BOTOX® Cosmetic is
indicated for the temporary improvement in the appearance of moderate to severe
glabellar lines associated with corrugator and/or procerus muscle activity in
patients 18 to 65 years of age.
Important Safety Information
BOTOX® Cosmetic is contraindicated in the presence of infection
at the proposed injection site(s) and in individuals with known
hypersensitivity to any ingredient in the formulation. There have been rare
reports of adverse events involving the cardiovascular system. Serious and/or
immediate hypersensitivity reactions have been reported rarely. These reactions
include anaphylaxis, urticaria, soft-tissue edema, and dyspnea.
The most common adverse events following injection include blepharoptosis and
nausea. Localized pain, infection, inflammation, tenderness, swelling, erythema
and/or bleeding/bruising may be associated with the injection. Patients with
neuromuscular disorders such as ALS, myasthenia gravis, or Lambert-Eaton
syndrome may be at increased risk of serious adverse events.
Please see the additional
safety information and full
prescribing information.
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