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Would you have Overactive bladder (Urge incontinence) when you have Rheumatoid arthritis?





Summary: Overactive bladder is found among people with Rheumatoid arthritis, especially people who are female, 50-59 old, also have Osteopenia, and take medication Fosamax.

We study 19 people who have Overactive bladder (Urge incontinence) 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 Overactive bladder >>>

Rheumatoid arthritis

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)

Overactive bladder

Overactive bladder (a condition in which the bladder squeezes urine out at the wrong time) has been reported by people with osteoporosis, osteopenia, depression, high blood pressure, multiple myeloma.(latest reports from Overactive bladder 1,086 patients)

On Nov, 26, 2014: 19 people who have rheumatoid arthritis and Overactive Bladder are studied.

Trend of Overactive bladder in rheumatoid arthritis reports

Gender of people who have rheumatoid arthritis and experienced Overactive bladder * :

FemaleMale
Overactive bladder96.55%3.45%

Age of people who have rheumatoid arthritis and experienced Overactive bladder * :

0-12-910-1920-2930-3940-4950-5960+
Overactive bladder0.00%0.00%0.00%0.00%0.00%0.00%18.18%81.82%

Severity of the symptom * :

leastmoderateseveremost severe
Overactive bladder0.00%0.00%100.00%0.00%

Top co-existing conditions for these people * :

  1. Osteopenia (19 people, 100.00%)
  2. Osteoporosis (17 people, 89.47%)
  3. Hypertension (10 people, 52.63%)
  4. Arthralgia (6 people, 31.58%)
  5. Prophylaxis (6 people, 31.58%)
  6. Breast cancer (6 people, 31.58%)
  7. Anxiety (1 people, 5.26%)
  8. Bipolar (1 people, 5.26%)
  9. Add (1 people, 5.26%)
  10. Urge incontinence (1 people, 5.26%)

Most common drugs used by these people * :

  1. Fosamax (19 people, 100.00%)
  2. Leflunomide (17 people, 89.47%)
  3. Alendronate sodium (15 people, 78.95%)
  4. Methotrexate (12 people, 63.16%)
  5. Raloxifene hydrochloride (9 people, 47.37%)
  6. Norvasc (9 people, 47.37%)
  7. Medrol (9 people, 47.37%)
  8. Arava (9 people, 47.37%)
  9. Prednisolone (9 people, 47.37%)
  10. Humira (9 people, 47.37%)

* 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 Overactive Bladder?

You are not alone! Join a mobile support group:
- support group for people who have Overactive Bladder and Rheumatoid arthritis
- support group for people who have Rheumatoid arthritis
- support group for people who have Overactive Bladder

Could your drug cause:

Other conditions that could cause:

Can you answer these questions (Ask a question):

  • Is it safe to use oxytrol and vagifem on the day ?
    I have just been given Oxytrol and Vagifem to take and was wondering does anyone know if it is okay for me to use them both on the same day as the instructions on the packets are both the same to be used twice per week ?
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  • 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?
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  • 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!!!
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  • I am a 56 year old female with rheumatoid arthritis. i also have found out i have osteoporosis. i keep getting right breast sensitivity also tingling and tenderness in right scapula area... (2 answers)
    I am a 56 year old female with tingling in my right shoulder blade and some tenderness. I have occasional breast discomfort in the same side and sometimes my rt. nipple feels sensitive. If I touch the area, the symptom on the nipple vanishes. at times the tingling travels into my neck and symptoms seem more noticeable in the evening. If I shower in a warm shower the symptoms will vanish for a time.. All my mammograms have been normal and never miss any but it has me very worried. I check my breasts often for lumps. From time to time it also seems like I have tenderness along the sternum on that side. I have rhematoid arthritis as well as was recently told I have osteoporosis. I had a thoracic x-ray and they can see loss of bone density and some vertebrae degeneration. Take methotrexate each week and folic acid every day....Any ideas out there???? Thanks
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  • Does enablex delay menstruation?
    I started taking enablex 7.5mg a month ago and my period is late this month. I've always been getting my period every 21 days, I'm always spot on. I'm just wondering if starting this medication will throw my cycle off? Thanks.
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More questions for: Rheumatoid arthritis, Overactive bladder

You may be interested at these reviews (Write a review):

  • Why has my bloodpresher now shot up
    My blood pressure was always low 120/68 now since being treated for rheumatoid arthritis it has shot up to 175/92
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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.
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  • 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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  • Vasculitis from enbrel
    I have deep scars on my legs from vasculitis. This was caused by Enbrel. Initially no one would connect the two: per my rheumatologist 'no one has ever reported vasculitis as a side effect of enbrel.' (2003)

    I had to suspend the enbrel for 8 weeks in preparation for complex abdominal surgery. The vasculitis started to heal. Several weeks after the surgery I resumed enbrel and the vasculitis returned by the second or third enbrel shot. The Dr was reluctantly willing to concede that 'it may have been the enbrel.'

    The vasculitis was horrific. I've never felt so much pain, pain that wasn't abated in the least by pain medicine. My dermatologist describe it as being equivalent to a third degree burn: the skin dies, nerves start to regenerate but aren't protected by the dermis.

    The scars look like I had flesh torn from my legs that didn't quite 'fill in.'

    Rheumatologists are too pushy about these biological medicines. They brush past even the most serious side effects. Anything for mobility... I'd prefer not to skip to dialysis sessions or treatment for other organ failure!
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  • Spiriva caused me to swell up like a hippo.
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More reviews for: Rheumatoid arthritis, Overactive bladder

Comments from related drug studies (Check your drugs):

  • I have had overactive bladder for over eight years, but it is getting worse. I go to the bathroom at least 9-10 times a night. I usually go at least once every hour. Now I am having some resistance when I try to urinate. I have to bend over and push hard to get all the urine out of my bladder. T ...
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  • upset stomach. extreme weight loss, 50 pounds in 4 months. muscle weakness, confusion, unsteady gait. stomach pain, anemic, need of blood transfusion, dry mouth, extreme tiredness, unable to eat or drink.
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  • I have been taking Humira for 6-1/2 months. All of a sudden about a month ago I developed a new Type 2 Allergic reaction to Bananas. I always ate bananas. It is a latex like reaction after ingesting from what I read on the internet. I have not been feeling well and do not eat often because I don ...
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  • I find I can read something but have a difficult time relating what I have just read to another person. Although I understand what I have read, I just seem to have great difficulty putting it into words to relate
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  • The resulting cause of the ulcerations is a large amount of fluid under the skin. This fluid creates enough pressure that it has to be expressed whenever you can't stand the pain anymore. The fluid is clear and dries yellow. It appears that it also has crystals when dried. The reaction of thes ...
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More related studies for: Rheumatoid arthritis, Overactive bladder

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