(Reuters)—On April, the U.S. Food and Drug Administration (FDA) cautioned against the use of malaria drug hydroxychloroquine (HCQ) in COVID-19 patients even as President Donald Trump, who has touted it as a “game changer,” advocated for an additional review.
The drug, first approved in 1955, provided no benefit and potentially higher risk of death for patients at U.S. veterans hospitals, according to an analysis that has been submitted for an expert review on Tuesday.
“You hear it both ways,” Pres. Trump told reporters at the White House on Friday after the FDA announcement. “I’m not a doctor. A study has to be done. If it helps, it’s great. If it doesn’t work, don’t do it,” he said.
Trump said he had just spoken with the president of Honduras, who had touted the drug when calling to ask for ventilators. “If it works I think everyone would be in favor of it … check with him, call him.”
The FDA said on Friday it was aware of increased use of HCQ and chloroquine through outpatient prescriptions and the malaria drugs could cause abnormal heart rhythms and dangerously rapid heart rate.1
COVID-19, the disease caused by the new coronavirus, has no approved treatment or vaccine. But HCQ has been widely used in an attempt to alter the course of the COVID-19 illness based on anecdotal reports that it may provide some benefit.
There are several randomized trials underway in the U.S. and elsewhere, with the National Institutes of Health last week starting a study to evaluate the safety and the effectiveness of HCQ.
A research team in Marseilles, France, published data showing that out of 80 mild COVID-19 patients treated with HCQ and antiobiotic azithromycin, 93% had no detectable levels of the virus after eight days.
Doctors have questioned the value of the Marseille study and several papers from China as being too small or poorly designed to offer hard evidence of benefit.
The FDA’s announcement comes a day after the E.U.’s drug regulator warned of side effects of the drugs, urging medical professionals to closely monitor patients on the medicines.
The FDA has allowed healthcare providers to use the drugs for COVID-19 through its emergency use authorization, but has not approved them to treat the disease.
The heart rhythm risks may increase when the medicines are combined with other drugs, such as antibiotic azithromycin, as well as in patients with existing heart and kidney disease, the agency said.2