Fluid retention is found among people with Rheumatoid arthritis, especially for people who are female, 60+ old, take medication Enbrel and have Pain. We study 645 people who have Fluid retention and Rheumatoid arthritis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
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Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) can be treated by Methotrexate, Methotrexate sodium, Enbrel, Prednisone, Humira (latest reports from 447,233 Rheumatoid arthritis patients)
Fluid retention (an abnormal accumulation of fluid in the blood) has been reported by people with primary pulmonary hypertension, pulmonary hypertension, high blood pressure, diabetes, multiple sclerosis (latest reports from 35,387 Fluid retention patients).
On Oct, 23, 2016
645 people who have Rheumatoid Arthritis and Fluid Retention are studied.
* Approximation only. Some reports may have incomplete information.
How to use the study: print a copy of the study and bring it to your health teams to ensure drug risks and benefits are fully discussed and understood.
I am away from home right now and don't have access to a scale. I feel definitely that I am retaining water. When I am home, I will be able to use a scale which gives an indication of the percentage of water one has in one's body. It's not terribly accurate but at least I will have ball park figures from (essentially) week to week. What do others who may be retaining water do to combat this problem?
Hi everyone. I am new to this support group. I am 48 years old and have RA. I am currently struggling with fluid retention. My weight is up 10-12lbs and I am feeling miserable. Does anyone have any suggestions? I am taking Lasix 20 mg a day and have been receiving Vodders massage but still the fluid remains. Thanks everyone. Cindi
About two weeks after beginning Zetia, I started to have severe itching after a shower. It also happened when I washed my hands or face. The itching was in the areas that touched water, except for my torso area. It is unrelenting for about 45 minutes. It is like being tortured for 45 minutes. I tried hydrocortizone, moisturizer, took oral benedryl. Nothing worked except for time. I discontinued Zetia today and hope to be itch-free soon!
Have been on Cimzia 3 months and 2 weeks ago started with leg, butt and upper arm Muscle Pain. Has anyone else had this happen? If so did the pain go away when you stopped Cimzia and how long did it take to subside? Did you try to go back on Cimzia again or move on to another Biologic? I can't ...
Not sure what details they want here? erm still alive and so far no more new diagnoses as each year seem to get diagnosed with something else. The main thing that is really annoying is that apart from the above illnesses is the various other things such as six car accidents, (I wouldn't mind but ...
Helping a friend who can not ask this herself. My friend has ongoing finger joint pain, and when it flares one finger joint in particular pains like an SOB. She tells me she's tried many things to no avail. I wonder if someone can direct me to a good resource, or your own good ideas, to deal ...
About two weeks after beginning Zetia, I started to have severe itching after a shower. It also happened when I washed my hands or face. The itching was in the areas that touched water, except for my torso area. It is unrelenting for about 45 minutes. It is like being tortured for 45 minutes. I ...
I am away from home right now and don't have access to a scale. I feel definitely that I am retaining water. When I am home, I will be able to use a scale which gives an indication of the percentage of water one has in one's body. It's not terribly accurate but at least I will have ball park ...
I was recently diagnosed with rheumatoid arthritis. I was first prescribed sulfasalazine but didn't improve on it after 7 weeks. My doc recently switched me to methotrexate and folic acid. She also gave me meloxicam and predisone to take as needed. I have not taken these last two. I've ...
Hi, I was on embrel until the insurance stopped paying for it. After two does of Humira I started seeing psoriasis spots. My RA doctor is trying to get Simponi approved. If anyone has very mild to moderate psoriasis, did you have a problem with Simoni making it worse?
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