Would you have Constipation when you have Rheumatoid arthritis?
Summary: Constipation is found among people with Rheumatoid arthritis, especially people who are female, 50-59 old, also have Osteoporosis, and take medication Humira.
We study 781 people who have Constipation and Rheumatoid arthritis from FDA and social media. Find out below who they are, other conditions they have and drugs they take.
You are not alone: join a mobile support group for people who have Rheumatoid arthritis and Constipation >>>
Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) can be treated by Methotrexate, Enbrel, Prednisone, Methotrexate Sodium, Humira, Plaquenil. (latest reports from Rheumatoid Arthritis 218,505 patients)
Constipation has been reported by people with osteoporosis, pain, high blood pressure, depression, high blood cholesterol.(latest reports from Constipation 80,049 patients)
On Nov, 25, 2014: 782 people who have rheumatoid arthritis and Constipation are studied.
Gender of people who have rheumatoid arthritis and experienced Constipation * :
Age of people who have rheumatoid arthritis and experienced Constipation * :
Severity of the symptom * :
|least||moderate||severe||most severe |
Top co-existing conditions for these people * :
- Osteoporosis (220 people, 28.13%)
- Hypertension (125 people, 15.98%)
- Pain (121 people, 15.47%)
- Vitamin supplementation (86 people, 11.00%)
- Prophylaxis (86 people, 11.00%)
- Gastrooesophageal reflux disease (66 people, 8.44%)
- Hypothyroidism (53 people, 6.78%)
- Depression (46 people, 5.88%)
- Restless legs syndrome (45 people, 5.75%)
- Ulcer (38 people, 4.86%)
Most common drugs used by these people * :
- Humira (436 people, 55.75%)
- Methotrexate (419 people, 53.58%)
- Folic acid (282 people, 36.06%)
- Enbrel (223 people, 28.52%)
- Prednisone (197 people, 25.19%)
- Remicade (155 people, 19.82%)
- Fosamax (127 people, 16.24%)
- Prednisolone (117 people, 14.96%)
- Celebrex (109 people, 13.94%)
- Aspirin (102 people, 13.04%)
* 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.
Do you have Rheumatoid Arthritis and Constipation?
You are not alone! Join a mobile support group:
- support group for people who have Constipation and Rheumatoid arthritis
- support group for people who have Rheumatoid arthritis
- support group for people who have Constipation
Could your drug cause:
Other conditions that could cause:
Can you answer these questions (Ask a question):
- What side effects do you experience from sulpfasalazine? (3 answers)
I began taking sulfasalazine 5 days ago for Rheumatoid arthritis. Since then I've had stomach cramps and bloating. Has anyone else experienced these side effects? If so, did the symptoms go away after using taking the meds for a while? And did the meds help the RA symptoms?
- Cymbalta r/t autonomic neuropathy
losartan 20 mg
tired all the time, dizziness, chronic constipation, stomach pains, pins and needles, diabetic type 2 hx alcoholism resolved, gerd, early satiety
- Is there a support group in the us for people with insulinomas? (1 answer)
SUPPORT GROUP IN UNITED STATES!!!
Hi, the only support group that I've been able to find for people with insulinomas is located in the UK... just wondering if there is one in the US. I had pancreatic surgery to remove my first insulinoma in 2012, we're thinking there's another because I'm still having problems with hypoglycemia... if anyone know anything, PLEASE CONTACT ME!!! :)
I know there can't just be a support group here for FERRETS!!! people are kind of important... I hate this song, but "Don't worry, BE HAPPY" is okay, I guess... I'm trying to force it upon myself. Things will get BETTER!!!
- Gastro with constipation in a 4 year old only cause pain at night?
In childrens hospital now have given the tag virus for stomach pain at night that is relieved by morphine
- Can my symptoms actually pinpoint a cause/condition? (1 answer)
I would just like insight on this. I'm on pain management right now, but it's just to manage the pain. Every thing else has really been not taken serious by any physican it office I've been to. Is this normal stuff many woman go through? I'm just sick of feeling like this between the constant pain & the daily having to pluck hairs it's insane. I'm in fantastic shape(used to be double my weight & now I'm 100lbs), the best looking I've ever been with a incredibly good looking husband & a wonderful family. My issues seem to detour a lot of things & while I'm young I'd like to get this solved or some type of solution to even maintain myself, not looking for a miracle, but would really appreciate answers.
More questions for: Rheumatoid arthritis, Constipation
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- Had nms in 2005, will trileptal increase chance of recurrence?
