Black Box Warnings and Medical Malpractice

Feb. 10, 2012 - PRLog -- A “black box” warning is the most severe warning category the U.S. Food and Drug Administration (FDA) uses in its medication safety classification system. The black box label is the most severe advisory that prescription drugs can contain without being pulled from the market in the United States.

In the recent past, drugs without black box warnings were eventually deemed unsafe and pulled from the market, while other medications only received black box warnings after lawsuits were filed by personal injury attorneys who practice product liability and/or medical malpractice law (also called a “medical malpractice attorney” http://www.daviddrexlerlaw.com/medical-malpractice-attorney-los-angeles.html ).

Public awareness of the importance of black box labels increased greatly in the early 2000s when medical malpractice cases received wide media attention from severe injury and deaths related to use of certain anti-inflammatory agents, antidepressants, and other classes of medications. Below are some important facts regarding black box warning labels.

The black box warning is intended to provide clear and obvious notification of safety issues associated with use of the medication. The black box warning is so named because of its appearance; as it has a black border around the warning text that appears on the label, package insert, and all other advertisements for that medication, such as advertisements in magazines. A black box warning is also called a “black label warning” or simply a “boxed warning”.

In order to be in compliance with FDA regulations, the boxed warning should include the following information:

a list of the specific side effects as reported by clinical study participants and patients
a list of all possible adverse conditions that have been reported or are likely to occur as a result from use of this drug
a statement advising you to read the manufacturer's patient Medication Guide and to weigh the risks and benefits of taking that drug with your MD
the FDA’s or the drug manufacturer's website
In the event that someone you love is harmed by one of these medications, it is important that you contact a personal injury attorney ( http://www.daviddrexlerlaw.com/ ) who specializes in medical malpractice, or specifically prescription malpractice in order to determine whether you have a case.

R. Klettke is a freelance writer. He writes about personal injury and medical malpractice law and other matters of jurisprudence.

Note: This article is not intended to provide legal advice upon which you should rely in making any decisions regarding the instituting or prosecuting of a legal claim. Laws and rules relating to the bringing of a claim vary widely from state to state. You should always contact a personal injury attorney to obtain information as to the rules and the laws pertaining to any claim you might have.