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Author Topic: fluid tablets  (Read 1995 times)
brenda seal
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« on: November 24, 2012, 07:09:37 AM »

Laurie was taking fruesimide - fluid tablets whilst on PD . when he became so sick and was dehydrated the doc stopped him taking them . Can you take fluid tablets when on haemo dialysis ? He cannot tolerate having more than 3 litres taken off at dialysis . He is trying extra hard to stick to fluid restriction - very hard to do in Australian summer conditions . He is still producing some urine .
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tiredandthirsty
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« Reply #1 on: November 24, 2012, 08:54:33 AM »

i have been doing in centre hemo since march.  take 2 furosemide in the morning and 2 in the evening.  helps me with my ascites.  with God's grace, haven't had a problem so far. don't know if this helps but just sharing my experience.

hope he feels better and keep feeling better forever.
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boswife
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us and fam easter 2013

« Reply #2 on: November 24, 2012, 09:20:55 AM »

once again,,, this is all up to the patient's tolleration (is that a word  ??? )  Bo takes 90 furosomide in the morn and eve,  and we take 1-2 Leaters off during D.  (we're on 3 off 1)  But!!  i *thought* that you need them even more for PD so it's going to be very individual im guessing...
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frankswife
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« Reply #3 on: November 24, 2012, 11:13:59 AM »

Frank takes 80 morning and nite, although it doesnt seem to be helping much anymore.
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amanda100wilson
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« Reply #4 on: November 24, 2012, 02:13:48 PM »

if you have any residual function,yes.  if not, furusemide tablets,will not do anything.  Managing fluid intake is how to limit too much fluid on-board.
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ESRD 22 years
  -PD for 18 months
  -Transplant 10 years
  -PD for 8 years
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Healthy people may look upon me as weak because of my illness, but my illness has given me strength that they can't begin to imagine.

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MightyMike
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« Reply #5 on: November 24, 2012, 04:22:49 PM »

I take 80mg on my off days because I still have residual function and I'm on hemo.  I take it mainly o remove excess potassium though.  But if you have no residual function they will not do a damn thing.  Best wishes.
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"The greatest pleasure in life is doing what people say you cannot do."
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December 2003 diagnosed with IgA Nephropathy 80% Function.
October 2004 started In-Center Hemo Dialysis Perma-Cath 5% Function.
September 2005 Living Related Donor (Mother) Transplant.
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August 2009 Upper Left Arm Fistula.
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« Reply #6 on: November 24, 2012, 09:30:41 PM »

if you're worried about the fluid pills, there are lots of little tricks... I use popsicles to keep my fluid intake down.. they feel like a lot more than they are.. one popsicle (both halves) are only 60mls... it's certainly NOT easy to watch the fluids in the heat, for sure..
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