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Would you have Memory impairment (Memory loss) when you have Rheumatoid arthritis?

Summary: Memory impairment is found among people with Rheumatoid arthritis, especially people who are female, 30-39 old, also have High blood pressure, and take medication Methotrexate.

We study 1,180 people who have Memory impairment (Memory loss) 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 Memory impairment >>>

 

 

 

 

Rheumatoid arthritis

Rheumatoid arthritis (a chronic progressive disease causing inflammation in the joints) can be treated by Methotrexate, Prednisone, Enbrel, Methotrexate Sodium, Humira, Plaquenil. (latest reports from 218,584 Rheumatoid Arthritis patients)

Memory impairment

Memory Impairment has been reported by people with multiple sclerosis, depression, pain, high blood pressure, high blood cholesterol. (latest reports from 63,328 Memory Impairment patients)

On Jan, 28, 2015: 1,180 people who have rheumatoid arthritis and Memory Impairment are studied.

Trend of Memory impairment in rheumatoid arthritis reports

Gender of people who have rheumatoid arthritis and experienced Memory impairment * :

FemaleMale
Memory impairment85.43%14.57%

Age of people who have rheumatoid arthritis and experienced Memory impairment * :

0-12-910-1920-2930-3940-4950-5960+
Memory impairment0.00%0.16%0.00%0.64%4.94%19.46%27.51%47.29%

Severity of the symptom * :

leastmoderateseveremost severe
Memory impairment28.12%50.00%15.62%6.25%

Top co-existing conditions for these people * :

  1. Hypertension (230 people, 19.49%)
  2. Pain (177 people, 15.00%)
  3. Depression (94 people, 7.97%)
  4. Osteoporosis (74 people, 6.27%)
  5. Gastric disorder (65 people, 5.51%)
  6. Insomnia (62 people, 5.25%)
  7. Prophylaxis (57 people, 4.83%)
  8. Hypothyroidism (54 people, 4.58%)
  9. Osteopenia (46 people, 3.90%)
  10. Diabetes mellitus (44 people, 3.73%)

Most common drugs used by these people * :

  1. Methotrexate (644 people, 54.58%)
  2. Humira (567 people, 48.05%)
  3. Enbrel (497 people, 42.12%)
  4. Folic acid (330 people, 27.97%)
  5. Remicade (286 people, 24.24%)
  6. Prednisone (255 people, 21.61%)
  7. Omeprazole (164 people, 13.90%)
  8. Aspirin (115 people, 9.75%)
  9. Prednisolone (107 people, 9.07%)
  10. Leflunomide (90 people, 7.63%)

* 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 Memory Impairment?

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

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More questions for: Rheumatoid arthritis, Memory impairment

