CLINICAL NEWS
Dasatinib (Sprycel, Bristol-Myers Squibb) may increase the risk of PAH, according to an FDA Drug Safety Communication issued to healthcare professionals. » More
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Middle-aged women with RLS may be at higher risk of developing high blood pressure, according to a study published online October 10 in Hypertension: Journal of the American Heart Association. » More |
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Resource Center: Oral Anticoagulation in Atrial Fibrillation
Atrial fibrillation afflicts more than 2.3 million persons in the United States and is expected to increase 2.5-fold by 2050. To find risk stratifying tools and articles on emerging oral anticoagulant therapies,
click here. |
According to a recent study, $5.8 billion was spent in 1 year on the unnecessary prescription of brand-name statins. » More |
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a) We follow the CMS-approved compendia. If a medication is listed, it is approved. We do not follow any pathway.
b) We follow the CMS-approved compendia, but a medication is only approved when it follows a pathway.
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Editor's Pick
THERAPY UPDATE
Tracking and preparing for the approval of generic products is 1 of the key components of proactive formulary management. Unfortunately, forecasting FDA approval of the first generic inhaled corticosteroid products is difficult. » Click here. |
FDA Commissioner Margaret A. Hamburg, MD, recently released a blueprint containing immediate steps that can be taken to drive biomedical innovation, while improving the health of Americans. » More |
The recent approval by FDA of an adult cancer therapy is 1 example of how children’s cancer research benefits patients of all ages. » More |
FDA ACTIONS
FDA has approved deferiprone (Ferriprox, ApoPharma) to treat patients with iron overload resulting from blood transfusions in patients with thalassemia. » More |
Vivus has resubmitted its NDA for Qnexa (phentermine/topiramate) to FDA. » More |
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