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FDA MEDWATCH ALERTS

December 18, 2014

0.9 Percent Sodium Chloride Injection USP in 100 mL MINI-BAG PLUS Container by Baxter: Recall - Particulate Matter

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FDA MedWatch Recall - Particulate Matter

November 21, 2014

FDA MedWatch - Respironics California, Esprit V1000 and V200 Ventilators: Class I Recall - Power Failure May Occur

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FDA MedWatch Respironics California Esprit V1000 and V200 Ventilators Class I Recall

November 21, 2014

FDA MedWatch - Highly Concentrated Potassium Chloride Injection, 10 mEq per 100 mL by Baxter: Recall - Mislabeled

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Highly Concentrated Potassium Chloride Injection 10 mEq per 100 mL by Baxter Recall Mislabeled

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House Passes Final FDA Bill, Key ASA Advanced Drug Shortage Provisions Included

Friday, June 22, 2012

Earlier this week, the U.S. House of Representatives voted overwhelmingly to pass the final version of legislation that contains important provisions to address drug shortages.

The legislation, S.3187, the "Food and Drug Administration (FDA) Safety and Innovation Act," was written principally to reauthorize the operations of the FDA’s prescription drug user fee program – a program that allows the FDA to collect fees from drug manufacturers to support the agency’s operations.  However, at the urging of ASA and other drug shortage stakeholders, lawmakers used this bill as the vehicle to address the national drug shortage issue.  Specifically, the bill includes an entire title or section consisting of provisions intended to help prevent and mitigate drug shortages.

Title X of S.3187 contains a number of ASA-advanced provisions that will help address shortages of anesthesia drugs.  Of particular note, the legislation includes "notification" language that requires manufacturers to notify the FDA when the production of certain drugs would be halted or interrupted.  ASA worked to ensure that the definition of these drugs to be reported included drugs used in the "treatment of a debilitating disease or condition," a definition that includes pain drugs; and drugs used "during surgery," a definition that includes anesthesia drugs.  This notification requirement will allow FDA to use its existing authority and resources to work with manufacturers to reverse or mitigate any production changes.

The legislation also includes language to require the Drug Enforcement Administration (DEA) to provide timely updates on decisions regarding controlled substance quota increases to manufacturers when such an increase could help address a drug shortage. 

These two key provisions were among the consensus recommendations of the ASA co-convened "Drug Shortage Summit" work group, a group of stakeholders that first met on November 5, 2010. 

The Food and Drug Administration (FDA) Safety and Innovation Act also includes ASA-endorsed provisions that:

• Direct the Secretary of Health and Human Services to establish a task force to enhance the Department’s response to shortages, and create a strategic plan to address stated aspects of shortages.

• Require the FDA to maintain a drug shortage list and provide patients, providers and the public with such information in order to prevent, mitigate, and manage drug shortages on the ground. 

• Authorize the Government Accountability Office (GAO) to conduct a study to examine the causes of drug shortages and issue recommendations on how to prevent or alleviate a drug shortage.  This provision would provide needed data on how the regulatory framework, manufacturing challenges, or other factors contribute to drug shortages, as well as recommendations to address such issues. 

The Senate is expected to vote on S.3187, the Food and Drug Administration (FDA) Safety and Innovation Act, next week, and the President is expected to sign the bill into law soon afterwards.

Review the legislation as passed by the House of Representatives.
Review a summary of the legislation.
Review ASA’s letter to the Senate and House negotiators.
Learn more about ASA’s work to address drug shortages.

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