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    Home » Newsletters » Drug Formulary Review Archives

    Drug Formulary Review Archives

    September 1, 2005

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    Drug Formulary Review 2005-09-01

    Joint Commission issues alert on vincristine administration

    Saying “tragic errors” related to vincristine administration continue to occur, the Joint Commission on Accreditation of Healthcare Organizations in Oakbrook Terrace, IL, issued a Sentinel Event Alert in July. Read More

    New law legally protects adverse event information

    Pharmacists should be encouraged to report medication adverse events (AEs) and their underlying causes under a new law signed by President Bush on July 29. Read More

    Study: Number of adverse events involves med errors

    A teaching hospital further improved its existing safety mechanisms after a study of critically ill patients found a significant number of adverse events involving medications. Read More

    Research News: Study: Customizing simple regimen raises adherence

    Hospital admissions related to poor medication adherence cost the United States billions of dollars a year. Two physicians recently reviewed the literature and discussed adherence to medication in the Aug. 5 issue of The New England Journal of Medicine. Read More

    News Briefs

    The FDA has asked Purdue Pharma LP to withdraw its pain management drug hydromorphone hydrochloride (Palladone) from the market. The agency made this request after acquiring new information about serious and potentially fatal adverse reactions that can occur when hydromorphone extended-release capsules are taken together with alcohol. Read More

    New FDA Approvals

    New indication for celecoxib (Celebrex) by Pfizer. The FDA has approved the selective COX-2 inhibitor celecoxib (Celebrex) for a new indication, the relief of the signs and symptoms associated with ankylosing spondylitis. Read More

    Drug Criteria & Outcomes: Drug evaluation: Dexmethylphenidate hydrochloride tablets (Focalin)

    Dexmethylphenidate, d-MPH (Focalin) is a new methylphenidate (d,l-MPH; MPH) formulation of the active enantiomer only. A variety of methylphenidate products are available but only dexmethylphenidate is the purified active enantiomer. Read More

    In The Pipeline

    Genelabs Technologies has received orphan drug designation for prasterone (Prestara), its investigational drug for lupus. Read More

    Drug Formulary Review Archives

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    Drug Formulary Review 2005-09-01
    September 1, 2005

    Table Of Contents

    Joint Commission issues alert on vincristine administration

    New law legally protects adverse event information

    Study: Number of adverse events involves med errors

    Research News: Study: Customizing simple regimen raises adherence

    News Briefs

    New FDA Approvals

    Drug Criteria & Outcomes: Drug evaluation: Dexmethylphenidate hydrochloride tablets (Focalin)

    In The Pipeline

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