Mac question: Arikayce Inhaler Antibiotic
hi all I have a question does anyone know if the medication from arikayce made them sort of feeling little bit more congested and do you think in a few months from being on this inhaler antibiotic pain in the lung will get better in time. i'm only on it for about 9 days now. getting frustrated already I feel like crying I have no voice and not sure if it will come back. I feel like I'm holding back from going to see family sometimes because I can't even speak with hardly no voice. I'm going to call the pharmacist today about those lozenges called strepfen to see if its safe to try them. has anyone found there voice was much better from trying them? I definitely need my voice I'm getting so frustrated thanks to anyone who can help thank you so much.
Interested in more discussions like this? Go to the MAC & Bronchiectasis Support Group.
Did you have Pseudomonas? Anyway I can get info is welcome.
Thanks,
Ellen
Hi Ellen - here is one discussion about pseudomonas that has been active recently: https://connect.mayoclinic.org/discussion/should-my-pseudomonas-be-treated/
Also, if you want to see more past conversations use the Search box and type pseudomonas, bronchiectasis - you will see a list of prior referenfcs, and can click on any that might interest you.
Sue
hi. I've been taking Arikayce since Oct 2020, with the predicted hoarse or absent voice and worsening tinnitus. It's the only thing that helps me cough out the tiny bit of sputum that I do. I'm used to it now, but the Arikayce rep said it just took a little time to get the voice back ... well, the voice is still not back and I'm just presuming that it won't come back until I stop taking the Arikayce. btw, I tried all sorts of lozenges, drinking hot water after, gargling with hot water or salt water ... nothing worked so I just deal with it. .... However, I'm very curious about the clofazimine -- my ID doc wants to start that and, from what I've read about it, I really am wary of it ... especially its 70-day half life! Please tell me how it is affecting you - like, did your skin turn orange-pink-brown??
I have been on Clofazamine for 2 1/2 months and have had minimal side effects. I have not turned orange, but my face does look a little tan. My skin is quite white and I expected the orange from what I had read. The most significant side effect has been weight loss and digestive issues. I have lost another 5 lbs on Clofazamine, and I am working hard to gain some back. My digestion was not good anyway because of the big 3, so it is hard to discern how much is due to Clofazamine, Like you, I cough up minimal sputum. I lost my voice with amikaycin, and it returned when I stopped taking it, I did not lose it with Arikayce but I only took 4 doses. Overall, I am ok with the Clofazamine, and am just hoping it will get rid of the resistant strain of MAC that I have.
@bnthorson My voice did not come back completely until I stopped the Arikayce but it wasn't bad like when I started and had no voice. I only ever had small sputum also but a tiny bit was enough to test for MAC which was great, take care Heather
It's good to hear that the voice will come back. Not being able to communicate verbally is isolating and discouraging, but we have to look for the greater good that will come out of this - like getting rid of as much of this horrible bacteria as possible. (My ID doc says we'll likely not get rid of it completely which makes me very sad, to put it mildly.) Thank you!
Thanks for your comments about the Clofazamine - I really am nervous about taking it. I previously had some serious adverse side effects from the main antibiotics (Rif and Eth) and had to stop taking them. I am currently taking the second-string of antibiotics which I understand are not as effective. 🙁 I've had digestive issues and diarrhea since Oct (when I started with Meropenem IV) since I've been on this alternate 4-atb regimen. (btw ... a little puzzled since amakacin and Arikayce are the same, aren't they?) *** anyone else taking clofazamine?? ***
@janeta I could not communicate for a few weeks but for the rest of the time on Arikayce I could communicate verbally, just a little but raspy. Yes a lot of us will not be able to get rid of this completely, I go to dr next week because my 3 antibiotics do not seem to be doing a lot, so I may be on the same regime as you, will be interesting. What 4 are you on ,Meropenem IV, arikayce, clofazimine and 1 other. yes amikacin is the IV version and arikayce the inhaled. So sorry you have had awful side effects, not nice. Take care Heather
I took amikaycin first because of insurance. I did take it inhaled. The difference between the two is how it is delivered. Arikayce is enclosed in a fat globule. My side effects were a little different but with both I developed a lump in my throat.
Thank you for the information on the other drugs. I had not heard of them. I have never completely been free of the bacteria since I was dx in 2002. This is my 3rd time on meds. Wishing you complete recovery!!!
I think I understand, then, that Arikayce is a brand name of the drug Amikacin. Amakacin is given IV or injected. The inhaled Arikayce I take now is liposomal - yes, encased in a fat globule. Subjectively, I feel that the Arikayce is the most effective in bringing up - or at least just clearing - the teeny-tiny bit of sputum that I have. SO many drugs and I'm trying to learn! I think I've finally understood that there are multiple ways to treat MAC/MAI, it affects everyone differently, and that just because the Mycobacterium isn't completely gone, I can still have a somewhat fair quality of life ... that it's not a death sentence as I initially thought. THANK YOU for your comments.