Systemic lupus erythematosus is found among people who take Folic Acid, especially for people who are female, 40-49 old , have been taking the drug for < 1 month, also take medication Methotrexate, and have Rheumatoid arthritis . We study 83,102 people who have side effects while taking Folic acid from FDA and social media. Among them, 296 have Systemic lupus erythematosus. Find out below who they are, when they have Systemic lupus erythematosus and more.
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Folic acid has active ingredients of folic acid. It is often used in vitamin supplementation. (latest outcomes from Folic acid 83,433 users)
Systemic lupus erythematosus (an autoimmune disease, which means the body's immune system mistakenly, attacks healthy tissue) has been reported by people with breathing difficulty, fever, rashes, drug ineffective, diarrhea (latest reports from 12,649 Systemic lupus erythematosus patients).
On Jul, 25, 2016
83,102 people reported to have side effects when taking Folic Acid.
Among them, 296 people (0.36%) have Systemic Lupus Erythematosus
* 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.
Hi i am Maddy and i am currently having tests for lupus. I was an incredibly fit person up to around 18 months ago. I had slightly raised blood pressure and was out on ramipril. I also got the flu and after that i have had recurring pleurisy symptoms accompanied by the most incredible fatigue i cant eat properly and i have lost a lot of weight. I also get sweats and chills and i did fet a butterfly rash one day when i went out in the sun but i thought it was the antibiotics i was on at the time. I suffer breathlessness and my shoulder muscles seize up. I am off the ramipril as i ran out and my blood pressure was okay so with the doctors consent i chose to stay off it. i've been off it a few weeks now but i am just recovering from a really bad bout of symptoms. I have paid to see consultants three times to try to get a diagnosis hence the blood tests relating to lupus. Does this all sound familiar to other ramipril users? Will my symptons eventually go?
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 am in pain everyday! My life sucks! I just want to know how to get some relief! Most days I don't want to get out of bed! My feet and legs hurt the most on me but lately my hands are starting to hurt! On my right foot I have a lump on the bottom of my foot, I have bunions(big) on both feet, ...
I've had RA for 26 years. I was on Methotrexate for 24 of those years. I've tried Xeljanz for a month. Made me weak, nauseous, major headaches etc. Tried Enbrel, results not good. Humira, results were no effect or side effects, can't afford. However it seems Zyrtec seems to help my allergies and ...
Hi i am Maddy and i am currently having tests for lupus. I was an incredibly fit person up to around 18 months ago. I had slightly raised blood pressure and was out on ramipril. I also got the flu and after that i have had recurring pleurisy symptoms accompanied by the most incredible fatigue i ...
I was diagnosed with lupus in 2002. Around the same time my doctor put me on losartan potassium. Also around the same time I began having a skin rash. I recently came across research that losartan can cause subcutaneous lupus. I have suffered from this skin rash for all these years. I am ...
Hi there, Just joining the group. I've had SLE for 28 years. This is the first time I have experienced Cellulitis. It started in my knee when I was on vacation. The ER Dr. gave me a script for Bactrim & Prednisone. The knee is looking better but I feel terrible! I am itchy all over. Has anybody ...
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