In Coding
Oct 15th, 2010
The U.S. Food and Drug Administration (FDA) has added information to the product label for GlaxoSmithKline’s rotavirus vaccine, which is marketed as Rotarix, after an interim analysis of a postmarketing study in Mexico indicated an increased risk of intussusception in the 31 days after the first dose of the vaccine. MayoClinic.com defines intussusception as a serious ...