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|Title:||Method for treating rosacea using oral or topical ivermectin|
|Abstract:||A method of treating rosacea in humans involving orally-administered or topically-applied ivermectin is disclosed. More specifically, oral ivermectin in a regimen of 200 micrograms per kilogram body weight per dose for 2 or 3 consecutive doses at least 3 and not more than 7 days apart as the preferred regimen or, alternatively, topical ivermectin compounded to a 2% concentration by weight in a cream, lotion, or gel carrier vehicle is administered as an effective treatment for all clinical stages and signs of rosacea in affected persons.|
|Inventor(s):||McDaniel; William Robert (Brentwood, TN)|
1. A method of treating rosacea by orally-administering or topically-applying ivermectin in a dosage sufficient to fill and eliminate Demodex folliculorum mites from hair
follicles in affected skin, resulting in cessation of the manifestations of allergic and vasomotor responses to the organism that cause the symptoms and signs of rosacea.
2. The method of claim 1, wherein one oral dose of ivermectin is about 200 micrograms per kilogram of body weight.
3. The method of claim 1, wherein said doses of oral ivermectin are repeated about two to four times with spacing of three to seven days between them.
4. The method of claim 1, wherein said rosacea affects facial skin or eyelids, or both.
5. The method of claim 1, wherein said topically-applied ivermectin is formulated in a carrier lotion, cream, or gel.
6. The method of claim 5, wherein the concentration of ivermectin in said topically-applied lotion, cream, or gel is about one to five percent by weight.
7. The method of claim 5, wherein said topically-applied ivermectin is applied to affected skin areas but not to eyelids.
8. The method of claim 5, wherein said topically-applied ivermectin is applied to affected skin areas at least once and not more than twice daily for a period of about two to four weeks.
9. The method of claim 5, wherein said topically-applied ivermectin is encapsulated inside microliposomes before being formulated into said carrier lotion, cream, or gel.
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