Medicines for ra

Common Questions and Answers about Medicines for ra

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Avatar n tn Your 2 problems are very different in causes, but both result in erosion of the joints and pain. One difficulty is that many of the newer medications such as remicade and enbrel are most effective for patients who are younger and recently diagnosed. This is because it can only prevent further damage frmo happening and if it's already happened, it can't heal that.
Avatar f tn I had earlier also stressed that when methotrexate is stopped,other medicines are started.These medicines are chosen such that they have no adverse effects on the RA as well as on the fetus.Pregnancy in RA is a very high risk case and the gynecologist that she will be consulting and the treating hospital should have all knowledge and facilities for high risk preganancy respectively.
Avatar n tn Serious problems require serious medicines and ALL medicines have side effects. The optimal thing is for you to be under the care of an ophthalmologist and a rheumatolgist. There are no quick fixes for your problem and you are receiving what sounds like excellent care.
Avatar m tn While there is not a cure for RA, there are treatments that can inhibit the progression of the disease and improve your quality of life. Did the doctor prescribe medication for your friend? What medications were prescribed?
1580703 tn?1651904887 I was diagnosed with Rheumatoid Arthritis about 5 years ago, I'm 24 years old right now, RA engaged my left ankle and my doctor prescribed prednisolone for me (six 5mg pill per a day) during my hospitalization as well as chloroquine, Folic Acid and calcium D. The treatment went well and after a while she decided to lower the dosage step by step, it took 2 years for me to walk normally again (July-August 2009), during that time the dosage for prednisolone was 1 per a week.
Avatar f tn You need to visit a good rheumatologist, who can start you on some good medications for RA. Along with the medicines, you need to be on physiotherapy so as to prevent joint stiffness as well as muscle atrophy. Regards. Please discuss, if you have any doubts.
Avatar m tn I am facing burning feet and shin while sitting since last 5 years. My NCS, RA Factor, ANA, ESR are normal. I have taken variety of medicines including Dulan, ronirol, tegral, prothyadine, cipralex, epival cr 500, sensival 25 etc. but my problem is still not resolved. During this problem i started walk which increased the problem. However, during walk i feel very normal i.e. no painful burning sensation, i feel. This is important that when i lay down i donot feel pain.
Avatar m tn I have one more question to you, well,as I saw in your profile you are mother, how old are your children and do they have some diagnose connected with RA, because we have one child he is very young only one year, for now everything is ok with him, but I am scared because this is inherited disease. I haven given birth to him before my husband got sick. Can you tell me also, do the medicines that patient take like corticosteroids, sulfasalasine , affect the fetus?
Avatar f tn Hello, I am a 45 yr old female 2007 I have recurring symptoms swollen with burning at times in knees,fingers, toes, elbows sometimes neck and shoulders I have been taking Prednisone off and on since 2007. Now I take it consistently. My primary has ordered blood test for RA, lupus, ms,gout and other things. All the test came back several times negative for these things.
494623 tn?1278279352 I have a Friend in Canada who has been on Minocycline for her RA for years and says she could not function without it,I asked my Doctor to prescribe this for me but he says it's not proven to be effective so wouldn't give me it !!! I have read that it IS effective not as a cure but by killing the bacteria that may be causing the RA symptoms. I am totally convinced it was the MRSA infection that caused my RA in the first place as I was absolutely fine before that happened ....
Avatar m tn i am bone TB patient docotr adviced me use medicines for 6 months .since last 5 months i am taking anti TB medicines ,in early days of using medicines i fells pains at nee joints & foot joints wirst joints.
Avatar f tn I started taking it against what my family dr said, but my RA specialist said you have nothing to loose, I took it for approximately 3 years and all my liver enzyme readings have gone to normal. I have been off of milk thistle for at least one and half years and my readings are all normal.. It may have been all my strong meds that affected the liver, but milk thistle repaired it.....read for yourself on the net about it and give it a try.
Avatar m tn Based on my own personal experience I would avoid the Tikosyn and the Flecainide based on experiences that I have had, however everyone responds differently and its important that you and your doctor maintain dialog about what works and what does not work for you. I have been in Afib for 3 years straight now and I have also been on Warfarin for that same period of time.
747443 tn?1233024111 I went back to the Rhemy last week and he put me on Sulfasalazine for the RA. My hands are beginning to twist and knot up. my elbows are knotted up also. You'll find the right combo of meds, just call your doc.
Avatar m tn I have had RA for 15 years, started after Golden Staph and heaps of antibiotics.'Have used all the usual drugs all of which caused all sorts of health problems without helping the RA. Have recently started to us Low Dose Naltrexone, 4.5mg each night. Pain has increased, fuzzy head, need to sleep more. Can anyoine tell me how long LDN takes tro kick in and are these symptoms normal. LND is OFF LABEL aqnd prepared for me by a compouding chemist.
Avatar n tn change of Angilock 50mg to Angilock 50 Plus Pladex 75mg - 0+1+0 Nitrin SR 2.6 mg - 1+0+1 Gerdo 2mg/Paricel 20mg - 1+0+1 Lexotanel 3mg - 0+0+1 (Sleeping pill) Frulac 20mg/50mg - 1+0+0 At first we thought it might be gastric problem, but after taking gastric medicines and food in control still the problem didn't gone.We are very worried about the block as the doctor said, and later he said we need to go for angiography to be sure about the blocks.
434698 tn?1207281597 I have been given the dx of RA, 5 years ago and have just recently been told that even though i have extreamly high levels of the ra factor in my blood i do not have RA it self, so for five years i have been giving myslef Methatrexate shots, which have landed me in the hospital with low white count levels on numourious occasions, ( sorry, about the spelling, i seem to be having a brain stall on how to spell at the moment, it has taking me at least 20 minutes to compose this darn post.
3486886 tn?1350410131 Is there anyone in the east coast(Pennsylvania) that knows how many people affected by mitochrondrial disease/disorders which is maternal. Is there any literature out there. My younger son was affected at about 14 and has the mt (DNA), possible MELAS, only thing is that doesn't fit is that he is about 6'5" not short staute, but doctors had no idea. He was taking a lot high powered medicines for his severe pain in thighs and back, trouble walking.
Avatar f tn Medications like Duloxetione, pregabalin and Milnacipram have been approved for treating fibromyalgia. See a psychologist for conselling. It will be best to discuss it with your doctor about which medication will be most suitable for you. Do keep us posted. Best luck and regards!