Would you have Night sweats when you have Rheumatoid arthritis?
Summary: Night sweats is found among people with Rheumatoid arthritis, especially people who are female, 40-49 old, also have Osteoporosis, and take medication Humira.
We study 567 people who have Night sweats 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 Night sweats >>>
Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) can be treated by Methotrexate, Enbrel, Methotrexate Sodium, Humira, Prednisone, Plaquenil. (latest reports from 218,584 Rheumatoid Arthritis patients)
Night sweats (sweating in night) has been reported by people with depression, rheumatoid arthritis, pain, osteoporosis, high blood pressure. (latest reports from 10,632 Night sweats patients)
On Jan, 26, 2015: 567 people who have rheumatoid arthritis and Night Sweats are studied.
Gender of people who have rheumatoid arthritis and experienced Night sweats * :
|Night sweats||72.08%||27.92% |
Age of people who have rheumatoid arthritis and experienced Night sweats * :
|Night sweats||0.00%||0.00%||0.00%||2.35%||4.39%||13.01%||37.30%||42.95% |
Severity of the symptom * :
|least||moderate||severe||most severe |
|Night sweats||6.67%||20.00%||66.67%||6.67% |
Top co-existing conditions for these people * :
- Osteoporosis (70 people, 12.35%)
- Hypertension (59 people, 10.41%)
- Pain (52 people, 9.17%)
- Restless legs syndrome (45 people, 7.94%)
- Vitamin supplementation (35 people, 6.17%)
- Prophylaxis (33 people, 5.82%)
- Hypothyroidism (23 people, 4.06%)
- Arthritis (21 people, 3.70%)
- Gastrooesophageal reflux disease (18 people, 3.17%)
- Nausea (15 people, 2.65%)
Most common drugs used by these people * :
- Humira (365 people, 64.37%)
- Methotrexate (324 people, 57.14%)
- Prednisone (203 people, 35.80%)
- Enbrel (194 people, 34.22%)
- Folic acid (165 people, 29.10%)
- Remicade (106 people, 18.69%)
- Celebrex (101 people, 17.81%)
- Arava (80 people, 14.11%)
- Fosamax (61 people, 10.76%)
- Diovan (57 people, 10.05%)
* 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 Night Sweats?
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- support group for people who have Night Sweats
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More questions for: Rheumatoid arthritis, Night sweats
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
- 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.
- Severe night sweats and hot flashes with cymbalta?
I am 24 years old and I have been having severe night sweats for about the last 2 and a half years. I have been on Cymbalta for about 4 and a half years. These night sweats are so severe that I typically wake up 2-4 times a night drenched in sweat where I have to change the sheets, get a new blanket, and change my clothes. This is usually happening to me about 4-6 times a week. I am not sure if this is related to Cymbalta or not. I have gone to my doctor and had all of the tests done, everything is normal. All of the doctors that I have gone to have been clueless as to what could be causing my night sweats. I am thinking of trying to change my Cymbalta to a different medication, however as I am sure most know, it is a pain in the butt to try and find a good antidepressant that works with your body and any other medications you may be taking. The only thing I am going to try before this is using Menopause medications vitamins. I have found a vitamin/supplement that is supposed to help with night sweats and hot flashes and does not have any hormones in it. I have only been taking it for 2 nights, so no results yet. I hope this works so I dont have to change off of Cymbalta.
- 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.
- 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!
More reviews for: Rheumatoid arthritis, Night sweats
Comments from related studies:
From this study (10 months ago):
I just begsn tx for rs using safest meds possible but did not yolerste pills so we are doing injections once a week but since we started I developed abdom ook nal edema plus whole body especially feet which subsided ptior to msjor orgsn testing hestt kidney bloodwotk a nd liver ultra sound. Results were normsl all in but kidney workup. We are trying to get to third week of methotrexate tx becausr the last uri which my ra dr treated immediately with snyibiotics my ra pain seemed much better I just had abdominal swelling and pressure on lungs thrn and yhis time entire body swelled dr rulled out ra it was edrma order err d tests with bed rest feet up over weekend causing edema to go away prior to echo and ultra sound. Tests were normal so went to pulmonologist to get help breathing and they were sfraid to use antibiotics just like my primary dr brgore they know nothing about my ra drugs so how am I supposed to stop this from going inyo pneumonia?
From this study (11 months ago):
Wake up after about 4 hours sleeps, bathed in sweat and can 'to go back to sleep for a couple of hours.
From this study (1 year ago):
Healed joint and soft tissue injuries (PID) return with increased pain and swelling. Pressure changes with position. Frequency and intensity of migraines increased with pressure symptoms. Genetic connective tissue disorder - Ehler Danlos Syndrome. Cardiac arrhythmia. History of rheumatic fever, pneumothorax, whooping cough, and severe allergic reactions.
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