Discover the surprising link between the COVID-19 pandemic and a rise in RSV cases!
The COVID-19 pandemic brought unexpected consequences beyond the virus itself, affecting other respiratory illnesses like Respiratory Syncytial Virus (RSV). Following the pandemic's onset, changes in RSV diagnostic platforms led to a surge in disease detection rates. This rise in RSV cases caused a significant impact on healthcare systems, with post-pandemic ICU admissions showing a notable increase, particularly for RSV-A cases. The interplay between these two respiratory viruses highlights the complex nature of viral interactions and the ripple effects of global health crises.
Changes in RSV diagnostic platforms after the COVID-19 pandemic led to increased disease detection, and post-pandemic ICU admissions were higher for RSV-A ...
Two studies highlight new respiratory syncytial virus (RSV) findings, with one estimating that the monoclonal antibody nirsevimab was 80% effective against ...
Respiratory syncytial virus (RSV) hospitalization–related features may help inform prevention approaches among children with the infection, according to one ...
A Short Communication published by the journal Influenza and Other Respiratory Diseases added to the research-based and real-world evidence the respiratory ...
A single dose of the vaccine showed long-lasting protection against RSV-associated lower respiratory tract disease in older adults.
Following this FDA decision, Arexvy is now the first available RSV vaccine for adults under the age of 60 who are not pregnant.
In a move that will make younger adults eligible for RSV vaccines, the FDA approved an expanded label for the GSK RSV vaccine, Arexvy (RSVPreF3 +AS01E), ...
The Food and Drug Administration has approved giving GSK's vaccine for respiratory syncytial virus down to age 50 years old, to those who are at higher risk ...
US approval adds complementary option to protein-based vaccines for respiratory syncytial virus. Moderna's mResvia vaccine has been approved to protect ...
GSK plc (LSE/NYSE: GSK) today announced that the US Food and Drug Administration (FDA) has approved Arexvy (Respiratory Syncytial Virus (RSV) Vaccine, ...
The FDA's expanded approval could help GSK maintain its dominance in the RSV market, which includes shots from Pfizer and Moderna.
Thanks to respiratory syncytial virus (RSV) shot Arexvy's new label expansion into a slightly younger pool of adults, GSK is more confident than ever that ...
The U.S. Food and Drug Administration approved the expanded use of GSK's respiratory syncytial virus (RSV) vaccine on Friday in adults aged between 50 and ...
RSV vaccines are approved for those above 60; Arexvy is 1st to be approved for this age group. Read more at straitstimes.com.