Brinsupri experience after 3+ months

Posted by scoop @scoop, Jan 2 10:34am

Brinsupri may take 3–6 months to reach full effect.
Please use this thread to share first-hand experiences only if you have been on Brinsupri for 3 months or longer.

To keep this discussion useful and focused, let’s limit comments to actual outcomes, side effects, or changes you’ve observed after at least 3 months of use.

General questions, early impressions (< 3 months), speculation, or unrelated discussions please post in a separate thread.

Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.

Profile picture for sweethighland @sweethighland

@mimmzy Glad that it is working for you. When you said the new drug thinned your mucus, I'm wondering was your mucus sticky with balls? I'm asking because I produce yellow/tan/green mucus everyday which is also sticky/slimy with mucus plugs/balls. I have not started the new drug yet fearing it will dry up the mucus and causes more infection. Are you on 10mg or 25mg?

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@sweethighland I've been on 25mg for almost 4 months and it is helping (less coughing ), but I still have the same mucus you described - sticky with balls. I had to up my hydration and take electrolyte pills since I've had a few dehydration episodes. My progress seems to go up and down depending on environmental challenges like pollen, ozone and humidity variations.

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Profile picture for mimmzy @mimmzy

@blm1007blm1007 yes it was a respiratory infection. My non-stop infections were pseudomonas. Difficulty clearing up the infections.

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@mimmzy how long have you been inhaling collistomethate? . How long have you had psuedanoma? Any side effects. Have you tried tobi. I go on cefipime IV picc when my psuedanoma aerigenosa attacks me. I had one severe attack this past jan/ feb. Bilateral lobe pnuemonia. Had been on 4 different antibiotics starting with cipro. Cefdiner, doxycycline. The psuedanoma got so bad that I wasn't sure even if cefipime would pull me out of this. Not on any inhaled yet

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I have been on Colistimethate now for 6 months. Will see my Infectious Disease Dr next month to evaluate. I had been battling pseudomonas for about 3 years. Each flare up came back within 2-3 months.. Have not had any flare ups with it since starting Brinsupri in October.

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Profile picture for mimmzy @mimmzy

I have been on Colistimethate now for 6 months. Will see my Infectious Disease Dr next month to evaluate. I had been battling pseudomonas for about 3 years. Each flare up came back within 2-3 months.. Have not had any flare ups with it since starting Brinsupri in October.

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@mimmzy im glad to here you are not having any flare ups lately. How did your doctors push back the psuedanoma. ? Which antibiotic? I have side effects on so many medications. My doctors mentioned tobi. But im not sure id make it through the side effects. So far ive been off any antibiotic since the cefipime . Just doing neb of ipratropium bromide and 7% sodium chloride. 2x daily. I use the percussion vest daily . Try to exercise use the aeribeka and pickle to get up mucus.

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Before Brinsupri I was on daily Azithromycin. Usually Levofloxacin and Z pack for flare ups. The Brinsupri and Colistimethate seems to work well. I also nebulizer 2X a day and use a flutter valve. I also exercise twice a week at Pulmonary Rehab. Mucinex and NAC to thin out mucus. A netty bottle to help with nasal mucus.

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