FDA Revokes Emergency Approval of Malaria Drugs for COVID-19

Declaring that the malaria drug “hydroxychloroquine was unlikely to be effective, the U.S. Food and Drug Administration revoked its emergency approval of the drug for COVID-19 in hospitalized patients. The agency also said the drugs had side effects they were concerned about, and that the benefits did not outweigh the risks. SOURCE: New York Times June 15, 2020  

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