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Xenon

Generic: Xenon XE-133

Verified·Apr 23, 2026
Manufacturer
Air Liquide
NDC
11994-127
Route
RESPIRATORY (INHALATION)
ICD-10 indication
Z01.89

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About Xenon

What is this medication? Xenon is an inhaled general anesthetic used to induce and maintain anesthesia during surgery. As a noble gas, it offers a unique profile compared to traditional anesthetics because it is chemically inert and not metabolized by the human body. It functions mainly as an NMDA receptor antagonist, allowing for a rapid onset of action and an equally fast recovery period, which helps patients wake up quickly once the gas administration is stopped. In addition to its role in surgery, xenon is valued for its cardiovascular stability and potential neuroprotective effects. It is often used for patients with compromised heart function because it does not lower blood pressure as significantly as other agents. Research also suggests it may help protect the brain and other organs from damage during periods of low oxygen or following a traumatic event, making it a versatile tool in both the operating room and intensive care environments.

Copay & patient assistance

Detailed copay and financial assistance information is not publicly available for this medication at this time. Please consult your pharmacist or the manufacturer's official patient support program for more details.

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Prescribing information

From the FDA-approved label for Xenon. Official source: DailyMed (NLM) · Label effective Nov 28, 2022

Indications and usage
INDICATIONS AND USAGE: Inhalation of Xenon Xe 133 Gas has proved valuable for the evaluation of pulmonary function and for imaging the lungs. It may also be applied to assessment of cerebral flow.
Dosage and administration
DOSAGE AND ADMINISTRATION: Xenon Xe 133 Gas is administered by inhalation from closed respirator systems or spirometers. The suggested activity range employed for inhalation by the average adult patient (70 kg) is: Pulmonary function including imaging: 74-1110MBq (2-30mCi) in 3 liters of air. Cerebral blood flow: 370-1110MBq (10-30mCi) in 3 liters of air. The patient dose should be measured by a suitable radioactivity calibration system immediately prior to administration. RADIATION DOSIMETRY The estimated absorbed radiation doses Method of Calculation: A Schema for Absorbed-Dose Calculation for Biologically Distributed Radionuclides, Supplement No. 1, MIRD pamphlet No. 1, J. Nucl. Med., p.7 (1968). to an average patient (70 kg) for pulmonary perfusion and cerebral blood flow studies from a maximum dose of 1110 MBq (30mCi) of Xenon Xe 133 in 3 liters of air are shown in Table 4. Table 4. Radiation Doses Effective Whole Half-Time Lungs 99% of activity is in lungs. Brain Body mGy/1110MBq (rads/30mCi) Pulmonary Perfusion 2 min. 2.5(0.25) 0.014(0.0014) 0.027(0.0027) Cerebral Blood Flow 5 min. 6.3(0.63) 0.035(0.0035) 0.068(0.0068)
Contraindications
CONTRAINDICATIONS: None known.
Warnings
WARNINGS: Xenon Xe 133 Gas delivery systems, i.e., respirators or spirometers, and associated tubing assemblies must be leakproof to avoid loss of radioactivity into the environs not specifically protected by exhaust systems. Xenon Xe 133 adheres to some plastics and rubber and should not be allowed to stand in tubing or respirator containers. The unrecognized loss of radioactivity from the dose for administration may render the study non-diagnostic. The vial stopper contains dry natural rubber latex and may cause allergic reactions in providers or patients who are sensitive to latex.
Adverse reactions
ADVERSE REACTIONS: Adverse reactions related to the use of this agent have not been reported to date.
Use in pregnancy
Pregnancy Animal reproductive studies have not been conducted with Xenon Xe 133 Gas. It is also not known whether Xenon Xe 133 Gas can cause fetal harm when administered to a pregnant woman or can affect reproduction capacity. Xenon Xe 133 Gas should be given to a pregnant woman only if clearly needed. Ideally, examination using radiopharmaceuticals, especially those elective in nature in a woman of childbearing capability, should be performed during the first few (approximately 10) days following the onset of menses.

Label text is reproduced as-is from the FDA-approved label. We do not paraphrase, summarize, or omit. Content above is for informational purposes only and is not medical advice. Always consult your prescribing clinician or pharmacist before making decisions about your medication.

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How this page is sourced

  • Drug identity verified against openFDA NDC Directory.
  • Label text (when shown) originates from NLM DailyMed.
  • Copay and assistance URLs verified periodically; if you hit a broken link, tell us.