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The U.S. Food and Drug Administration is warning consumers that homeopathic teething tablets and gels may pose a risk to infants and children. The FDA recommends that consumers stop using these products and dispose of any in their possession. Homeopathic…
FDA announced comment period for draft environmental assessment for genetically engineered mosquito. The Food and Drug Administration said genetically modifying mosquitos would not cause harm to other species. Male mosquitos would be modified to produce offspring that die shortly after…
Statement on Proposed Hydrocodone Reclassification from Janet Woodcock, M.D., Director, Center for Drug Evaluation and Research Over the past several years, the U.S. Food and Drug Administration (FDA) has been carefully evaluating and weighing the appropriate use of opioid analgesic…
The U.S. Food and Drug Administration said Monday that the drugs, including Depakote and Depacon, should never be taken by pregnant women for the prevention of migraine headaches. The FDA is alerting health care providers and patients that medications including…
An Ambien Warning from the FDA. The U.S. Food and Drug Administration today announced it is requiring the manufacturers of Ambien, Ambien CR, Edluar and Zolpimist, widely used sleep drugs that contain the active ingredient zolpidem, to lower current recommended…