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Order warning labels.


Byline: The Register-Guard

Ever done this? You've got a nuclear headache, so you start with three extra-strength painkillers to guarantee quick relief. No good, so you take two or three more a couple of hours later.

You're taking unnecessary risks with your health when you exceed recommended dosages of nonprescription non·pre·scrip·tion
adj.
Sold legally without a physician's prescription; over-the-counter.
 painkillers. Don't assume dosage dosage /dos·age/ (do´saj) the determination and regulation of the size, frequency, and number of doses.

dos·age
n.
1. Administration of a therapeutic agent in prescribed amounts.
 instructions for popular medications such as Tylenol are just conservative guidelines that can be ignored.

In fact, acetaminophen acetaminophen (əsēt'əmĭn`əfĭn), an analgesic and fever-reducing medicine similar in effect to aspirin. It is an active ingredient in many over-the-counter medicines, including Tylenol and Midol. , the active ingredient An active ingredient, also active pharmaceutical ingredient (or API), is the substance in a drug that is pharmaceutically active. Some medications may contain more than one active ingredient.  in Tylenol and hundreds of other common cold and pain-relief products, is toxic at high doses and can cause acute liver failure Acute liver failure is the appearance of severe complications rapidly after the first signs of liver disease (such as jaundice), and indicates that the liver has sustained severe damage (loss of function of 80-90% of liver cells). . About 100 people a year die after unintentionally overdosing on acetaminophen, according to according to
prep.
1. As stated or indicated by; on the authority of: according to historians.

2. In keeping with: according to instructions.

3.
 the Food and Drug Administration, and such overdoses lead to more than 56,000 emergency room visits a year.

To raise public awareness of the dangers, the FDA FDA
abbr.
Food and Drug Administration


FDA,
n.pr See Food and Drug Administration.

FDA,
n.pr the abbreviation for the Food and Drug Administration.
 launched a campaign last Thursday urging consumers to carefully follow dosage instructions for products containing acetaminophen and other nonprescription pain relievers. Drug store brochures and magazine ads have been developed to carry the message.

But the current effort needs a much stronger dose of financing and aggressiveness from the FDA. With just $20,000 committed to the campaign, the FDA is depending on pharmacy chains to put the brochure in stores and wants magazines to run the ads for free.

The best potential tool - bolder, clearer warning labels on painkiller packaging - still languishes unused in some state of study at the FDA, though it's not a new idea. Government advisory panels first made recommendations for stronger label warnings on nonprescription painkillers in 1977. Those recommendations were renewed by FDA scientists in 2002.

If the FDA is serious about protecting the public from this risk, it needs to finally heed 25 years of scientific advice and order manufacturers to put new warning labels on these products.
COPYRIGHT 2004 The Register Guard
No portion of this article can be reproduced without the express written permission from the copyright holder.
Copyright 2004, Gale Group. All rights reserved. Gale Group is a Thomson Corporation Company.

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Title Annotation:Editorials; FDA can do more to address overdose risk
Publication:The Register-Guard (Eugene, OR)
Article Type:Editorial
Date:Jan 26, 2004
Words:303
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