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  Vol. 295 No. 4, January 25, 2006 TABLE OF CONTENTS
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Black Box Warnings

Tracy Hampton, PhD

JAMA. 2006;295:377.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

An analysis by the Agency for Healthcare Research and Quality of automated claims data from nearly 930 000 enrollees in 10 geographically diverse health plans over a 30-month period reveals that more than 40% of patients received at least one medication that carried a black box warning that could potentially apply to them.

Physicians were less likely to comply with the warning recommendations when patients did not receive necessary laboratory tests before beginning new prescriptions. However, high levels of physician compliance were found when drugs were prescribed for pregnant women, and there was almost no coprescribing of contraindicated drugs with QT-interval-prolonging drugs that regulate heart rhythm.

The report, FDA Drug Prescribing Warnings: Is the Black Box Half Empty or Half Full, was published on November 18 in an online edition of Pharmacoepidemiology and Drug Safety (Wagner AK et al. Pharmacoepidemiol Drug Saf [online publication ahead of print]).



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