Luxiq
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Luxiq
SIDE EFFECTS
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 | ||
| Mild | Moderate | Severe | ||
| Luxiq Foam n=63 |
34 (54%) | 28 (44%) | 5 (8%) | 1 (2%) |
| Betamethasone valerate lotion n=63 |
33 (52%) | 26(41%) | 6 (10%) | 1 (2%) |
| Placebo Foam n=32 |
24 (75%) | 13(41%) | 7 (22%) | 41 (2%) |
| Placebo Lotion n=30 |
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 »
DRUG INTERACTIONS
No information provided.
Last reviewed on RxList: 9/29/2008
This monograph has been modified to include the generic and brand name in many instances.
Additional Luxiq Information
Luxiq - User Reviews
Report Problems to the Food and Drug Administration
You are encouraged to report negative side effects of prescription drugs to the FDA. Visit the FDA MedWatch website or call 1-800-FDA-1088.
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