Chiropractic Research, Principles and Human Interest articles and handouts to provide material for your patient education program.
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Welcome to the FDA Article Archive of In Touch Education Services' Health Care Research Center.

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Influenza Drug Tamiflu's Effectiveness Questioned
    A January 17, 2012 review of the influenza drug Tamiflu by the Cochrane Database of Systematic Reviews has raised questions about the effectiveness of the medication. Questions al . . . keep reading
FDA Renews Warning On Acetaminophen
    A December 22, 2011 warning from the U.S. Food and Drug Administration (FDA) says that 2009 guidelines for infant doses of acetaminophen may actually increase the possibilities of . . . keep reading
FDA Downplayed Stop-Smoking Drug Chantix Suicide Risk
    A November 3, 2011 report in the online edition of PLoS ONE, says that by focusing only on episodes of depression and suicidality that ended in hospitalization, a recent FDA revie . . . keep reading
FDA: Antipsychotic Drug Causes Severe Allergic Reactions
    On September 1, 2011, the U.S. Food and Drug Administration (FDA) published a warning that the antipsychotic drug Saphris can cause life-threatening allergic reactions, even at th . . . keep reading
FDA Warns Anti-Nausea Drug May Trigger Heart Arrhythmias
    A September 15, 2011 warning from the U.S. Food and Drug Administration (FDA) says a drug used to treat nausea and vomiting may trigger dangerous and possibly lethal changes in he . . . keep reading
FDA Issues Warning On Antipsychotic Drug Saphris
    On September 1, 2011, the U.S. Food and Drug Administration (FDA) issued a warning that the antipsychotic drug Saphris can cause life-threatening allergic reactions, sometimes as . . . keep reading
Drug Ads Ignore FDA Regulations
    The August 22, 2011 online edition of Public Library of Science One reports on a study that found most advertisements for drugs are not in compliance with FDA regulations. &n . . . keep reading
FDA Warns Of Bladder Cancer Risk With Diabetes Drug Actos
    On June 15, 2011, the U.S. Food and Drug Administration (FDA) issued a warning that patients taking the diabetes drug Actos for more than a year may run an increased risk of devel . . . keep reading
FDA Warns Of Myocardial Infarction and Circulatory Risk With Chantix
    On June 16, 2011, the U.S. Food and Drug Administration (FDA) announced label changes to the stop-smoking drug Chantix and issued a warning that smokers with a history of heart a . . . keep reading
FDA Recommends Limited Use Of Anesthesia In Kids
    On March 10, 2011, a U.S. Food and Drug Administration (FDA) advisory panel has recommended that the use of anesthesia in young children should be limited because children exposed . . . keep reading
FDA Orders New Danger Labels For Antipsychotic Drugs
    In a February 22, 2011 announcement, the U.S. Food and Drug Administration (FDA) has ordered that all antipsychotic drugs must contain new label information regarding the dangers . . . keep reading
FDA Limits Amount Of Acetaminophen In Combination Pain Medications
    On January 13, 2011, the US Food and Drug Administration (FDA) issued an order restricting the amount of acetaminophen that could be used in combination pain medications due to t . . . keep reading
FDA Issues Warning On Cough Drug After Child Deaths
    On December 14, 2010, the U.S. Food and Drug Administration (FDA) issued new label warnings for the prescription cough medication Tessalon (generic name benzonatate) after reviewi . . . keep reading
FDA Device Oversight Found Lacking
    The November 2, 2010 online edition of the British Medical Journal features an article by journalists Jeanne Lenzer and Shannon Brownlee charging the U.S. Food and Drug Administra . . . keep reading
Drug Maker Pulls Diet Drug Meridia From Market
    On October 8, 2010 the U.S. Food and Drug Administration (FDA) announced that drug maker Abbot has agreed to remove the diet drug Meridia (generic name sibutramine) from the U.S. . . . keep reading
FDA Sets New Rules For Reporting Adverse Trial Events
    On September 29, 2010 the U.S. Food and Drug Administration (FDA) announced they have finalized new procedures they claim will speed up reporting and analysis of potential safety . . . keep reading
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