Immunosuppressive Forums (Page 7)

what the cost of one injection ## Infliximab is most commonly used to treat auto-immune disorders. As to the price, I cannot give you a definitive answer, as it will vary depending on where you live. The price may vary some, from pharmacy to pharmacy. Have you tried calling a few to check? ## what is the role of fleximab on patients of rhemotied arthirits or ankylosing spondilits ## Hi I have severe systemic behcet, s VASCULITIS DO YOU RECOMEND FLIXAMAP For this disease and whaf Are the side effects and are they with the risks.....

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In the nearby future i can participate for a testcase in Belgium taking tofacitinib for CA. I only have to be stabil with 16mg medrol (corticoïds) to participate and that's just the problem. I hope I don't get a placebo wich is possible during the study. I hope I can help, not only myself but many others who has the same (agressive) desease. Is there nothing else wich can help my upcoming CA? I take colitofalk and cortisones, Imuran is not possible anymore after a high value of bloodinfection last year. Remikade has helped during a year but as shown in recent results a high amount of this medicinal product in my blood doesn't help me anymore.

In the nearby future i can participate for a testcase in Belgium taking tofacitinib for CA. I only have to be stabil with 16mg medrol (corticoïds) to participate and that's just the problem. I hope I don't get a placebo wich is possible during the study. I hope I can help, not only myself but many others who has the same (agressive) desease. Is there nothing else wich can help my upcoming CA? I take colitofalk and cortisones, Imuran is not possible anymore after a high value of bloodinfection last year. Remikade has helped during a year but as shown in recent results a high amount of this medicinal product in my blood doesn't help me anymore.

I have been taken off humira because I have to start treatment for latent tb. I have severe RA and am wondering when the severe pain is going to kick in. I have been off it a month and am feeling very little pain so far. I'm kind of nervous. Also, when I restart the humira, will I start feeling better right away? ## Based on my research, Humira (Adalimumab) is used in the treatment of rheumatoid arthritis. It works by blocking the action of TNF, a substance in the body that causes inflammation. Unfortunately, there's no way of knowing ahead of time how well a particular medication might end up working for you. Doctor's can only assume that it will be effective based on medical records, health, age, weight, whether or not you're taking other medications, body chemistry, e...

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I have been taking humara now for 7 months and at about month 5 my gums started to bleed with the lightest touch, I also started to look like a teenager again with acne. And in the last month my skin has exploded with pimple like sores that pop to look like ulcers. I was just wondering if anyone else has had this happen. My doc does not seemed to be to concerned with it but it sucks! ## Based on my research, there are some side effects of Humira (adalimumab) that could explain what you've been experiencing with the acne breakouts; but I have yet to find anything on the bleeding gums: nlm.nih.gov/medlineplus/druginfo/meds/a603010.html Have you asked your doctor about any other alternative medications to help treat your condition?

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I am travelling to Australia for one year in the next few weeks. I have 5 pens that will keep me going but was wondering if anyone knew the cost of the pens in Australia or if there was any scheme available over there which would cover costs for Humira patients?? Any information would be greatly appreciated. Thanks

I have Psoriatic arthritis and I have taken Enbrel and Humira and they gave me financial help with thier injections. I had to go to Remicade infusions, which are $3,600 per time & i had the 1st three close together. My insurance only pays 60% which leaves me with a huge bill.....all my take-home pay for one month. Johnson & Johnson says they reserve their help for people with No insurance. I'd like to see them get up stiff as a board every morning; hurting from head to toe; but dragging yourself to work anyway....then you have to give all your money to them! This country is not for the middle class people who want to work. Thanks for nothing Johnson & Johnson....I'm going back to Humira that care about their patients! ## I am sorry that you are having trouble getting...

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I have Psoriatic arthritis and I have taken Enbrel and Humira and they gave mefinancial help with thier injections. I had to go to Remicade infusions, which are $3,600 per time & i had the 1st three close together. My insurance only pays 60% which leaves me with a huge bill.....all my take-home pay for one month. Johnson & Johnson says they reserve their help for people with No insurance. I'd like to see them get up stiff as a board every morning; hurting from head to toe; but dragging yourself to work anyway....then you have to give all your money to them! This country is not for the middle class people who want to work. Thanks for nothing Johnson & Johnson....I'm going back to Humira that care about their patients! ## I'm very sorry that you were refused assist...

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I have been on neoral for almost one year it has helped my skin disease by 50 percent but I have suffered many consequences. I now have high blood pressure and I'm on another med. My gums are bad and I'm getting gum disease. I now am up 6 times a night going the bathroom I'm getting worried and wondering if I should just go off it or will my skin disease come back full force ## Hi tara, Depending on the type of skin disease you have, it seems as though you may be better off with a more natural alternative that gets the job done without these unwanted side effects. In my opinion, just the fact that you're questioning the efficacy of this medication is enough to tell me that you're not entirely satisfied with taking it. Personally, I think changing medications is worth...

