Taking Hydroxychloroquine ‘Ultimately a Decision Between a Patient and Their Doctor:’ FDA

Taking Hydroxychloroquine ‘Ultimately a Decision Between a Patient and Their Doctor:’ FDA
A pharmacist displaying a box of hydroxychloroquine (HCQ) tablets in his store in Hyderabad, India, on April 28, 2020. Noah Seelam/AFP via Getty Images
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A day after President Donald Trump admitted to taking a regimen of hydroxychloroquine and zinc to lower his COVID-19 risk, the Food and Drug Administration (FDA) appeared to soften its stance on widespread use of the anti-malarial drug, saying the decision should be made by a patient and their doctor.

“The decision to take any drug is ultimately a decision between a patient and their doctor,” FDA Commissioner Stephen Hahn told The Hill in a statement on Tuesday. “Hydroxychloroquine and chloroquine are already FDA-approved for treating malaria, lupus, and rheumatoid arthritis.”
Isabel van Brugen
Isabel van Brugen
Reporter
Isabel van Brugen is an award-winning journalist. She holds a master's in newspaper journalism from City, University of London.
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