Elexacaftor 50 mg / ivacaftor 37.5 mg / tezacaftor 25 mg Oral Tablet
RxNorm 2557214
Concept Hierarchy & Relationship Mapping
RxNorm Concept Unique Identifier (RxCUI) 2557214 represents a standardized clinical drug concept used for cross-system interoperability. This concept aggregates multiple Atom IDs (AUIs), which are specific naming variations and synonyms used across pharmaceutical databases to ensure accurate medication mapping for: elexacaftor 50 mg / ivacaftor 37.5 mg / tezacaftor 25 mg Oral Tablet.
The following semantic concepts and normalized strings are associated with this clinical entity:
This clinical crossover tool is designed for healthcare professionals, pharmacists, and data analysts to safely compare substitute products and manage medication interoperability.
SCDPrescribable
Semantic Clinical Drug (SCD):
Elexacaftor 50 mg / ivacaftor 37.5 mg / tezacaftor 25 mg Oral Tablet
(Atom ID: 12646237)
PSNPrescribable
Prescribable Name (PSN):
Elexacaftor 50 mg / ivacaftor 37.5 mg / tezacaftor 25 mg Oral Tablet
(Atom ID: 12646251)
PTPrescribable
Designated preferred name (PT):
Elexacaftor 50 mg and ivacaftor 37.5 mg and tezacaftor 25 mg oral tablet
(Atom ID: 12902469)
FNPrescribable
Full form of descriptor (FN):
Product containing precisely elexacaftor 50 mg and ivacaftor 37.5 mg and tezacaftor 25 mg/1 each conventional release oral tablet (clinical drug)
(Atom ID: 12903752)
Patient Education
Elexacaftor, Tezacaftor, and Ivacaftor
The combination of elexacaftor, tezacaftor, and ivacaftor is used to treat certain types of cystic fibrosis (an inborn disease that causes problems with breathing, digestion, and reproduction) in adults and children 12 years of age and older. It should be used only in people with a certain genetic make-up. Your doctor may order a blood test to help decide if this medication is right for you. Elexacaftor and tezacaftor are in a class of medications called cystic fibrosis transmembrane conductance regulator (CFTR) correctors. Ivacaftor is in a class of medications called cystic fibrosis transmembrane conductance regulator (CFTR) potentiators. These medications work by improving the function of a protein in the body to decrease the build-up of thick mucus in the lungs and improve other cystic fibrosis symptoms.
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