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Following the listing of the combination on the Pharmaceutical Benefits Scheme in 2022, the cost for people aged twelve years of age or older with cystic fibrosis who have at least one F508del mutation in the cystic fibrosis transmembrane conductance regulator gene is $30.00 per month, or $7.30 for concession card holders. [48]
Elexacaftor is a medication that acts as cystic fibrosis ... is used to treat people with cystic fibrosis who are ... for the treatment of cystic fibrosis. ...
Ivacaftor is a medication used to treat cystic fibrosis in people with certain mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene (primarily the G551D mutation), who account for 4–5% cases of cystic fibrosis. [ 5 ][ 6 ] It is also included in combination medications, lumacaftor/ivacaftor, tezacaftor/ivacaftor ...
Cystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
Lumacaftor/ivacaftor. Lumacaftor/ivacaftor, sold under the brand name Orkambi among others, is a combination of lumacaftor and ivacaftor used to treat people with cystic fibrosis who have two copies of the F508del mutation. [6] It is unclear if it is useful in cystic fibrosis due to other causes. [6] It is taken by mouth.
Sweat test. Sweat test. Purpose. measures concentration of chloride. The sweat test measures the concentration of chloride that is excreted in sweat. It is used to screen for cystic fibrosis (CF). [1] Due to defective chloride channels (CFTR), the concentration of chloride in sweat is elevated in individuals with CF.