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

  • Methadone and forgetting basic things.
    I have been in MMT (Methadone Maintenance Treatment) for around 7 1/2 years for chronic pain. I have gotten to where I forget things that I never would or did before and the longer in time the worse it has gotten I am currently looking at some different meds for treatment. The loss of memory is everything from childhood memories to what I did yesterday I may pay something and if I dont write it diwn I will forget it things I have known all my life I have forgotten. I can't say 100% it is from the MMT or not however I will sag I had no such problems before and I am at age 38 so I believe I am much too young to have severe memory loss that I am currently experiencing and whats scary is what if it never comes back and continues to decline?
  • Percocet and memory loss
    A close friend of mine has been using prescription Percocet for 5 to 6 years. Her MD first prescribed the lowest dosage possible to be taken 3 to 4 times daily for pain. I am aware that this medication frequently needs to be increased because it will become less effective. I don't know how many times he has increased the dosage but it has been many times. I believe now she is taking the highest dosage of it up to four to six times daily and six tablets at a time. I have made several attempts to tell her the information I know about Percocet and to have her to ask her MD about her now short and long term memory problems. Her response is to shout at me, telling me she needs that much for pain and to mind my own business when I tell her about the negative side effects I see, especially her daily and hourly memory problems. She has also said she has no reason to speak to her doctor about memory problems. I think that is because she fears he might lower the dosage. My concern about her poor memory only causes her to tell me I am the one with a bad memory, even though the only pain meds I infrequently take are OTC ones. According to my MD, I have been told my memory for my age of 63 is perfectly fine and better than most for my age. Also I take no medications with the side effects that cause memory problems. In addition when my MD prescribes new medication I always read the info that accompanies them, do research online and pay attention to all warnings and side effect info. The few times I have had side effects they have only been GI problems and I have consulted my MD regarding those and work with my MD for an alternative medication. My friend NEVER EVER reads any of the accompanying material that comes with her prescriptions. Also she never looks up her medications online to get additional information, including possible side effects. I worry about her very much and fear she now has an addiction to Percocet. Several years ago she asked her MD for Chantix to stop smoking, never reading the info supplied with the prescription. I urged to read the info and side effects. She declined, telling me she knew what she was doing. After two weeks of using Chantix she had a mental break down and ended up on the psych ward of our local hospital for 3 weeks. That medication was the first that began to cause her to have memory problems. She accepted that fact for about a month then dismissed it claiming her memory problems were over. They weren't because she was still taking Percocet. I understand no one wants to be told by a friend they suspect that person has memory problems, but I haven't done so to be mean or cruel, but only out of great love and concern. At this point with all the Percocet she takes daily she really is at a level to be considered an addict and I fear soon she will convince her MD to increase the dosage because it no longer controls her pain. I've written this review as a cautionary tale to inform others to be vigilant with their family, friends and loved ones as Percocet can and does cause short and long term memory loss. Although all my efforts to assist and speak to my friend have failed, please don't give up on those in your life who you notice are experiencing memory loss signs that take Percocet. If possible speak to them or their MD. Oh, and be prepared to be yelled at that you are the one with memory problems or to be told to mind your own business. And please, please read the information that accompanies all of your medications.
  • 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.
  • Higher than a kite, and dumber than one of those saying i can no longer remember!
    I told my shrink I didn't want to try anymore antidepressants... that they make me crazy-stupid(pristiq), crazy-nympho(wellbutrin), or crazy-sloth(lexapro). I have complex ptsd, did, and gad. I really don't want to take anything... I just want to work out, eat right, and try to put myself back on track. It seems like every time I try these pills I get pushed off course. Anyways here's my experience with pristiq. Day1) dilation ofpupils was noticed with in a few hours, it started to feel like I was on sshrooms....I'd look in the mirror and feel so much love...just stand there staring. I slept better than I did in months. Day 2) Sadly though, when I woke up I couldn't climax, it was like I was numb. My pupils were still dilated and I still felt an out pouring of love and admiration while looking at myself. I tried hard not to fixate and get ready for work. I noticed that my tummy wasn't bloated anymore, I hadn't felt this much releaf in months. As I took my daily 50mg I reassured myself that it was ok not to climax in favor of all the good things I'm feeling now. Pristiq didn't interfere with my routine other than climaxing. Day 3) I awoke well rested with a happy tummy and it didn't bother me a bit not to climax, I jumped out of bed and started my day with vigor. The moment I took my dose and left the house is the last thing I remember! From what I wrote in my calendar, the notes I took, and my phone history I can piece together the things I did for 7 more days!!! I went to work, but my coworker was on holidays so it was just me alone in the office, I have no family or friends in this country (I moved to get away from a bad situation, hence cptsd) anyways I had no interaction. The only thing that brought me out was probably that I stopped taking the medication on day7 (According to the amount of medication left)....it's taken 14 more days to get out of the pristiq fog. During that time I've experienced nightly vivid dreams/ nightmares, extreme sweating and high body temperature, my stomach discomfort fluctuates but I can control it through diet, I'm able to climax again though it takes time, my pupils returned to normal a few days after I returned to myself...I seem to have memory impairment.

More reviews for: Rheumatoid arthritis, Memory impairment

Comments from related studies:

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