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.
PRECAUTIONS
General
Xenon Xe 133, as well as other radioactive drugs, must be
handled with care and appropriate safety measures should be used to minimize
radiation exposure to clinical personnel. Also, care should be taken to
minimize radiation exposure to patients consistent with proper patient
management.
Exhaled Xenon Xe 133 gas should be controlled in a manner
that is in compliance with the appropriate regulations of the government agency
authorized to license the use of radionuclides.
Radiopharmaceuticals should be used only by physicians
who are qualified by training and experience in the safe use and handling of
radionuclides and whose experience and training have been approved by the
appropriate government agency authorized to license the use of radionuclides.
Carcinogenesis, Mutagenesis, Impairment Of Fertility
No long term animal studies have been performed to
evaluate carcinogenic potential or whether Xenon Xe 133 affects fertility in
males or females.
Pregnancy Category C
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.
Nursing Mothers
It is not known whether Xenon Xe 133 is excreted in human
milk. Many drugs are excreted in human milk, therefore formula feedings should
be substituted for breastfeeding, because of the potential for adverse
reactions in nursing infants.
Pediatric Use
Safety and effectiveness in the pediatric population has
not been established.
Geriatric Use
Clinical studies of Xenon Xe 133 Gas did not include
sufficient numbers of subjects aged 65 and over to determine whether they
respond differently from younger subjects. Other reported clinical experience
has not identified differences in responses between the elderly and younger
patients. In general, dose selection for an elderly patient should be cautious,
usually starting at the low end of the dosage range, reflecting the greater
frequency of decreased hepatic, renal, or cardiac function, and of concomitant
disease or other drug therapy.