"The US Food and Drug Administration (FDA) has approved the tumor necrosis factor inhibitor adalimumab (Humira, AbbVie) for the treatment of moderate to severe hidradenitis suppurativa (HS), making it the first and only FDA-approved therapy"...
The most frequent adverse event was burning/itching/stinging at the application site; the incidence and severity of this event were as follows:
|Incidence and severity of burning/itching/stinging|
|Product||Total incidence||Maximum severity|
|34 (54%)||28 (44%)||5 (8%)||1 (2%)|
|Betamethasone valerate lotion
|33 (52%)||26(41%)||6 (10%)||1 (2%)|
|24 (75%)||13(41%)||7 (22%)||41 (2%)|
|20 ( 6 7%)||12(40%)||5 (17%)||31 (0%)|
Other adverse events which were considered to be possibly, probably, or definitely related to Luxiq (betamethasone valerate foam) occurred in 1 patient each; these were paresthesia, pruritus, acne, alopecia, and conjunctivitis.
The following additional local adverse reactions have been reported with topical corticosteroids, and they may occur more frequently with the use of occlusive dressings. These reactions are listed in an approximately decreasing order of occurrence: irritation; dryness; folliculitis; acneiform eruptions; hypopigmentation; perioral dermatitis; allergic contact dermatitis; secondary infection; skin atrophy; striae; and miliaria.
Systemic absorption of topical corticosteroids has produced reversible hypothalamic-pituitary-adrenal (HPA) axis suppression, manifestations of Cushing's syndrome, hyperglycemia, and glucosuria in some patients.
Read the Luxiq (betamethasone valerate foam) Side Effects Center for a complete guide to possible side effects
Last reviewed on RxList: 9/29/2008
Additional Luxiq Information
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