Home >  Term: boxed warning
boxed warning

The strongest form of warning required by the Food and Drug Administration (FDA) for prescription drug labeling. A boxed warning alerts health care providers and consumers to increased risk of serious adverse reactions associated with use of a drug or to restrictions on use of a drug. The boxed warning is presented in a box surrounded by a black border and is placed on the drug label and any package inserts or promotional materials intended for the prescriber or patient.

0 0

Penulis

© 2024 CSOFT International, Ltd.