References

  1. Pseudomonas. Cystic Fibrosis Foundation Website. https://www.cff.org/Living-with-CF/Germs-and-Staying-Healthy/What-Are-Germs/Pseudomonas. Accessed January 13, 2017.
  2. Cunningham JC, Taussig, LM. Respiratory System. In: An Introduction to Cystic Fibrosis: For Patients and Their Families. 6th ed. Cystic Fibrosis Foundation; 2013:43.
  3. Cystic Fibrosis. US National Library of Medicine Website. https://ghr.nlm.nih.gov/condition/cystic-fibrosis. Updated January 24, 2017. Accessed January 29, 2017.
  4. Data on file, Gilead Sciences, Inc.
  5. Mogayzel PJ Jr, Naureckas ET, Robinson KA, et al. Cystic fibrosis pulmonary guidelines. Chronic medications for maintenance of lung health. Am J Respir Crit Care Med. 2013;187:680-9.
  6. Cystic Fibrosis Foundation. 2015 CF Foundation Patient Registry Annual Data Report. https://www.cff.org/Our-Research/CF-Patient-Registry/2015-Patient-Registry-Annual-Data-Report.pdf. Published August 2016. Accessed January 13, 2017.
  7. Retsch-Bogart GZ, Quittner AL, Gibson RL, et al. Efficacy and safety of inhaled aztreonam lysine for airway Pseudomonas in cystic fibrosis. Chest. 2009;135:1223-1232.