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Articles tagged with "FDA"

FDA Requires Naloxone Discussion to Be Part of Opioid Labeling, Prescribing

August 13, 2020

Opioid use following otolaryngology surgical procedures has received increased interest, with many studies recommending shorter-term prescriptions for opioids to avoid dependence on the drugs. In response to a continuing opioid crisis in the United States, the FDA announced on July 23 that it will require that labeling for opioid pain medicine and medicine to treat […]

FDA Recalls Zantac

April 3, 2020

Updated April 10, 2020.  The U.S. Food and Drug Administration announced on April 1 that it is immediately pulling all prescription and over-the-counter ranitidine (brand name Zantac) drugs from the market because of an impurity issue. Although most recalls are the result of contamination that occurs at some point during the drug production cycle, this […]

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Off-Label Cochlear Implantation Common

March 1, 2018

A new study concludes that cochlear implantation is commonly performed for indications beyond those included in FDA-approved labeling

FDA Works to Increase Consumer Access to Hearing Aids

February 15, 2017

The FDA takes steps to better support consumer access to hearing aids.

Lecturer describes shift in healthcare from 1946 through the ACA

Reducing Costs in the Changing Fabric of Healthcare

July 10, 2016

Lecturer describes shift in healthcare from 1946 through the ACA

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How the U.S. FDA Approves Medical Devices

How the U.S. FDA Approves Medical Devices

May 6, 2015

Outline of steps in the federal approval route, from idea phase to implementation

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FDA’s Unique Identifier Program Has Benefits, Drawbacks

April 5, 2013

The proposed rule may assist with safety, but be costly.

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FDA Seeks to Prevent Surgical Fires

April 6, 2012

While surgical fires are exceedingly rare they can have devastating consequences. The FDA and a coalition of health care providers recently launched the Preventing Surgical Fires Initiative to help physicians manage the risk of surgical fire.

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