What's your experience wtih Brinsupr (brensocatib)?
It seems a bunch of us have started Brinsupri. Let's use this thread for discussion. If you are taking Brinsupri have you noticed anything different, including changes to bronchiectasis or side effects? How long have you been on it?
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Connect

@whitemarsh
I have BE and MAC. I started the 3 antibiotic treatment in September '25 and Brinsupri in December '25. I'm tolerating the antibiotics well as long as I keep up the daily kefir and the only negative with the Brinsupri is mild headache on occasion.
I am starting my second month on Brinsupri. (I have Bronchiectasis and MAC. ) I am experiencing a reduction in sputum. I find it helpful to photograph with my iphone what I cough up periodically with a penny next to it to gauge size, to track what is happening, and document for my pulmonologist rather than rely on verbal descriptions.
@kristia Hello, I see you have been around Connect for a bit, I'm glad you have good news to share in your first post. We have moved it to a continuing discussion where those using Brinsupri share their experience with the rest of us.
How long have you been living with Bronchiectasis? What else do you do to stay healthy?
-
Like -
Helpful -
Hug
1 ReactionI was diagnosed with BE about 2years ago and MAC about a year ago. I have been on Brinsupri for 6 months. The only side effect I have had is some dry patches on my skin. My last scan showed no advancement so I consider that a win. Because of this, my pulmonologist and I have decided not to put me on antibiotics for the MAC. I nebulize and do a nasal rinse twice a day. I feel this plus the Brinsupri are keeping me stable.