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Category: FDA

FDA Investigating Risk of Testosterone Causing Cardiovascular Events

The U.S. Food & Drug Administration is investigating the risk of testosterone treatments causing an increased rate of cardiovascular events such as heart attacks and stroke, according to a drug safety communication from the…

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Help Make Generic Drug Manufacturers Accountable for Safety by Signing Take Justice Back Petition

FDA proposes rule changes to hold generic drug manufacturers accountable for injuries The FDA has proposed new rules that would improve generic drug manufacturer accountability. More than 80 percent of prescriptions are…

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FDA Issues Black Box Warning on Two Cancer Drugs

The hepatitis B warnings on two blood cancer drugs were recently strengthened by the Food and Drug Administration (FDA), according to Fox News. The strengthened warnings were issued to reflect the risk of…

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FDA Strengthens Warning on Lariam, Anti-Malaria Drug

Recently, the Food and Drug Administration (FDA) announced that the commonly used anti-malaria drug, called mefloquine hydrochloride (brand name Lariam) must have a “black box” warning on its label. The drug has…

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FDA To Revisit Rule Blocking Lawsuits Against Generic Drug Makers

The U.S. Food & Drug Administration has indicated it might allow generic drug manufacturers to revise their products’ safety labels independent of their name brand counterparts. If this change is made, consumers harmed by…

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