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Revtorpyk is intended to treat patients with advanced breast cancer whose tumors have low levels of a protein called HER2 and no mutation in a gene called PIK3CA. …
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The U.S. FDA said the drug was approved within 50 days of the company filing for approval, one of the fastest approval times for any drug. …
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The FDA approved the original version of mifepristone in 2000 and gradually eased access over time. …
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The effort launched by U.S. Health Secretary Robert F. Kennedy Jr., dubbed “Operation Stork Speed,” is the first deep look at the ingredients in formula since 1998. …
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The Food and Drug Administration said several lots of six products containing benzoyl peroxide are being recalled, though it stressed consumers faced little risk. …
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A meeting of a committee which advises the U.S. Food and Drug Administration on vaccine policy has been canceled, a committee member told Reuters. …
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The drugmaker Novo Nordisk can meet present and future demand in the U.S. for its drugs including Ozempic and Wegovy, the U.S. Food and Drug Administration said. …
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The FDA has proposed removing phenylephrine, a common ingredient in decongestants, due to its ineffectiveness, which may prompt Canada to review its approval of the drug. …
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The U.S. FDA has launched an investigation into the safety of tampons following a study that found trace amounts of toxic metals, such as arsenic and lead, in various brands. …
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