In 2005 I had NMS, which was not detected by my drs for 4 months. I'd been on Lexapro & Seroquel for 2 yrs, but was weaned from Lexapro & placed on Lamictal 3/05. Began getting low-grade fevers, which I was told were not caused by the Lamictal. I quit taking it anyway, fevers (along with uncontrollable shivering) continued & got higher. By 5/05 my temps were reaching 105 deg F. Husband said I became combative, refused to go to hospital. Early June/05 he came home to find me wrapped in blankets, with a temp over 105 F. He tried to place me in a tub of cold water, said I was rigid & screamed when he tried to move me. I was in the tub, speaking "in tongues" (his description, I have no memory of this). He called 911, took me to hospital. I woke, no idea where I was or why. After a lumbar puncture & 2 days in ICU I went home. The fevers continued...2 weeks later he came home to find me wrapped in sheets, towels, blankets, with the heat on full (it was in the 90's outside) he called ambulance again. I awoke to find myself under an ice blanket with nurses pushing large vials of dantrolene into both arms, several liters. Another LP, a stint in ICU...this time they told me it was NMS. The dr who dxd me said he was surprised I was alive, & not a vegetable, as my temp had peaked at 109 deg F. I suffered brain damage; short-term memory loss, brain can't control my body temp, my blood pressure went up. An arteriogram showed completely healthy heart & arteries, no plaque at all. I lost all body fat as well as some muscle mass. The fevers continued even after stopping the Seroquel. I visited my PCP for a checkup in 9/05, temp was normal. I started shuddering, my temp went up a full degree every 5 minutes. PCP admitted me to ER, my heart rate was over 272 B/M; they stopped my heart 3 times to "reset" it, which didn't work. I spent 3 days in hospital. Several months later my P doc tried me on Lamictal alone; I got Stevens-Johnson syndrome. I stopped the drug as soon as the signs appeared. I've been untreated, except for Neurontin & Primidone, until my manic episodes became unlivable. 3 weeks ago I went 8 days with no sleep, became psychotic. My P doc gave me Trileptal, which has evened my moods, but I've been getting low-grade fevers (highest was 103.6). Would having had NMS in the past make me more prone to falling to it again with the Trileptal? It's the only new med I've taken in over a year.
- I need advise, badly ckd!! (1 response)
The orthostatic BP started in mid April, I was only dizzy upon wakening then it would subside. I have never been a big breakfast eater so I started doing that. We were in Disney later in April and I was extremely fatigued, to the point of not wanting to walk, Disney would be the first time I passed out when getting dizzy. I of course said I had gotten too warm and was exhausted from work the previous week. The dizziness continued in the mornings & I passed out several more times. On May 1st, I passed out while putting my make-up on and hit my eye on the faucet and head on the tile floor, despite that I went to work thinking it would subside, it didn't. I went to the ER directly after work. They ran a B-met on me and my GFR was 11 and creatinine 3.95. They admitted me to a larger hospital for evaluation. While in there, they pumped me with fluids continuously, saying I had severe dehydration. My kidney function improved, my creatinine levels went back down to 1.34. After 5 days I was discharged and told to see a cardiologist and endo. The endo doc cancelled my appointment on the basis it was not his area. I had had a cortisol and ACTH testing which I guess was normal. I saw the cardiologist, who said it wasn't cardio. I had had an echocardiogram in the hospital and EKG monitoring. Cardio sent me to neurology, the PNRN did a basic neurological exam and drew blood for disease markers such as Lupus, sjorgens, hepatitis, ect. All disease markers came back negative, but my GFR was at 11 again and creatinine was 4.25, BUN 50 along with an elevated ACE level. They called me and said I sarcoidosis. I really don't have any of the primary S/S of this autoimmune disease. I don't know where to go from here, they are referring me to another neurologist at a bigger hospital. I can't live my normal life, can't walk on my feet due extreme pain and I pass out at least 2x a week, which is not good for my old body. My BP upon laying and sitting runs like 117/72, upon standing it drops to like 70/50-50/30. I am on 0.1 mg of florinef, I tried increasing it but then my legs swelled up for a gain of 23#. I talked to Mayo Clinic today and all there specialists are booked out thru December. I have to be able to work, I can't stay home any longer than September 8th! Please advise me!
- Sulfasalazine and the never ending menstrual cycle
I started this drug and never had menstrual problems begore. Within 3 months, I started my period and it never stopped even with stopping the drug for 3 mon ths. I ended up going my gyne and he prescribed megace. I had been bleeding for a total of 6 months. Made an appt with my rhuemy and explained this situation. His words were "it hasn't been listed in the literature as a side effect". Keep taking it. I started it again. Same situation and same treatment. Never took it again and changed rheumy.
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