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my father had a severe and almost fatal experience with Ketek. His physician did not feel that his episode (stopped breathing) was related. I feel that every situation with a medication should be evaluated. Fortunately help arrived in time, he was intubated and rushed to the hospital. Every doctor should be aware that ANY medication can cause a reaction, especially when you have Myasthenia.
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Shortly after Ketek was approved by the FDA, the FDA began receiving reports that Ketek was causing severe liver damage, including deaths. As a result, by February 2007, the FDA added a black box warning (which is the strongest warning that the FDA placed on a prescription drug) about liver damage to the Ketek label.
Schlichter, Bogard & Denton, a law firm in St. Louis, Missouri, is handling cases for a number of individuals that have been harmed by Ketek. You can visit their website at www.uselaws.com or contact kkraft@uselaws.com for a free evaluation. |
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