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February 06, 2012
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Drug Litigation News

 

FDA Commemorates a Century of Protecting and Promoting Public Health

The U.S. Food and Drug Administration (FDA) today will celebrate the centennial of the Pure Food and Drugs Act of 1906 at an event dedicated to the agency's past, present and future service to the nation. The ceremony, which will be held at the FDA's Harvey W. Wiley federal building, will feature U.S. Health and Human Services Secretary Michael O. Leavitt and Acting FDA Commissioner Andrew C. von Eschenbach, M.D.  Also in attendance will be senior leaders of the agency, and scores of current and former FDA employees and special guests including former Commissioners of Food and Drugs, representatives of consumer and trade groups, and descendants of Dr. Harvey W. Wiley, the scientist whose early support of food and drug regulations earned him the title of "Father of the Pure Food and Drugs Act.

Dr. Wiley served as the first director of the Bureau of Chemistry of the United States Department of Agriculture, which later became the FDA. In addition to presentations by Secretary Leavitt and Acting Commissioner Dr. von Eschenbach, the program's highlights include an overview of the coming public health opportunities and challenges by FDA's Deputy Commissioners and other senior leaders of the agency. Sean K. Sullivan, Associate Publisher of Good Housekeeping magazine, will speak about Dr. Wiley's work following government service as Director of the Bureau of Foods, Sanitation and Health for Good Housekeeping magazine.

The modern FDA dates its origin to June 1906, when President Theodore Roosevelt signed the Food and Drugs Act and Congress embarked on a policy of continuous strengthening of public health protections and of their enforcement, first by the Bureau of Chemistry, and later by the FDA. Since then, Americans have benefited from increasingly comprehensive, science-based safeguards for a myriad products essential for health, survival and high quality of life.

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Did You Know?    
 
 
Many over the counter drugs were once prescription drugs
Americans buy about 5 billion over-the-counter drugs each year, according to government estimates, to treat their headaches, heartburn, coughs and colds, and other routine health problems. According to the Consumer Healthcare Products Association, a trade

 


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News about Drug Litigation cases in Indiana and nationwide:

Experts Fault New FDA Drug Label Changes
WEDNESDAY, June 7 (HealthDay News) -- Experts say the new labeling system for prescription drugs about to launch in the United States will not radi...
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Study Shows Lag Time
Study Shows Lag Time in Reporting Drug Withdrawal Decisions to Healthcare Professionals

Charlottesville, Va., May 23, 2006...

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Drugs Into The U.S. Marketplace
It will focus in particular on whether certain "later-listed" patents or inappropriate patent submissions by the sponsors of innovator drug product...
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Drug Litigation Terms

 


Today's Terms

Marketing Status

Definition:
Marketing status indicates how a drug product is sold in the United States.

Generic Drug

Definition:
A generic drug is the same as a brand name drug in dosage, safety, strength, how it is taken, quality, performance, and intended use.

Over-the-Counter Drugs (OTC)

Definition:
FDA defines OTC drugs as safe and effective for use by the general public without a doctor's prescription.

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Drug Litigation Resources

 


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Drug Litigation Hot Topics

 


Topics Related to Drug Litigation:

  • Adverse Effects
  • Prescription Drugs
  • Over the Counter Drugs
  • Drug Recalls
  • Dosage Errors
  • Drug Company Liability
  • Drug Company Negligence
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