How does Symdeko work?
Symdeko contains ivacaftor and tezacaftor. Ivacaftor allows the defective CFTR protein to work better, improving the exchange of chloride ions across cell membranes within the airways. Tezacaftor moves the defective CFTR protein to the cell membrane so that it can facilitate the transfer of chloride ions across the membrane. Ivacaftor boost the function of the defective CFTR protein and tezacaftor corrects its location. This combined approach helps maintain a good balance of salt and water within the lungs and provides superior treatment compared to either drug alone.
Symdeko consists of 2 different tablets. A yellow tablet that contains both ivacaftor and tezacaftor which is taken once daily in the morning, and a blue tablet containing only ivacaftor that is taken 12 hours later in the evening. Two different strengths of Symdeko are available.
Symdeko needs to be taken with food that contains fat, such as butter, cheese pizza, eggs, peanut butter, or whole-milk dairy products.
Symdeko was approved in February 2018, the third disease-modifying medicine to become available for the treatment of adults and adolescents with cystic fibrosis (CF) over the age of six. Symdeko is suitable for people with CF who have two copies of the F508del mutation, or with at least one mutation that responds to treatment with Symdeko.
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What is Fluimucil used for?
Fluimucil is a brand name for acetylcysteine sachets and tablets which may be used to clear phlegm and liquefy thick and viscous mucus secretions caused by respiratory conditions such as acute bronchitis, chronic bronchitis, cystic fibrosis, pneumonia, pulmonary emphysema, or bronchiectasis. It is a type of mucolytic. Fluimucil is available over the counter (without a prescription) in most countries that have it. Continue reading
What is Trikafta?
Trikafta is a triple combination therapy that contains elexacaftor, ivacaftor, and tezacaftor, which is approved for adults and children 2 years of age and older with at least one F508del mutation in the CFTR gene, or a mutation in the CFTR gene that is responsive to Trikafta based on in vitro data. Continue reading
How does Kalydeco work?
Kalydeco specifically targets the underlying cause of cystic fibrosis (CF) and is approved for adults, children, and infants aged 4 months and older with CF with one or more specific mutations in their CFTR gene that is responsive to Kalydeco. It allows the defective CFTR protein to work better and increases salt and water movement within the airways. This thins the mucus and makes it easier to cough out. Continue reading
Related medical questions
- What is the difference between Symdeko and Orkambi?
- What is the difference between Symdeko and Kalydeco?
- How do the warnings differ between Symdeko and Orkambi?
- Can you take Symdeko with birth control pills?
- How are Symdeko tablets taken?
- How do you take Orkambi?
Drug information
Related support groups
- Symdeko (6 questions, 3 members)
- Ivacaftor/tezacaftor (3 questions, 3 members)
- Cystic Fibrosis (10 questions, 29 members)