Federal regulators approved the first direct-to-consumer test for the BRCA genes, which increase the risk of breast and ovarian cancer, the agency announced on Tuesday

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First, make sure the FDA stays involved

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Jessica Porten went to a women’s clinic in Sacramento, CA that accepts her Medicaid coverage, to talk about medication options and therapy. Porten admitted to the nurse that she was having some violent thoughts. “I described maybe hitting myself or squeezing the baby too tight,” she said. “But I was very adamant through the entire appointment that I was not going to hurt myself and I was not going to hurt my children.”

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Critics wonder why

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It’s the first attempt by the UN health agency to assess the problem. Experts reviewed 100 studies involving more than 48,000 medicines. Drugs for treating malaria and bacterial infections accounted for nearly 65 percent of fake medicines

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How Anne Wojcicki led her company from the brink of failure to scientific pre-eminence

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That’s dangerous. When the results of clinical trials aren’t made public, the consequences can be dangerous — and potentially deadly

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