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Last week the Food and Drug Administration (FDA) listened to presentations and comments from several members of an expert FDA advisory committee regarding the benefit-to-risk ratio of Long Acting Beta-agonist drugs (LABAs). The advisory panel consisted of 27 voting health care professionals representing subcommittees in pulmonary and allergy medicine, safety and risk, and pediatric advisory.
The medications of interest were LABAs prescribed for treatment... Read moreBlack box warnings are a type of labeling that the Federal Drug Administration (FDA, for short) requires pharmaceutical companies to use... Read more »
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There have been treatments for asthma for at least a thousand years. The ancients used jimson weed to relax the muscles surrounding the... Read more »
HealthCentral launched a new site this week on health care issues and how our political candidates stand on these issues:drug pricesthe... Read more »
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The U.S. Food and Drug Administration (FDA) has requested that asthma drugs in the leukotriene receptor agonists category be given a "precaution" on... Read more »
What is the concern about Singulair (montelukast)?Singulair is a major drug in asthma treatment – it is important to review recent developments and... Read more »
Doctors who participate in the clinical trial of an asthma medication are more likely to prescribe that medication, a new Danish study has found. The... Read more »
The U.S. Food and Drug Administration (FDA) has called for warnings to be added to four common asthma medications, including Advair, Foradil,... Read more »
The U.S. Food and Drug Administration is reviewing data that may link the asthma drug Xolair to heart problems such as heart attacks and strokes,... Read more »