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We thank all the patients who took part in this trial; the members of the data and safety monitoring board, Andrea Apter, Serpil Erzurum, Barbara Layman, Yancy Phillips, Bruce Psaty, and James Sheller; and our study coordinators, Denise Beaver, Kelly Bixler, Jennifer Brandorff, Terry Britton, Peggy Cadbury, Alyson Clayborn, Vanessa Curtis, Mary Gill, Robert Hmieleski, Donna Jinwright, Christena Kolakowski, Jeffrey Krings, Lauren Leshak, Aimee Merchlinski, Barbara Miller, Surinder Narula, Brenda Patterson, Melanie Payton, Jean Schenkkan, Ann Sexton, Kerrie Sheaffer, Allen Stevens, Melissa Thrasher, Suzanne Vogt, Rhonda Webb, Lynda Weichel-Williams, Cheryl Wilmoth, Tiffany Wirth, Muhammad Zahid, Ronald Zimmerman, and Kathy Zheng.

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Tell your doctor if you have ever had any unusual or allergic reaction to this medicine or any other medicines.

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Patients should keep an ongoing record of their peak flow readings to help them detect worsening of their condition.

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Adverse event data taken from over 26 clinical trials demonstrated the safety profile consistent with original registration trials.

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There is positive evidence of human fetal risk based on adverse reaction data from investigational or marketing experience or studies in humans, but potential benefits may warrant use of the drug in pregnant women despite potential risks.

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