In early December 2008, the Food and Drug Administration (FDA)held an unusual joint meeting of the Pulmonary–AllergyDrugs Advisory Committee, the Drug Safety and Risk ManagementAdvisory Committee, and the Pediatric Advisory Committee toconsider the safety of long-acting beta-agonists (LABAs). Themeeting is described in detail in a Perspective in this issueof the Journal by Kramer,1 who points out that decision makingby the advisers and the FDA was hampered by the lack of dataabout the safety of LABAs.
LABAs, which are administered by inhalation, act by effectingprolonged stimulation of the β2-adrenergic receptor. They. . . [Full Text of this Article]
Source Information
From the Department of Medicine, McMaster University, and the Firestone Institute of Respiratory Health, St. Joseph's Hospital (P.M.O) — both in Hamilton, ON, Canada.
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Agarwal, A., Knobil, K., Kramer, J. M., O'Byrne, P. M., Drazen, J. M.
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Jaeschke, R., Angus, D. C.
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