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RE: methotrexate side effects
AngylHeart
Wednesday, August 15, 2007 at 06:41 PMre: RE: methotrexate side effects
AngylHeart
Wednesday, August 15, 2007 at 06:59 PMSorry - accidentally hit the "post comment"!
Lyrica is a fairly new drug that is for neuropathy and was recently approved to treat fibromyalgia - the first RX to be approved to treat FMS (which I also have).
I am convinced that the nerve damage is from taking the methotrexate. The Lyrica is very helpful in controlling the night time pain in my feet. I don't know if your pain issues are similar to mine or not - but I think that it is important that you take quick acton.
I think it is important that you see your physician asap. If you are suffering so much, you need to see if you can resolve this problem before your pain becomes chronic.
Good luck!
AngylHeart
re: re: RE: methotrexate side effects
tiff
Sunday, December 30, 2007 at 01:47 AMre: re: re: RE: methotrexate side effects
AngylHeart
Tuesday, January 01, 2008 at 06:55 PMSorry for the delay - holidays and all.
I would not recommend surgery based on my personal experience with two surgeries on each foot from the methotrexate nerve damage - and I continue to have problems with swelling & pain, which Lyrica helps a bit. However, I am not a physician and would suggest that she see her dr.
When I have a lot problems with trigger finger in thumb, etc., I find injections of steroids to be very helpful.
re: re: re: re: RE: methotrexate side effects
tif
Wednesday, January 02, 2008 at 05:05 AMre: re: RE: methotrexate side effects
barbara
Sunday, March 02, 2008 at 12:26 AMre: RE: methotrexate side effects
barbara
Sunday, March 02, 2008 at 12:19 AMhi..............am on metho. for lupus and lots of nausea,feeling faint,leg cramping and am hoping it gets better and will help.on 10mg a week for about 6 weeks now.on it for inflammation and vasculitis and on a small dose of prednisone too.am pretty frustrated and sick but do trust my doctors.any advie or help?thanks............barbarare: RE: methotrexate side effects
pat
Sunday, May 10, 2009 at 10:36 PMI have only taken the first weeks dose for my auto immune disorder as they try to transition me from over a year at high doses of predisone and leg pains in my calves are growing daily. This concerns me. I'd like to know if others have this and it is managable or if it means this drug is not a good choice for me. pat
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methotrexate side effects
karin
Tuesday, September 18, 2007 at 08:50 PM -
Untitled Comment
tania
Wednesday, September 19, 2007 at 05:15 PM -
Methotrexate side effects.
Louise Richmond
Thursday, October 11, 2007 at 07:35 PMI was on Methotrexate a couple years ago andhad no problem, then my RA went into remission for 2 years. I am now back on the medication, and I have been having problems with leg and top of my feet cramping and very much pain. I have also being troubled with itching in my hair. I would like to know if you have had this problem. Louisere: re: Methotrexate side effects.
Louise Richmond
Tuesday, October 16, 2007 at 08:43 AMre: Methotrexate side effects.
barbara
Sunday, March 02, 2008 at 12:14 AM -
methotrexate side effects
Jaimie
Thursday, December 20, 2007 at 09:12 AMI was on methotrexate for 3 months and developed pneumonia. I stopped taking everything and went to an alternative doctor. She put me ona diet and supplements. I went from not being able to walk and being on 25 mlgs of prednisone to wearing high heels again and only 5 mlgs of prednisone. This diet does work along with the supplements. If you want more information you can email me at JaMac77@yahoo.com. I don't think anyone can completely understand what it is like to live with RA unless you have it.re: methotrexate side effects
Anonymous
Thursday, June 18, 2009 at 08:49 AMwhat type of diet. I have Ra and I was on mex a few years ago and it worked well for me but I had to go off due to breast cancer . It has been about 2 yr. now and I feel good but I can feel my Ra starting up again. I am on drugs for inflamation and 2 Plaquiniel a day so I would like to find about your diet
Sandy
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Mexotrexate and side effects
Randy S
Tuesday, January 01, 2008 at 12:42 PMBob,
My name is Randy and I have RA and Psoratic arthritis. I am 56 years old and my RA comes from many years of sports ranging from football to breaking horses in my 40's. I take an injection of Humira 40mg every 2 weeks and 8 Mexorexate once a week meaning all at one time per my doctors direction. The Humira has helped substantially but my kidney funtions are showing signs of perfomance which could lead to failure in the future. Have you had your blood tested for this side effect. My doctor checks my blood for inflamation (C-Reactive Protien), metabolics, CBC and Sedimentation rates every 3 months. Please let me know your knowledge on this.
re: Mexotrexate and side effects
robgsc@infonline.net
Wednesday, January 02, 2008 at 11:40 AMRandy,
Thanks for the information. I also am 56 years old and very active. Racquetball, long distant running, backpacking and cross country skiing. I have had to give up racquetball and running but I walk daily as well as backpack and I still cross country ski. My Dr. has me on 5 tablets of metotrexate once a week and 15 mg. of meloxicam daily. My amount of attacks have reduced dramatically but I still have have them on occasion. My Dr. does check my blood levels every two to three months and at one time I was taking 6 tablets of methotrexate and he reduced it after one of my blood tests and says now that my levels are back to normal. I do not drink alcohol and he has expressed to me that that is very important to completely abstain from drinking while taking methotrexate. How well do you feel that the Humira is working for you?
