Millions of them.
One of you.
Stand up to your symptoms and breathe better with CAYSTON.
Patients with cystic fibrosis and chronic Pseudomonas aeruginosa (Pa) can experience respiratory symptoms such as coughing, wheezing, and mucus production. CAYSTON is an inhaled antibiotic that helps suppress Pa bacteria and could reduce your symptoms. Ask your doctor how CAYSTON can help you breathe better.

CAYSTON is a prescription inhaled antibiotic used to improve breathing symptoms in people with cystic fibrosis (CF) who have a lung infection due to Pseudomonas aeruginosa (Pa). CAYSTON is not a treatment for infections caused by other bacteria or viruses, such as the common cold. CAYSTON is used only with the Altera® Nebulizer System. It is not known if CAYSTON is safe and effective in children under the age of 7 or in patients with FEV1 <25% or >75% predicted.

My Cayston Partner

My Cayston Partner is a free educational support program designed to help you stick to your CAYSTON treatment plan. It features a mobile-friendly personal page, helpful videos, personal stories from CF patients and caregivers, up-to-date refill and pharmacy information, and optional dosing and refill reminders.

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Learn more about the impact chronic Pseudomonas aeruginosa (Pa) can have on your lungs.

About half of all people with cystic fibrosis have a type of bacteria in their lungs called Pa.1 Over time, Pa can cause serious damage to the lungs and airways that may not go away.2

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Fast treatment time and flexible dosing

CAYSTON is an inhaled antibiotic that attacks Pa at the source. Nebulization time is typically 2-3 minutes, 3 times a day, at least 4 hours apart. To ensure that you get your complete dose of CAYSTON, make sure you are in an environment with a flat, stable surface and sitting in an upright position. Click below to see how CAYSTON can fit into your daily life.

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