Descovy, a daily pre-exposure prophylaxis treatment, is approved to reduce the risk of contracting HIV upon exposure to the virus.
The drug, manufactured by Gilead, is designed for at risk adults and adolescents who weigh at least 77 pounds.
Descovy is not for individuals at risk of HIV infection from receptive vaginal sex, as the effectiveness on that population hasn’t been tested.
The clinical trial for Descovy showed it was similar to Truvada, Gilead’s other HIV prevention drug, in reducing the risk of acquiring HIV.
The most common adverse reaction in patients without HIV taking Descovy was diarrhea.
The FDA warned that Descovy could exacerbate Hepatitis B symptoms. It also warned Descovy shouldn’t be taken by HIV-positive people or people with an unknown HIV status.
Read the full news release here.
More articles on pharmacy:
Eli Lilly and Bayer dodge suits claiming they used nurses to push drugs
At the Becker's 11th Annual IT + Revenue Cycle Conference: The Future of AI & Digital Health, taking place September 14–17 in Chicago, healthcare executives and digital leaders from across the country will come together to explore how AI, interoperability, cybersecurity, and revenue cycle innovation are transforming care delivery, strengthening financial performance, and driving the next era of digital health. Apply for complimentary registration now.