The evaluation of drug safety in clinical trials is a critical element of the drug development process, ensuring that therapeutic benefits outweigh potential harms. Clinical trials, particularly in ...

Almost one quarter of hospital patients in the U.S. experience an adverse event such as medication-related harm, a pressure injury or infection during their care, according to a new study. The ...

Clinical trials utilize multiple methods of tracking, categorizing, and assessing any side effects at each trial stage. A negative side effect during clinical trials, whether expected as a potential ...

NEW DELHI: The All India Institute of Medical Sciences (AIIMS), New Delhi, has established a dedicated committee to monitor and report adverse events related to drugs and medical devices used in ...

The CDC requests and reviews medical records, including hospital records, clinic records, death certificates, and autopsy reports, for each report labeled as “serious.” VAERS staff do not decide if ...