Remdesivir can now be administered intravenously by healthcare providers in the U.S. as it undergoes further study.
an emergency use authorization for remdesivir, an antiviral drug that has shown some promising preliminary results in early clinical trials.... [+]
Ebola drug Remdesivir in particularly severely ill patients in Hamburg, northern Germany on April 8, 2020.The emergency use authorization allows health care providers to administer the drug to patients with severe cases of COVID-19, meaning they have low blood oxygen levels or are in need of oxygen therapy or a ventilator.that provides information about remdesivir and its potential side effects.
While the FDA warned that more information is still needed, clinical trial data released this week by the National Institute of Allergy and Infectious DiseasesThe action does not mean that the agency has approved the drug, but doctors can give it to patients as it undergoes more study. The normal approval process can take years. in The Lancet, found no statistically significant improvement in time to recovery.
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