Abstract
In the absence of a rational therapeutic approach to the basic molecular defect in cystic fibrosis (CF), contemporary therapy remains an amalgam of variably effective empiric treatments aimed at various clinical manifestations and components of this complex and protean disease. The result is a remarkable polypharmaceutical regimen of antibiotics, pancreatic enzymes, nutritional supplements, bronchodilators, and assorted other medications. In this chapter, I will review the two components of this polypharmacy that have resulted in significant problems with allergic reactions, not only in CF patients, but also (in some cases) in their caretakers. These two components are antibiotic and pancreatic enzyme therapy. Among the antibiotics used to treat pulmonary infection in CF, antipseudomonal semisynthetic penicillin derivative and cephalosporin β-lactam drugs have caused most of the allergic problems found in patients; accordingly, the major focus of this review will be on these compounds.
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Moss, R.B. (1990). Drug Allergy in Cystic Fibrosis. In: Moss, R.B. (eds) Cystic Fibrosis. Allergy and Immunology, vol 1. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-4612-0475-6_12
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DOI: https://doi.org/10.1007/978-1-4612-0475-6_12
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