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Please note: In order to qualify to use Latisse, you must be over age 18, not pregnant or nursing, have glaucoma or other chronic eye conditions, recent eye surgery, or be allergic to the ingredients in the solution.
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As with any drug, there are the intended therapeutic effects as well as unintended side effects and complications. Some of the side effects may be deleterious while others may eventuate in a new indication for the drug.
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The reactions, which have been chosen for inclusion due to either their seriousness, frequency of reporting, possible causal connection to LATISSE, or a combination of these factors, include: eye swelling, eyelid edema, hypersensitivity (local allergic reactions lacrimation increased, madarosis and trichorrhexis (temporary loss of a. Patients should be advised about the potential for increased brown iris pigmentation, which is likely to be permanent. Bimatoprost has been reported to cause pigment changes (darkening) to periorbital pigmented tissues and eyelashes.
Cardiovascular System There have been reports following administration of BOTOX of adverse events involving the cardiovascular system, including arrhythmia and myocardial infarction, some with fatal outcomes. Some of these patients had risk factors including pre-existing cardiovascular disease.
Important Safety Information Warnings and Precautions: In patients using. LUMIGAN (bimatoprost ophthalmic solution) or other prostaglandin analogs for the treatment of elevated intraocular pressure (IOP the concomitant use of LATISSE may interfere with the desired reduction in IOP.
If such reactions occur, further injection of BOTOX Cosmetic should be discontinued and appropriate medical therapy immediately instituted. One fatal case of anaphylaxis has been reported in which lidocaine was used as the diluent and, consequently, the causal agent cannot be reliably determined.
The safety and effectiveness of BOTOX for unapproved uses have not been established. Hypersensitivity Reactions Serious and/or immediate hypersensitivity reactions have been reported. These reactions include anaphylaxis, serum sickness, urticaria, soft-tissue edema, and dyspnea.
Patients using prostaglandin analogs including. LUMIGAN for IOP reduction should only use. LATISSE after consulting with their physician and should be monitored for changes to their intraocular pressure. Increased iris pigmentation has occurred when bimatoprost solution was administered.
Postmarketing reports indicate that the effects of BOTOX Cosmetic and all botulinum toxin products may spread from the area of injection to produce symptoms consistent with botulinum toxin effects. These may include asthenia, generalized muscle weakness, diplopia, ptosis, dysphagia, dysphonia, dysarthria, urinary incontinence and breathing.