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Williams Kherkher Law Firm, L.L.P.
8441 Gulf Freeway, Suite 600, Houston, TX 77017-5051 USA
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Office: 832-369-8296
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Blogroll
Dietary supplement recalled after mistaken for antibiotic
Posted on May 10th, 2011
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Multi-Mex Distributors Inc., have announced the recall of their dietary product after it was mistaken for amoxicilin and used to treat children. The issue arose when it was discovered that the dietary product, Amoxilina, and the antibiotic amoxicilin were confused by the parents of four Hispanic children in Texas. Buy Amoxil The children were taken [...]
Houston defective drug attorney, Houston defective pharmaceutical product lawyers
Houston defective pharmaceutical product attorneys, Houston defective pharmaceutical product lawyers
Tagged Houston defective pharmaceutical product attorneys, Houston defective pharmaceutical product lawyers
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Tylenol recall update: Criminal charges possible
Posted on May 27th, 2010
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The Federal Drug Administration has been investigating the Tylenol recall and now has put the case in the criminal investigation division. One of the problems associated with the recalled products is the excess amount of acetaminophen. The issue being investigated by the FDA is a matter of non-compliance with the FDA warnings and also the [...]
Tylenol recalls investigated by FDA
Posted on May 25th, 2010
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The Food and Drug Administration continues to investigate the drug manufacturer McNeil (a division of Johnson & Johnson) after reports of 775 serious side effects were reported by consumers. McNeil has initiated four recalls in the past seven months and recently shut down operations at a Fort Washington, Pennsylvania location. The FDA typically considers adverse [...]
Increased cancer risk tied to diabetes drug Byetta
Posted on April 13th, 2010
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New data from the U.S. Food and Drug Administration suggests that the once-weekly intravenous Byetta show similar signs of cancer in rats as do similar drugs such as Victoza. This new data may indicate that Byetta will carry the same boxed warning as Victoza, alerting patients of the risk of thyroid tumors commonly associated with [...]
Raptiva Recalled Due to Risk of Neurological Disease
Posted on April 9th, 2009
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Raptiva (efalizumab) a psoriasis drug manufactured and marketed by Genentech, Inc., was recently recalled by the company in response to concerns about the drug's association with progressive multifocal leukoencephalopathy (PML), a rare and deadly brain disease. In October 2008, the FDA changed Raptiva's label to warn about the increased risk of PML. By early 2009, [...]