CLL + nephrotic syndrome: furosemide problem - CLL Support

CLL Support

23,140 members39,744 posts

CLL + nephrotic syndrome: furosemide problem

BMFCDRW profile image
5 Replies

Hello, I'm here to share something with the community that may be important for those who have had nephrotic syndrome related to an infiltration of CLL in the kidneys. Normally, when there is a lot of swelling, it's common to be prescribed furosemide. In my case, I'm being treated with obinutuzumab, which has improved a little, but then I was prescribed 60 mg/day of furosemide (Lasix) to help with swelling. The problem is that it's done exactly the opposite and has overloaded my kidneys. I was already retaining some albumin and I lost it again. After some research, I realised that in this specific case, furosemide can damage the glomeruli and have an adverse effect. I don't know if anyone else has had this experience but I wanted to share it with you in the hope that it might help someone.

Written by
BMFCDRW profile image
BMFCDRW
To view profiles and participate in discussions please or .
Read more about...
5 Replies
studebaker profile image
studebaker

sorry for your troubles. Why was the dose of Furosemide so high to begin with and I truly hope it is reversible situation. 🤞🏻

Good luck 😉

Dana

BMFCDRW profile image
BMFCDRW in reply to studebaker

Thank you! They are trying to see if it makes something with the Nephrotic syndrome but I think it’s the opposite.

Ptown profile image
Ptown

Hello and thank you for sharing this information with our community. Pooling our experiences only serves to strengthen our collective knowledge. Take good care and let us know how you are getting along, if you have time. Carolyn

Poodle2 profile image
Poodle2

Sorry to hear this. I hope things will start taking a turn to better. Keep us posted, you deserve some relief.

BMFCDRW profile image
BMFCDRW

Thank you so much! It really hasn't been easy! But I think at the moment most of the problems I have are more from the kidneys than the CLL. I've had my third treatment with obinituzumab and it's been a lot easier. Now I really just need to see what's going to happen with the kidneys. Especially the fact that my stomach and feet are very swollen. Thank you all

Not what you're looking for?

You may also like...

New to the CLL site

I am new to the site...have posted a couple of things this week but didn't introduce myself. I...

New To CLL and I had Covid in March 2020.

Hello, I'm 49 and I was diagnosed with CLL in November of this year. It's been quite a year. Both...

I'm trying to find out more about the connection of the Spleen and CLL.

I was diagnosed with CLL in 2015. After six months chemo treatments, I am now on a three month...

Liver damaged by CLL soon since beginning

Hi All, I'd like to share my concerns with you guys, as I am worried that my CLL which was...

Sepsis and CLL

I'd really like to ask anyone who has had experience of CLL if they have ever been admitted to...