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Acne Treatment, Finally Some Facts
Copyright 2005 George ForganSmith Acne is, perhaps, the single treated skin disorder and has been addressed in a wide variety of ways. Often the wisest step is to develop a program in consultation with a dermatologist or medical practitioner....
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Skin Care For Acne
Caring for your skin is important for good health and beauty,
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The Essential Oil Home Medicine Chest – Part I: The Oils
Essential oils provide a wonderful natural-medicine alternative to common ailments we see at home. Their actions are broad and diverse, ranging from topical antiseptics and anti-inflammatories to analgesics, digestive system tonics, and...
The First Step To Curing
The first step to curing acne is knowing what type of acne you have. This information gives you precious insight to what may have actually triggered the acne outset. Once you know your acne trigger, you are one step closer to removing the acne...
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Acne: FDA Approved Aczone For Acne Treatment
The U.S. Food and Drug Administration (FDA) approved to market
Aczone (dapsone) Gel, 5 per cent for acne vulgaris topical
treatment. But patients who have the enzyme deficiency, G6PD
(Glucose 6-phosphate dehydrogenase), will need to be monitored
with regular blood counts to detect if they are predisposed to
one type of anemia (hemolytic anemia).
Aczone, a trademark of QLT USA Inc., is an aqueous topical gel
which contains 5 per cent dapsone. According to scientific
research, combining dapsone in a Solvent Microparticulate (SMP)
gel enables dapsone to be applied topically and safely. This
product achieved significant per cent reduction in the number of
acne lesions and better success rate on the Global Acne
Assessment Score in two randomized double-blind, vehicle
controlled clinical studies in 3000 acne patients.
Oiliness/peeling, dryness, and erythema were the most common
adverse events reported from controlled clinical trials.
However, there were no significant differences in the adverse
event rates between Aczone Gel and vehicle control treated
patients.
1.4 per cent of about 3500 patients had the enzyme deficiency
-in the Aczone clinical trial program- which is consistent with
the incidence in the general North American
population.
The company QLT will undertake a post-approval Phase IV study in
50 acne patients who have G6PD deficiency and follow them for 6
months, after which QLT expects to submit an application to the
FDA to re-evaluate the Aczone label.
The President and Chief Executive Officer of QLT Inc., Paul
Hastings, stated that "Aczone represents an important clinical
advance in dermatology, has demonstrated safety and efficacy in
over 4,000 patients. We are very pleased with the FDA's decision
and confident in Aczone's potential as a new class of treatment
for acne patients". Article written by Hector Milla, editor of
http://www.acnetreatment
stips.com , a website pointing acne treatment tips
and http://www.acnesoluti
onsproducts.com , visit for reviews and acne solution
products information . Thanks for use this article in your
website or ezine keeping a live link.
About the author:
Hector Milla, editor of many websites in different
topics:Moreover he has a degree in business administration.
http://www.disorderskin.com
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