Brittle nails is found among people with Rheumatoid arthritis, especially for people who are female, 60+ old, take medication Humira and have Rheumatoid arthritis. We study 10 people who have Brittle nails 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 212,673 Rheumatoid arthritis patients)
Brittle nails has been reported by people with central obesity, abnormal faeces, limb asymmetry, orthostatic hypertension, lung cancer - non-small cell (latest reports from 610 Brittle nails patients).
On Jul, 22, 2016
10 people who have Rheumatoid Arthritis and Brittle Nails 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 was officially diagnosed July 2015. So now it is officially one year. I have had an incredibly difficult time finding meds that do not make me sick. I have been on Methotrexate, Lefludomide, Hydroxychloriquine, Pregabalin, Humira, Orencia....I also added several other conditions ie CAD and Non Hodgkin Lymphoma etc. How many are taken out by "co morbidity". For those of you that are new to the world of RD take heart. The one true thing is it is not the same for two people. The disease is so complex it does not affect people the same way. This makes it difficult to diagnose and treat. Find someone you trust and buckle up. It make take time but they will find a combination that works for you. Also, do ignore the socioeconomic implications of chronic disease. Particularly, one so poorly understood.
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 ...
This is for my father. Shortly after starting methotrexate injections and cortisone for Rheumatoid arthritis my father started having language difficulties and now has dementia. He was diagnosed with Pick's disease. Could it be caused by these drugs? He is still taking them.
I've lost 30 pounds since I started taking sulfasalazine 4 months ago. I stopped the med last week but I haven't gained any weight back yet. I actually lost a few more pounds since I stopped taking it. I am very underweight now. Has anyone had this happen to them, and how long did it take to ...
Methotrexate Sodium can cause Bone And Joint Pain, what should be done to correct this? My pain is worse than before taking Methotrexate, constant pain in all extremities , hands, wrists, fingers, elbows, shoulders, legs etc.
I was officially diagnosed July 2015. So now it is officially one year. I have had an incredibly difficult time finding meds that do not make me sick. I have been on Methotrexate, Lefludomide, Hydroxychloriquine, Pregabalin, Humira, Orencia....I also added several other conditions ie CAD and Non ...
Hi was diagnosed with ra in May of 2016. I am 50 and have urinary incontinence. I don't think it's from meds because I have had it before diagnosis. I also think I had ra for 5 years before being diagnosed.
I took cialis one 10mg tablet only once a week for the past 8 years. It has caused my RA factor elevation, small nodules in middle joints of fingers, pain & stiffness of all fingers while sleeping. I am really scared. I self diagnosed as I stopped taking cialis and after few weeks my joint pain ...
Several years ago in 2013 I was"diagnosed" with RA. I went through every medication including, humira, embral, to now IV fusions of remicade which has been almost a year. I am not feeling any better and body aches and joint pains getting worse. I started researching my symptoms and lyme kept ...
My body is covered in welts or blisters of sorts. It turns out it is a drug reaction and not psoriasis yahoo👍 There are no effective treatments, so I am thrilled to know this will go away in time. I also saw my Rheumy on Tuesday. I now have non Hodgkin's lymphoma...very very early..the good ...
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