FDA approval Mupirocin - Bactroban clinical trails
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FDA approval for Mupirocin - Bactroban

The world of antibiotics was first introduced in 1940’s.Initially it was labeled as the “miracle drugs”. With its effectiveness to deal with bacterial infections it has achieved a secure place in the medication world. Mupirocin, an ointment used in the treatment of bacterial infections, more accurately an antibiotic that is used as a tropical treatment for impetigo. It was on 24th October 2005 that the Taro Pharmaceutical Industries Ltd announced its approval in USA from the Food and Drug Administration.

This approval was for the manufacturing of USP, 2% ointment. This ointment by this industry better known as TARO turns out to be equivalent to that made by the GlaxoSmithKline’s Bactroban ointment. Analysis and reports based on the six clinical trails that were taken to evaluate the effectiveness of mupirocin or the bactroban showed positive results. It had also been found that those patients using Mupirocin under the brand name Bactroban cured their problem up to 905 to 91%.

While those using the same under the brand name Placebo showed results only up to 7-8 percent. Not only this but also the post effects of the drugs of both when compared were found to be astonishing.Bactroban showed that 75% of patients were completely bacteria free after 3-4 four weeks, this number was outstanding as compared to just 10% result of Placebo. According to the surveys conducted it was noticed that mupriocin is an ointment which has an annual sale of more than $77.00 million in US.

With this pace of the sale it can be predicted that this drug has a bright future in the antibiotic category.
 

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