Search Results

The US FDA has proposed removing oral phenylephrine as an active ingredient in over-the-counter medications for temporary nasal congestion relief. (Representational Image: Pixabay)
Sai Sindhuja K
3 min read
The US FDA's primary responsibility is ensuring drugs are both safe and effective
FDA reviews the recalls for medical devices and analyze its potential use and damage that it can cause
(Representational image: Unsplash)
MBT Desk
9 min read
What are the associated factors that lead to Recalling of the medical devices and what are the options other than 'removal' of medical devices in such cases?
The first emergency treatment for potentially fatal allergic reactions without the use of needles is ARS Pharmaceuticals' nasal spray. (Representational image: Unsplash)
Priyanka Pandey
2 min read
The spray, which will be marketed under the name Neffy, is thought to be a viable substitute for the EpiPen and other autoinjectors that contain epinephrine
According to the FDA, MLD is assessed to affect one in every 40,000 individuals in the US.

 (Representational image: Unsplash)
Lavanya Beeraboina
3 min read
The FDA said that the one time therapy, branded as Lenmeldy in the U.S., is authorized for children in certain stages of disease progression.
The Chikungunya virus is transmitted by the Aedes aegypti and Aedes albopictus mosquitoes, which can also transmit dengue and Zika viruses 
(Representational image: CDC PHIL)
Lavanya Beeraboina
2 min read
The US Food and Drug Administration approved Ixchiq, the first chikungunya vaccine, for individuals 18 years of age and older who are more vulnerable to mosquito-borne viruses.
A person donates blood in Yorba Linda, California, March 31, 2020. (VOA)
MBT Desk
2 min read
The U.S. Food and Drug Administration on Friday proposed revisions to its guidelines to make it easier for gay and bisexual men to donate blood
Read More
logo
Medbound
www.medboundtimes.com