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Important Safety Information: If no improvement is seen after 6 months of use, VANIQA should be discontinued. The most frequent adverse events related to treatment with VANIQA were mild and skin related. Please see full prescribing information for VANIQA.

You are encouraged to report negative side effects of prescription drugs to the FDA. Visit www.FDA.gov/medwatch or call 1-888-INFO-FDA

VANIQA is covered by U.S. Patent 5,648,394