It is the FDA that tells a drug company when they must put a black box warning in their drug's literature,package inserts,and advertisements.

Question

Quizplus · Accepted Answer

The FDA has the authority to require a drug company to add a black box warning to their drug's labeling and advertising. This is typically done when there is significant evidence of a serious or life-threatening risk associated with the drug. The decision to require a black box warning is based on a thorough review of the available data on the drug's safety and effectiveness.

It Is the FDA That Tells a Drug Company When