Chronic fatigue syndrome is found among people who take Remicade, especially for people who are female, 20-29 old , have been taking the drug for 6 - 12 months, also take medication Accutane, and have Folliculitis . We study 83,100 people who have side effects while taking Remicade from FDA and social media. Among them, 20 have Chronic fatigue syndrome. Find out below who they are, when they have Chronic fatigue syndrome and more.
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Remicade has active ingredients of infliximab. It is often used in rheumatoid arthritis. (latest outcomes from Remicade 83,346 users)
Chronic fatigue syndrome (disorder that causes extreme fatigue) has been reported by people with pain, drug ineffective, insomnia, memory loss, fatigue (latest reports from 2,451 Chronic fatigue syndrome patients).
On Jul, 27, 2016
83,100 people reported to have side effects when taking Remicade.
Among them, 20 people (0.02%) have Chronic Fatigue Syndrome
* Approximation only. Some reports may have incomplete information.
** Reports from social media are used.
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.
Long term Depression and anxiety CFS, Low testosterone and thyroid Stated 2 years ago Have had some improvement but still not living independent Gave home health aid 7 days a week As I write this my son is driving my Dr Poddel in Summit NJ for consultation Anyone use Dr Podell and if so what was your experience Paul
I am 71 years old. I have a meninginoma brain tumor & RA. I had brain surgery May 5, 2010. About 2/3 of the meninginoma was removed. The 1/3 that was left shrank to about 3%. In 2013 it started growing back. It had grown back to about original size in 3/2015. Annual check up July 2016 MRI showed that the tumor has doubled in the last 1.5 years. I started remicade infusion at about the same time. COINCIDENCE????
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 ...
I have been dx with fms/cfs since 1999. Recently received my MJ card & tried a few items from the weed store. I have not been able to find a product that gives me the feeling of a clear head & energy. Is it out there? I've tried vap, the orange one, edibles, strawberry cough joint which did ...
I am 71 years old. I have a meninginoma brain tumor & RA. I had brain surgery May 5, 2010. About 2/3 of the meninginoma was removed. The 1/3 that was left shrank to about 3%. In 2013 it started growing back. It had grown back to about original size in 3/2015. Annual check up July ...
I have just learned I have developed food allergies due to remicade. Unfortunately I have not been seen by allergist yet to determine which allergies. How to deal and cope with unknowingly eating foods I am allergic to?
Hi, My son has Crohns and after his recent flare and non response to intravenous steroids Remicade was offered (he is responding well and is also taking pure gum based turpentine (1 drop on a white sugar cube initially) which produced a white slimy mucous covered stool which we thought might ...
Long term Depression and anxiety CFS, Low testosterone and thyroid Stated 2 years ago Have had some improvement but still not living independent Gave home health aid 7 days a week As I write this my son is driving my Dr Poddel in Summit NJ for consultation Anyone use Dr Podell and if so ...
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