PRECAUTIONSThe initial prescription and renewal of the medication order
beyond 20 mL should be made by a physician only after examination of the patient
with the aid of magnification, such as a slit lamp biomicroscopy and, where
appropriate, fluorescein staining.
The possibility of persistent fungal infections of the cornea should be
considered after prolonged corticosteroid dosing.
PregnancyPregnancy Category C. Dexamethasone has been shown to be
teratogenic in mice and rabbits following topical ophthalmic application in
multiples of the therapeutic dose.
In the mouse, corticosteroids produce fetal resorptions and a specific
abnormality, cleft palate. In the rabbit, corticosteroids have produced fetal
resorptions and multiple abnormalities involving the head, ears, limbs, palate,
etc.
There are no adequate or well-controlled studies in pregnant women. Neomycin
and polymyxin B sulfates and dexamethasone ophthalmic suspension should be used
during pregnancy only if the potential benefit to the mother justifies the
potential risk to the embryo or fetus. Infants born of mothers who have received
substantial doses of corticosteroids during pregnancy should be observed
carefully for signs of hypoadrenalism.
Nursing MothersSystemically administered corticosteroids appear in human milk
and could suppress growth, interfere with endogenous corticosteroid production,
or cause other untoward effects. It is not known whether topical administration
of corticosteroids could result in sufficient systemic absorption to produce
detectable quantities in human milk. Because many drugs are excreted in human
milk, caution should be exercised when neomycin and polymyxin B sulfates and
dexamethasone ophthalmic suspension is administered to a nursing woman.
Pediatric UseSafety and effectiveness in pediatric patients have not been
established.