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What are the most common side effects of Neoral? ## Hi tara, Side effects of Neoral (Cyclosporine) can include: headache diarrhea heartburn gas increased hair growth on the face, arms, or back growth of extra tissue on the gums acne flushing uncontrollable shaking of a part of your body burning or tingling in the hands, arms, feet, or legs muscle or joint pain cramps pain or pressure in the face ear problems breast enlargement in men depression difficulty falling asleep or staying asleep Some side effects can be serious. If you experience any of the following symptoms, or those listed in the IMPORTANT WARNING section, call your doctor immediately: unusual bleeding or bruising pale skin yellowing of the skin or eyes seizures loss of consciousness changes in behavior or mood difficulty co...

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IPlease help. In 5 weeks I'm taking an extended motoring holiday of Europe and will sometimes not have refrigeration available. I need a method which does not involve ice of keeping my humira syringes between 3-8degrees for up to 24hrs. I've spoken to Abbott Australasia reps twice and was extremely disappointed that they could not advise me on how to successfully travel with humira :) for this period of time. From other internet sites, I was recommended FRIO travel wallet/pack but it seems FRIO doesn't achieve 3-8degrees. I can't be the only one to have this problem. Any and all advice very welcome. Many thanks Annie ## I'm sorry about the problems you are having, but in reality planning such travel and trying to keep a medication at precise temperatures really isn&#...

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Developed a sinus infection and was prescribed Sulfameth/TMP antibiotics and was told not to take HUMIRA until finished. Not sure how long to wait.. thhank you ## Did you ask your doctor? There aren't any interactions listed that I can find, so I'm not sure of the specifics. I'd assume it should be at least 24 hours after you finish the antibiotic, but you should check with your doctor or pharmacist to be safe.

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My doctor has approved a drop from 2000/day to 1000/day and I am experiencing a fogginess and lack of pep. I use it with prednesone for myasthenia gravis. Has anyone had adverse issues when using a lower dose of cellcept? Bob ## It is completely normal to experience withdrawal type symptoms any time you lower the dosage of a medication, or stop taking it. It occurs because your body was used to the previous dosage you were taking. Have the symptoms tapered of by now? This should happen, once your body adjusts to the new lower dosage.

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Lately I've noticed swelling on the sides of both lower shins. I have numbness in the right foot (Big Toe.. the upper tip) only. I also noticed that there is indentations around the top of my (to the ankle)sport socks. I exercise daily but have never had this problem before. I am a 58 yr. old female. Wt. 96lbs. 5'1" with rheumatoid arthritis......Thanks for any info. P.S. I have taken Humira, Methotrexate,Armor Thyroid, Nasacort Nasal Spray for a few years without a problem. ## I am taking Oxycodone W/APAP 5/325 Tab I have experience swelling in my feet and ankles ## Have either one of you contacted your doctors, yet? The swelling could be a sign of edema, which can lead to serious health problems, such as congestive heart failure. It may be caused by the mentioned medicatio...

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Do you know when you body has had enough of this type of medication. ## I'm not quite sure what you're asking. Could you please clarify? CellCept contains a form of Mycophenolic Acid and it is used to as an immunosuppressant. It is very important to use it according to your doctor's instructions to get the best results for your health and well being.

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I have been on Myfortic for a year to treat auto-immune disorders. There have been days where I will be riddled with tremors and have had my potassium and sodium levels drop to dangerous levels. Has anyone else experienced the uncontrollable shaking? Is it related to the Myfortic? Is there anything I can do next time it happens so I don't have to go to the ER? ## Myfortic contains the active ingredient Mycophenolic Acid, it is used for immune suppression. Have you consulted your regular doctor about this? None of these are listed as common side effects of the medication, but there is really no way to say what long-term use may do to any particular person. Has the hospital been able to provide with information on what's causing the problems? You may need to supplement your levels...

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PILL that is yellow round A seperation line Z? ## This tablet contains 50mg of Azathioprine, which is used to prevent organ rejection following organ transplantation and to treat a vast array of autoimmune diseases, including rheumatoid arthritis, pemphigus, inflammatory bowel disease (such as Crohn's disease and ulcerative Colitis), multiple sclerosis, autoimmune hepatitis, atopic dermatitis, Myasthenia Gravis, Neuromyelitis Optica, restrictive lung disease, and others. For more information about this drug, please refer to the link below... If you have any more questions or concerns, please post back and I will be happy to help you.

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orange oblong ## The pill which you are describing is Mycophenolate mofetil (500 mg). Mycophenolate mofetil is indicated for the prevention of organ transplant rejection in adults and renal transplant rejection in children over 2 years More details about this medication are available at: Do you have any other questions or information to add? Please post back if you do...

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round peach or pink 477 at bottom ## I located a match to a purple oblong pill with 93 above 7477, this pill is Mycophenolate Mofetil 500 mg. Mycophenolate Mofetil is an immunosuppressant drug used to prevent rejection in organ transplantation. To learn more click on the link below... Do you have any more questions or information to add? Please post back if you do.

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i need suppllier in india with reasonable rate ## i am patent of 'AS' since last three year.doctor gave me injection of ramicade . now i cant afford it because it so much costly to me.now my disease grow up once again.i want to take ramicade injection as soon as possible in india. please response me how can i get it. thank you

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