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FDA advisory committees recommend removing Chantix boxed warning
SILVER SPRING, Md. — The Food and Drug Administration’s advisory committees on psychopharmacologic drugs and drug safety risk management held a recommended Wednesday that the boxed warning accompanying Pfizer’s smoking cessation drug Chantix be removed.FDA approves Shire’s Cuvitru
LEXINGTON, Mass. — The Food and Drug Administration has approved Shire’s latest treatment Cuvitru (immune globulin subcutaneous (human) 20% solution). The drug is indicated to treat adults and pediatric patients ages two years and older with primary immunodeficiency, a group of more than 300 genetic disorders in which a part of the immune system functions improperly or is missing.