Trump ‘personally’ pressured CDC, FDA, NIH to allow untested malaria drugs to be used to treat coronavirus: report

President Donald Trump personally intervened in the medical approval process, calling top officials from three of the nation's leading federal government medical agencies to pressure them to allow drugs untested for use in treating the novel coronavirus to be used for that purpose.

Top officials at the Centers for Disease Control and Prevention (CDC), the Food and Drug Administration (FDA), and the National Institutes of Health (NIH) received telephone calls from the President of the United States, who "personally pressed" them to make the malaria drugs, chloroquine and hydroxychloroquine available.

"Rarely, if ever, has a U.S. president lobbied regulators and health officials to focus their efforts on specific unproven drugs," Reuters reveals in its exclusive report. "Shortly afterward, the federal government published highly unusual guidance informing doctors they had the option to prescribe the drugs, with key dosing information based on unattributed anecdotes rather than peer-reviewed science."

His calls launched a "cascade of federal action."

Trump's focus came after a Fox News interview in mid-March of a a lawyer the conservative cable network said was associated with a small French study, who said “we have strong reason to believe that a preventative dose of hydroxychloroquine is going to prevent the virus from attaching to the body and just get rid of it completely.”

Two days later, that same attorney, appears on Fox News again, declaring, the president “has the authority to authorize the use of hydroxychloroquine against coronavirus immediately.”

Just one day later Trump began his campaign to promote the malaria drugs, despite only anecdotal evidence and that one small French study.

"On March 19, Trump vowed to make the drugs more widely available. 'It’s shown very encouraging – very, very encouraging early results,' he said at a press conference. 'And we’re going to be able to make that drug available almost immediately. And that’s where the FDA has been so great. They – they’ve gone through the approval process; it’s been approved. And they did it – they took it down from many, many months to immediate.'

The drugs had not, in fact gone through the FDA's "approval process" to treat coronavirus, nor had they been approved by the FDA to do so.

Two days after that. Trump posted these tweets:

"Now, millions of hydroxychloroquine and chloroquine pills are on their way to the public, donated by drugmakers, including Novartis’ Sandoz, Bayer and Teva Pharmaceutical Industries Ltd. The FDA issued an emergency authorization on March 28 allowing them to be prescribed and distributed from the Strategic National Stockpile."