with hanger) vial or a To-be-Diluted vial. AKYNZEO for injection requires dilution prior to administration. See full prescribing information for information on preparation, administration, and incompatibilities for each product.

Source: US FDA prescribing information

Warnings and precautions

Hypersensitivity reactions, including anaphylaxis, have been reported in patients receiving palonosetron, one of the components of AKYNZEO, with or without known hypersensitivity to other 5-HT 3 receptor antagonists. Serotonin syndrome has been reported with 5-HT 3 receptor antagonists alone but particularly with concomitant use of serotonergic drugs. If such symptoms occur, discontinue AKYNZEO and initiate supportive treatment. If concomitant use of AKYNZEO with other serotonergic drugs is clinically warranted, patients should be made aware of a potential increased risk for serotonin syndrome.

Source: US FDA prescribing information

Side effects

The following clinically significant adverse reactions are found elsewhere in the labeling: Hypersensitivity Reactions Serotonin Syndrome Most common adverse reactions (≥3%) for AKYNZEO capsules are headache, asthenia, dyspepsia, fatigue, constipation and erythema. The safety profile of AKYNZEO for injection was generally similar to that seen with AKYNZEO capsules.

Source: US FDA prescribing information

Interactions

CYP3A4 Substrates: inhibition of CYP3A4 by netupitant can result in increased plasma concentrations of the concomitant drug for 6 days after single dosage administration of AKYNZEO, avoid concomitant CYP3A4 substrates for one week, if feasible. If not avoidable, consider dose reduction of the CYP3A4 substrate. CYP3A4 Inducers (e.g., rifampin): decreased plasma concentrations of netupitant, avoid use

Source: US FDA prescribing information

Storage

Storage AKYNZEO capsules should be stored at 20 °C to 25 °C (68 °F to 77 °F), excursions permitted from 15 °C to 30 °C (59 °F to 86 °F). NDC # 69639-102-01: pack of one vial of lyophilized powder Storage Store AKYNZEO for injection in carton, protected from light at 2° to 8°C (35.6 F to 46.4°F). NDC # 69639-106-01: pack of one vial of solution with hanger (Ready-to-Use) NDC # 69639-105-01: pack of one vial of solution (To-be-Diluted) Storage Store AKYNZEO injection in carton, protected from light at 20°C to 25°C (68°F to 77°F).

Source: US FDA prescribing information

For healthcare professionals and buyers. This is not medical advice. Treatment decisions belong to the prescriber.

All presentations

1 presentations of Fosnetupitant and Palonosetron, sorted by availability.

MedicineActive ingredientManufacturerRegisterAvailability
Akynzeo 260 mg/0.28 mg per 20 mL injectionIntravenous Cold chainFosnetupitant and PalonosetronHelsinn TherapeuticsUS FDAAvailable on request

Brands by market

1 brand names across 1 markets.

Brand names by country

United States

Manufacturers

Regulatory status

Approval facts from US FDA, EMA and CDSCO data, and registration status by country where we hold register data.

RegisterStatusSource
US FDAFirst approved 19 April 2018Drugs@FDA
EU (EMA)Not recorded—
India (CDSCO)Not yet confirmed against CDSCO approval lists—
United StatesRegisteredUS FDA (NDC directory, openFDA)Checked 12 November 2026

Questions and answers

Is Fosnetupitant and Palonosetron available for export from India?

Yes, on request. MedsAcross lists 1 presentations of Fosnetupitant and Palonosetron and sources them for licensed hospitals, importers and physicians against valid import documents.

What brand names does Fosnetupitant and Palonosetron have?

The catalogue lists 1 brand names for Fosnetupitant and Palonosetron, including Akynzeo.

Is Fosnetupitant and Palonosetron approved by the US FDA?

Yes. The US FDA first approved Fosnetupitant and Palonosetron on 19 April 2018, according to Drugs@FDA.

Does Fosnetupitant and Palonosetron need cold chain shipping?

At least one listed presentation of Fosnetupitant and Palonosetron must be kept cold, so it is shipped in temperature-controlled packaging. Check the storage line on each presentation.

References

  1. AKYNZEO prescribing information (Helsinn Therapeutics). U.S. National Library of Medicine, DailyMed. Retrieved 23 June 2026

Request Fosnetupitant and Palonosetron for export supply

Tell us the strength, quantity and destination country. Our team replies with availability, lead time and the import documents needed.