Thank you,
Rob
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Untitled Comment
robin
Monday, May 19, 2008 at 07:42 PMare you taking your folic acid/leucovorin calcium? I just admitted to a doctor at my college campus clinic that I forget all the time and he responded by begging me to take it because it negates the side effects of methotrexate. I've never had cramping, but severe nausea...so my doctor switched me to the methotrexate injections instead because it bypasses your digestive system that way. Also, if you get a cough or cold while you're on it, you need to halve your dose or just skip it all together that week b/c it will severely suppress your immune system (i know you know this, but not many people take the innitiative and reduce their dosage). Otherwise you risk not recovering, as I am dealing with this very moment.
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Untitled Comment
anne
Friday, June 20, 2008 at 05:47 PMHi Rob ... In 2006 I had treatment for breast cancer, I had a combi chemo treatment called epirubicen/ cmf .. The M stood for mehtotrextate and I have to say I don't can't say which chemo drug caused severe joint pain ...BUT I can say that it only began when the CMF started ...I felt crippled like an old old lady :-( After treatment ended the pain eased but did not leave completely so I got referred to the RA (rheumatoid arthtirits clinic.
I am now on several drugs to treat my RA but since I started methotrexate again I suffer joint pains especially leg cramps at night ...not mild cramps but really sore ones ...I wake up at night and get out of bed in an attempt to relieve them ...
I see you posted this a while ago so I hope you are ok and not suffering
Anne xXxx
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Leg cramps
Rob Burton
Monday, February 23, 2009 at 02:10 PMI am also on methotrexate for RA. Ever since I started taking the drug I have been experiencing severe nightly lower leg and feet cramps. Whether or not this medication is the exact culprit I don't know. I am waiting to here back from my doctor. I will add that I have suffered these types of cramps all of my adult life but not every night and not all year round.
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Methotraxare side effects
Anonymous
Sunday, May 17, 2009 at 04:16 PMAsk your doctor to check you vitamin D levels, Methotraxate eats the calcium in your body thus the ability to absord vitamin D. You could also try taking multivitamins with vitamin D, calcium and magnasium in it. Good luck!
re: Methotraxare side effects
practicemakespermanent
Tuesday, May 26, 2009 at 10:48 PMI was on Humira for 8 months for RA and 6 months into my treatment I was put on methotrexate. What started as moving numbness and tingling in my feet and hands turned into terrible cramping in my legs and feet at night. I was taken off of the Humira & methotrexate in late February and while the symptoms subsided, they didn't completely go away. I had a nerve velocity conduction study, and emg, and MRIs of my brain and spinal cord which all came back normal (thank God). I switched rheumatologists because my initial one really brushed off the numbness and tingling I felt for a whole month and still kept me on Humira (which can cause the onset of MS and MS-like symptoms). My new rheumatologist has changed my diet, has me taking fish oil, magnesium citrate, and Vitamin D. Overall my joints felt immensely better as did the rest of me. Due to my visible knuckle swelling and occassional joint pain he began me on methotrexate again. I took my first injection two days ago and am at this very moment experiencing pain and cramping in my legs and feet. While I am not glad that others are having these experiences as well, I am relieved to know that this may be directly associated with the use of methotrexate and knowing that others have felt this way, I feel better equipped to discuss my theories with my doctor.
re: re: Methotraxare side effects
Discouragedone
Thursday, August 27, 2009 at 06:01 AMDear Practicemakespermanent!
I am also an RA patient and be on the weekly intake of 25 mg Methotrexate [next to REMICADE transfusions]. As you, I am awakened at night with terrible cramps in my lower extremities; I am actually catapulted out of bed because they are so severe.
My Rheumatologist prescribed 2 capsules of 300mg Magnesium, in addition of the recommendation of eating bananas and apricots. Being on that regimen for the past three weeks, but still suffer of these horribly painful cramps. It worries me if this could finally lead to a more severe problem!?
It would be really helpful in hearing from someone who had a successful treatment to prevent or subdue these cramps.
Thanks, Discouragedone :-(
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Greetings.
I have RA and took methotrexate in 2004 for about only 3 months. While taking this RX, I developed nerve pain in both my feet. I also began having problems with extreme swelling of my feet, ankles & calfs. Even though I discontinued taking the methotrexate, the swelling and agonizing nerve pain in my feet persisted. I ended up having 4 surgeries on my feet (2 each) to have the troublesome nerve removed. The second set of surgeries helped slightly, but I still suffer tremendous pain, especially at night.
My Rheumatologist gave me some samples of "Lyrica" (originally for neuropathy