FDA appears to soften stance on hydroxychloroquine after Trump says he takes malaria drug

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FDA appears to soften stance on hydroxychloroquine after Trump says he takes malaria drug
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The FDA advised consumers against taking hydroxychloroquine for Covid-19 outside a hospital or formal clinical trial setting due to the risk of 'serious heart rhythm problems.'

A bottle of Prasco Laboratories Hydroxychloroquine Sulphate is arranged for a photograph in the Queens borough of New York, U.S., on Tuesday, April 7, 2020.The U.S. Food and Drug Administration said Tuesday that taking hydroxychloroquine is "ultimately" a choice between patients and their health-care providers, appearing to soften its earlier advisory against taking the anti-malaria drug outside of a hospital.

The comments came a day after President Donald Trump said he has been taking hydroxychloroquine daily forHe said he asked his White House physician about the drug. "I asked him, 'What do you think?' He said, 'Well, if you'd like it.' I said, 'Yeah, I'd like it. I'd like to take it.

Hydroxychloroquine, which has been repeatedly touted by Trump as a potential game-changer in fighting the coronavirus, is also often used by doctors to treat rheumatoid arthritis and lupus. White House physician Dr. Sean Conley released a memo Monday evening, which said that after discussing evidence for and against hydroxychloroquine with Trump, they concluded "the potential benefit from treatment outweighed the relative risks."

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