FluMist is a nasal spray manufactured by AstraZeneca that has been used to protect against influenza in the United States since 2003. It’s currently available in pharmacies and other health care settings for people ages 2 to 49 who have a prescription.
Friday’s approval from the FDA adds a second option for those eligible to receive the vaccine: It can be taken at home, through self-administration by adults or to children with the help of a caregiver.
AstraZeneca plans to make the vaccine available for self-administration through a third-party online pharmacy, which will prescribe and ship the vaccine after reviewing a screening and eligibility assessment. It expects this option to be available in time for the start of next year’s respiratory virus season.
“Today’s approval of the first influenza vaccine for self- or caregiver-administration provides a new option for receiving a safe and effective seasonal influenza vaccine potentially with greater convenience, flexibility and accessibility for individuals and families,” Dr. Peter Marks, director of the FDA’s Center for Biologics Evaluation and Research, said in a statement.
“Getting vaccinated each year is the best way to prevent influenza, which causes illness in a substantial proportion of the U.S. population every year and may result in serious complications, including hospitalization and death,” he said. “This approval adds another option for vaccination against influenza disease and demonstrates the FDA’s commitment to advancing public health.”