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US Revokes Emergency Use Of Hydroxychloroquine Touted By Trump Vs. Virus


U.S. regulators on Monday revoked emergency authorization for malaria drugs promoted by President Donald Trump for treating COVID-19 amid growing evidence they don’t work and could cause serious side effects.

The Food and Drug Administration said the drugs hydroxychloroquine and chloroquine are unlikely to be effective in treating the coronavirus. Citing reports of heart complications, the FDA said the drugs’ unproven benefits “do not outweigh the known and potential risks.”

The decades-old drugs, also prescribed for lupus and rheumatoid arthritis, can cause heart rhythm problems, severely low blood pressure and muscle or nerve damage. The agency reported Monday that it had received nearly 390 reports of complications with the drugs, including more than 100 involving serious heart problems. Such reports represent an incomplete snapshot of complications with the drugs because many side effects go unreported.

FDA’s move means that shipments of the drugs obtained by the federal government will no longer be distributed to state and local health authorities for use against the coronavirus. The drugs are still available for alternate FDA-approved uses, so U.S. doctors could still prescribe them for COVID-19 — a practice known as off-label prescribing.

Dr. Steven Nissen, a Cleveland Clinic researcher who has been a frequent FDA adviser, agreed with the decision and said he would not have granted emergency access in the first place.

“There has never been any high-quality evidence suggesting that hyrdoxychloroquine is effective” for treating or preventing coronavirus infection, he said, but there is evidence of serious side effects.

On Thursday, a National Institutes of Health panel of experts revised its recommendations to specifically recommend against the drug’s use except in formal studies, and “that, I’m sure, had influence on the FDA,” Nissen said.

The actions by FDA and NIH send a clear signal to health professionals against prescribing the drugs for coronavirus.

Trump aggressively pushed the drug beginning in the first weeks of the outbreak and stunned medical professionals when he revealed he took the drug preemptively against infection. After Trump’s repeated promotions, prescriptions for hydroxychloroquine soared, contributing to shortages for patients using the drugs for established uses.

No large, rigorous studies have found the drugs safe or effective for preventing or treating COVID-19. And a string of recent studies made clear they could do more harm than good.

Dr. Peter Lurie, a former FDA associate commissioner and an Obama administration appointee, said the agency had tarnished its reputation by clearing the drugs based on scant evidence and under apparent political pressure.

“This is an agency that gains its credibility from the strength of its scientific pronouncements,” said Lurie, now president of the nonprofit Center for Science in the Public Interest. “The lesson of this whole tawdry episode is that it’s the old, painstaking ways of science that ultimately deliver safe and effective therapies.”

The only remaining drug with FDA authorization against COVID-19 is remdesivir, an intravenous drug that has been shown to help severely ill, hospitalized patients recover faster.

The FDA granted emergency use of the drugs for coronavirus patients in late March at the same time the U.S. government accepted 30 million doses of hydroxychloroquine and chloroquine that had been donated by two foreign drug manufacturers. Millions of those doses were shipped to U.S. hospitals to treat patient who weren’t enrolled in clinical trials.

But the FDA previously warned doctors that it had seen reports of dangerous side effects and heart problems reported to poison control centers and other health systems.

The agency said it revoked the authorization in consultation with the Biomedical Advanced Research and Development Authority, or BARDA, which had requested the emergency use.

BARDA’s former director said in April that he was removed from his job because he resisted political pressure from Trump appointees to allow widespread use of the malaria drugs. Rick Bright said he worked with FDA senior staff to limit the drugs’ authorization to patients hospitalized with COVID-19 and under professional supervision.

Among other issues, Bright objected to the fact that some of the doses imported were manufactured at facilities in India and Pakistan that had not been inspected by the FDA.

The FDA says it sampled and tested the imported drugs to confirm they met the agency’s standards for safety and quality.

(AP)



5 Responses

  1. Yet another hit job by YWN using AP against President Trump and his suggestion for dealing with this virus. In Dr. Zelenko’s new report and statistical study of the proper way to use HCQ/Zn/Z-Pack all the issues in this article are effectively addressed and disproven. If someone has a political agenda, They don’t care how many people may die as long as their agenda succeeds.
    I wish there was another good Jewish news web site that reflected real Torah values that is politically conservative.

  2. Dr. Peter Lurie, a former FDA associate commissioner and an Obama administration appointee […] now president of the nonprofit Center for Science in the Public Interest.

    Which means nothing he has to say is of the slightest value. CSPI is a sham organization, a left-wing propaganda unit that manipulates science to pursue its political agenda.

    We all know what’s really “wrong” with this drug — Trump supported it. Had he not done so everyone would be hailing it.

  3. I don’t get how you can suddenly discover that a medicine that has been used prophylactically for more than fifty years, has serious side effects. I mean, they were dishing it out like candy to anyone going to a country that had even a slight malaria problem, by their “new findings” shouldn’t we have seen hundreds of thousands of people develop serious heart issues over the last half-century from taking this drug?!

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