(Reuters) -The Biden administration has decided to stretch out its limited supply of monkeypox vaccine by allowing a different method of injection that uses one-fifth as much per shot, the New York Times reported on Monday, citing senior officials familiar with the planning.
The United States declared monkeypox a public health emergency last week, in an effort to bolster the U.S. response to contain the outbreak.
For U.S. Food and Drug Administration (FDA) to authorize the intradermal injection, which requires injecting one-fifth of the current dose into the skin instead of a full dose into underlying fat, the Department of Health and Human Services (HHS) will need to issue a new emergency declaration, the report said, allowing regulators to invoke the FDA’s emergency use powers.
The announcement is expected as early as Tuesday afternoon, according to the newspaper. (https://nyti.ms/3P7QSFZ)
White House, HHS and FDA did not immediately respond to Reuters’ requests for comment.
Earlier this month, Biden appointed two federal officials to coordinate his administration’s response to monkeypox, following declarations of emergencies by California, Illinois and New York.
Of late more than 80 countries where monkeypox is not endemic have reported outbreaks of the viral disease, which the World Health Organization has declared a global health emergency, as confirmed cases crossed 27,800 and non-endemic countries reported their first deaths.
First identified in monkeys in 1958, the disease has mild symptoms including fever, aches and pus-filled skin lesions, and people tend to recover from it within two to four weeks, the WHO says. It spreads through close physical contact and is rarely fatal.
(Reporting by Akriti Sharma in Bengaluru; Editing by Christopher Cushing & Simon Cameron-Moore)