Brinsupri follow-up
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.
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@blm1007blm1007 I'm curious about why are you considering antibiotics now, when it seems your self-care routine has you stable.
Do you have any worsening symptoms? Does your CT show increasing nodules or cavities? Is your bronchiectasis becoming more severe (based on images)? Is the MAI "load" increasing in your sputum cultures?
I'm thinking about what I would do in your place (at 74), and unless my answer was "Yes" to at least three of the questions above, I would not entertain antibiotic therapy again. I quit before I was negative, continued 7% saline & airway clearance. My last two sputum cultures (2 years apart) were negative. I am about to reach 6 years without antibiotics, and I can still recall how awful I felt.
Remember, even on antibiotic therapy, you have to keep up everything you are doing now, so it's not as though they would simplify your life. And the antibiotics are HARD on the body, especially causing fatigue in many people (I was one!), possible unpleasant side effects and weight loss. Therapy will up your self-care burden - scheduling when to take the meds, monitoring vision and hearing, probable need for probiotics...
So I'm really curious what has led you to this possible change.
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4 Reactions@sueinmn Sue, thanks for taking time to discuss all this with me again.
Yes, to only one of your questions regarding it all. Worsening mucus plugging in the lower left lobe. PFT was good. I was not doing my the postural drainage routine on the left and right side.....I am now putting that into my A.M. and P.M. BE postural drainage therapy routines. Hope that will get it up and out, those mucus plugs.
You are truly right about not simplifying one's life. I just came off of being on an antibiotic for an infection that developed on my leg after the dermatologist burnt one of those areas they call pre cancerous, That one antibiotic did change some of my timing and did make me think of what it would be like with doing the antibiotics for BE.
I am so disappointed with having the mucus clearing bouts after I eat that takes a bit of time before the feeling of the need to clear stops. That is what limits me socially. I know I need to find my way around that and I will with giving time and thought to it. Therefore the reason for my possible change of thought about the antibiotics.
Thanks for reminding me of your experience(s). You may not be a financial counselor (that I know of) but you sure are a great BE health counselor for me...THANKS so very much. I needed to hear all you said and asked.
Barbara
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1 Reaction@hopefuldan Welcome to the group, Dan. Thanks for sharing your experience. Many of us are hopeful about this drug and I hope you see improvement.
I second what Sue said!
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1 Reaction@blm1007blm1007 Here is what my pulmonologist said about looking for mucus plugs when I asked about the significance in my CT - she looks for them to see if I need to increase my airway clearance or other efforts.
The absence of plugs in my CT last winter led her to suggest I didn't need as much mucus-thinning medication (in my case, I use plain extended-release Mucinex) and we reduced it to once per day. Now we are in cold/flu season, and I seem to have a bit of mucus all day, so I am increasing it back to twice a day, and using my Aerobika once a day in addition to exercise to move the mucus. Fingers crossed, this will be enough because unless I get sick, my next CT isn't until a year from now (every 2 years to limit exposure.)
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3 Reactions@irenea8 Irene you may have seen it by now but there is a person on the thread Sue started "Overwhelmed by Bronchiectasis "Must Do's". Watch this Video." They asked about others with Pseudomonas and thought about you and your journey.
Hope things are going well for you with your BE routine today and decisions about the Plan D and Brinsupri.
Barbara
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2 ReactionsHello out there.
I do not cough. Had only one coughing bout in September in which I coughed up four small globs of gray mucus. Yeah! I had been on amoxicillin for four days for a lung infection diagnosed from a low grade fever, fatigue, oxy levels at 90 and breathing limits. I have been well now for a month while limiting exposure to crowds due to low immunity. My CT scan last month showed the nodules from a year ago were the same size. But much mucus plugging noted in lungs. I have gerd; sleep on my right side for that and have mucus in throat a lot. Spit up when I can. Why don't i cough. How do I clear my lungs?
I have been diagnosed with brochiectasis this last year. Last month my pulmonologist has given me the option of trying Brinsupri and I am waiting to have it all processed and sent as there are several steps for insurance approval, etc., etc. Meanwhile, as I am medicine adverse, I am questioning whether to take it or not even though I have said yes and the process has begun.
Rare risks are skin cancer, gingavitus, etc. I had a squamos cell carcinoma removed from my lip this last September.
It seems some of you who have started brinsupri are coughing and have more pronounced symptoms. Mine are just on the CT scan and shortness of breath.
Any opinions will be welcomed.
Thank you.
Mary
I'm about to start on this drug, and am very interested in the feedback.
@cool I can relate to you, when I was diagnosed with BE in 2021 , was never told about airway clearance, until I found out this group forum, which I learned a lot. I had mucus plugs in my CT , through this group I started nebulizing 7% saline ( my pulmonologist did believe in it initially) so I started it on my own, my last check up he said my lungs sounded better, less shortness of breath, doing airway clearance, started the free app Autogenic draining, watching videos. Don’t know when my next CT hopefully those mucus plugs are gone my next appointment in December. Also he started me on
Mucinex 1200 mg. Some days I get a lot of mucus out, but not everyday. Just keep on trying and I thank everyone here for their input. May God bless us all.
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4 Reactions@nickraosr Welcome to the group. As you can see, there's a lot of interest in the medicine here and I hope you share your experience with it here, too. I hope it works great.
If you have other questions, tell us a little about your situation with bronchiectasis and we'll try to help.