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The acne drug Accutane is one of the most dangerous products on the market today. The drug causes serious side-effects, most notably birth defects. This combination—unique efficacy coupled with unique risk—has posed a serious challenge for the Food and Drug Administration FDA. Over the past two decades, FDA has grappled with how manage the completely preventable but persistently serious problem of Accutane-induced birth defects. On several occasions, the product spurred FDA to take unprecedented regulatory action. In when American researchers for Hoffmann-La Roche began studying the chemical, isotretinoin, they were struck by its remarkable effectiveness.

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DermNet provides Google Translate, a free accutane sale translation service. Note that this may not provide an exact translation in all languages. Isotretinoin cis retinoic acid is a vitamin-A derivative retinoid. Isotretinoin was developed in the s, but only started being used in the mid s. Isotretinoin is a very effective medication for the treatment of acne.

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Accutane is derived from Vitamin A, which has been used to fight acne since Different companies have developed numerous Vitamin-A based acne treatments over the years, including retin-A, isotretinoin and Accutane. Before the release of Accutane, severe acne was primarily treated with oral antibiotics like tetracyclines and erythromycin. While these drugs worked for some patients, they were only effective against one of the bacteria that cause acne, Propionibacterium. Over time, these antibiotics grew less and less effective as the bacteria developed more resistant strains.

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Michael Gambon, the actor best known for playing Dumbledore in the 'Harry Potter' films, dies at Remains found in Colorado are identified as Suzanne Morphew, a mom who disappeared in The mother of a man suspected of killing a Baltimore tech CEO urged him to surrender, fearing police would try to kill him. A national registry on Friday began accepting names of Americans who take the anti-acne drug Accutane, part of a federal effort to limit use of the birth-defect-causing drug by pregnant women. The Food and Drug Administration has tried for more than 20 years to limit the exposure of fetuses to the drug, prescribed to about, Americans a month.

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