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LOTRISONE (BETAMETHASONE DIPROPIONATE, CLOTRIMAZOLE) CREAM: PATIENT COUNSELING INFORMATION
Advise the patient to read the FDA-approved patient labeling (Patient Information).
Inform the patient of the following:
Use Lotrisone cream as directed by the physician. It is for external use only.
Avoid contact with the eyes, the mouth, or intravaginally.
Advise patients to report any visual symptoms to their healthcare providers.
Do not use Betamethasone, Clotrimazole (Lotrisone) cream on the face or underarms.
Do not use more than 45 grams of Lotrisone cream per week.
When using Betamethasone Dipropionate, Clotrimazole (Lotrisone) cream in the groin area, patients should use the medication for 2 weeks only, and apply the cream sparingly. Patients should wear loose-fitting clothing. Notify the physician if the condition persists after 2 weeks.
Do not use this drug for any disorder other than that for which it was prescribed.
Do not bandage, cover or wrap the treatment area unless directed by the physician. Avoid use of Lotrisone cream in the diaper area, as diapers or plastic pants may constitute occlusive dressing.
Report any signs of local adverse reactions to the physician. Advise patients that local reactions and skin atrophy are more likely to occur with occlusive use or prolonged use.
This medication is to be used for the full prescribed treatment time, even though the symptoms may have improved. Notify the physician if there is no improvement after 1 week of treatment for tinea cruris or tinea corporis, or after 2 weeks for tinea pedis.
Manufactured and distributed by Merck, Schering-Plough pharmaceutical companies and their divisions.
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